NZ795268A - Systems and methods for one-shot guide RNA (ogRNA) targeting of endogenous and source DNA - Google Patents

Abstract

Engineered nucleic acids encoding genome editing system components are provided, as are engineered RNA-guided nucleases that include inserts encoded in part by cellular genomic or other sequences recognized by guide RNAs.

Description

Engineered nucleic acids encoding genome editing system components are provided, as are engineered RNA-guided ses that include inserts encoded in part by cellular genomic or other sequences recognized by guide RNAs.

NZ 795268 S AND METHODS FOR OT GUIDE RNA (ogRNA) TARGETING OF ENDOGENOUS AND SOURCE DNA CROSS-REFERENCE TO RELATED APPLICATION This application is a divisional application of New Zealand ation No. 754072, a National Phase application submitted on 30 May 2019, and is related to International Patent Application No. , filed on 5 December 2017, and claims priority to U.S. Provisional Application No.: 62/430,154 filed on 5 December 2016, and to U.S. Provisional ation No.: 62/503,640 filed on 9 May 2017, the content of which is incorporated by reference in its entirety, and to which priority is claimed.

SEQUENCE LISTING This application contains a Sequence g, which was submitted in ASCII format via EFS-Web, and is hereby incorporated by nce in its entirety. The ASCII copy, created on December 4, 2017, is named 0841770163SEQLISTING.TXT and is 92,969bytes in size.

FIELD This disclosure relates to genome editing systems and related methods and itions for editing a target nucleic acid sequence, or modulating sion of a target c acid sequence, and applications thereof. More particularly, the disclosure relates to engineered self-regulating genome editing systems.

CRISPRs (Clustered Regularly Interspaced Short Palindromic s) d in bacteria and archaea as an adaptive immune system to defend against viral attack.

Upon exposure to a virus, short segments of viral DNA are integrated into the CRISPR locus. RNA is transcribed from a portion of the CRISPR locus that includes the viral sequence. That RNA, which contains sequence complementary to the viral genome, mediates targeting of a Cas9 protein to a target sequence in the viral genome. The Cas9 protein, in turn, cleaves and thereby silences the viral target.

Recently, the CRISPR/Cas system has been adapted for genome editing in eukaryotic cells. The introduction of site-specific double strand breaks (DSBs) allows for target sequence alteration through endogenous DNA repair mechanisms, for example non-homologous end-joining (NHEJ) or homology-directed repair (HDR).

The use of CRISPR/Cas-based genome editing systems as a tool for the treatment of inherited diseases is widely recognized. The US. Food and Drug Administration (FDA), for example, held a Science Board Meeting on er 15, 2016, addressing the use of such systems and ial regulatory issues they may pose. In that meeting, the FDA noted that while Cas9/guide RNA (gRNA) ribonucleoprotein (RNP) complexes may be customized to generate precise edits at a locus of interest, the complexes may also interact with, and cut at, other “off-target” loci. The potential for off-target cuts (“off-targets”), in turn, raises at least a regulatory risk with t to approval of CRISPR/Cas therapeutics.

One strategy for reducing rget risk is to include, in a vector encoding a Cas9, a “governing guide RNA,” (ggRNA) which is a guide RNA targeted to the Cas9 coding ce. When this vector is delivered to a subject, Cas9, which might ise be constitutively and/or stably expressed by y transduced cells, is expressed only transiently. Over time, the Cas9 coding domain in the vector is disrupted by cutting mediated by the governing guide RNA.

SUMMARY The instant disclosure provides genome editing systems and related methods which adapt gRNAs targeted to specific loci to ally limit the genome editing activity of these systems in a manner distinct from conventional ggRNAs. These adapted gRNAs are referred to as “one-shot guide RNAs” or “ogRNAs”. For clarity, ogRNAs described herein can be ecular or modular, as discussed in greater detail below. tion of gRNAs into ogRNAs is achieved by engineering cellular DNA sequences recognized by such gRNAs into nucleic acid sequences encoding an RNA- guided nuclease, e. g., a Cas9 nuclease or a Cpfl nuclease or a vector backbone. In certain embodiments, the RNA-guided nuclease is Cas9. In certain embodiments, the RNA-guided nuclease is Cpfl.

In one aspect, this disclosure relates to an ed c acid encoding an RNA-guided se, which isolated nucleic acid includes an, exogenous, substituted, inserted or engineered nucleic acid sequence, such as a eukaryotic nucleic acid sequence.

The eukaryotic or otherwise ous sequence is generally 17 nucleotides or greater in length, and either comprises or is adjacent to a protospacer adjacent motif (PAM) that is recognized by the RNA-guided nuclease. Certain embodiments of the isolated nucleic acid also encode a gRNA (for instance, an ogRNA) having a targeting domain that is complementary to a portion of the exogenous or eukaryotic nucleic acid sequence that is adjacent to the PAM, which targeting domain is optionally greater than 16 nucleotides or 16—24 nucleotides in length. In certain ments, the complementarity of the targeting domain to a portion of the exogenous or eukaryotic nucleic acid sequence is sufficient to allow for modification of the nucleic acid sequence encoding the RNA- guided nuclease. In certain embodiments, the targeting domain is complementary to at least about 50%, about 60%, about 70%, about 80%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, about 99% of the exogenous or eukaryotic nucleic acid sequence. In certain embodiments, the RNA- guided nuclease is a Cas9 protein. In some embodiments, the eukaryotic nucleic acid sequence is within an RNA-guided nuclease coding sequence, where it can encode at least part of a modified portion of the protein. In instances wherein the exogenous sequence encodes all or part of a modified portion of the ided nuclease, that sequence can be positioned within a region that is flanked by codons for glycine, alanine or valine at each of its 3’ and 5’ ends. In some cases, the region of the RNA-guided nuclease coding sequence comprising the exogenous nucleic acid ce encodes an amino acid having a sequence of G—(X)6-10—G. In embodiments where the RNA-guided nuclease is Cas9, the proteins d by these ces can comprise ions (relative to SEQ ID NO: 2) such as E271_N272insGX6_10G, 372insGX6_10G, and/or Q73 7_A738insGX6.10G, and/or ions at or near the N-terminus of a Cas9 e, and/or sequences of at least 95% identity (e. g. 95%, 96%, 97%, 98%, 99% or r identity) to SEQ ID NOS: 3-5 and 10.

Continuing with this aspect of the disclosure, the isolated nucleic acid can include an insertion (relative to SEQ ID NO: 6) c.8l3_814insN27-36, c. l l 13_l l l4insN27-36, and/or c221 l_2212insN27-3 6, and/or insertions at or near the coding ce of the N- terminus of a Cas9 peptide, and/or have at least 95% (e. g. 95%, 96%, 97%, 98%, 99% or greater identity) sequence identity to SEQ ID NOS: 7-9 and 11. The isolated nucleic acid can, alternatively or onally include an insertion of c.157insN19.36 and/or share at least 80% (e.g. 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% or greater identity) sequence identity with SEQ ID NO: 1. Isolated nucleic acids ing to this aspect of this disclosure are optionally incorporated into vectors such as plasmids, viral vectors, naked DNA vectors, etc. In some instances, an adeno-associated virus (AAV) vector incorporates isolated nucleic acids ing to this aspect of the disclosure. In certain embodiments, a target site for the gRNA is within the vector backbone. The vectors can be used to alter both a cellular endogenous target gene and the RNA-guided nuclease expression.

In n embodiments, the RNA-guided nuclease is Cpf1. In certain embodiments, the amino acid sequence of a Cpf1 protein is set forth in SEQ ID NO: 13.

In certain embodiments, the Cpf1 n can comprise an insertion such as a GX6.10G insertion. In certain embodiments, the ion (relative to SEQ ID NO: 13) is positioned between amino acid positions 147 and 148, anywhere between amino acid positions 484 and 492, anywhere between amino acid positions 568 and 590, anywhere between amino acid positions 795 and 855, anywhere between amino acid positions 1131 and 1140, or anywhere between amino acid positions 1160 and 1173. In certain embodiments, the insertion is positioned at or near the N—terminus of a Cpfl peptide. In certain embodiments, the amino acid sequence of the Cpf1 n comprising the insertion has at least 95% sequence identity (e. g. 95%, 96%, 97%, 98%, 99% or greater identity) to SEQ ID NO: 13.

In certain embodiments, an isolated nucleic acid ce encoding a Cpf1 protein is set forth in SEQ ID NO: 14. In n embodiments, the isolated Cpf1 nucleic acid can comprise an ion such as an N24-36 insertion. In certain embodiments, the insertion (relative to SEQ ID NO: 14) is positioned between nucleic acid positions 441 and 442, anywhere between c acid positions 1452 and 1474, anywhere between nucleic acid positions 1704 and 1768, anywhere between nucleic acid positions 2385 and 2563, anywhere between nucleic acid positions 3393 and 3418, or anywhere n nucleic acid ons 3480 and 3517. In certain embodiments, the insertion does not alter the g frame of the isolated Cpfl nucleic acid. In certain embodiments, the insertion is positioned at or near the N—terminus of a Cpf1 peptide. In certain embodiments, the nucleic acid sequence of the Cpf1 protein comprising the insertion has at least 95% (e. g. 95%, 96%, 97%, 98%, 99% or greater identity) sequence identity to SEQ ID NO: 14. ed nucleic acids according to this aspect of this disclosure are optionally incorporated into vectors such as plasmids, viral vectors, naked DNA vectors, etc. In some ces, an adeno-associated virus (AAV) vector incorporates isolated c acids according to this aspect of the disclosure. In certain embodiments, a target site for the gRNA is within the vector backbone. The vectors can be used to alter both a cellular endogenous target gene and the RNA-guided nuclease expression.

In another aspect, the disclosure s to transiently active genome editing s that include a guide RNA with a targeting domain that is complementary to a eukaryotic nucleotide sequence and an engineered RNA-guided se encoded by a c acid comprising a eukaryotic nucleic acid sequence as described above. In certain embodiments, the RNA-guided nuclease is a Cas9 protein. The gRNA and engineered Cas9 can form a Cas9/gRNA complex, which complex may in turn cleave or otherwise alter or inactivate the nucleic acid encoding the engineered Cas9 protein. In certain ments, the Cas9/gRNA complex can cleave a nucleic acid encoding a cellular endogenous target gene. The transiently active genome g system can be used to alter both the cellular nous target and the RNA-guided nuclease expression. As discussed above, the eukaryotic nucleic acid sequence can encode, at least in part, a modified portion (e.g., amino acid insertion or substitution) of the Cas9, which d portion has a sequence as described above. In certain embodiments, the engineered Cas9 n has at least about 80% nuclease activity of a wild-type Cas9 protein.

In certain embodiments, the RNA—guided nuclease is a Cpfl protein. The gRNA and ered Cpfl can form a Cpfl/gRNA complex, which complex may in turn cleave or otherwise alter or inactivate the nucleic acid encoding the engineered Cpfl protein. In certain embodiments, the Cpfl/gRNA x can cleave a nucleic acid ng a cellular nous target gene. The transiently active genome editing system can be used to alter both the cellular endogenous target and the RNA—guided nuclease expression. As discussed above, the eukaryotic nucleic acid sequence can encode, at least in part, a modified portion (e.g., amino acid insertion or substitution) of the Cpfl, which d portion has a sequence as bed above. In certain embodiments, the engineered Cpfl protein has at least about 80% nuclease activity of a wild-type Cpfl protein In yet another aspect, the disclosure relates to a RNA-guided nuclease comprising an amino acid insertion or substitution at least partially encoded by a eukaryotic nucleic acid sequence of at least 17 nucleotides in length. In certain embodiments, the RNA- guided nuclease having the amino acid insertion or substitution has at least about 80% se activity of a wild-type RNA-guided se. The eukaryotic sequence can be a mammalian sequence, and/or the ce of a human or animal subject. In certain embodiments, the RNA-guided nuclease can be a Cas9 protein and nucleic acids encoding the Cas9 protein according to this aspect of this disclosure are substantially as described above.

In another aspect, the disclosure relates to a method of altering a cell that involves delivering (eg, contacting, administering, introducing, transfecting, transducing, etc.) a transiently expressed genome editing system as described above. In certain embodiments, the method can be used to alter a target site in a cell. In certain embodiments, the method can be used to alter both a cellular endogenous target gene and the RNA-guided nuclease expression.

In still another aspect, this disclosure relates to a kit sing one or more components of a transiently active genome editing system, a nucleic acid and/or an RNA-guided se according to the various aspects of the disclosure presented above.

BRIEF DESCRIPTION OF THE DRAWINGS The accompanying drawings are intended to provide illustrative, and schematic rather than comprehensive, es of certain aspects and embodiments of the present disclosure. The drawings are not intended to be limiting or binding to any particular theory or model, and are not arily to scale. Without limiting the foregoing, nucleic acids and polypeptides may be depicted as linear ces, or as schematic two- or three-dimensional structures; these depictions are intended to be illustrative rather than limiting or binding to any particular model or theory regarding their structure.

Figure 1A is a diagram illustrating a SaCas9-gRNA complex targeting both an endogenous cellular target and a nucleic acid ng the SaCas9 in a viral vector.

Figure 1B is a cartoon diagram depicting a 2-vector system in which ered SaCas9 and gRNAs are encoded on separate viral genomes. Two types of ary sites in a recombinant adeno-associated virus (AAV) genome into which heterologous cellular ces can be engineered are marked by arrows.

Figure 2 is a ribbon diagram ing an S. aureus Cas9 n. Exemplary 3O regions which can be encoded by engineered heterologous sequences are identified by arrows.

Figures 3A-3C are schematic graphs showing exemplary peptide-encoding inserts orating heterologous cellular sequences.

Figure 4A is a cartoon diagram depicting exemplary constructs with target sites at four different positions in the SaCas9 coding sequence, as well as a gRNA expression plasmid.

Figure 4B depicts comparisons of transcription levels and translation levels of wild-type Cas9 constructs and self-inactivating Cas9 ucts.

Figures 4C-4E depict the levels of nuclease activity among wild-type and self- inactivating SaCas9 proteins.

Figure 5A depicts the experimental design in Example 3.

Figure 5B depicts self-inactivating AAVs maintain efficacy at target GFP plasmids while self-inactivating in HEK293 cells. The upper left panel shows the locations of target sites inserted in the self—inactivating Cas9 constructs. The lower left panel shows GFP expression levels in HEK293 cells with or without wild-type or self- inactivating SaCas9 constructs. The lower right panel shows Cas9 protein levels in HEK293 cells transduced with ype or self-inactivating SaCas9 constructs.

Figure 6A is a graph showing the editing levels of an endogenous target locus (mCEP290) with ype or self—inactivating SaCas9 constructs in mouse retinal explants.

Figure 6B is a graph demonstrating the % wild-type SaCas9 sequence levels in mouse retinal ts with wild-type or self-inactivating SaCas9 ucts.

Figure 7A depicts the editing levels of an endogenous target locus with wild—type or self-inactivating SaCas9 ucts in viva.

Figure 7B depicts the fold changes of c transcripts expressed through self- vating SaCas9 constructs compared to the wild-type SaCas9 construct.

DETAILED DESCRIPTION Definitions and Abbreviations Unless otherwise specified, each of the ing terms has the meaning associated with it in this section.

The indefinite articles “a” and “an” refer to at least one of the associated noun, and are used hangeably with the terms “at least one” and “one or more.” For example, “a module” means at least one module, or one or more modules.

The conjunctions “or” and “and/or” are used hangeably as non-exclusive disjunctions.

“Domain” is used to describe a t of a protein or nucleic acid. Unless otherwise indicated, a domain is not required to have any specific functional property.

An “indel” is an insertion and/or deletion in a nucleic acid ce. An indel may be the product of the repair of a DNA double strand break, such as a double strand break formed by a genome editing system of the present disclosure. An indel is most ly formed when a break is repaired by an “error prone” repair pathway such as the NHEJ pathway described below.

“Gene conversion” refers to the alteration of a DNA sequence by incorporation of an endogenous homologous sequence (e. g. a homologous sequence within a gene array).

“Gene correction” refers to the alteration of a DNA sequence by incorporation of an exogenous homologous sequence, such as an exogenous single- or double-stranded donor template DNA. Gene conversion and gene correction are products of the repair of DNA double-strand breaks by HDR pathways such as those described below.

Indels, gene conversion, gene correction, and other genome editing outcomes are 2O typically assessed by sequencing (most commonly by “next—gen” or ncing-by— sis” methods, though Sanger cing may still be used) and are quantified by the relative frequency of numelical changes (e. g., i1, i2 or more bases) at a site of interest among all sequencing reads. DNA samples for sequencing may be prepared by a variety of methods known in the art, and may involve the amplification of sites of interest by polymerase chain reaction (PCR), the capture ofDNA ends generated by double strand breaks, as in the GUIDEseq process described in Tsai et al. (Nat.

Biotechnol. 34(5): 483 (2016), incorporated by nce herein) or by other means well known in the art. Genome editing outcomes may also be assessed by in situ hybridization methods such as the ombTM system commercialized by Genomic Vision (Bagneux, France), and by any other suitable methods known in the art.

“Alt-HDR,” “alternative gy-directed repair,” or “alternative HDR” are used interchangeably to refer to the process of repairing DNA damage using a homologous nucleic acid (e.g., an endogenous homologous sequence, e.g., a sister chromatid, or an exogenous nucleic acid, e.g., a template nucleic acid). Alt-HDR is ct from cal HDR in that the process utilizes ent pathways from canonical HDR, and can be inhibited by the canonical HDR mediators, RAD51 and BRCA2. Alt-HDR is also distinguished by the involvement of a single- stranded or nicked homologous c acid template, whereas canonical HDR generally involves a double-stranded homologous template.

“Canonical HDR,” "canonical homology-directed repair" or “cHDR” refer to the process of repairing DNA damage using a homologous nucleic acid (e.g., an endogenous homologous sequence, e. g., a sister chromatid, or an exogenous nucleic acid, e. g., a te nucleic acid). Canonical HDR typically acts when there has been significant resection at the double strand break, forming at least one single-stranded portion of DNA. In a normal cell, cHDR typically involves a series of steps such as recognition of the break, ization of the break, resection, ization of —stranded DNA, formation of a DNA crossover intermediate, resolution of the crossover intermediate, and ligation. The process requires RAD51 and BRCA2, and the homologous nucleic acid is typically double-stranded.

Unless indicated otherwise, the term “HDR” as used herein encompasses both canonical HDR and alt-HDR.

“Non-homologous end joining” or “NHEJ” refers to ligation mediated repair and/or nontemplate mediated repair including canonical NHEJ (cNHEJ) and alternative NHEJ (altNHEJ), which in turn includes microhomology-mediated end joining (MMEJ), -strand annealing (SSA), and synthesis-dependent microhomology-mediated end joining (SD-MMEJ).

“Replacement” or “replaced,” when used with reference to a modification of a molecule (e. g. a nucleic acid or protein), does not require a process limitation but merely indicates that the replacement entity is present.

“Subject” means a human or non-human animal. A human subject can be any age (e. g, an infant, child, young adult, or adult), and may suffer from a e, or may 3O be in need of alteration of a gene. Alternatively, the subject may be an animal, which term includes, but is not limited to, mammals, birds, fish, es, amphibians, and more particularly non-human primates, rodents (such as mice, rats, hamsters, etc), rabbits, guinea pigs, dogs, cats, and so on. In certain ments of this disclosure, the subject is livestock, e.g., a cow, a horse, a sheep, or a goat. In certain embodiments, the subject is poultry.

“Treat,” “treating,” and ment” mean the treatment of a disease in a subject (e. g., a human subject), including one or more of inhibiting the disease, i.e., arresting or preventing its development or progression; relieving the disease, ie., causing regression of the disease state; relieving one or more symptoms of the disease; and curing the disease, “Prevent, 3) (Lpreventing,” and ntion” refer to the prevention of a disease in a mammal, e.g., in a human, including (a) avoiding or precluding the disease; (b) affecting the predisposition toward the disease, or (c) preventing or delaying the onset of at least one symptom of the disease.

A “Kit” refers to any collection of two or more ents that together constitute a functional unit that can be employed for a specific purpose. By way of illustration (and not limitation), one kit ing to this disclosure can e a guide RNA complexed or able to complex with an RNA—guided nuclease, and accompanied by (e. g. suspended in, or suspendable in) a pharmaceutically acceptable carrier. The kit can be used to uce the complex into, for example, a cell or a subject, for the purpose of causing a desired c alteration in such cell or subject. The components of a kit can be packaged together, or they may be separately packaged. Kits according to this disclosure also optionally e directions for use (DFU) that describe the use of the kit e. g., according to a method of this disclosure. The DFU can be physically ed with the kit, or it can be made available to a user of the kit, for instance by electronic means.

The terms “polynucleotide)3 eotide sequence7’ (Lnucleic acid”, ic acid 7 , molecule”, “nucleic acid sequence”, and “oligonucleotide” refer to a series of nucleotide bases (also called otides”) in DNA and RNA, and mean any chain of two or more nucleotides. These terms refer to compositions that can be chimeric mixtures or derivatives or modified versions thereof, single-stranded or double-stranded. These terms also refer to compositions that can be modified at the base moiety, sugar moiety, or phosphate backbone, for e, to improve stability of the molecule, its hybridization parameters, etc. A nucleotide sequence typically s genetic information, including, but not limited to, the information used by cellular machinery to make proteins and enzymes. These terms include double- or single-stranded genomic DNA, RNA, any tic and genetically manipulated polynucleotide, and both sense and antisense polynucleotides. These terms also include nucleic acids containing modified bases.

Conventional IUPAC notation is used in tide sequences presented herein, as shown in Table 1, below (see also h-Bowden A, Nucleic Acids Res, 1985 May , l3(9):3021-30, incorporated by reference herein). It should be noted, however, that “T” denotes “Thymine or Uracil” in those instances where a ce may be encoded by either DNA or RNA, for example in gRNA targeting domains, Table 1: IUPAC nucleic acid notation Adenine Thymine or Uracil Guanine Uracil G or T/U C or T/U A or T/U — C, G or T/U A=CorG A, C or T/U “ A, G or T/U A, C, G or T/U The terms “protein,)7 <4peptide” and “polypeptide” are used hangeably to refer to a sequential chain of amino acids linked together Via peptide bonds. The terms include individual proteins, groups or complexes of proteins that associate together, as well as fragments or portions, variants, derivatives and analogs of such proteins, Peptide ces are presented herein using conventional notation, beginning with the amino or N-tenninus on the left, and proceeding to the carboxyl or C-terminus on the right. Standard one-letter or three-letter abbreviations can be used.

Overview In general terms, this disclosure concerns genome editing systems, including, but not limited to, transiently active genome editing systems, comprising ided ses and gRNAs that are targeted to specific, y cellular, DNA ces. The gRNAs used in these genome editing systems are referred to throughout this disclosure as “one-shot guide RNAs” or ogRNAs, to distinguish them from governing guide RNAs that are specifically targeted to nucleic acid sequences encoding RNA-guided nucleases such as Cas9. In the various embodiments of this disclosure, the nucleic acids ng genome editing systems are modified to introduce sites recognized by ogRNAs, allowing them to function as ggRNAs without altering their ability to recognize the specific cellular sequences they have been designed to target. As such, in certain ments, the genome editing system can edit the endogenous target locus as well as the c acid encoding the RNA—guided nuclease. Figure 1A is a diagram illustrating a SaCas9- gRNA complex targeting the endogenous ar locus as well as an engineered Cas9 sequence comprising an ogRNA target sequence in a viral vector.

For y of presentation, and as illustrated in Figure 1B, the sites that are introduced into nucleic acids encoding genome editing systems are d into (a) sites introduced into nucleic acid vector backbones, e. g. viral genome backbones, and/or (b) sites introduced into RNA-guided nuclease encoding sequences, for example, sequences encoding a Cas9 nuclease. This grouping is not intended to be limiting or binding to any particular theory or model, and (a) and (b) are not mutually exclusive. The introduction of ogRNA target sites into sequences ng genome editing systems or vectors containing such sequences has several advantages over other self-inactivation strategies.

For one thing, the introduction of an ogRNA target site into such nucleic acids allows self-inactivating genome editing systems to be designed and implemented without the need for a separate ggRNA. This in turn permits self-inactivating genome editing systems to be ed in comparatively less space to facilitate, for example, a self- inactivating system comprising multiple gRNAs to be packaged in a single vector (a “one-shot” configuration) such as an AAV vector with a ing limit of about 4.7 kb.

Another advantage is a potential improvement in the tability of the behavior of the ogRNA relative to ggRNA systems due to, for example, the elimination of variation due to ences in expression or cutting efficiency between a genomically-targeted gRNA and a ggRNA. Further advantages of the embodiments of this disclosure will be evident to those of skill in the art. In certain embodiments, sites introduced into the RNA-guided nuclease do not alter the nuclease activity of the RNA-guided nuclease as compared to the wild-type n. In certain ments, the engineered RNA guided-nuclease has at least about 80%, about 85%, about 90%, about 95%, or about 99% nuclease activity of the wild-type protein.

Turning first to the introduction of engineered sequences into vector backbones, it will be understood by those of skill in the art that many vector nucleic acids, such as plasmids, artificial chromosomes, and/or recombinant viral vector genomes, comprise “backbone” sequences that do not encode RNA-guided nucleases. By engineering one or more ogRNA target sites into these backbone sequences, the genome editing system orating the ogRNA can recognize and alter the vector, for example by forming single- or double-strand breaks, point mutations, or other modifications as described in greater detail below. This alteration, in turn, can reduce or eliminate transcription of one or more components of the genome editing system and thereby limit the activity of the genome editing system.

An ogRNA target site, whether it is incorporated into a vector backbone or an RNA-guided nuclease coding sequence, will generally comprise a 16-24 nucleotide sequence (a “protospacer” sequence) that is complementary to a ing domain sequence (or “spacer”, 16—24 nucleotide in length) of the ogRNA; the protospacer is adjacent to a pacer Adjacent Motif (or “PAM”) that is, generally, between 3 and 6 nucleotides in length depending on the s of RNA-guided se used. Certain examples in this disclosure focus on target sites for use with S. aureus Cas9, which recognizes an NNGRRT or NNGRRV PAM that is immediately 3’ of the pacer sequence as visualized on the “top” or “complementary” strand. Without ng the foregoing, an exemplary S. aureus ogRNA target site can be 22-30 nucleotides in length, comprising a 16-24 nucleic acid sequence in the eukaryotic gene and a 6 nucleotide PAM that is recognized by the S. aureus Cas9. ot guide RNA target sites can be engineered into vector backbones in any suitable position, though it may be advantageous in certain cases to position ogRNA target sites in proximity to sites or ts that (a) are required for the stability of the vector in viva, (b) that will lose function, rather than gain function, when disrupted by, e. g. an indel; and/or (c) that are required for the expression of functional RNA-guided nuclease. These sites or elements may include, without tion, promoter sequences for gRNAs and/or RNA-guided ses; inverted terminal repeats, gRNA coding sequences, etc.

In n ments where the ogRNA target site is introduced into a nucleic acid vector backbone, the target site is located within or adjacent to the promoter sequence of a gRNA and/or a RNA-guided nuclease. In certain embodiments, the target site is located upstream of a transcription start site of the promoter sequence, e.g., 0 bp, about 1 bp, about 10 bp, about 50 bp, about 100 bp, about 200 bp, about 500 bp, about 1000 bp, or any intermediate distance or ranges thereof upstream of the transcription start site. In certain embodiments, the target site is located downstream of a transcfiption start site of the er sequence, e.g., 0 bp, about 1 bp, about 10 bp, about 50 bp, about 100 bp, about 200 bp, about 500 bp, about 1000 bp, or any intermediate distance or ranges thereof downstream of the transcription start site. In certain embodiments, the target site comprises a transcription start site.

In certain ments where the ogRNA target site is introduced into a nucleic acid vector ne, the target site is located within or adjacent to a 5' untranslated region (5’ UTR) of a RNA-guided nuclease. In certain embodiments, the target site is located upstream of a translation start site of the promoter sequence, e.g., 0 bp, about 1 bp, about 10 bp, about 50 bp, about 100 bp, about 200 bp, about 500 bp, about 1000 bp, or any intermediate distance or ranges thereof upstream of the translation start site. In certain embodiments, the target site is located within or adjacent to a 3’ untranslated region (3’ UTR) of a RNA—guided nuclease. In certain embodiments, the target site is located downstream of a translation stop codon (e.g., TGA, TAA and TAG), e.g., 0 bp, about 1 bp, about 10 bp, about 50 bp, about 100 bp, about 200 bp, about 500 bp, about 1000 bp, or any intermediate distance or ranges thereof downstream of the translation stop site.

Table 2, below, includes one exemplary AAV backbone into which a target site (denoted by N’s) is ered near the 5’ end (c.157insN19.30) Table 2: Exemplary in-backbone target sequence TTGGCCACTCCCTCTCTGCGCGCTCGCTCGCTCACTGAGGCCGGGCGACCAAAGGTCGCCCGACG CTTTGCCCGGGCGGCCTCAGTGAGCGAGCGAGCGCGCAGAGAGGGAGTGGCCAACTCCA TCACTAGGGGTTCCTCAGATCTGAATTNNNNNNNNNNNNNNNNNNNNNNNNNNCTAGCGCTTAAG TCGCGCATTGATTATTGACTAGTTATTAATAGTAATCAATTACGGGGTCATTAGTTCATAGCCCA TATATGGAGTTCCGCGTTACATAACTTACGGTAAATGGCCCGCCTGGCTGACCGCCCAACGACCC CCGCCCATTGACGTCAATAATGACGTATGTTCCCATAGTAACGCCAATAGGGACTTTCCATTGAC GTCAATGGGTGGACTATTTACGGTAAACTGCCCACTTGGCAGTACATCAAGTGTATCATATGCCA AGTACGCCCCCTATTGACGTCAATGACGGTAAATGGCCCGCCTGGCATTATGCCCAGTACATGAC GGACTTTCCTACTTGGCAGTACATCTACGTATTAGTCATCGCTATTACCATGGTGATGC GGTTTTGGCAGTACATCAATGGGCGTGGATAGCGGTTTGACTCACGGGGATTTCCAAGTCTCCAC CCCATTGACGTCAATGGGAGTTTGTTTTGGCACCAAAATCAACGGGACTTTCCAAAATGTCGTAA CAACTCCGCCCCATTGACGCAAATGGGCGGTAGGCGTGTACGGTGGGAGGTCTATATAAGCAGAG CTGGTTTAGTGAACCGTCAGATCCGCTAGAGATCCGCTCTAGAGGATCCGGTACTCGAGGAACTG AAAAACCAGAAAGTTAACTGGTAAGTTTAGTCTTTTTGTCTTTTATTTCAGGTCCCGGATCCGGT GGTGGTGCAAATCAAAGAACTGCTCCTCAGTGGATGTTGCCTTTACTTCTAGGCCTGTACGGAAG TGTTACGCGGCCGCCACCATGGGACCGAAGAAAAAGCGCAAGGTCGAAGCGTCCATGAAAAGGAA CTACATTCTGGGGCTGGACATCGGGATTACAAGCGTGGGGTATGGGATTATTGACTATGAAACAA GGGACGTGATCGACGCAGGCGTCAGACTGTTCAAGGAGGCCAACGTGGAAAACAATGAGGGACGG AGAAGCAAGAGGGGAGCCAGGCGCCTGAAACGACGGAGAAGGCACAGAATCCAGAGGGTGAAGAA GTTCGATTACAACCTGCTGACCGACCATTCTGAGCTGAGTGGAATTAATCCTTATGAAG CCAGGGTGAAAGGCCTGAGTCAGAAGCTGTCAGAGGAAGAGTTTTCCGCAGCTCTGCTGCACCTG GCTAAGCGCCGAGGAGTGCATAACGTCAATGAGGTGGAAGAGGACACCGGCAACGAGCTGTCTAC AAAGGAACAGATCTCACGCAATAGCAAAGCTCTGGAAGAGAAGTATGTCGCAGAGCTGCAGCTGG AACGGCTGAAGAAAGATGGCGAGGTGAGAGGGTCAATTAATAGGTTCAAGACAAGCGACTACGTC AAAGAAGCCAAGCAGCTGCTGAAAGTGCAGAAGGCTTACCACCAGCTGGATCAGAGCTTCATCGA TACTTATATCGACCTGCTGGAGACTCGGAGAACCTACTATGAGGGACCAGGAGAAGGGAGCCCCT TCGGATGGAAAGACATCAAGGAATGGTACGAGATGCTGATGGGACATTGCACCTATTTTCCAGAA AGAAGCGTCAAGTACGCTTATAACGCAGATCTGTACAACGCCCTGAATGACCTGAACAA CCTGGTCATCACCAGGGATGAAAACGAGAAACTGGAA1ACTATGAGAAGTTCCAGATCATCGAAA TTAAGCAGAAGAAAAAGCCTACACTGAAACAGATTGCTAAGGAGATCCTGGTCAACGAA GAGGACATCAAGGGCTACCGGGTGACAAGCACTGGAAAACCAGAGTTCACCAATCTGAAAGTGTA TCACGATATTAAGGACATCACAGCACGGAAAGAAATCATTGAGAACGCCGAACTGCTGGATCAGA TTGCTAAGATCCTGACTATCTACCAGAGCTCCGAGGACATCCAGGAAGAGCTGACTAACCTGAAC AGCGAGCTGACCCAGGAAGAGATCGAACAGATTAGTAATCTGAAGGGGTACACCGGAACACACAA CCTGTCCCTGAAAGCTATCAATCTGATTCTGGATGAGCTGTGGCATACAAACGACAATCAGATTG CAATCTTTAACCGGCTGAAGCTGGTCCCAAAAAAGGTGGACCTGAGTCAGCAGAAAGAGATCCCA ACCACACTGGTGGACGATTTCATTCTGTCACCCGTGGTCAAGCGGAGCTTCATCCAGAGCATCAA AGTGATCAACGCCATCATCAAGAAGTACGGCCTGCCCAA1GATATCATTATCGAGCTGGCTAGGG AGAAGAACAGCAAGGACGCACAGAAGATGATCAATGAGATGCAGAAACGAAACCGGCAGACCAAT GAACGCATTGAAGAGATTATCCGAACTACCGGGAAAGAGAACGCAAAGTACCTGATTGAAAAAAT CAAGCTGCACGATATGCAGGAGGGAAAGTGTCTGTATTCTCTGGAGGCCATCCCCCTGGAGGACC TGCTGAACAATCCATTCAACTACGAGGTCGATCATATTATCCCCAGAAGCGTGTCCTTCGACAAT TCCTTTAACAACAAGGTGCTGGTCAAGCAGGAAGAGAACTCTAAAAAGGGCAATAGGACTCCTTT CCAGTACCTGTCTAGTTCAGATTCCAAGATCTCTTACGAAACCTTTAAAAAGCACATTCTGAATC TGGCCAAAGGAAAGGGCCGCATCAGCAAGACCAAAAAGGAGTACCTGCTGGAAGAGCGGGACATC AACAGATTCTCCGTCCAGAAGGATTTTATTAACCGGAATCTGGTGGACACAAGATACGCTACTCG CGGCCTGATGAATCTGCTGCGATCCTATTTCCGGGTGAACAATCTGGATGTGAAAGTCAAGTCCA TCAACGGCGGGTTCACATCTTTTCTGAGGCGCAAATGGAAGTTTAAAAAGGAGCGCAACAAAGGG TACAAGCACCATGCCGAAGATGCTCTGATTATCGCAAATGCCGACTTCATCTTTAAGGAGTGGAA AAAGCTGGACAAAGCCAAGAAAGTGATGGAGAACCAGATGTTCGAAGAGAAGCAGGCCGAA1CTA TGCCCGAAATCGAGACAGAACAGGAGTACAAGGAGATTTTCATCACTCCTCACCAGATCAAGCAT GATTTCAAGGACTACAAGTACTCTCACCGGGTGGATAAAAAGCCCAACAGAGAGCTGAT CAATGACACCCTGTATAGTACAAGAAAAGACGATAAGGGGAATACCCTGATTGTGAACAATCTGA ACGGACTGTACGACAAAGATAATGACAAGCTGAAAAAGCTGATCAACAAAAGTCCCGAGAAGCTG CTGATGTACCACCATGATCCTCAGACATATCAGAAACTGAAGCTGATTATGGAGCAGTACGGCGA CGAGAAGAACCCACTGTATAAGTACTATGAAGAGACTGGGAACTACCTGACCAAGTATAGCAAAA AGGATAATGGCCCCGTGATCAAGAAGATCAAGTACTATGGGAACAAGCTGAATGCCCATCTGGAC ATCACAGACGATTACCCTAACAGTCGCAACAAGGTGGTCAAGCTGTCACTGAAGCCATACAGATT CGATGTCTATCTGGACAACGGCGTGTATAAATTTGTGACTGTCAAGAATCTGGATGTCATCAAAA AGGAGAACTACTATGAAGTGAATAGCAAGTGCTACGAAGAGGCTAAAAAGCTGAAAAAGATTAGC AACCAGGCAGAGTTCATCGCCTCCTTTTACAACAACGACCTGATTAAGATCAATGGCGAACTGTA TAGGGTCATCGGGGTGAACAATGATCTGCTGAACCGCATTGAAGTGAATATGATTGACATCACTT ACCGAGAGTATCTGGAAAACATGAATGATAAGCGCCCCCCTCGAATTATCAAAACAATTGCCTCT AAGACTCAGAGTATCAAAAAGTACTCAACCGACATTCTGGGAAACCTGTATGAGGTGAAGAGCAA AAAGCACCCTCAGATTATCAAAAAGGGCGGATCCCCCAAGAAGAAGAGGAAAGTCTCGAGCGACT ACCATGACGGTGATTATAAAGATCATGACATCGATTACAAGGATGACGATGACAAGTAG CAATAAAGGATCGTTTATTTTCATTGGAAGCGTGTGTTGGTTTTTTGATCAGGCGCGTCCAAGCT TGCATGCTGGGGAGAGATCTAGGAACCCCTAGTGATGGAGTTGGCCACTCCCTCTCTGCGCGCTC GCTCGCTCACTGAGGCCGCCCGGGCAAAGCCCGGGCGTCGGGCGACCTTTGGTCGCCCGGCCTCA GAGCGAGCGCGCAGAGAGGGAGTGGCCAA [SEQ ID NO:1] While the exemplary backbone sequence of Table 2 includes a single target site, this disclosure also encompasses backbones into which 2, 3, 4, 5 or more identical or non-identical target sequences are engineered into the vector. onally, it will be appreciated by those of skill in the art that certain sequences within the vector ne may be similar to ns of the target site, and that these sites may be easily d to create target sites. For example, there can be multiple PAMs within the vector backbone, and the sequence immediately 5’ (as visualized on the complementary or top strand) can be modified to differ by 0, l, 2, 3 or more nucleotides from the protospacer sequence recognized by the ogRNA. atively, a PAM sequence may be introduced into a sequence encoding a gRNA targeting domain for example by modifying the residues of the gRNA immediately 3’ of the ing domain. In certain embodiments, an ed c acid encoding a Cas9 protein having a eukaryotic sequence can share at least 80% (eg. 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% or greater identity) sequence identity with SEQ ID NO: 1. In certain embodiments, an isolated nucleic acid encoding a Cpfl protein having a eukaryotic sequence can share at least 80% (e. g. 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% or greater identity) sequence identity with SEQ ID NO: 14.

Turning next to systems in which a target site is introduced into a sequence 2O encoding an RNA-guided nuclease, this disclosure provides certain engineered S. aureus Cas9 proteins that are encoded by DNA sequences comprising target sites as bed above. Short (eg. 24-42 base pair, or 8-13 amino-acid) sequences comprising such target sites are referred to as “inserts” when they are implemented in Cas9-coding sequences and/or engineered Cas9 proteins, whether they are inserted into the sequence, or replace a portion of the sequence. Figures 3A-3C are schematic graphs showing exemplary peptide—encoding inserts orating heterologous cellular sequences.

Skilled ns will appreciate that the design criteria for inserts include certain conditions that are not necessarily applicable to target sites in the “backbone” sequence of a DNA . For one thing, the length of the insert in certain embodiments is divisible by three to avoid the introduction of a frameshift mutation that may affect the function of the engineered RNA-guided nuclease. In instances where c target sites have a length that is not divisible by three, one or two additional nucleotides are added to the insert as necessary to preserve the reading frame of the coding sequence comprising the insert.

Another design ion that is met by certain embodiments of this disclosure is minimal tion of the structure of the engineered protein comprising the insert. This requirement is met in some instances by (a) locating the insert in a region of the nuclease protein where the addition of amino acids is well tolerated, and/or (b) selecting inserts that will tend not to disrupt the structure of the surrounding protein. These two design elements are dealt with in turn: With respect to the location of the insert, Figures 1B and 2 depict four exemplary sites (AC1, AC2, AC3, NT) in the S. aureus Cas9 n into which an insert is added in various embodiments of this disclosure, e. g. E271_N272insGX6-10G, L371_N372insGX6.10G, Q737_A73 8insGX6.10G, and/or at or near the N—terminus (NT).

The peptide ces corresponding to each of these positions are presented in Table 3 2O below. In the table, residues within the insert are denoted by X. The sequences ted include amino acid inserts for clarity, however, the insert can have any suitable length.

In certain embodiments, an insert “at or near the N—terminus” is positioned within about 20 amino acid residues from the first amino acid residue of an RNA-guided nuclease (e. g., Cas9 or Cpf1) peptide. In certain embodiments, an insert at or near the N- nus is positioned at about 0, about 1, about 2, about 3, about 4, about 5, about 6, about 7, about 8, about 9, about 10, about 11, about 12, about 13, about 14, about 15, about 16, about 17, about 18, about 19, or about 20 amino acid es from the first amino acid residue of an RNA-guided nuclease (e.g., Cas9 or Cpfl) peptide. In certain 3O embodiments, an insert at or near the inus is positioned upstream of the first amino acid residue of an RNA-guided nuclease (e.g., Cas9 or Cpfl) peptide. In certain embodiments, an insert at or near the N-terminus is positioned downstream of the first amino acid residue of an RNA-guided nuclease (e.g., Cas9 or Cpf1) peptide. In certain embodiments, an insert at or near the N—terminus is positioned between a nuclear localization sequence (NLS) and the coding sequence for the ided se peptide. In certain embodiments, the NLS comprises a peptide sequence set forth in SEQ ID NO: 12 GPKKKRKVEAS [SEQ ID NO: 12].

In certain embodiments, an insert at or near the N—terminus is positioned within about 9 amino acid residues from the first amino acid residue of a Cas9 e. In certain embodiments, an insert at or near the N—terminus is positioned at about 0, about 1, about 2, about 3, about 4, about 5, about 6, about 7, about 8, about 9 amino acid residues from the first amino acid residue of a Cas9 peptide. In certain embodiments, an insert at or near the N-terminus is positioned within about 20 amino acid es from the first amino acid residue of a Cpf1 peptide. In certain embodiments, an insert at or near the N—terminus is positioned at about 0, about 1, about 2, about 3, about 4, about 5, about 6, about 7, about 8, about 9, about 10, about 11, about 12, about 13, about 14, about 15, about 16, about 17, about 18, about 19, or about 20 amino acid residues from the first amino acid residue of a Cpf1 peptide.

In certain embodiments, the insert can comprise a translational start codon (i.e., ATG). In n embodiments, the translational start codon (i.e., ATG) is in-frame with the RNA—guided nuclease coding sequence. In certain embodiments, an insert at or near the N—terminus of the RNA-guided nuclease coding sequence is positioned between a translational start codon (i.e., ATG) and the RNA-guided nuclease coding sequence.

Additionally, skilled artisans will appreciate that RNA-guided nuclease ces (e. g., Cas9 or Cpf1 n sequences) may be modified in ways that do not disrupt the operation of the ogRNA, and that these sequences may be modified to have 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 or more amino acid changes. Said another way, in n embodiments, sequences will have more than 95% sequence identity to the corresponding naturally occurring RNA-guided nuclease. In certain embodiments, s added in these three exemplary sites do not alter the nuclease activity of the RNA- guided nuclease protein as compared to the wild-type RNA-guided nuclease. In n embodiments, the RNA-guided nuclease with inserts added in the exemplary sites will have at least about 40%, about 50%, about 60%, about 70%, about 80%, about 85%, about 90%, about 95%, or about 99% nuclease activity of the wild-type ided nuclease.

Table 3: Exemplary engineered Cas9 proteins JDIGITSVGYGIIDYETRDVIDAGV? .TJHSTLSGINPYTARVKGLSQKLST..

RNSKAAEEKYVAEAQLERAKKDGEVRGSINRF QRTYYEG?GEGSPTGWKD:KEWYEMLWGHCTYTPEELRSVKYAYNADLYNA.

Cas9 EYYTKEQIIEVVF<QKKK?TLKQIAKTILVNT. ?EFTNL DQIAKIJTIYQSSEDIQEELTNLNSEJ " <GYTGTHN. aureus sequence ITWRLK. <DAQKWINEMQKRVRQTNITRIEEII EVDHIIPRSVSFDNSFNNKVLVKQ..

Sample peptlde _ NKGYKHHAEDALIIANADFIF TY<TIFIT?{QIKilKDFKDY<YSHRVDKKPNRT KK4_NKSPEKALMYHHDPQTYQKLKLIMEQYGDEKNPLYKYYEETGNYAT {LSLKPYRFDVYLDVGVYKTVTVKNLDVI EFTASFYNVDLIKINGELYRVIGVNVDLLNRIEVNWIDITYQEYLEWMNDKR?? JGNLYEV<SKKHPQIIKKG [SEQ ID NO:2] .DTGITSVGYGIIDYETRDVIDAGV .FKEANVH A§QLKRRRQl .TJHST.SGINPYTARVKGTSQKLS TTbSAAL QQGVjNVNLVbEDTGWT 8% EMQKRVQQTNE .." BBQ QSVSFJVSFNNKV. .3VKVKSIVGGFTSF_ <F<KERNKGYKHHAIT [\ QATSMPbITTbeY<. ?{QIKHIK3FKDY<YSJRVDK<_ _ HI 4N64YDKJNDXLKK4:NKSPEKgLMYHHDPQTYQKLKLIMEQYGDEK VG?VIKKI JVAHLDITDDYPNS .SWKPYRFDVYLD EVNSKCYT. {ISNQAEFIASFYNVDLIKINGI QVIGVNND RITKTIASKTQSIKKYSTDILGNJYEVKSKKHPQI:KKG JDIGITSVGYGIIDYETRDVI 4F .

.TJHSELSGINPYEARVKGLSQKLSb.fltSAAL RYSKATERKYVAETQLERTKKDGEVRGSINRFKTSDYVKEAKQTTK EG?GEGS?TGWKDI JWGHCTYF?EELRSVKYAYNA N372insGX6_10G ' {QKK _ {TILVNT.DIKGY%VTSTG Position L371 Q " " . YSJRVDK<- Z 3WDKLKKTTWKSPFKTTMYHHDPQTYQKL(LIMEQYGDEKNPTYKYYERTG V _ JVAHLDITDDYPNSQNKVV<.SWKPYRFDVYLDNGVYKFVTVKNLDVI{KENYY EVNSKCY. {ISNQAITFIASFYNVDLIKINGELYRVIGVNNDLLVRIEVNWIDTTYREYLENM NDKRPPRIIKTIASKTQSIKKYSTDILGNLYEVKSKKHPQIIXKG [SEQ ID NO: 4] LDIGITSVGYGIIDYETRDVIDAGVRLTKEANVENNEGRRSKRGARQLKRRRRi _ .TDHSTLSGINPYTARVKGLSQKLSTTTESAAL.H.AK%RGVHNVNTVEEDTGV.

LEEKYVAELQLERLKKDGEVQGSINRFKTSDYV<EAKQLLKVQKAY{QLDQSFI QTYYEG?GEGSPFGWKD:KEWYEMLWGHCTYTPEELRSVKYAYNADLYNA.

T<bQIIRWVFKQKK<?TLKQIAKTILVV.TDIKGYQVHSTGK?EFTNL .DQIAKILTIYQSSTDIQEEL"WLNST . <GYTGTHN. 3 8insGX6_10G FWRLKLVPKKVDLSQQKEIP"TLVD SIKVINAIIKKYG Position DAQKWIWEMQKTWRQTNERIEEIITr . . {LHDMQTGKCLYS ?RSVSFDNSFNNKV.VKQTTWSKKGWQTPFQYLSSSDSKISYEZ 7_A73 SKTKKEYLLEERDINRFSVQKDF_NRNLVJTRYATRGLMNLLRSYFRVNNLDVKVKS_NGGF {TKKERVKGYKHTAEDALIIANADF:FKEWKKLDKAKKVMENQMFEEKQXXXXXXXXXXX Q73 <TIFIT?{QIKHIK3F LIWDTLYSTR<DDKGWT_JIVNN LINKSPE<LLMYHH PLYKYYIT JGNYLTKYSKKD _ _ _ IKKENYY {ISNQAT _ LNRIEVYMIDITYQEYLENM {TQSIK :5] DVIDAGV _ .SGINPYEARVKGTMSQKISTTEFSAAT.LHLAK RRGVflNVNEVEEDTGNELSTKEQ:SRNSKALEEKYVAELQLERLKKDGEVRGS-NRFKTSDYVKEAKQ YYEGPGEGSPFGWKDIKEWYEMLMGHCTYFPE LRSVKYA TVVFKQKKK?TLKQIAKEI. {GYRVr‘Sr1 . . {ILTIYQSSLDIQTTLUNLNSbLTQb.LIbQISN_J NT LSLKAIVLILDELWHTNDWQIAIFNRLKLVPKKVD.SQQKPIPTTLVDDFILSPVVKRSF IQSIKVINAIIKKYGL?NDIIITLART{VSKDAQ{WINEMQKRVRQTVLRIEEIIQTTGKTNAKYLIT Position <I<LHDMQEGKCLYSITAIP.TDLLNN?FNYEVD{IIPRSVSFDNSFVVKVLV<Q.TENSK<GNRTPFQ YLSSSDSK:SYETFKKHILNLAKGKGRISKTKKEYLLEERDINRFSVQKDFINRNLVDTRYATRGLMN LLRSYFRVY LDVKV " _ T<WKFKKLRNKGYKHHAEDALIIANADFIFKEW<KLDKAK< fifiKQAbSM?fl:ETfiQfiYKbIbITBHQI{{IKDFKDYKYS{TVDKKPVRELINDTLYSTRKD VNNLNGLYJKDNDKLKKLINKSPEKLLMYHHDPQTYQKLKLIMEQYGDEKNPLYKYYEETG NYLTKYSKKDNGPVIKK:KYYGVKLNAHLDITDDY?NSRNKVVKLSLKPYRFDVYLDNGVYKTVTVKW .DVIKKTVYYEVNSKCYEEA<KLKKISVQAEFIASFYNNDLIKINGT.YRVIGVNVDLLNRIEVNWID LEVMNDKRPPR-IKTIASKTQSIKKYSTDILGNLYEVKSKKiPQIIKKG [SEQ ID NO:lO] The engineered Cas9 ns presented in Table 3 are encoded by the exemplary nucleic acids sequences listed in Table 4. In the table, the nucleotides within the insert are denoted by N, and insert positions corresponding to amino acid positions 1-3 are c.813_814insN27_36, _1114insN27_36, and c.2211_2212insN27-36, respectively.

Table 4: Exemplary nucleic acid sequences encoding engineered Cas9 proteins AGGAACTACATTCTGGGGCTGGACATCGGGATTACAAGCGTGGGGTATGGGATTATTGACTA AAGGGACGTGATCGACGCAGGCGTCAGACTGTTCAAGGAGGCCAACGTGGAAAACAATGAGG GACGGAGAAGCAAGAGGGGAGCCAGGCGCCTGAAACGACGGAGAAGGCACAGAATCCAGAGGGTGAAG AAACTGCTGTTCGATTACAACCTGCTGACCGACCATTCTGAGCTGAGTGGAATTAATCCTTATGAAGC CAGGGTGAAAGGCCTGAGTCAGAAGCTGTCAGAGGAAGAGTTTTCCGCAGCTCTGCTGCACCTGGCTA AGCGCCGAGGAGTGCATAACGTCAATGAGGTGGAAGAGGACACCGGCAACGAGCTGTCTACAAAGGAA CAGATCTCACGCAATAGCAAAGCTCTGGAAGAGAAGTATGTCGCAGAGCTGCAGCTGGAACGGCTGAA GAAAGATGGCGAGGTGAGAGGGTCAATTAATAGGTTCAAGACAAGCGACTACGTCAAAGAAGCCAAGC AGCTGCTGAAAGTGCAGAAGGCTTACCACCAGCTGGATCAGAGCTTCATCGATACTTATATCGACCTG CTGGAGACTCGGAGAACCTACTATGAGGGACCAGGAGAAGGGAGCCCCTTCGGATGGAAAGACATCAA GAATGGTACGAGATGCTGATGGGACATTGCACCTATTTTCCAGAAGAGCTGAGAAGCGTCAAGTACG TTATAACGCAGATCTGTACAACGCCCTGAATGACCTGAACAACCTGGTCATCACCAGGGATGAAAAC GAAACTGGAA"1ACTATGAGAAGTTCCAGATCATCGAAAACGTGTTTAAGCAGAAGAAAAAGCCTAC CTGAAACAGATTGCTAAGGAGATCCTGGTCAACGAAGAGGACATCAAGGGCTACCGGGTGACAAGCA (D ACCAGAGTTCACCAATCTGAAAGTGTATCACGATATTAAGGACATCACAGCACGGAAAGAA Q) TCATTGAGAACGCCGAACTGCTGGATCAGATTGCTAAGATCCTGACTATCTACCAGAGCTCCGAGGA C" GGAAGAGCTGACTAACCTGAACAGCGAGCTGACCCAGGAAGAGATCGAACAGATTAGTAATC (/1 TGAAGGGGTACACCGGAACACACAACCTGTCCCTGAAAGCTATCAATCTGATTCTGGATGAGCTGTGG (0 CATACAAACGACAATCAGATTGCAATCTTTAACCGGCTGAAGCTGGTCCCAAAAAAGGTGGACCTGAG 0 TCAGCAGAAAGAGATCCCAACCACACTGGTGGACGATTTCATTCTGTCACCCGTGGTCAAGCGGAGCT E TCATCCAGAGCATCAAAGTGATCAACGCCATCATCAAGAAGTACGGCCTGCCCAATGATATCA" R GAGCTGGCTAGGGAGAAGAACAGCAAGGACGCACAGAAGATGATCAATGAGATGCAGAAACGAAACCG E GCAGACCAATGAACGCATTGAAGAGATTATCCGAACTACCGGGAAAGAGAACGCAAAGTACCTGATTG (/5 AAAAAATCAAGCTGCACGATATGCAGGAGGGAAAGTGTCTGTATTCTCTGGAGGCCATCCCCCTGGAG O) GACCTGCTGAACAATCCATTCAACTACGAGGTCGATCATATTATCCCCAGAAGCGTGTCCTTCGACAA --—1 T“CCTTTAACAACAAGGTGCTGGTCAAGCAGGAAGAGAACTCTAAAAAGGGCAATAGGACTCCTTTCC 4.: AGTACCTGTCTAGTTCAGATTCCAAGATCTCTTACGAAACCTTTAAAAAGCACATTCTGAATCTGGCC 9 AAAGGAAAGGGCCGCATCAGCAAGACCAAAAAGGAGTACCTGCTGGAAGAGCGGGACATCAACAGATT S CTCCGTCCAGAAGGATTTTATTAACCGGAATCTGGTGGACACAAGATACGCTACTCGCGGCCTGATGA 'U ATCTGCTGCGATCCTATTTCCGGGTGAACAA".1CTGGATGTGAAAGTCAAGTCCATCAACGGCGGGTTC O ACATCTTTTCTGAGGCGCAAATGGAAGTTTAAAAAGGAGCGCAACAAAGGGTACAAGCACCATGCCGA -—1 AGATGCTCTGATTATCGCAAATGCCGACTTCATCTTTAAGGAGTGGAAAAAGCTGGACAAAGCCAAGA g AAGTGATGGAGAACCAGATGTTCGAAGAGAAGCAGGCCGAATCTATGCCCGAAATCGAGACAGAACAG (I) GAGTACAAGGAGATTTTCATCACTCCTCACCAGATCAAGCATATCAAGGATTT AAGGACTACAAGTA CTCTCACCGGGTGGATAAAAAGCCCAACAGAGAGCTGATCAATGACACCCTGTATAGTACAAGAAAAG ACGATAAGGGGAATACCCTGATTGTGAACAATCTGAACGGACTGTACGACAAAGATAATGACAAGCTG CTGATCAACAAAAGTCCCGAGAAGCTGCTGATGTACCACCATGATCCTCAGACATATCAGAA ACTGAAGCTGATTATGGAGCAGTACGGCGACGAGAAGAACCCACTGTATAAGTACTATGAAGAGACTG GGAACTACCTGACCAAGTATAGCAAAAAGGATAATGGCCCCGTGATCAAGAAGATCAAGTACTATGGG AACAAGCTGAATGCCCATCTGGACATCACAGACGATTACCCTAACAGTCGCAACAAGGTGGTCAAGCT GTCACTGAAGCCATACAGATTCGATGTCTATCTGGACAACGGCGTGTATAAATTTGT ACTGTCAAGA ATCTGGATGTCATCAAAAAGGAGAACTACTATGAAGTGAATAGCAAGTGCTACGAAGAGGCTAAAAAG CTGAAAAAGATTAGCAACCAGGCAGAGTTCATCGCCTCCTTTTACAACAACGACCTGATTAAGATCAA TGGCGAACTGTATAGGGTCATCGGGGTGAACAATGATCTGCTGAACCGCATTGAAGTGAA".1ATGATTG ACATCACTTACCGAGAGTATCTGGAAAACATGAATGATAAGCGCCCCCCTCGAATTATCAAAACAATT GCCTCTAAGACTCAGAGTATCAAAAAGTACTCAACCGACATTCTGGGAAACCTGTATGAGGTGAAGAG CAAAAAGCACCCTCAGATTATCAAAAAGGGC [SEQ ID NO:6] ATGAAAAGGAACTACATTCTGGGGCHGGACATCGGGATHACAAGCGTGGGGTATGGGATTATTGACTA TGAAACAAGGGACG”GATCGACGCAGGCGTCAGACTGT"CAAGGAGGCCAACGTGGAAAACAA"GAGG GACGGAGAAGCAAGAGGGGAGCCAGGCGCCTGAAACGACGGAGAAGGCACAGAATCCAGAGGGTGAAG AAACTGCTGTTCGAHTACAACCTGCHGACCGACCATTCHGAGCTGAGTGGAATTAAHCCTTATGAAGC CAGGGTGAAAGGCC”GAGTCAGAAGCTGTCAGAGGAAGAGTTTTCCGCAGCTCTGC"GCACCTGGCTA AGCGCCGAGGAGTGCATAACGTCAATGAGG"GGAAGAGGACACCGGCAACGAGCTG"CTACAAAGGAA TCACGCAATAGCAAAGCZ JGGAAGAGAAGTATGTCGCAGAGCTGCAGCTGGAACGGCTGAA GAAAGATGGCGAGG”GAGAGGG"CAATTAA"AGGTTCAAGACAAGCGAC"ACGTCAAAGAAGCCAAGC AGCTGCTGAAAGTGCAGAAGGC""ACCACCAGCTGGATCAGAGCTTCA"CGATAC""ATATCGACCTG CTGGAGACTCGGAGAACCTACTATGAGGGACCAGGAGAAGGGAGCCCCTTCGGATGGAAAGACATCAA GGAATGGTACGAGA”GCTGATGGGACATTGCACCTATTTTCCAGAAGAGCTGAGAAGCGTCAAGHACG C""ATAACGCAGATCTGTACAACGCCCTGAATGACCTGAACAACCTGG"CA"CACCAGGGA"GAA§EE NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAACGAGAAACTGGAATACTATGAGAAGTTCCAGAT CA”CGAAAACG”GT”TAAGCAGAAGAAAAAGCCTACACTGAAACAGAT”GCHAAGGAGATCCTGGTCA ACGAAGAGGACATCAAGGGCTACCGGGTGACAAGCAC"GGAAAACCAGAG""CACCAATCTGAAAGTG TA"CACGATA"TAAGGACATCACAGCACGGAAAGAAA"CATTGAGAACGCCGAAC"GCTGGATCAGAT TGCTAAGA”CC”GACTATCTACCAGAGCTCCGAGGACATCCAGGAAGAGC”GACTAACCTGAACAGCG AGCTGACCCAGGAAGAGATCGAACAGATTAGHAATC"GAAGGGGTACACCGGAACACACAACC"GHCC CTGAAAGC"A"CAATC"GATTCTGGATGAGC"GTGGCATACAAACGACAA"CAGA"TGCAATC"TT CCGGCTGAAGCTGGTCCCAAAAAAGGTGGACCTGAGTCAGCAGAAAGAGATCCCAACCACACTGGTGG ACGATTTCAHHCTG”CACCCGTGGTCAAGCGGAGCT"CATCCAGAGCATCAAAGHGATCAACGCCATC [i A"CAAGAAG"ACGGCC"GCCCAATGATATCA"TATCGAGCTGGCTAGGGAGAAGAACAGCAAGGACGC ~% ACAGAAGATGATCAATGAGATGCAGAAACGAAACCGGCAGACCAATGAACGCATTGAAGAGATTATCC in GAACTACCGGGAAAGAGAACGCAAAGTACCTGATTGAAAAAA"CAAGCTGCACGATATGCAGGAGGGA .ti.—‘ AAG"GTCTG"A"TCTC"GGAGGCCATCCCCC"GGAGGACCTGCTGAACAA"CCA”TCAACTACGAGGT O CGA"CATAT"ATCCCCAGAAGCG"GTCCT"CGACAAT"CCTT"AACAACAAGGTGC"GGTCAAGCAGG r—1 AAGAGAAC”CTAAAAAGGGCAAHAGGACTCC”TTCCAGTACC”GTCTAGT”CAGAT”CCAAGATCTCT °°. TACGAAACC"T”AAAAAGCACA""CTGAA"C”GGCCAAAGGAAAGGGCCGCATCAGCAAGACCAAAAA GGAGTACC"GC"GGAAGAGCGGGACATCAACAGATTC"CCG"CCAGAAGGATTTTA""AACCGGAATC ACACAAGATACGCTACTCGCGGCCTGATGAATCTGCTGCGATCCTATTTCCGGGTGAACAAT CTGGATGTGAAAGTCAAGTCCA”CAACGGCGGGTTCACATCHHTTCTGAGGCGCAAAHGGAAGTTTAA AAAGGAGCGCAACAAAGGGTACAAGCACCA"GCCGAAGATGC"CTGA”TA"CGCAAA"GCCGACTTCA TCTTTAAGGAGTGGAAAAAGCTGGACAAAGCCAAGAAAGTGATGGAGAACCAGATGTTCGAAGAGAAG GAATCHATGCCCGAAA"CGAGACAGAACAGGAGTACAAGGAGAT"TTCATCACTCCTCACCA GA"CAAGCATA"CAAGGAflTTCAAGGAC"ACAAG”ACTCTCACCGGG”GGATAAAAAGCCCAACAGAG AGC"GATCAA"GACACCCTGTA"AGTACAAGAAAAGACGATAAGGGGAATACCCTGATTGTGAACAAT CTGAACGGAC”GTACGACAAAGATAATGACAAGC”GAAAAAGC”GATCAACAAAAGTCCCGAGAAGC” GC"GATGTACCACCA"GA”CCTCAGACAmA"CAGAAACTGAAGCTGAHTATGGAGCAGTACGGCGACG ACCCACTGTA"AAGTACTATGAAGAGACTGGGAACTACCT ACCAAGTA"AGCAAAAAGGAT AATGGCCCCGTGATCAAGAAGATCAAGTACTATGGGAACAAGCTGAATGCCCATCTGGACATCACAGA CGATHACccmAACAG”CGCAACAAGGTGG”CAAGCTG”CACTGAAGCCATACAGA”TCGATG”CTATC TGGACAACGGCGTG”A"AAATT"G"GAC"G"CAAGAA"CTGGA"GT ATCAAAAAGGAGAAC"ACTAr1 GAAGTGAATAGCAAGTGCTACGAAGAGGCTAAAAAGCTGAAAAAGATTAGCAACCAGGCAGAGZ I CGCC”CCTTMTACAACAACGACCTGATTAAGATCAATGGCGAACTGTATAGGGTCATCGGGGMGAACA ATGA"CTGC"GAACCGCA"TGAAG"GAA"A"GAT”GACATCAC"TACCGAGAGTA"CTGGAAAACATG AATGATAAGCGCCCCCCTCGAATTATCAAAACAATTGCCTCTAAGACTCAGAGTA"CAAAAAG"ACTC AACCGACAT”CTGGGAAACCTGTA”GAGGTGAAGAGCAAAAAGCACCCTCAGATTATCAAAAAGGGC [SEQ ID NO:7] ATGAAAAGGAACTACATTCTGGGGCTGGACATCGGGATTACAAGCGTGGGGTATGGGATTATTGACTA TGAAACAAGGGACGTGATCGACGCAGGCGTCAGACTGTTCAAGGAGGCCAACGTGGAAAACAATGAGG GACGGAGAAGCAAGAGGGGAGCCAGGCGCCTGAAACGACGGAGAAGGCACAGAATCCAGAGGGTGAAG AAACTGCTGTTCGATTACAACCTGCTGACCGACCATTCTGAGCTGAGTGGAATTAATCCTTATGAAGC CAGGGTGAAAGGCCTGAGTCAGAAGCTGTCAGAGGAAGAGTTTTCCGCAGCTCTGCTGCACCTGGCTA ZX(3(I(3(3(I(3]\(3(3]\(311(3(3]XU1]\ZX(I(ST1(31%]X"3(31X(3(3"1(3(3]XZX(§Z\(§(3ZX(IZX(I(I(3(3(I]\ZX(I(EZX(3(IZ1(3"1(311}\(3]X]\Z\(3(3]XZX CAGATCTCACGCAATAGCAAAGCTCTGGAAGAGAAGTATGTCGCAGAGCTGCAGCTGGAACGGCTGAA GAAAGATGGCGAGGTGAGAGGGTCAATTAATAGGTTCAAGACAAGCGACTACGTCAAAGAAGCCAAGC AGCTGCTGAAAGTGCAGAAGGCTTACCACCAGCTGGATCAGAGCTTCATCGATACTTATATCGACCTG CTGGAGACTCGGAGAACCTACTATGAGGGACCAGGAGAAGGGAGCCCCTTCGGATGGAAAGACATCAA GTACGAGATGCTGATGGGACATTGCACCTATTTTCCAGAAGAGCTGAGAAGCGTCAAGTACG CTTATAACGCAGATCTGTACAACGCCCTGAATGACCTGAACAACCTGGTCATCACCAGGGATGAAAAC GAGAAACTGGAATACTATGAGAAGTTCCAGATCATCGAAAACGTGTTTAAGCAGAAGAAAAAGCCTAC ACTGAAACAGATTGCTAAGGAGATCCTGGTCAACGAAGAGGACATCAAGGGCTACCGGGTGACAAGCA CTGGAAAACCAGAGTTCACCAATCTGAAAGTGTATCACGATAT"1AAGGACATCACAGCACGGAAAGAA ATCATTGAGAACGCCGAACTGCTGGATCAGATTGCTAAGATCCTGACTATCTACCAGAGCTCCGAGGA CATCCAGGAAGAGCTGACTAACCTGNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAACAGCG AGCTGACCCAGGAAGAGATCGAACAGATTAGTAATCTGAAGGGGTACACCGGAACACACAACCTG CTGAAAGCTAT CAA"-1CTGATTCTGGATGAGCTGTGGCATACAAACGACAATCAGATTGCAATCTT " CCGGCTGAAGCTGGTCCCAAAAAAGGTGGACCTGAGTCAGCAGAAAGAGATCCCAACCACACTGGC \9 TCATTCTGTCACCCGTGGTCAAGCGGAGCTTCATCCAGAGCATCAAAGTGATCAACGCCATC z” ATCAAGAAGTACGGCCTGCCCAATGATATCATTATCGAGCTGGCTAGGGAGAAGAACAGCAAGGACGC (\l (I) ACAGAAGATGATCAATGAGATGCAGAAACGAAACCGGCAGACCAATGAACGCATTGAAGAGATTATCC E ”—1 GAACTACCGGGAAAGAGAACGCAAAGTACCTGATTGAAAAAATCAAGCTGCACGATATGCAGGAGGGA ’5 v—1 -—1 v—1 AAGTGTCTGTATTCTCTGGAGGCCATCCCCCTGGAGGACCTGCTGAACAATCCATTCAACTACGAGGT V) —1 0 CGATCATATTATCCCCAGAAGCGTGTCCTTCGACAATTCCTTTAACAACAAGGTGCTGGTCAAGCAGG DA m r—1 AAGAGAACTCTAAAAAGGGCAATAGGACTCCTTTCCAGTACCTGTCTAGTTCAGATTCCAAGATCTCT —1 TACGAAACCTTTAAAAAGCACATTCTGAATCTGGCCAAAGGAAAGGGCCGCATCAGCAAGACCAAAAA 0 GGAGTACCTGCTGGAAGAGCGGGACATCAACAGATTCTCCGTCCAGAAGGATTTTATTAACCGGAATC TGGTGGACACAAGATACGCTACTCGCGGCCTGAT CTGCTGCGATCCTATTTCCGGGTGAACAAT GTGAAAGTCAAGTCCATCAACGGCGGGTTCACATCTTTTCTGAGGCGCAAATGGAAGTTTAA AAAGGAGCGCAACAAAGGGTACAAGCACCATGCCGAAGATGCTCTGATTATCGCAAATGCCGACTTCA TCTTTAAGGAGTGGAAAAAGCTGGACAAAGCCAAGAAAGTGATGGAGAACCAGATGTTCGAAGAGAAG CAGGCCGAATCTATGCCCGAAATCGAGACAGAACAGGAGTACAAGGAGATTTTCATCACTCCTCACCA GATCAAGCATATCAAGGATTTCAAGGACTACAAGTACTCTCACCGGGTGGATAAAAAGCCCAACAGAG AGCTGATCAA"1GACACCCTGTATAGTACAAGAAAAGACGATAAGGGGAATACCCTGATTGTGAACAAT CTGAACGGACTGTACGACAAAGATAATGACAAGCTGAAAAAGCTGATCAACAAAAGTCCCGAGAAGCT GTACCACCATGATCCTCAGACATATCAGAAACTGAAGCTGATTATGGAGCAGTACGGCGACG AGAAGAACCCACTGTATAAGTACTATGAAGAGACTGGGAACTACCT ACCAAGTATAGCAAAAAGGAT AATGGCCCCGTGATCAAGAAGATCAAGTACTATGGGAACAAGCTGAATGCCCATCTGGACATCACAGA CGATTACCCTAACAGTCGCAACAAGGTGGTCAAGCTGTCACTGAAGCCATACAGATTCGATGTCTATC TGGACAACGGCGTGTATAAATTTGTGACTGTCAAGAATCTGGATGT ATCAAAAAGGAGAACTACTAT GAAGTGAATAGCAAGTGCTACGAAGAGGCTAAAAAGCTGAAAAAGATTAGCAACCAGGCAGAG'L 1 CGCCTCCTTTTACAACAACGACCTGATTAAGATCAATGGCGAACTGTATAGGGTCATCGGGGTGAACA ATGATCTGCTGAACCGCATTGAAGTGAATATGATTGACATCACTTACCGAGAGTATCTGGAAAACATG AATGATAAGCGCCCCCCTCGAATTATCAAAACAA'L1TGCCTCTAAGACTCAGAGTATCAAAAAGTACTC AACCGACATTCTGGGAAACCTGTATGAGGTGAAGAGCAAAAAGCACCCTCAGATTATCAAAAAGGGC [SEQ ID NO:8] AGGAACTACATTCTGGGGCTGGACATCGGGATTACAAGCGTGGGGTATGGGATTATTGACTA TGAAACAAGGGACGTGATCGACGCAGGCGTCAGACTGTTCAAGGAGGCCAACGTGGAAAACAATGAGG GACGGAGAAGCAAGAGGGGAGCCAGGCGCCTGAAACGACGGAGAAGGCACAGAATCCAGAGGGTGAAG AAACTGCTGTTCGATTACAACCTGCTGACCGACCATTCTGAGCTGAGTGGAATTAATCCTTATGAAGC CAGGGTGAAAGGCCTGAGTCAGAAGCTGTCAGAGGAAGAGTTTTCCGCAGCTCTGCTGCACCTGGCTA ZX(3(I(3(3(I(3]\(3(3]\(311(3(3]XU1]\ZX(I(ST1(31%]X"3(31X(3(3"1(3(3]XZX(§Z\(§(3ZX(IZX(I(I(3(3(I]\ZX(I(EZX(3(IZ1(3"1(311}\(3]X]\Z\(3(3]XZX CAGATCTCACGCAATAGCAAAGCTCTGGAAGAGAAGTATGTCGCAGAGCTGCAGCTGGAACGGCTGAA GAAAGATGGCGAGGTGAGAGGGTCAATTAATAGGTTCAAGACAAGCGACTACGTCAAAGAAGCCAAGC AGCTGCTGAAAGTGCAGAAGGCTTACCACCAGCTGGATCAGAGCTTCATCGATACTTATATCGACCTG CTGGAGACTCGGAGAACCTACTATGAGGGACCAGGAGAAGGGAGCCCCTTCGGATGGAAAGACATCAA GGAATGGTACGAGATGCTGATGGGACATTGCACCTATTTTCCAGAAGAGCTGAGAAGCGTCAAGTACG CTTATAACGCAGATCTGTACAACGCCCTGAATGACCTGAACAACCTGGTCATCACCAGGGATGAAAAC CTGGAATACTATGAGAAGTTCCAGATCATCGAAAACGTGTTTAAGCAGAAGAAAAAGCCTAC ACTGAAACAGATTGCTAAGGAGATCCTGGTCAACGAAGAGGACATCAAGGGCTACCGGGTGACAAGCA CTGGAAAACCAGAGTTCACCAATCTGAAAGTGTATCACGATAT"1AAGGACATCACAGCACGGAAAGAA ATCATTGAGAACGCCGAACTGCTGGATCAGATTGCTAAGATCCTGACTATCTACCAGAGCTCCGAGGA GGAAGAGCTGACTAACCTGAACAGCGAGCTGACCCAGGAAGAGATCGAACAGATTAGTAATC TGAAGGGGTACACCGGAACACACAACCTGTCCCTGAAAGCTATCAATCTGATTCTGGATGAGCTGTGG CATACAAACGACAATCAGATTGCAATCTTTAACCGGCTGAAGCTGGTCCCAAAAAAGGTGGACCTGAG TCAGCAGAAAGAGATCCCAACCACACTGGTGGACGATTTCATTCTGTCACCCGTGGTCAAGCGGAGCT m TCATCCAGAGCATCAAAGTGATCAACGCCATCATCAAGAAGTACGGCCTGCCCAATGATATCATTATC N GAGCTGGCTAGGGAGAAGAACAGCAAGGACGCACAGAAGATGATCAATGAGATGCAGAAACGAAACCG % GCAGACCAATGAACGCATTGAAGAGATTATCCGAACTACCGGGAAAGAGAACGCAAAGTACCTGATTG ”K: AAAAAATCAAGCTGCACGATATGCAGGAGGGAAAGTGTCTGTATTCTCTGGAGGCCATCCCCCTGGAG as GACCTGCTGAACAATCCATTCAACTACGAGGTCGATCATATTATCCCCAGAAGCGTGTCCTTCGACAA o TTCCTTTAACAACAAGGTGCTGGTCAAGCAGGAAGAGAACTCTAAAAAGGGCAA"1AGGACTCCTTTCC I—1 AGTACCTGTCTAGTTCAGATTCCAAGATCTCTTACGAAACCTTTAAAAAGCACATTCTGAATCTGGCC N. AAAGGAAAGGGCCGCATCAGCAAGACCAAAAAGGAGTACCTGCTGGAAGAGCGGGACATCAACAGATT O CTCCGTCCAGAAGGATTTTATTAACCGGAATCTGGTGGACACAAGATACGCTACTCGCGGCCTGATGA ATCTGCTGCGATCCTATTC TGTGAAAGTCAAGTCCATCAACGGCGGGTTC ACATCTTTTCTGAGGCGCAAA GGAGCGCAACAAAGGGTACAAGCACCATGCCGA AGATGCTCTGATTATCGCAAATGCCGAC"1CATCTTTAAGGAGTGGAAAAAGCTGGACAAAGCCAAGA AAGTGATGGAGAACCAGATGT-TCGAAGAGAAGCAGNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN EEEGCCGAATCTATGCCCGAAATCGAGACAGAACAGGAGTACAAGGAGATTTTCATCACTCCTCACCA GATCAAGCATATCAAGGATTTCAAGGACTACAAGTACTCTCACCGGGTGGATAAAAAGCCCAACAGAG AGCTGATCAA"1GACACCCTGTATAGTACAAGAAAAGACGATAAGGGGAATACCCTGATTGTGAACAAT CTGAACGGACTGTACGACAAAGATAATGACAAGCTGAAAAAGCTGATCAACAAAAGTCCCGAGAAGCT GCTGATGTACCACCATGATCCTCAGACATATCAGAAACTGAAGCTGATTATGGAGCAGTACGGCGACG AGAAGAACCCACTGTATAAGTACTATGAAGAGACTGGGAACTACCT ACCAAGTATAGCAAAAAGGAT AATGGCCCCGTGATCAAGAAGATCAAGTACTATGGGAACAAGCTGAATGCCCATCTGGACATCACAGA CGATTACCCTAACAGTCGCAACAAGGTGGTCAAGCTGTCACTGAAGCCATACAGATTCGATGTCTATC TGGACAACGGCGTGTATAAATTTGTGACTGTCAAGAATCTGGATGT ATCAAAAAGGAGAACTACTAT GAAGTGAATAGCAAGTGCTACGAAGAGGCTAAAAAGCTGAAAAAGATTAGCAACCAGGCAGAG". 1 CGCCTCCTTTTACAACAACGACCTGATTAAGATCAATGGCGAACTGTATAGGGTCATCGGGGTGAACA ATGATCTGCTGAACCGCATTGAAGTGAATATGATTGACATCACTTACCGAGAGTATCTGGAAAACATG AATGATAAGCGCCCCCCTCGAATTATCAAAACAA"1TGCCTCTAAGACTCAGAGTATCAAAAAGTACTC AACCGACATTCTGGGAAACCTGTATGAGGTGAAGAGCAAAAAGCACCCTCAGATTATCAAAAAGGGC [SEQ ID NO:9] ATGGGACCGAAGAAAAAGCGCAAGGTCGAAGCGTCCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAT GAACTACATTCTGGGGCTGGACATCGGGATTACAAGCGTGGGGTATGGGATTATTGACTATG AAACAAGGGACGTGATCGACGCAGGCGTCAGACTGTTCAAGGAGGCCAACGTGGAAAACAATGAGGGA CGGAGAAGCAAGAGGGGAGCCAGGCGCCTGAAACGACGGAGAAGGCACAGAATCCAGAGGGTGAAGAA GTTCGATTACAACCTGCTGACCGACCATTCTGAGCTGAGTGGAATTAA“CCTTATGAAGCCA GGGTGAAAGGCCTGAGTCAGAAGCTGTCAGAGGAAGAGTTTTCCGCAGCTCTGCTGCACCTGGCTAAG GGAGTGCATAACGTCAA_ 3GGAAGAGGACACCGGCAACGAGCTGTCTACAAAGGAACA GA“C”CACGCAATAGCAAAGCTCTGGAAGAGAAGTATGTCGCAGAGCTGCAGCTGGAACGGCTGAAGA AAGATGGCGAGGTGAGAGGGTCAA"1T-AA" .1T CAAGACAAGCGACTACGTCAAAGAAGCCAAGCAG CTGCTGAAAGTGCAGAAGGCTTACCACCAGCTGGATCAGAGCTTCATCGATACTTATATCGACCTGCT GGAGACTCGGAGAACCTACTATGAGGGACCAGGAGAAGGGAGCCCCTTCGGATGGAAAGACATCAAGG AATGGTACGAGATGCTGATGGGACATTGCACCTATTTTCCAGAAGAGCTGAGAAGCGTCAAGTACGCT TATAACGCAGATCTGTACAACGCCCTGAATGACCTGAACAACCTGGTCATCACCAGGGATGAAAACGA GGAATACTATGAGAAGTTCCAGATCATCGAAAACGTGTTTAAGCAGAAGAAAAAGCCTACAC TGAAACAGATTGCTAAGGAGATCCTGGTCAACGAAGAGGACATCAAGGGCTACCGGGTGACAAGCACT GGAAAACCAGAGTTCACCAATCTGAAAGTGTATCACGATATTAAGGACATCACAGCACGGAAAGAAAT CATTGAGAACGCCGAACTGCTGGATCAGATTGCTAAGATCCTGACTATCTACCAGAGCTCCGAGGACA TCCAGGAAGAGCTGACTAACCTGAACAGCGAGCTGACCCAGGAAGAGATCGAACAGATTAGTAATCTG AAGGGGTACACCGGAACACACAACCTGTCCCTGAAAGCTATCAATCTGATTCTGGATGAGCTGTGGCA TACAAACGACAA".1CAGATTGCAATCTTTAACCGGCTGAAGCT GG".1CCCAAAAAAGGTGGACCTGAGTC AGCAGAAAGAGATCCCAACCACACTGGTGGACGATTTCATTCTGTCACCCGTGGTCAAGCGGAGCTTC ATCCAGAGCATCAAAGTGATCAACGCCATCATCAAGAAGTACGGCCTGCCCAATGATATCATTATCGA [—‘ GCTGGCTAGGGAGAAGAACAGCAAGGACGCACAGAAGATGATCAATGAGATGCAGAAACGAAACCGGC ATGAACGCATTGAAGAGATTATCCGAACTACCGGGAAAGAGAACGCAAAGTACCTGATTGAA o AAAA" 1GCACG TATGCAGGAGGGAAAGTGTCTGTATTCTCTGGAGGCCATCCCCCTGGAGGA '51 CCTGCTGAACAA".1CCAT "1CAACTACGAGGTCGATCATATTATCCCCAGAAGCGTGTCCTTCGACAATT c.- CCTTTAACAACAAGGTGCTGGTCAAGCAGGAAGAGAACTCTAAAAAGGGCAATAGGACTCCTTTCCAG TACCTGTCTAGTTCAGATTCCAAGATCTCTTACGAAACCTTTAAAAAGCACATTCTGAATCTGGCCAA AGGAAAGGGCCGCATCAGCAAGACCAAAAAGGAGTACCTGCTGGAAGAGCGGGACATCAACAGATTCT CCGTCCAGAAGGA TTTATTAACCGGAATCTGGTGGACACAAGATACGCTACTCGCGGCCTGATGAAT CTGCTGCGATCCTATTTCCGGGTGAACAA"1CTGGATGTGAAAGTCAAGTCCATCAACGGCGGGTTCAC ATCTTTTCTGAGGCGCAAATGGAAGTTTAAAAAGGAGCGCAACAAAGGGTACAAGCACCATGCCGAAG ATGCTCTGATTATCGCAAATGCCGACTTCATCTTTAAGGAGTGGAAAAAGCTGGACAAAGCCAAGAAA GTGATGGAGAACCAGATGTTCGAAGAGAAGCAGGCCGAATCTATGCCCGAAATCGAGACAGAACAGGA GTACAAGGAGATTTTCATCACTCCTCACCAGATCAAGCATATCAAGGATTTCAAGGACTACAAGTACT CTCACCGGGTGGATAAAAAGCCCAACAGAGAGCTGATCAA"1GACACCCTGTATAGTACAAGAAAAGAC GATAAGGGGAATACCCTGATTGTGAACAATCTGAACGGACTGTACGACAAAGATAATGACAAGCTGAA GATCAACAAAAGTCCCGAGAAGCTGCTGATGTACCACCATGATCCTCAGACATATCAGAAAC TGAAGCTGATTATGGAGCAGTACGGCGACGAGAAGAACCCACTGTATAAGTACTATGAAGAGACTGGG AACTACCT ACCAAGTATAGCAAAAAGGATAA"-1GGCCCCGT ATCAAGAAGATCAAGTACTATGGGAA CAAGCTGAATGCCCATCTGGACATCACAGACGATTACCCTAACAGTCGCAACAAGGTGGTCAAGCTGT CACTGAAGCCATACAGATTCGATGTCTATCTGGACAACGGCGTGTATAAATTTGTGACTGTCAAGAAT CTGGATGTCATCAAAAAGGAGAACTACTATGAAGTGAATAGCAAGTGCTACGAAGAGGCTAAAAAGCT GAAAAAGATTAGCAACCAGGCAGAGTTCATCGCCTCCTTTTACAACAACGACCTGATTAAGATCAATG GCGAACTGTATAGGGTCATCGGGGTGAACAATGATCTGCTGAACCGCATTGAAGTGAATATGATTGAC ATCACTTACCGAGAGTATCTGGAAAACATGAATGATAAGCGCCCCCCTCGAATTATCAAAACAATTGC CTCTAAGACTCAGAGTATCAAAAAGTACTCAACCGACATTCTGGGAAACCTGTATGAGGTGAAGAGCA AAAAGCACCCTCAGATTATCAAAAAGGGC [SEQ ID NO:11] In certain embodiments, the RNA-guided nuclease is Cpf1. In certain embodiments, the amino acid sequence of a Cpf1 protein is set forth in SEQ ID NO: 13.

In certain embodiments, the Cpr protein can comprise an insertion such as a G insertion. In certain embodiments, the insertion (relative to SEQ ID NO: 13) is positioned between amino acid positions 147 and 148, anywhere between amino acid positions 484 and 492, anywhere between amino acid positions 568 and 590, anywhere between amino acid positions 795 and 855, anywhere between amino acid positions 1131 and 1140, or anywhere between amino acid positions 1160 and 1173. In certain embodiments, the insertion is positioned at or near the N-terminus of a Cpfl peptide. In certain embodiments, the amino acid sequence of the Cpf1 protein comprising the insertion has at least 95% sequence identity (e. g. 95%, 96%, 97%, 98%, 99% or greater identity) to SEQ ID NO: 13.

MTQFEGFINLYQVSKTLRFELIPQGKTLKHIQEQGFIEEDKARNDHYKEL KPIIDRIYKTYADQCLQLVQLDWENLSAAIDSYRKEKTEETRNALIEEQATYRNA IHDYFIGRTDNLTDAINKRHAEIYKGLFKAELFNGKVLKQLGTVTTTEHENALLR SFDKFTTYFSGFYENRKNVFSAEDISTAIPHRIVQDNFPKFKENCHIFTRLITAVPS LREHFENVKKAIGIFVSTSIEEVFSFPFYNQLLTQTQIDLYNQLLGGISREAGTEKI KGLNEVLNLAIQKNDETAHIIASLPHRFIPLFKQILSDRNTLSFILEEFKSDEEVIQS FCKYKTLLRNENVLETAEALFNELNS[DLTHIFISHKKLETISSALCDHWDTLRNA LYERRISELTGKITKSAKEKVQRSLKHEDINLQEIISAAGKELSEAFKQKTSEILSH AHAALDQPLPTTLKKQEEKEILKSQLDSLLGLYHLLDWFAVDESNEVDPEFSAR LTGIKLEMEPSLSFYNKARNYATKKPYSVEKFKLNFQMPTLASGWDVNKEKNN GAILFVKNGLYYLGIMPKQKGRYKALSFEPTEKTSEGFDKMYYDYFPDAAKMIP KCSTQLKAVTAHFQTHTTPILLSNNFIEPLEITKEIYDLNNPEKEPKKFQTAYAKK 2O TGDQKGYREALCKWIDFTRDFLSKYTKTTSIDLSSLRPSSQYKDLGEYYAELNPL LYHISFQRIAEKEIMDAVETGKLYLFQIYNKDFAKGHHGKPNLHTLYWTGLFSPE IKLNGQAELFYRPKSRMKRMAHRLGEKMLNKKLKDQKTPIPDTLYQE HRLSHDLSDEARALLPNVITKEVSHEIIKDRRFTSDKFFFHVPITLNYQA ANSPSKFNQRVNAYLKEHPETPIIGIDRGERNLIYITVIDSTGKILEQRSLNTIQQFD NREKERVAARQAWSVVGTIKDLKQGYLSQVIHEIVDLMIHYQAVVVL FKSKRTGIAEKAVYQQFEKMLIDKLNCLVLKDYPAEKVGGVLNPYQL TDQFTSFAKMGTQSGFLFYVPAPYTSKIDPLTGFVDPFVWKTIKNHESRKHFLEG FDFLHYDVKTGDFILHFKMNRNLSFQRGLPGFMPAWDIVFEKNETQFDAKGTPF IAGKRIVPVIENHRFTGRYRDLYPANELIALLEEKGIVFRDGSNILPKLLENDDSH AIDTMVALIRSVLQMRNSNAATGEDYINSPVRDLNGVCFDSRFQNPEWPIVHDAD ANGAYHIALKGQLLLNHLKESKDLKLQNGISNQDWLAYIQELRN [SEQ ID NO: In certain embodiments, an isolated c acid sequence encoding a Cpfl protein is set forth in SEQ ID NO: 14. In certain embodiments, the isolated Cpf1 nucleic acid can comprise an insertion such as an N24-36 insertion. In certain embodiments, the insertion (relative to SEQ ID NO: 14) is positioned between nucleic acid positions 441 and 442, anywhere between nucleic acid positions 1452 and 1474, anywhere between nucleic acid positions 1704 and 1768, anywhere between nucleic acid positions 2385 and 2563, anywhere between nucleic acid ons 3393 and 3418, or anywhere between nucleic acid positions 3480 and 3517. In certain embodiments, the insertion does not alter the reading frame of the ed Cpfl nucleic acid. In certain embodiments, the insertion is positioned at or near the N—terminus of a Cpf1 peptide. In certain embodiments, the nucleic acid sequence of the Cpf1 protein sing the insertion has at least 95% (e. g. 95%, 96%, 97%, 98%, 99% or greater identity) sequence identity to SEQ ID NO: 14. ed nucleic acids according to this aspect of this disclosure are optionally incorporated into vectors such as plasmids, viral vectors, naked DNA vectors, etc. In some instances, an adeno-associated virus (AAV) vector orates isolated nucleic acids according to this aspect of the sure. In n embodiments, a target site for the gRNA is within the vector backbone. The vectors can be used to alter both a cellular endogenous target gene and the RNA-guided nuclease expression.

ATGACACAGTTCGAGGGCTTTACCAACCTGTATCAGGTGAGCAAGAC 2O ACTGCGGTTTGAGCTGATCCCACAGGGCAAGACCCTGAAGCACATCCAGGA GCAGGGCTTCATCGAGGAGGACAAGGCCCGCAATGATCACTACAAGGAGCT GAAGCCCATCATCGATCGGATCTACAAGACCTATGCCGACCAGTGCCTGCAG CTGGTGCAGCTGGATTGGGAGAACCTGAGCGCCGCCATCGACTCCTATAGAA AGGAGAAAACCGAGGAGACAAGGAACGCCCTGATCGAGGAGCAGGCCACA TATCGCAATGCCATCCACGACTACTTCATCGGCCGGACAGACAACCTGACCG ATGCCATCAATAAGAGACACGCCGAGATCTACAAGGGCCTGTTCAAGGCCG TTAATGGCAAGGTGCTGAAGCAGCTGGGCACCGTGACCACAACCG AGCACGAGAACGCCCTGCTGCGGAGCTTCGACAAGTTTACAACCTACTTCTC CGGCTTTTATGAGAACAGGAAGAACGTGTTCAGCGCCGAGGATATCAGCAC AGCCATCCCACACCGCATCGTGCAGGACAACTTCCCCAAGTTTAAGGAGAAT TGTCACATCTTCACACGCCTGATCACCGCCGTGCCCAGCCTGCGGGAGCACT TTGAGAACGTGAAGAAGGCCATCGGCATCTTCGTGAGCACCTCCATCGAGGA GGTGTTTTCCTTCCCTTTTTATAACCAGCTGCTGACACAGACCCAGATCGACC TGTATAACCAGCTGCTGGGAGGAATCTCTCGGGAGGCAGGCACCGAGAAGA TCAAGGGCCTGAACGAGGTGCTGAATCTGGCCATCCAGAAGAATGATGAGA CAGCCCACATCATCGCCTCCCTGCCACACAGATTCATCCCCCTGTTTAAGCAG ATCCTGTCCGATAGGAACACCCTGTCTTTCATCCTGGAGGAGTTTAAGAGCG ACGAGGAAGTGATCCAGTCCTTCTGCAAGTACAAGACACTGCTGAGAAACG AGAACGTGCTGGAGACAGCCGAGGCCCTGTTTAACGAGCTGAACAGCATCG ACCTGACACACATCTTCATCAGCCACAAGAAGCTGGAGACAATCAGCAGCG CCCTGTGCGACCACTGGGATACACTGAGGAATGCCCTGTATGAGCGGAGAAT CTCCGAGCTGACAGGCAAGATCACCAAGTCTGCCAAGGAGAAGGTGCAGCG CAGCCTGAAGCACGAGGATATCAACCTGCAGGAGATCATCTCTGCCGCAGGC CTGAGCGAGGCCTTCAAGCAGAAAACCAGCGAGATCCTGTCCCAC GCACACGCCGCCCTGGATCAGCCACTGCCTACAACCCTGAAGAAGCAGGAG GAGAAGGAGATCCTGAAGTCTCAGCTGGACAGCCTGCTGGGCCTGTACCACC ACTGGTTTGCCGTGGATGAGTCCAACGAGGTGGACCCCGAGTTCTC TGCCCGGCTGACCGGCATCAAGCTGGAGATGGAGCCTTCTCTGAGCTTCTAC AACAAGGCCAGAAATTATGCCACCAAGAAGCCCTACTCCGTGGAGAAGTTC AAGCTGAACTTTCAGATGCCTACACTGGCCTCTGGCTGGGACGTGAATAAGG AGAAGAACAATGGCGCCATCCTGTTTGTGAAGAACGGCCTGTACTATCTGGG CATCATGCCAAAGCAGAAGGGCAGGTATAAGGCCCTGAGCTTCGAGCCCAC AGAGAAAACCAGCGAGGGCTTTGATAAGATGTACTATGACTACTTCCCTGAT GCCGCCAAGATGATCCCAAAGTGCAGCACCCAGCTGAAGGCCGTGACAGCC CACTTTCAGACCCACACAACCCCCATCCTGCTGTCCAACAATTTCATCGAGCC TCTGGAGATCACAAAGGAGATCTACGACCTGAACAATCCTGAGAAGGAGCC AAAGAAGTTTCAGACAGCCTACGCCAAGAAAACCGGCGACCAGAAGGGCTA CAGAGAGGCCCTGTGCAAGTGGATCGACTTCACAAGGGATTTTCTGTCCAAG TATACCAAGACAACCTCTATCGATCTGTCTAGCCTGCGGCCATCCTCTCAGTA TAAGGACCTGGGCGAGTACTATGCCGAGCTGAATCCCCTGCTGTACCACATC AGCTTCCAGAGAATCGCCGAGAAGGAGATCATGGATGCCGTGGAGACAGGC AAGCTGTACCTGTTCCAGATCTATAACAAGGACTTTGCCAAGGGCCACCACG GCAAGCCTAATCTGCACACACTGTATTGGACCGGCCTGTTTTCTCCAGAGAA CCTGGCCAAGACAAGCATCAAGCTGAATGGCCAGGCCGAGCTGTTCTACCGC CCTAAGTCCAGGATGAAGAGGATGGCACACCGGCTGGGAGAGAAGATGCTG AACAAGAAGCTGAAGGATCAGAAAACCCCAATCCCCGACACCCTGTACCAG GAGCTGTACGACTATGTGAATCACAGACTGTCCCACGACCTGTCTGATGAGG CCAGGGCCCTGCTGCCCAACGTGATCACCAAGGAGGTGTCTCACGAGATCAT CAAGGATAGGCGCTTTACCAGCGACAAGTTCTTTTTCCACGTGCCTATCACA CTGAACTATCAGGCCGCCAATTCCCCATCTAAGTTCAACCAGAGGGTGAATG TGAAGGAGCACCCCGAGACACCTATCATCGGCATCGATCGGGGCGA GAGAAACCTGATCTATATCACAGTGATCGACTCCACCGGCAAGATCCTGGAG CAGCGGAGCCTGAACACCATCCAGCAGTTTGATTACCAGAAGAAGCTGGAC AACAGGGAGAAGGAGAGGGTGGCAGCAAGGCAGGCCTGGTCTGTGGTGGGC ACAATCAAGGATCTGAAGCAGGGCTATCTGAGCCAGGTCATCCACGAGATC GTGGACCTGATGATCCACTACCAGGCCGTGGTGGTGCTGGCGAACCTGAATT TCGGCTTTAAGAGCAAGAGGACCGGCATCGCCGAGAAGGCCGTGTACCAGC AGTTCGAGAAGATGCTGATCGATAAGCTGAATTGCCTGGTGCTGAAGGACTA TCCAGCAGAGAAAGTGGGAGGCGTGCTGAACCCATACCAGCTGACAGACCA GTTCACCTCCTTTGCCAAGATGGGCACCCAGTCTGGCTTCCTGTTTTACGTGC CTGCCCCATATACATCTAAGATCGATCCCCTGACCGGCTTCGTGGACCCCTTC GTGTGGAAAACCATCAAGAATCACGAGAGCCGCAAGCACTTCCTGGAGGGC TTCGACTTTCTGCACTACGACGTGAAAACCGGCGACTTCATCCTGCACTTTAA GATGAACAGAAATCTGTCCTTCCAGAGGGGCCTGCCCGGCTTTATGCCTGCA TGGGATATCGTGTTCGAGAAGAACGAGACACAGTTTGACGCCAAGGGCACC CCTTTCATCGCCGGCAAGAGAATCGTGCCAGTGATCGAGAATCACAGATTCA CCGGCAGATACCGGGACCTGTATCCTGCCAACGAGCTGATCGCCCTGCTGGA GGAGAAGGGCATCGTGTTCAGGGATGGCTCCAACATCCTGCCAAAGCTGCTG GAGAATGACGATTCTCACGCCATCGACACCATGGTGGCCCTGATCCGCAGCG TGCTGCAGATGCGGAACTCCAATGCCGCCACAGGCGAGGACTATATCAACA GCCCCGTGCGCGATCTGAATGGCGTGTGCTTCGACTCCCGGTTTCAGAACCC AGAGTGGCCCATGGACGCCGATGCCAATGGCGCCTACCACATCGCCCTGAAG GGCCAGCTGCTGCTGAATCACCTGAAGGAGAGCAAGGATCTGAAGCTGCAG AACGGCATCTCCAATCAGGACTGGCTGGCCTACATCCAGGAGCTGCGCAAC SEQHDNOJA] Skilled artisans will be aware that the exemplary sequences presented herein may 3O be modified in ways that do not affect the ing ples of the genome editing systems they embody. Accordingly, modified nucleotide or amino acid sequences that are ted, fused to other sequences, or otherwise modified to have >50%, >60%, >7096,>8096,>8596,>9096,>9196,>9296,>9396,>9496,>9596,>9696,>9796,>9896or >99% sequence identity relative to the sequences presented herein are within the scope of this sure. So too are amino acid or nucleic acid sequences differing by l, 2, 3, 4, , 6, 7, 8, 9, 10, 15, 20 or more residues from the sequences presented herein.

Turning next to the selection of s that will minimize disruption of nuclease structure, many of the inserts within the scope of this sure have been ered to satisfy one or more of the following requirements: (i) the insert includes, at its 3’ and 5’ ends, 3-nucleotide codons for e or another small, flexible residue (e. g., alanine or valine), and encodes an amino acid sequence such as: G G, where “X” denotes any amino acid, subject to the constraints set forth here, (ii) the insert does not introduce a stop codon, splice donor or acceptor, or other undesirable domain in the coding sequence; (iii) X is characterized by a hydrophilicity or hydrophobicity that will not disrupt the folding of the engineered protein or its final structure (e.g. phenylalanine), and (iv) X is not bulky (e.g. tryptophan), and is not a cysteine, proline or other amino acid that could disrupt the structure of the Cas9 by introducing a bend or causing steric interference with the surrounding protein, forming a sulfur bridge, etc.

In certain cases, inserts according to this disclosure can be generated according to the following tic: 1. For a target site (protospacer and PAM) within a cellular gene target of interest, identify all possible amino acid sequences that may be d by the target site sequence in all six possible reading frames; 2. Discard any nucleotide sequence reading frames that do not meet the design criteria set forth above (e.g., that encode a stop codon, or that encode peptides that would likely disrupt the structure of the nding protein due to hydrophobicity, bulk, etc; 3. For each nucleotide sequence that is not ded in step 2, a. add glycine codons to the 3’ and 5’ ends of the target site, b. if necessary, insert on the 5’ end of the sequence between the glycine codon and the target site, one or two nucleotides to shift the target site sequence into a desired reading frame, and c. if necessary, insert, on the 3’ end of the sequence n the target site and the glycine codon, one or two nucleotides to keep the 3’ glycine codon and the subsequent peptide sequence in frame.

It should be noted that the inserts of the present disclosure are broadly compatible with RNA—guided nucleases, including without limitation Cas9, Cpfl, and other Class 2 nucleases and the various orthologs thereof, and nucleic acids ng the same. In certain embodiments, the ided nuclease is Cas9. In certain embodiments, the RNA-guided nuclease is Cpfl. While certain examples of this disclosure focus on the use of inserts to regulate expression of S. aureus Cas9, the skilled artisan will appreciate that an insert of this disclosure may be adapted for use with other nucleases or orthologs.

By way of example, an insert may be d for use in another nuclease or ortholog by (i) selecting an appropriate target site comprising a PAM sequence recognized by the nuclease or ortholog, and (ii) selecting an insertion site that is within a peptide loop that is (a) located on a surface of the nuclease protein, and/or (b) predicted to tolerate the insertion of the insert without alterations in folding or structure.

In use, the engineered nucleic acids ing to this disclosure simultaneously provide a template for transcription and sion of genome editing system components and a substrate for cleavage or other editing by genome editing systems once expressed. In many (though not arily all) embodiments, cleavage of the engineered nucleic acid decreases or eliminates expression of one or more genome editing system components encoded by the engineered nucleic acid. Alternatively, or additionally, cleavage of the engineered nucleic acids can result in the formation of indel mutations that decrease the function of the genome editing system components These outcomes, in turn, can provide a temporal limit to the genome editing activity caused by delivery of the ered nucleic acids as compared to non-engineered nucleotides encoding similar components. For e, where a nucleic acid vector encoding a RNA-guided nuclease and gRNA under the l of constitutive promoters would be expected to drive ongoing, constitutive genome editing ty, the inclusion of an ogRNA target site in the same vector (whether in the backbone or the RNA-guided nuclease coding sequence) will result in a limited period of high expression of system components and a transient peak in genome editing activity, which will decrease as copies of the vector within each cell are cleaved and inactivated, over a period of hours, days, or weeks. It will be clear to the d artisan that temporal tion of genome editing activity using the transiently active genome editing systems bed herein can be advantageous in certain settings, for ce to limit the potential for off-target cutting, or to limit any potential ar response to the genome editing system components.

In certain embodiments, the activity of the RNA-guided nuclease can be modulated via the nature of the ogRNA target ce inserted into either the vector backbone or the RNA-guided nuclease coding sequence. For example, if the ogRNA target sequence comprises a consensus PAM ce, the RNA-guided nuclease will edit the nucleic acid encoding the RNA-guided nuclease at a higher efficiency than a target ce comprising a sub—optimal PAM. Accordingly, if a consensus PAM sequence is employed, expression of the RNA-guided nuclease will reflect a burst dose, while if a sub-optimal PAM sequence is employed, sion of the RNA—guided nuclease will reflect an extended dose. Exemplary consensus and sub-optimal PAM sequences for S. aureus Cas9 are listed in Table 5.

Table 5: Consensus and sub-optimal S. aureus Cas9 PAM sequences HYRV Sub-optimal PAM — substitution ofH for G, Rl, V for T HRYV Sub-optimal PAM — substitution ofH for G, R2, V for T HYYV timal PAM — substitution ofH for G, R1, R2, V for T This overview has focused on a handful of exemplary embodiments that rate the principles of certain engineered nucleic acid vectors and engineered RNA—guided nucleases. For clarity, however, this disclosure encompasses modifications and variations that will be evident to those of skill in the art. For example, editing of the nucleic acid encoding the RNA-guided se and the nuclei acid encoding the cellular endogenous target gene, as described herein, can be simultaneous or concomitant, however there is not necessarily a temporal restriction of such editing. With that in mind, the following disclosure is intended to illustrate the operating principles of genome editing systems more generally. What follows should not be understood as limiting, but rather illustrative of certain ples of genome editing systems, which, in combination with the instant disclosure, will inform those of skill in the art about onal implementations of and modifications that are within the scope of this disclosure.

Genome g systems The term “genome editing system” refers to any system having RNA-guided DNA editing activity. Genome editing systems of the present disclosure e at least two components adapted from naturally ing CRISPR systems: a guide RNA (gRNA) and an ided nuclease. These two ents form a complex that is capable of associating with a specific nucleic acid sequence and editing the DNA in or around that nucleic acid sequence, for instance by making one or more of a single strand break (an SSB or nick), a double strand break (a DSB) and/or a point mutation. In certain embodiments, the genome editing system is a transiently active genome editing system. In certain embodiments, the genome g system can alter both a cellular endogenous target gene and the RNA-guided-nuclease expression. In certain ments, the gRNA/RNA-guided se complex can cleave both the c acid encoding the RNA-guided nuclease and the nucleic acid encoding the cellular 2O endogenous target gene.

Naturally occurring CRISPR systems are organized evolutionarily into two classes and five types (Makarova et al. Nat Rev Microbiol. 2011 Jun, 9(6): 467—477 (Makarova), incorporated by reference herein), and while genome editing s of the present disclosure may adapt components of any type or class of naturally occurring CRISPR system, the embodiments presented herein are generally adapted from Class 2, and type II or V CRISPR systems. Class 2 systems, which encompass types 11 and V, are characterized by relatively large, multidomain RNA-gmided se proteins (e.g., Cas9 or Cpfl) and one or more guide RNAs (e.g, a chNA and, optionally, a trachNA) that form ribonucleoprotein (RNP) complexes that associate with (i.e. target) and cleave specific loci complementary to a targeting (or spacer) sequence of the chNA. Genome editing systems according to the present disclosure similarly target and edit cellular DNA sequences, but differ significantly from CRISPR systems occurring in nature. For example, the unimolecular guide RNAs described herein do not occur in nature, and both guide RNAs and RNA-guided nucleases according to this disclosure may incorporate any number of non-naturally occurring modifications.

Genome editing systems can be implemented (e. g. administered or delivered to a cell or a t) in a variety of ways, and different implementations may be suitable for distinct applications. For instance, a genome editing system is implemented, in n embodiments, as a protein/RNA complex (a ribonucleoprotein, or RNP), which can be ed in a pharmaceutical composition that ally includes a pharmaceutically acceptable carrier and/or an encapsulating agent, such as a lipid or polymer micro- or nano-particle, micelle, liposome, etc. In certain embodiments, a genome editing system is implemented as one or more nucleic acids encoding the RNA-guided nuclease and guide RNA components described above (optionally with one or more additional components); in certain embodiments, the genome editing system is implemented as one or more vectors comprising such nucleic acids, for instance a viral vector such as an adeno-associated virus; and in certain embodiments, the genome editing system is implemented as a combination of any of the foregoing. Additional or modified implementations that operate ing to the ples set forth herein will be nt to the skilled artisan and are within the scope of this disclosure.

It should be noted that the genome editing systems of the present disclosure can be targeted to a single specific nucleotide sequence, or may be targeted to — and capable of editing in parallel — two or more specific nucleotide sequences through the use of two or more guide RNAs. The use of multiple gRNAs is referred to as “multiplexing” throughout this sure, and can be employed to target multiple, unrelated target sequences of st, or to form le SSBs or DSBs within a single target domain and, in some cases, to generate specific edits within such target domain. For example, International Patent Publication No. is incorporated by reference herein, bes a genome g system for correcting a point mutation (C.2991+l655A to G) in the human CEP29O gene that results in the creation of a cryptic splice site, which in turn reduces or eliminates the function of the 3O gene. The genome editing system of Maeder utilizes two guide RNAs targeted to sequences on either side of (i.e. g) the point mutation, and forms DSBs that flank the mutation. This, in turn, promotes deletion of the intervening sequence, including the mutation, y eliminating the cryptic splice site and restoring normal gene function.

As another example, Ramusino”), incorporated by reference herein, describes a genome g system that es twogRNAs in combination with a Cas9 nickase (a Cas9 that makes a single strand nick such as S. pyogenes D10A), an arrangement termed a “dual-nickase system.” The dual—nickase system of Cotta—Ramusino is configured to make two nicks on opposite s of a sequence of interest that are offset by one or more tides, which nicks combine to create a double strand break having an overhang (5’ in the case of Cotta— Ramusino, though 3’ overhangs are also possible). The ng, in turn, can facilitate homology directed repair events in some stances. And, as another example, WO 2015/070083 by Palestrant et a1. (“Palestrant”, incorporated by reference herein) describes a gRNA targeted to a nucleotide sequence encoding Cas9 (referred to as a “governing RNA”), which can be included in a genome editing system comprising one or more additional gRNAs to permit transient expression of a Cas9 that might otherwise be constitutively expressed, for example in some virally transduced cells. These multiplexing applications are intended to be exemplary, rather than limiting, and the skilled n will appreciate that other applications of multiplexing are generally compatible with the genome editing systems described here.

Genome editing systems can, in some instances, form double strand breaks that are ed by cellular DNA double-strand break mechanisms such as NHEJ or HDR. 2O These mechanisms are described throughout the literature, for example by Davis & Maizels, PNAS, 111(10):E924-932, March 11, 2014 (Davis) (describing Alt-HDR); Frit et al. DNA Repair 17(2014) 81-97 (Frit) (describing Alt-NHEJ); and Iyama and Wilson 111, DNA Repair (Amst) 2013-Aug, 12(8): 6 (Iyama) (describing canonical HDR and NHEJ pathways generally).

Where genome g systems e by forming DSBs, such systems optionally include one or more components that promote or facilitate a ular mode of double-strand break repair or a particular repair outcome. For instance, Cotta- Ramusino also describes genome editing systems in which a single—stranded oligonucleotide “donor template” is added; the donor template is incorporated into a target region of cellular DNA that is cleaved by the genome editing system, and can result in a change in the target sequence.

In certain embodiments, genome editing systems modify a target sequence, or modify sion of a gene in or near the target ce, without causing single- or -strand breaks. For example, a genome editing system may include an RNA- guided nuclease fused to a functional domain that acts on DNA, thereby modifying the target sequence or its expression. As one example, an RNA-guided nuclease can be connected to (eg. fused to) a cytidine deaminase functional domain, and may e by generating targeted C-to-A substitutions. Exemplary nuclease/deaminase fusions are described in Komor et al. Nature 533, 420—424 (19 May 2016) (“Komor”), which is incorporated by reference. Alternatively, a genome g system may utilize a ge-inactivated (i.e. a “dead”) nuclease, such as a dead Cas9 (dCas9), and may operate by forming stable complexes on one or more targeted regions of cellular DNA, thereby interfering with functions involving the targeted region(s) including, without limitation, mRNA transcfiption, tin remodeling, etc.

Guide RNA RNA molecules The terms “guide RNA” and “gRNA” refer to any nucleic acid that promotes the specific association (or “targeting”) of an RNA-guided nuclease such as a Cas9 or a Cpf1 to a target sequence such as a genomic or episomal sequence in a cell. gRNAs can be unimolecular ising a single RNA molecule, and referred to alternatively as chimeric), or modular (comprising more than one, and typically two, separate RNA 2O molecules, such as a chNA and a trachNA, which are y associated with one another, for instance by duplexing). gRNAs and their component parts are described throughout the literature, for instance in Briner et al. (Molecular Cell 56(2), 333-339, October 23, 2014 (Briner), which is incorporated by reference), and in Cotta—Ramusino.

In bacteria and archaea, type II CRISPR systems generally comprise an RNA- guided nuclease n such as Cas9, a CRISPR RNA (chNA) that includes a 5’ region that is complementary to a foreign sequence, and a trans-activating chNA (trachNA) that includes a 5’ region that is complementary to, and forms a duplex with, a 3’ region of the chNA. While not intending to be bound by any theory, it is t that this duplex facilitates the formation of— and is necessary for the ty of— the RNA complex. As type II CRISPR systems were adapted for use in gene editing, it was discovered that the chNA and trachNA could be joined into a single unimolecular or chimeric guide RNA, for ce, but not by way of limitation, by means of a four nucleotide (e. g. GAAA) “tetraloop” or “linker” sequence bridging complementary regions of the chNA (at its 3’ end) and the A (at its 5’ end).

(Mali et al. Science. 2013 Feb 15; 339(6121): 823—826 (“Mali”); Jiang et al. Nat hnol. 2013 Mar; 31(3): 233—239 (“Jiang”); and Jinek et al., 2012 Science Aug. 17; 337(6096): 816-821 (“Jinek”), all of which are incorporated by reference herein.) Guide RNAs, whether unimolecular or modular, include a “targeting domain” that is fully or lly complementary to a target domain within a target ce, such as a DNA sequence in the genome of a cell where editing is desired. Targeting domains are referred to by various names in the literature, including without limitation “guide sequences” (Hsu et al., Nat Biotechnol. 2013 Sep; 31(9): 827—832, (“Hsu”), incorporated by reference herein), “complementarity regions” -Ramusino), “spacers” (Briner) and generically as “chNAs” (Jiang). Irrespective of the names they are given, targeting s are lly 10—30 nucleotides in length, and in certain embodiments are 16-24 nucleotides in length (for ce, 16, 17, 18, 19, 20, 21, 22, 23 or 24 nucleotides in length), and are at or near the 5’ terminus of in the case of a Cas9 gRNA, and at or near the 3’ terminus in the case of a Cpfl gRNA.

In addition to the targeting domains, gRNAs typically (but not arily, as discussed below) include a plurality of domains that may influence the formation or activity of gRNA/Cas9 complexes. For instance, as mentioned above, the duplexed structure formed by first and ary complementarity domains of a gRNA (also referred to as a repeatzanti—repeat duplex) interacts with the recognition (REC) lobe of Cas9 and can e the formation of Cas9/gRNA complexes. (Nishimasu et al., Cell 156, 93 5—949, February 27, 2014 (Nishimasu 2014) and Nishimasu et al., Cell 162, 1113- 1126, August 27, 2015 (Nishimasu 2015), both incorporated by reference herein). It should be noted that the first and/or second complementarity domains may contain one or more poly-A tracts, which can be ized by RNA polymerases as a termination signal. The sequence of the first and second complentarity domains are, therefore, optionally modified to eliminate these tracts and promote the complete in vitro transcription of gRNAs, for instance through the use of A—G swaps as described in Briner, or A-U swaps. These and other similar modifications to the first and second mentarity domains are within the scope of the present disclosure.

Along with the first and second complementarity domains, Cas9 gRNAs typically e two or more additional duplexed regions that are involved in nuclease activity in viva but not necessarily in vitro. masu 2015). A first stem-loop one near the 3’ portion of the second complementarity domain is referred to variously as the “proximal domain,” (Cotta-Ramusino) “stem loop 1” (Nishimasu 2014 and 2015) and the “nexus” (Briner). One or more additional stem loop structures are generally present near the 3’ end of the gRNA, with the number varying by species: S. pyogenes gRNAs typically e two 3’ stem loops (for a total of four stem loop structures including the repeatzanti-repeat duplex), while S. aureus and other species have only one (for a total of three stem loop structures). A description of conserved stem loop structures (and gRNA structures more generally) organized by species is provided in Briner.

While the foregoing description has focused on gRNAs for use with Cas9, it should be appreciated that other RNA-guided nucleases have been (or may in the future be) discovered or invented which utilize gRNAs that differ in some ways from those bed to this point. For instance, Cpf1 (“CRISPR from Prevotella and Franciscella 1”) is a recently discovered RNA-guided nuclease that does not require a trachNA to function. (Zetsche et al., 2015, Cell 163, 1 October 22, 2015 (Zetsche I), incorporated by reference herein). A gRNA for use in a Cpfl genome editing system generally includes a targeting domain and a complementarity domain (alternately 2O referred to as a e”). It should also be noted that, in gRNAs for use with Cpfl, the targeting domain is usually t at or near the 3’ end, rather than the 5’ end as bed above in connection with Cas9 gRNAs (the handle is at or near the 5’ end of a Cpfl gRNA).

Those of skill in the art will appreciate, however, that although structural differences may exist between gRNAs from different prokaryotic species, or between Cpf1 and Cas9 gRNAs, the principles by which gRNAs operate are generally consistent.

Because of this consistency of operation, gRNAs can be defined, in broad terms, by their targeting domain sequences, and skilled artisans will iate that a given targeting domain sequence can be incorporated in any suitable gRNA, ing a unimolecular or modular gRNA, or a gRNA that includes one or more chemical modifications and/or sequential ations (substitutions, additional nucleotides, truncations, etc.) Thus, for economy of presentation in this disclosure, gRNAs may be described solely in terms of their targeting domain sequences.

More generally, skilled artisans will appreciate that some aspects of the present disclosure relate to systems, methods and compositions that can be implemented using multiple RNA-guided nucleases. For this reason, unless otherwise ed, the term gRNA should be understood to encompass any suitable gRNA that can be used with any RNA-guided nuclease, and not only those gRNAs that are compatible with a particular species of Cas9 or Cpf1. By way of illustration, the term gRNA can, in certain embodiments, include a gRNA for use with any RNA-guided nuclease occurring in a Class 2 CRISPR system, such as a type II or type V or CRISPR system, or an RNA- guided nuclease derived or d therefrom. gRNA desigfl Methods for selection and validation of target sequences as well as off-target analyses have been described previously, e.g., in Mali; Hsu; Fu et al., 2014 Nat hnol 32(3): 279-84, Heigwer et al., 2014 Nat methods 11(2): 122-3, Bae et al. (2014) Bioinformatics 30(10): 1473—5, and Xiao A et al, (2014) Bioinformatics 30(8): 1180-1182. Each of these references is incorporated by reference herein. As a non— limiting example, gRNA design can involve the use of a software tool to ze the choice of potential target sequences corresponding to a user’s target sequence, e. g., to minimize total off-target activity across the genome. While off-target activity is not limited to cleavage, the cleavage efficiency at each off-target sequence can be predicted, e.g., using an mentally-derived weighting scheme. These and other guide selection methods are described in detail in Maeder and Cotta-Ramusino. gRNA modifications The activity, stability, or other characteristics of gRNAs can be altered through the incorporation of n modifications. As one example, transiently expressed or delivered nucleic acids can be prone to degradation by, e. g., cellular nucleases.

Accordingly, the gRNAs bed herein can contain one or more d nucleosides or nucleotides which introduce stability toward nucleases. While not wishing to be bound by theory it is also believed that certain modified gRNAs described herein can exhibit a reduced innate immune response when introduced into cells. Those of skill in the art will be aware of certain cellular responses commonly observed in cells, e.g., mammalian cells, in se to ous nucleic acids, ularly those of viral or bacterial origin. Such responses, which can e induction of cytokine expression and release and cell death, may be reduced or eliminated altogether by the modifications presented herein.

Certain exemplary modifications discussed in this n can be included at any position within a gRNA sequence including, without limitation at or near the 5’ end (e.g., within 1-10, 1-5, or 1-2 tides of the 5’ end) and/or at or near the 3’ end (e.g., within 1-10, 1-5, or 1-2 tides of the 3’ end). In some cases, modifications are oned within functional motifs, such as the repeat-anti—repeat duplex of a Cas9 gRNA, a stem loop structure of a Cas9 or Cpfl gRNA, and/or a targeting domain of a gRNA.

As one example, the 5’ end of a gRNA can include a otic mRNA cap structure or cap analog (e.g., a G(5 )ppp(5 QG cap analog, a m7G(5 )ppp(5 )6 cap analog, or a 3 ’-O-Me-m 7G(5 ’)ppp(5 9G anti reverse cap analog (ARCA)), as shown below: The cap or cap analog can be included during either chemical synthesis or in vitro transcription of the gRNA.

Along similar lines, the 5’ end of the gRNA can lack a 5’ triphosphate group.

For instance, in vitro transcribed gRNAs can be phosphatase-treated (e.g., using calf intestinal alkaline phosphatase) to remove a 5’ sphate group.

Another common modification involves the addition, at the 3’ end of a gRNA, of a plurality (e.g., 1—10, 10-20, or 25-200) of adenine (A) residues referred to as a polyA tract. The polyA tract can be added to a gRNA during al synthesis, following in vitro transcription using a polyadenosine polymerase (e.g., E. coli Poly(A)Polymerase), or in vivo by means of a polyadenylation sequence, as described in Maeder.

It should be noted that the modifications described herein can be ed in any suitable manner, e. g. a gRNA, whether transcribed in vivo from a DNA vector, or in vitro transcribed gRNA, can include either or both of a 5’ cap structure or cap analog and a 3’ polyA tract.

Guide RNAs can be modified at a 3’ terminal U ribose. For example, the two terminal hydroxyl groups of the U ribose can be oxidized to aldehyde groups and a itant opening of the ribose ring to afford a modified nucleoside as shown below: wherein “U” can be an unmodified or modified uridine.

The 3’ terminal U ribose can be modified with a 2’3’ cyclic phosphate as shown below: wherein “U” can be an unmodified or modified uridine.

Guide RNAs can contain 3’ nucleotides which can be stabilized against degradation, e.g., by incorporating one or more of the modified nucleotides described herein. In certain ments, uridines can be replaced with modified es, e.g., 5- (2-amino)propyl uridine, and o uridine, or with any of the modified uridines described herein; adenosines and guanosines can be replaced with modified adenosines and guanosines, e.g., with ations at the 8-position, e.g., 8-bromo guanosine, or with any of the modified adenosines or guanosines described herein.

In certain embodiments, sugar-modified ribonucleotides can be incorporated into the gRNA, e.g., wherein the 2’ OH-group is replaced by a group selected from H, -OR, - R (wherein R can be, e.g., alkyl, lkyl, aryl, l, heteroaryl or sugar), halo, —SH, -SR (wherein R can be, e.g., alkyl, cycloalkyl, aryl, l, heteroaryl or sugar), amino in amino can be, e.g., NHZ; alkylamino, dialkylamino, heterocyclyl, arylamino, diarylamino, heteroarylamino, diheteroarylamino, or amino acid); or cyano (—CN). In certain ments, the phosphate backbone can be modified as described , e.g., with a phosphothioate (Pth) group. In n embodiments, one or more of the nucleotides of the gRNA can each independently be a modified or unmodified nucleotide including, but not limited to 2’-sugar modified, such as, 2’-O-methyl, 2’-O- methoxyethyl, or oro modified including, e.g., 2’-F or 2’-O-methyl, ine (A), 2’-F or 2’-O-methyl, cytidine (C), 2’-F or 2’-O-methyl, uridine (U), 2’-F or 2’-O-methyl, thymidine (T), 2’—F or 2’-O-methyl, ine (G), 2’-O-methoxyethylmethyluridine (Teo), 2’-O-methoxyethyladenosine (Aeo), 2’-O-methoxyethylmethylcytidine (mSCeo), and any combinations thereof.

Guide RNAs can also include “locked” nucleic acids (LNA) in which the 2’ OH- group can be connected, e.g., by a Cl-6 ne or Cl-6 heteroalkylene bridge, to the 4’ carbon of the same ribose sugar. Any suitable moiety can be used to provide such bridges, include without limitation methylene, propylene, ether, or amino bridges; 0- amino (wherein amino can be, e.g., NHz, alkylamino, dialkylamino, heterocyclyl, arylamino, diarylamino, heteroarylamino, or diheteroarylamino, ethylenediamine, or polyamino) and aminoalkoxy or O(CH2)n-amino (wherein amino can be, e.g., NHZ; alkylamino, dialkylamino, heterocyclyl, ino, diarylamino, arylamino, or diheteroarylamino, ethylenediamine, or polyamino).

In certain embodiments, a gRNA can include a modified nucleotide which is multicyclic (e.g., tricyclo; and “unlocked” forms, such as glycol nucleic acid (GNA) (e. g., R-GNA or S—GNA, where ribose is replaced by glycol units attached to phosphodiester bonds), or threose nucleic acid (TNA, where ribose is replaced with Ot-L- threofuranosyl-(3 ’—>2’)).

Generally, gRNAs include the sugar group ribose, which is a 5-membered ring having an oxygen. Exemplary d gRNAs can include, without limitation, replacement of the oxygen in ribose (e.g., with sulfur (S), selenium (Se), or alkylene, such as, e.g., methylene or ethylene), addition of a double bond (e.g., to replace ribose with cyclopentenyl or cyclohexenyl); ring contraction of ribose (e. g., to form a 4- membered ring of cyclobutane or oxetane); ring expansion of ribose (e.g., to form a 6- or ered ring having an additional carbon or heteroatom, such as for example, anhydrohexitol, altritol, mannitol, cyclohexanyl, cyclohexenyl, and morpholino that also has a oramidate backbone). Although the majority of sugar analog alterations are localized to the 2’ position, other sites are amenable to modification, including the 4’ position. In certain embodiments, a gRNA comprises a 4’—S, 4’-Se or a 4’-C— aminomethyl-2’ -O-Me modification.

In certain embodiments, deaza nucleotides, e. g., 7-deaza-adenosine, can be incorporated into the gRNA. In certain embodiments, O- and N—alkylated tides, e.g, N6-methyl adenosine, can be incorporated into the gRNA. In certain embodiments, one or more or all of the nucleotides in a gRNA are ucleotides.

RNA-guided nucleases RNA-guided nucleases according to the present sure include, but are not limited to, naturally-occurring Class 2 CRISPR nucleases such as Cas9, and Cpf1, as well as other nucleases derived or obtained therefrom. In functional terms, ided nucleases are defined as those nucleases that: (a) interact with (e. g. complex with) a gRNA, and (b) together with the gRNA, associate with, and optionally cleave or , a target region of a DNA that includes (i) a sequence complementary to the targeting domain of the gRNA and, optionally, (ii) an additional sequence referred to as a “protospacer adjacent motif,” or “PAM,” which is described in greater detail below. As the following examples will illustrate, RNA—guided nucleases can be defined, in broad terms, by their PAM specificity and cleavage activity, even though variations may exist between individual RNA-guided nucleases that share the same PAM specificity or ge ty. Skilled artisans will appreciate that some aspects of the present disclosure relate to systems, methods and compositions that can be implemented using any suitable RNA-guided nuclease having a certain PAM city and/or cleavage activity. For this reason, unless ise specified, the term RNA—guided nuclease should be understood as a generic term, and not limited to any particular type (e. g. Cas9 vs. Cpfl), species (e. g. S. pyogenes vs. S. aureus) or variation (e. g. full-length vs. truncated or split; naturally-occurring PAM specificity vs. engineered PAM specificity, etc.) of RNA-guided se. 3O The PAM sequence takes its name from its sequential relationship to the spacer” sequence that is complementary to gRNA targeting domains (or “spacers”). er with protospacer sequences, PAM sequences define target regions or sequences for specific RNA-guided nuclease / gRNA combinations.

Various RNA-guided nucleases may e different sequential relationships between PAMs and protospacers. In general, Cas9s recognize PAM sequences that are 3’ of the protospacer as visualized on the bottom or non-complementary strand: ’ ----------------------- [protospacer] ------------3 ’ complementary 3 ’ ——————————————[PAM] -----------------------------------5 ’ non- complementary Cpf1, on the other hand, generally recognizes PAM sequences that are 5’ of the pacer as visualized on the bottom or non-complementary strand: ’ ------------------- [protospacer] ----------------------------3 ’ complementary 3 ’ -----------------------------------[PAM] -------------------5 ’ non- complementary In addition to recognizing specific sequential orientations ofPAMs and protospacers, RNA-guided nucleases can also recognize specific PAM sequences. S. aureus Cas9, for instance, recognizes a PAM sequence ofNNGRRT or NNGRRV, wherein the N residues are ately 3’ of the region recognized by the gRNA targeting domain. S. pyogenes Cas9 recognizes NGG PAM sequences. And F. da 2O Cpf1 izes a TTN PAM sequence. PAM sequences have been identified for a variety of RNA-guided nucleases, and a strategy for identifying novel PAM sequences has been described by Shmakov et al., 2015, Molecular Cell 60, 385—397, November 5, 2015. It should also be noted that engineered ided nucleases can have PAM specificities that differ from the PAM specificities of nce molecules (for instance, in the case of an engineered RNA—guided nuclease, the reference le may be the naturally occurring variant from which the RNA-guided nuclease is derived, or the naturally occurring variant having the greatest amino acid sequence homology to the engineered RNA-guided nuclease).

In addition to their PAM specificity, RNA-guided nucleases can be characterized by their DNA cleavage activity: naturally-occurring RNA-guided nucleases typically form DSBs in target nucleic acids, but engineered variants have been produced that generate only SSBs (discussed above) Ran & Hsu, et al., Cell , 1380—1389, ber 12, 2013 (Ran), incorporated by reference herein), or that do not cut at all.

Crystal structures have been determined for S. pyogenes Cas9 (Jinek 2014), and for S. aureus Cas9 in complex with a unimolecular guide RNA and a target DNA (Nishimasu 2014; Anders 2014, and Nishimasu 2015).

A naturally occurring Cas9 protein comprises two lobes: a recognition (REC) lobe and a nuclease (NUC) lobe, each of which comprise particular structural and/or functional domains. The REC lobe comprises an arginine-rich bridge helix (BH) domain, and at least one REC domain (e.g. a RECl domain and, optionally, a REC2 domain). The REC lobe does not share ural similarity with other known proteins, ting that it is a unique functional domain. While not wishing to be bound by any theory, mutational analyses suggest specific functional roles for the BH and REC domains: the BH domain appears to play a role in gRNA:DNA recognition, while the REC domain is thought to interact with the repeat:anti-repeat duplex of the gRNA and to mediate the formation of the Cas9/gRNA complex.

The NUC lobe comprises a Rqu domain, an HNH domain, and a PAM- interacting (PI) domain. The Rqu domain shares structural rity to retroviral integrase superfamily s and cleaves the non-complementary (i.e. bottom) strand of the target nucleic acid. It may be formed from two or more split Rqu motifs (such as Rqu I, Rqu II, and Rqu III in S. pyogenes and S. aureus). The HNH domain, ile, is urally similar to HNN clease motifs, and cleaves the mentary (i.e. top) strand of the target nucleic acid. The PI domain, as its name suggests, contributes to PAM city.

While certain functions of Cas9 are linked to (but not necessarily fully determined by) the specific domains set forth above, these and other functions may be mediated or influenced by other Cas9 domains, or by multiple domains on either lobe.

For instance, in S. pyogenes Cas9, as described in Nishimasu 2014, the repeat:antirepeat duplex of the gRNA falls into a groove between the REC and NUC lobes, and nucleotides in the duplex interact with amino acids in the BH, PI, and REC domains.

Some nucleotides in the first stem loop structure also interact with amino acids in multiple domains (PI, BH and RECl), as do some nucleotides in the second and third stem loops (Rqu and PI domains).

The crystal structure of Acidaminococcus Sp. Cpfl in complex with chNA and a double-stranded (ds) DNA target including a TTTN PAM sequence has been solved by Yamano et al. (Cell. 2016 May 5; 165(4): 2 (Yamano), incorporated by reference herein). Cpfl, like Cas9, has two lobes: a REC (recognition) lobe, and a NUC (nuclease) lobe. The REC lobe includes RECl and REC2 s, which lack similarity to any known protein structures. The NUC lobe, ile, includes three Rqu domains , -II and —III) and a BH domain. However, in contrast to Cas9, the Cpfl REC lobe lacks an HNH , and includes other domains that also lack similarity to known protein structures: a structurally unique PI domain, three Wedge (WED) domains (WED-I, -II and -III), and a nuclease (Nuc) domain.

While Cas9 and Cpfl share rities in structure and function, it should be appreciated that n Cpfl activities are mediated by structural domains that are not analogous to any Cas9 domains. For ce, cleavage of the complementary strand of the target DNA appears to be mediated by the Nuc domain, which differs sequentially and spatially from the HNH domain of Cas9. Additionally, the non-targeting n of Cpfl gRNA (the handle) adopts a pseudoknot structure, rather than a stem loop structure formed by the repeatzantirepeat duplex in Cas9 gRNAs.

Modifications 01 RNA-guided nucleases The RNA—guided nucleases described above have activities and ties that can be useful in a variety of applications, but the skilled artisan will appreciate that RNA-guided nucleases can also be modified in certain instances, to alter cleavage activity, PAM specificity, or other structural or functional features.

Turning first to modifications that alter cleavage activity, mutations that reduce or eliminate the activity of domains within the NUC lobe have been described above.

Exemplary mutations that may be made in the Rqu domains, in the Cas9 HNH domain, or in the Cpfl Nuc domain are described in Ran and Yamano, as well as in Cotta- no. In general, ons that reduce or eliminate activity in one of the two nuclease domains result in RNA—guided nucleases with nickase activity, but it should be noted that the type of nickase activity varies depending on which domain is inactivated.

As one e, inactivation of a Rqu domain of a Cas9 will result in a nickase that cleaves the complementary or top strand as shown below (where C denotes the site of cleavage): ’ ------------------- [protospacer]--[C] ---------------------3 a 3 3 ______________________________________________________________5 3 On the other hand, inactivation of a Cas9 HNH domain results in a nickase that cleaves the bottom or non-complementary strand: ’ ------------------- [protospacer] ---------------------------3 3 3 ’ ------------------------------------- [C] ---------------------5 ’ Modifications ofPAM specificity relative to lly occurring Cas9 reference les have been described by Kleinstiver et al. for both S. pyogenes (Kleinstiver et al., Nature. 2015 Jul 23,523(7561):481-5 (Kleinstiver 1) and S. aureus (Kleinstiver et al., Nat Biotechnol. 2015 Dec; : 1293—1298 (Klienstiver 11)). tiver et al. have also described modifications that improve the targeting fidelity of Cas9 (Nature, 2016 January 28; 529, 490-495 (Kleinstiver 111)). Each of these references is incorporated by reference herein.

RNA-guided nucleases have been split into two or more parts, as described by Zetsche et al. (Nat Biotechnol. 2015 Feb;33(2):139-42 (Zetsche II), incorporated by reference), and by Fine et al. (Sci Rep. 2015 Jul 1,5: 10777 (Fine), incorporated by reference).

RNA-guided nucleases can be, in certain embodiments, size-optimized or truncated, for ce via one or more deletions that reduce the size of the nuclease while still retaining gRNA association, target and PAM ition, and cleavage activities. In certain ments, RNA guided nucleases are bound, covalently or non- covalently, to another polypeptide, nucleotide, or other structure, optionally by means of a linker. Exemplary bound nucleases and linkers are bed by Guilinger et al., Nature Biotechnology 32, 577—5 82 (2014), which is incorporated by reference for all purposes herein.

RNA-guided nucleases also optionally include a tag, such as, but not limited to, a nuclear localization signal to facilitate movement of RNA—guided se protein into the nucleus. In certain embodiments, the RNA-guided nuclease can incorporate C- and/or N—terminal nuclear zation s. Nuclear localization sequences are known in the art and are described in Maeder and elsewhere.

The foregoing list of modifications is intended to be exemplary in nature, and the skilled artisan will appreciate, in view of the instant disclosure, that other modifications may be possible or desirable in certain applications. For brevity, therefore, exemplary systems, methods and compositions of the present sure are presented with reference to particular RNA-guided nucleases, but it should be understood that the RNA- guided nucleases used may be d in ways that do not alter their operating principles. Such modifications are within the scope of the present disclosure.

Nucleic acids encoding RNA-guided ses Nucleic acids encoding RNA-guided nucleases, e.g., Cas9, Cpfl or functional fragments thereof, are provided herein. ary nucleic acids encoding RNA-guided nucleases have been described previously (see, e. g., Cong 2013; Wang 2013; Mali 2013; Jinek 2012).

In some cases, a nucleic acid encoding an RNA-guided nuclease can be a synthetic nucleic acid ce. For example, the synthetic nucleic acid molecule can be chemically modified. In certain embodiments, an mRNA encoding an RNA-guided nuclease will have one or more (e.g., all) of the following properties: it can be capped; 2O polyadenylated, and substituted with 5-methylcytidine and/or pseudouridine.

Synthetic nucleic acid ces can also be codon optimized, e. g., at least one mmon codon or less—common codon has been replaced by a common codon. For example, the synthetic nucleic acid can direct the synthesis of an optimized messenger mRNA, e.g., optimized for expression in a mammalian expression system, e. g., described herein. Examples of codon zed Cas9 coding ces are ted in Cotta- Ramusino.

In addition, or alternatively, a nucleic acid encoding an RNA—guided nuclease may comprise a nuclear localization ce (NLS). Nuclear localization sequences are known in the art.

Functional analysis of candidate les Candidate RNA-guided nucleases, gRNAs, and complexes thereof, can be evaluated by standard methods known in the art. See, e. g. Cotta-Ramusino. The stability ofRNP complexes may be evaluated by differential scanning fluorimetry, as described below.

Differential Scanning Fluorimetry (DSF) The thermostability of ribonucleoprotein (RNP) complexes comprising gRNAs and RNA—guided nucleases can be measured via DSF. The DSF technique measures the thermostability of a protein, which can se under ble conditions such as the addition of a binding RNA molecule, e.g., a gRNA.

A DSF assay can be performed according to any suitable protocol, and can be employed in any suitable setting, including without limitation (a) testing different conditions (e. g. different stoichiometric ratios of gRNA: RNA-guided nuclease protein, ent buffer solutions, etc.) to identify l conditions for RNP formation; and (b) testing modifications (e.g. chemical modifications, alterations of ce, etc.) of an RNA-guided nuclease and/or a gRNA to identify those modifications that improve RNP formation or stability. One readout of a DSF assay is a shift in melting temperature of the RNP complex; a relatively high shift suggests that the RNP complex is more stable (and may thus have greater activity or more favorable kinetics of formation, kinetics of degradation, or another functional teristic) relative to a nce RNP complex characterized by a lower shift. When the DSF assay is deployed as a ing tool, a threshold g temperature shift may be specified, so that the output is one or more RNPs having a g ature shift at or above the threshold. For instance, the threshold can be 5—10°C (e.g. 5°, 6°, 7°, 8°, 9°, 10°) or more, and the output may be one or more RNPs characterized by a melting temperature shift greater than or equal to the threshold.

Two miting examples of DSF assay conditions are set forth below: To determine the best solution to form RNP complexes, a fixed concentration (e. g. 2 pM) of Cas9 in water+10x SYPRO Orange® (Life Technologies cat#S-6650) is dispensed into a 384 well plate. An equimolar amount of gRNA diluted in solutions with varied pH and salt is then added. After incubating at room temperature for 10’ and brief centrifugation to remove any bubbles, a Bio-Rad CFX3 84TM Real-Time System C1000 TouchTM Thermal Cycler with the Bio-Rad CFX Manager software is used to run a gradient from 20°C to 90°C with a 1°C increase in temperature every 10 seconds.

The second assay consists of mixing various concentrations of gRNA with fixed concentration (e. g. 2 uM) Cas9 in optimal buffer from assay 1 above and ting (e. g. at RT for 10’) in a 384 well plate. An equal volume of optimal buffer + 10x SYPRO Orange® (Life Technologies cat#S—6650) is added and the plate sealed with Microseal® B adhesive (MSB-1001). Following brief centrifugation to remove any bubbles, a Bio- Rad CFX3 84TM Real-Time System C1000 M Thermal Cycler with the Bio-Rad CFX Manager software is used to run a gradient from 20°C to 90°C with a 1°C increase in temperature every 10 seconds.

Genome editing strategies The genome editing systems described above are used, in various embodiments of the present disclosure, to generate edits in (i.e. to alter) targeted regions of DNA within or obtained from a cell. s strategies are bed herein to generate particular edits, and these strategies are lly described in terms of the desired repair outcome, the number and positioning of individual edits (e.g. SSBs or DSBS), and the target sites of such edits.

Genome g strategies that involve the formation of SSBs or DSBs are 2O terized by repair outcomes including: (a) deletion of all or part of a targeted region, (b) insertion into or replacement of all or part of a targeted region; or (c) interruption of all or part of a targeted region. This grouping is not intended to be limiting, or to be binding to any particular theory or model, and is offered solely for economy of presentation. Skilled artisans will appreciate that the listed outcomes are not mutually ive and that some repairs may result in other outcomes. The description of a particular editing strategy or method should not be understood to require a particular repair e unless otherwise specified.

Replacement of a targeted region generally es the ement of all or part of the existing ce within the targeted region with a homologous sequence, for 3O instance through gene correction or gene conversion, two repair outcomes that are mediated by HDR pathways. HDR is promoted by the use of a donor template, which can be single-stranded or double-stranded, as described in greater detail below. Single- or double—stranded templates can be exogenous, in which case they will promote gene correction, or they can be endogenous (e. g. a gous sequence within the cellular genome), to promote gene conversion. Exogenous tes can have asymmetric overhangs (i.e. the portion of the template that is complementary to the site of the DSB may be offset in a 3’ or 5’ direction, rather than being centered within the donor te), for instance as described by Richardson et al. (Nature Biotechnology 34, 339— 344 (2016), rdson), incorporated by reference). In instances where the template is single-stranded, it can pond to either the complementary (top) or non— complementary m) strand of the targeted region.

Gene conversion and gene correction are tated, in some cases, by the formation of one or more nicks in or around the targeted region, as described in Ran and Cotta-Ramusino. In some cases, a dual—nickase strategy is used to form two offset SSBs that, in turn, form a single DSB having an overhang (e. g. a 5’ overhang).

Interruption and/or deletion of all or part of a targeted sequence can be achieved by a variety of repair outcomes. As one example, a sequence can be deleted by simultaneously generating two or more DSBs that flank a ed region, which is then excised when the DSBs are repaired, as is described in Maeder for the LCAlO mutation.

As another e, a sequence can be interrupted by a deletion generated by formation of a double strand break with single-stranded overhangs, followed by exonucleolytic processing of the overhangs prior to repair.

One specific subset of target sequence interruptions is mediated by the formation of an indel within the targeted sequence, where the repair outcome is typically mediated by NHEJ pathways (including Alt—NHEJ). NHEJ is referred to as an “error prone” repair pathway because of its association with indel mutations. In some cases, however, a DSB is repaired by NHEJ without alteration of the ce around it (a so-called “perfect” or “scarless” repair); this generally requires the two ends of the DSB to be perfectly ligated. , meanwhile, are thought to arise from enzymatic processing of free DNA ends before they are ligated that adds and/or removes tides from either or both strands of either or both free ends.

Because the tic processing of free DSB ends may be stochastic in nature, indel mutations tend to be variable, occurring along a distribution, and can be influenced by a y of factors, including the specific target site, the cell type used, the genome g strategy used, etc. It is possible to draw limited generalizations about indel formation: ons formed by repair of a single DSB are most commonly in the 1-50 bp range, but can reach greater than 100-200 bp. Insertions formed by repair of a single DSB tend to be shorter and often include short duplications of the sequence immediately surrounding the break site. However, it is possible to obtain large insertions, and in these cases, the inserted sequence has often been traced to other regions of the genome or to plasmid DNA present in the cells.

Indel mutations — and genome editing systems configured to produce indels — are useful for interrupting target sequences, for example, when the generation of a specific final sequence is not required and/or where a frameshift mutation would be tolerated.

They can also be useful in settings where particular sequences are preferred, insofar as the certain sequences desired tend to occur entially from the repair of an SSB or DSB at a given site. Indel mutations are also a useful tool for ting or screening the ty of particular genome editing systems and their components. In these and other gs, indels can be characterized by (a) their relative and absolute frequencies in the genomes of cells contacted with genome editing systems and (b) the distribution of numerical differences relative to the unedited sequence, e. g. i1, i2, 13, etc. As one example, in a lead-finding setting, multiple gRNAs can be screened to identify those gRNAs that most efficiently drive cutting at a target site based on an indel t under controlled conditions. Guides that produce indels at or above a threshold frequency, or that e a particular distribution of indels, can be selected for further study and development. Indel frequency and distribution can also be useful as a readout for ting different genome editing system implementations or formulations and delivery methods, for instance by g the gRNA constant and varying certain other reaction ions or delivery methods.

Multiglex Strategies While exemplary strategies discussed above have focused on repair outcomes ed by single DSBs, genome editing systems according to this disclosure may also be employed to generate two or more DSBs, either in the same locus or in different loci.

Strategies for editing that involve the formation of multiple DSBs, or SSBs, are described in, for instance, Cotta-Rarnusino.

Donor template design Donor template design is described in detail in the literature, for instance in Cotta-Ramusino. DNA oligomer donor templates (oligodeoxynucleotides or ODNs), which can be single-stranded (ssODNs) or double-stranded (dsODNs), can be used to facilitate HDR-based repair of DSBs, and are particularly useful for introducing alterations into a target DNA sequence, inserting a new sequence into the target sequence, or replacing the target sequence altogether.

Whether single-stranded or double-stranded, donor templates generally include regions that are gous to s ofDNA within or near (eg. flanking or adjoining) a target sequence to be cleaved. These homologous regions are referred to here as “homology arms,” and are illustrated schematically below: [5’ homology arm] — [replacement sequence] —- [3’ homology arm].

The homology arms can have any suitable length (including 0 nucleotides if only one homology arm is used), and 3’ and 5’ homology arms can have the same length, or can differ in length. The selection of appropriate homology arm s can be influenced by a variety of factors, such as the desire to avoid homologies or microhomologies with certain sequences such as Alu repeats or other very common elements. For example, a 5’ homology arm can be shortened to avoid a sequence repeat element. In other embodiments, a 3’ homology arm can be shortened to avoid a sequence repeat element. In some embodiments, both the 5’ and the 3’ homology arms can be shortened to avoid ing certain sequence repeat elements. In on, some homology arm designs can e the efficiency of editing or increase the frequency of a d repair outcome. For example, Richardson et al. Nature Biotechnology 34, 339— 344 (2016) (Richardson), which is incorporated by reference, found that the relative asymmetry of 3’ and 5’ homology arms of single-stranded donor templates influenced repair rates and/or outcomes.

Replacement sequences in donor templates have been described elsewhere, including in Cotta—Ramusino et al. A replacement ce can be any suitable length (including zero nucleotides, where the desired repair outcome is a deletion), and lly includes one, two, three or more ce modifications relative to the naturally—occurring sequence within a cell in which editing is d. One common sequence ation involves the alteration of the naturally-occurring sequence to repair a on that is related to a disease or condition of which treatment is desired.

Another common sequence modification involves the alteration of one or more sequences that are complementary to, or code for, the PAM sequence of the RNA-guided nuclease or the targeting domain of the gRNA(s) being used to generate an SSB or DSB, to reduce or eliminate repeated cleavage of the target site after the replacement sequence has been orated into the target site.

Where a linear ssODN is used, it can be configured to (i) anneal to the nicked strand of the target c acid, (ii) anneal to the intact strand of the target nucleic acid, (iii) anneal to the plus strand of the target nucleic acid, and/or (iv) anneal to the minus strand of the target nucleic acid. An ssODN may have any le length, e.g., about, or no more than 150-200 nucleotides (e.g., 150, 160, 170, 180, 190, or 200 nucleotides).

It should be noted that a template nucleic acid can also be a nucleic acid vector, such as a viral genome or circular double-stranded DNA, e.g., a plasmid. Nucleic acid s comprising donor templates can include other coding or non—coding elements.

For example, a template nucleic acid can be delivered as part of a viral genome (e. g. in an AAV or lentiviral genome) that includes n genomic backbone elements (e.g. ed terminal repeats, in the case of an AAV genome) and optionally includes additional ces coding for a gRNA and/or an RNA-guided se. In certain embodiments, the donor template can be adjacent to, or flanked by, target sites recognized by one or more gRNAs, to facilitate the formation of free DSBs on one or both ends of the donor template that can participate in repair of corresponding SSBs or DSBs formed in cellular DNA using the same gRNAs. Exemplary c acid vectors suitable for use as donor templates are described in Cotta-Ramusino.

Whatever format is used, a template nucleic acid can be designed to avoid undesirable sequences. In certain embodiments, one or both homology arms can be shortened to avoid overlap with certain sequence repeat elements, e. g., Alu repeats, LINE elements, etc.

Target cells Genome editing systems according to this disclosure can be used to manipulate or 3O alter a cell, e. g., to edit or alter a target c acid. The manipulating can occur, in various embodiments, in vivo or ex vivo.

A variety of cell types can be manipulated or altered according to the embodiments of this disclosure, and in some cases, such as in vivo applications, a plurality of cell types are altered or manipulated, for example by delivering genome editing systems according to this disclosure to a plurality of cell types. In other cases, however, it may be desirable to limit manipulation or alteration to a particular cell type or types. For instance, it can be desirable in some instances to edit a cell with limited differentiation potential or a terminally differentiated cell, such as a photoreceptor cell in the case of Maeder, in which modification of a genotype is expected to result in a change in cell phenotype. In other cases, however, it may be desirable to edit a less differentiated, multipotent or pluripotent, stem or progenitor cell. By way of e, the cell may be an embryonic stem cell, induced pluripotent stem cell (iPSC), hematopoietic stem/progenitor cell (HSPC), or other stem or progenitor cell type that differentiates into a cell type of relevance to a given application or indication.

As a corollary, the cell being altered or manipulated is, sly, a dividing cell or a non-dividing cell, depending on the cell type(s) being targeted and/or the desired g outcome.

When cells are manipulated or altered ex vivo, the cells can be used (e. g. administered to a subject) immediately, or they can be maintained or stored for later use.

Those of skill in the art will iate that cells can be maintained in e or stored (e. g. frozen in liquid nitrogen) using any suitable method known in the art.

Implementation of genome g systems: delivem, formulations, and routes of administration As discussed above, the genome editing systems of this disclosure can be implemented in any suitable manner, meaning that the ents of such systems, including without limitation the ided nuclease, gRNA, and optional donor template nucleic acid, can be delivered, formulated, or administered in any suitable form or combination of forms that results in the transduction, expression or introduction of a genome g system and/or causes a desired repair outcome in a cell, tissue or t.

Tables 6 and 7 set forth several, non-limiting examples of genome editing system implementations. Those of skill in the art will appreciate, however, that these listings are not comprehensive, and that other entations are possible. With reference to Table 6 in particular, the table lists several exemplary implementations of a genome editing system comprising a single gRNA and an optional donor template. However, genome editing systems according to this disclosure can incorporate multiple gRNAs, multiple RNA-guided nucleases, and other components such as proteins, and a y of implementations will be evident to the skilled artisan based on the ples illustrated in the table. In the table, [N/A] indicates that the genome editing system does not include the indicated component.

Table 6 Genome Editin_ S stem Com - onents RNA-guided Donor Comments An R\A-gu1ded nuclease protein -:-:-Protein [N/A] cRNomplexed with a gRNA molecule m leX) An R\P complex as described above plus a single--stranded or double- stranded donor tem late.

An R\A— uided nuclease rotein lus “!gRNA-encodingDNA and a separateDNA donor temlate.An R and a donor template.

A Dl\A or DNA vector encoding an donor tem o late.

Two separate DNAs, or two separate DNA vectors, encoding the RNA- DNA DNA [N/A] guided nuclease and the gRNA, res ectivel .

---Three separate DNAs, or three separate DNA vectors, encoding the RNA-guided nuclease, the gRNA and the donor temolate, tivel . orDNAvectorencoding anRNA-guided nuclease and a g A first DNA or DNA vector ng an RNA-guided nuclease and a gRNA, DNA DNA and a second DNA or DNA vector encoding a donor template.

A first DNA or DNA vector encoding an RNA-guided nuclease and second DNA DNA DNA or DNA vector encoding a gRNA and a donor template.

A first DNA or DNA vector ng an RNA-guided nuclease and a donor template, and a second DNA or DNA vector encoding a gRNA A DNA or DNA vector encoding an RNA-guided nuclease and a donor tem-late, and a gRNA An RNA or RNA vector encoding an RNA-guided nuclease and comprising a gRNA An RNA or RNA vector encoding an RNA-guided nuclease and comprising a gRNA, and a DNA or DNA vector encoding a donor template.

Table 7 summarizes s delivery methods for the components of genome editing systems, as described herein. Again, the listing is intended to be exemplary rather than limiting.

Table 7 Delivery Type Of into Non- Duration of Genome Delivery Vector/Mode MOIecule Dividing Expression Integration Delivered Cells Physical (e.g., electroporation, ent Nucleic Acids particle gun, Calcium and Proteins Phosphate transfection, cell compression or squeezing) Viral Retrovirus RNA irus YES/NO with modifications Adenovirus Transient DNA Adeno- YES Stable NO DNA Associated Virus (AAV) Vaccinia Virus YES Very NO DNA Transient Herpes Simplex YES Stable DNA Virus Non-Viral Cationic Transient Depends on Nucleic Acids mes whatis and Proteins delivered Polymeric Transient Depends on Nucleic Acids Nanoparticles what is and Proteins delivered Biological Attenuated Transient Nucleic Acids Non-Viral Bacteria Delivery Engineered Transient Nucleic Acids Bacteriophages Mammalian Transient Nucleic Acids Virus-like Particles Biological Transient Nucleic Acids Erythrocyte Ghosts and Exosomes Nucleic acid—based delivefl of genome editing systems Nucleic acids encoding the various elements of a genome editing system according to the t sure can be stered to subjects or delivered into cells by art-known methods or as described herein. For example, RNA-guided nuclease- encoding and/or gRNA-encoding DNA, as well as donor template nucleic acids can be delivered by, e. g., vectors (e. g., viral or non-viral vectors), non-vector based methods (e. g., using naked DNA or DNA complexes), or a combination thereof.

Nucleic acids encoding genome editing systems or components thereof can be delivered directly to cells as naked DNA or RNA, for ce by means of transfection or electroporation, or can be conjugated to molecules (e. g., N-acetylgalactosamine) promoting uptake by the target cells (e. g., erythrocytes, HSCs). Nucleic acid vectors, such as the vectors summarized in Table 7, can also be used.

Nucleic acid vectors can comprise one or more sequences encoding genome editing system components, such as an RNA-guided nuclease, a gRNA and/or a donor template. A vector can also comprise a sequence encoding a signal peptide (e. g., for r localization, nucleolar zation, or mitochondrial localization), ated with (e. g., ed into or fused to) a sequence coding for a protein. As one example, a nucleic acid vectors can include a Cas9 coding sequence that includes one or more nuclear localization sequences (e.g., a nuclear zation sequence from SV40).

The c acid vector can also e any suitable number of regulatory/control elements, e.g., promoters, enhancers, introns, polyadenylation signals, Kozak consensus sequences, or internal ribosome entry sites (IRES). These ts are well known in the art, and are described in Cotta-Ramusino.

Nucleic acid vectors according to this disclosure include recombinant viral s. Exemplary viral vectors are set forth in Table 7, and additional suitable viral s and their use and production are described in Cotta—Ramusino. Other viral vectors known in the art can also be used. In addition, viral particles can be used to deliver genome editing system components in nucleic acid and/or peptide form. For example, “empty” viral les can be assembled to contain any suitable cargo. Viral vectors and viral particles can also be ered to incorporate targeting ligands to alter target tissue specificity.

In addition to viral vectors, non-viral vectors can be used to deliver nucleic acids encoding genome editing systems according to the present disclosure. One important category of non-viral c acid vectors are nanoparticles, which can be organic or inorganic. Nanoparticles are well known in the art, and are summarized in Cotta- Ramusino. Any suitable nanoparticle design can be used to deliver genome editing system components or nucleic acids encoding such components. For instance, organic (e. g. lipid and/or polymer) nanoparticles can be le for use as delivery vehicles in certain embodiments of this disclosure. Exemplary lipids for use in nanoparticle ations, and/or gene transfer are shown in Table 8, and Table 9 lists exemplary polymers for use in gene transfer and/or nanoparticle formulations.

Table 8: Lipids Used for Gene Transfer l,2-Dioleoyl-sn-glycero-3 -phosphatidylcholine DOPC l,2-Dioleoyl-sn-glycero-3 -phosphatidylethanolamine DOPE Cholesterol _- N—[ l -(2,3 yloxy)propyl]N,MN—trimethylammonium chloride N-(3 -Aminopropyl)-N,N-dimethyl-2,3 -bis(dodecyloxy)—l — 1 -Dioleoyloxypropy1)--2,,6-trimethylpyridinium _-' 2,3 -Dioleyloxy-N-[2(sperrninecarboxamido-ethy1] -N,N—dimethyl-l - DOSPA Cationic propanaminium trifluoroacetate 1,2-Dioley1-3 -trimethy1ammonium-propane DOPA N-(2-Hydroxyethyl)-N,N-dimethy1-2,3 -bis(tetradecyloxy) MDRIE Cationic aminium bromide 3B-[N—(N’,N’-Dimethy1aminoethane)—carbamoyl]cholesterol Bis-guanidium-tren-cholesterol 1,3 -Diodeoxy(6-carboxy—spermy1)—propy1amide 2,3 -Dioctadecyloxypropy1)(2-hydroxyethy1)] -dimethy1ammonium CLIP-1 Cationic chloride rac-[2(2,3 -Dihexadecyloxypropy1- CLIP-6 Cationic oxymethyloxy)ethyl]trimethylammonium bromide 1,2-Distearyloxy-N,N-dimethyl-3 -aminopropane 1,2-Dimyristoy1-trimethy1ammonium propane 0, 0 ’-Dimyristy1-N-lysy1 aspartate 1,2-Distearoy1-sn-glycer0 -3 —ethy1phosphocholine N—Palmitoyl D-erythro-sphingosy1 carbamoyl-spermine N—l‘—Buty1—N0—tetradecy1-3 -tetradecylaminopropionamidine Octadecenolyoxy[ethylheptadeceny1-3 hydroxyethyl] imidazolinium DOTIM Cationic chloride N1 -Cholesteryloxycarbony1-3,7-diazanonane-1,9-diamine CDAN 2-(3-[Bis(3 -amino-propy1)—amino]propy1amino)-N— RPR209120 Cationic ditetradecylcarbamoylme-ethy1-acetamide 1,2-dilinoleyloxy-3 - dimethylaminopropane A 2,2-di1inoley1din1ethy1aminoethy1-[1,3]—dioxolane DLin-KCZ-DMA leyl- methyldimethylaminobutyrate DLin-MC3-DMA Table 9: Polymers Used for Gene Transfer Polymer Abbreviation Poly(ethylene)glycol PEG Polyethylenimine PEI bis(succinimidylpropionate) DSP Dimethy1-3 ,3 ’ -dithiobispropionimidate DTBP Poly(ethylene imine) biscarbamate PEIC Poly(L-1ysine) PLL Histidine modified PLL Poly(N-Vinylpyrrolidone) PVP ropylenimine) PPI Poly(amidoamine) PAMAM Poly(amido ethylenimine) SS-PAEI Triethylenetetramine TETA Poly(B-aminoester) -hydroxy-L-proline ester) PHP Poly(allylamine) Poly(ot-[4-aminobutyl] -L-g1ycolic acid) PAGA Poly(D,L-lactic-co-glycolic acid) PLGA Poly(N—ethylVinylpyridinium bromide) Poly(phosphazene)s PPZ Poly(phosphoester)s PPE Poly(phosphoramidate)s PPA Poly(N—2-hydroxypropy1methacrylamide) pHPMA Poly (2-(dimethylamino)ethyl methacrylate) pDMAEMA Poly(2-aminoethyl propylene phosphate) PPE-EA Chitosan Galactosylated chitosan N—Dodacylated chitosan Histone Non-viral vectors ally include targeting modifications to improve uptake and/or selectively target certain cell types. These targeting ations can include e.g., cell c antigens, monoclonal antibodies, single chain antibodies, aptamers, polymers, sugars (e. g., N-acetylgalactosamine c)), and cell penetrating peptides.

Such vectors also optionally use fusogenic and endosome-destabilizing peptides/polymers, undergo acid-triggered conformational changes (e.g., to accelerate endosomal escape of the cargo), and/or incorporate a stimuli-cleavable polymer, e. g., for release in a cellular compartment. For example, disulfide-based cationic polymers that are cleaved in the reducing cellular environment can be used.

In certain embodiments, one or more nucleic acid molecules (e. g., DNA molecules) other than the components of a genome editing system, e.g., the RNA-guided nuclease component and/or the gRNA component described herein, are delivered. In n embodiments, the nucleic acid molecule is delivered at the same time as one or more of the components of the genome editing system. In certain embodiments, the nucleic acid molecule is delivered before or after (e. g., less than about 30 minutes, 1 hour, 2 hours, 3 hours, 6 hours, 9 hours, 12 hours, 1 day, 2 days, 3 days, 1 week, 2 weeks, or 4 weeks) one or more of the ents of the genome editing system are delivered. In n embodiments, the nucleic acid molecule is delivered by a different 2O means than one or more of the components of the genome editing system, e.g., the RNA- guided nuclease component and/or the gRNA component, are delivered. The nucleic acid molecule can be delivered by any of the delivery methods described herein. For example, the nucleic acid molecule can be delivered by a viral vector, e. g., an integration-deficient lentivirus, and the RNA-guided se molecule ent and/or the gRNA ent can be delivered by electroporation, e.g., such that the toxicity caused by nucleic acids (e.g., DNAs) can be reduced. In n embodiments, the nucleic acid molecule encodes a therapeutic protein, e. g., a protein described herein.

In certain ments, the nucleic acid molecule encodes an RNA molecule, e. g., an RNA molecule described herein. ry of RNPs and/or RNA encoding genome g system comgonenis RNPs (complexes of gRNAs and ided nucleases, i.e., ribonucleoprotein complexes) and/or RNAs encoding RNA-guided nucleases and/or gRNAs, can be delivered into cells or administered to subjects by art-known methods, some of which are described in Cotta-Ramusino. In vitro, RNA-guided nuclease-encoding and/or gRNA- encoding RNA can be delivered, e.g., by microinjection, electroporation, transient cell compression or squeezing (see, e. g., Lee 2012). mediated transfection, peptide- mediated delivery, GalNAc- or other conjugate-mediated delivery, and combinations thereof, can also be used for delivery in vitro and in vivo.

In vitro, delivery via electroporation comprises mixing the cells with the RNA ng RNA-guided nucleases and/or gRNAs, with or without donor template nucleic acid molecules, in a cartridge, chamber or cuvette and applying one or more electrical impulses of defined on and amplitude. Systems and protocols for electroporation are known in the art, and any suitable electroporation tool and/or protocol can be used in connection with the various embodiments of this disclosure.

Route of administration Genome g systems, or cells altered or manipulated using such s, can be administered to subjects by any suitable mode or route, whether local or systemic.

Systemic modes of administration include oral and parenteral routes. Parenteral routes 2O include, by way of example, intravenous, intramarrow, intrarterial, intramuscular, intradermal, subcutaneous, intranasal, and intraperitoneal routes. Components administered systemically can be d or formulated to target, e. g., HSCs, hematopoietic stem/progenitor cells, or erythroid progenitors or precursor cells.

Local modes of administration include, by way of example, intramarrow injection into the trabecular bone or intrafemoral ion into the marrow space, and infusion into the portal vein. In certain embodiments, significantly smaller s of the components (compared with systemic approaches) can exert an effect when administered y (for e, directly into the bone marrow) compared to when administered systemically (for example, intravenously). Local modes of administration can reduce or eliminate the incidence of potentially toxic side effects that may occur when eutically effective amounts of a component are administered systemically. stration can be provided as a periodic bolus (for example, intravenously) or as continuous infusion from an internal reservoir or from an external reservoir (for example, from an intravenous bag or implantable pump). Components can be stered locally, for example, by continuous release from a sustained release drug delivery device.

In addition, components can be formulated to permit e over a prolonged period of time. A release system can include a matrix of a biodegradable al or a material which releases the incorporated components by diffusion. The components can be homogeneously or heterogeneously buted within the release system. A variety of release systems can be useful, however, the choice of the appropriate system will depend upon rate of release required by a particular application. Both non-degradable and degradable e systems can be used. Suitable e systems include polymers and polymeric matrices, non-polymeric matrices, or inorganic and c excipients and diluents such as, but not limited to, calcium carbonate and sugar (for example, trehalose). e systems may be natural or tic. However, synthetic release systems are preferred because generally they are more reliable, more reproducible and produce more defined release profiles. The release system material can be selected so that ents having different molecular weights are released by diffusion through or degradation of the al.

Representative synthetic, biodegradable polymers include, for example: polyamides such as poly(amino acids) and poly(peptides); polyesters such as poly(lactic acid), poly(glycolic acid), poly(lactic-co-glycolic acid), and poly(caprolactone), poly(anhydrides); polyorthoesters; polycarbonates; and chemical derivatives thereof (substitutions, additions of al groups, for example, alkyl, alkylene, hydroxylations, oxidations, and other modifications routinely made by those skilled in the art), copolymers and es thereof. Representative synthetic, non-degradable polymers include, for example: polyethers such as poly(ethylene oxide), poly(ethylene glycol), and poly(tetramethylene oxide), vinyl polymers-polyacrylates and polymethacrylates such as methyl, ethyl, other alkyl, hydroxyethyl methacrylate, acrylic and methacrylic acids, and others such as inyl alcohol), poly(vinyl pyrolidone), and poly(vinyl acetate); poly(urethanes); cellulose and its derivatives such as alkyl, hydroxyalkyl, ethers, esters, nitrocellulose, and various cellulose acetates, polysiloxanes, and any chemical derivatives f (substitutions, additions of al groups, for example, alkyl, alkylene, hydroxylations, oxidations, and other modifications ely made by those skilled in the art), copolymers and mixtures thereof.

Poly(lactide-co-glycolide) microsphere can also be used. Typically the microspheres are composed of a r of lactic acid and glycolic acid, which are structured to form hollow spheres. The spheres can be approximately 15-30 microns in diameter and can be loaded with components described herein.

Mum-modal 0r diflerential delivefl of comgonems Skilled artisans will appreciate, in view of the instant disclosure, that ent components of genome editing systems disclosed herein can be delivered together or separately and simultaneously or nonsimultaneously. Separate and/or asynchronous delivery of genome editing system ents can be particularly desirable to provide temporal or spatial control over the function of genome editing systems and to limit certain effects caused by their activity. ent or differential modes as used herein refer to modes of delivery that confer different pharmacodynamic or pharmacokinetic properties on the subject component molecule, e. g., a RNA-guided se molecule, gRNA, template nucleic acid, or payload. For example, the modes of ry can result in different tissue distribution, different half-life, or different al bution, e.g., in a selected tment, tissue, or organ.

Some modes of delivery, e.g., delivery by a nucleic acid vector that persists in a cell, or in progeny of a cell, e.g., by autonomous replication or insertion into cellular nucleic acid, result in more persistent expression of and ce of a component. es include viral, e.g., AAV or lentivirus, delivery.

By way of example, the components of a genome editing system, e.g., a RNA- guided nuclease and a gRNA, can be delivered by modes that differ in terms of resulting half-life or persistent of the delivered component the body, or in a particular compartment, tissue or organ. In certain embodiments, a gRNA can be delivered by such modes. The RNA-guided nuclease le component can be delivered by a mode which results in less persistence or less exposure to the body or a particular compartment 3O or tissue or organ.

More generally, in certain embodiments, a first mode of delivery is used to r a first component and a second mode of delivery is used to deliver a second component. The first mode of delivery confers a first pharmacodynamic or pharrnacokinetic property. The first pharmacodynamic property can be, e. g, distribution, persistence, or exposure, of the component, or of a nucleic acid that encodes the component, in the body, a tment, tissue or organ. The second mode of delivery confers a second pharmacodynamic or pharrnacokinetic property. The second pharmacodynamic property can be, e. g., distribution, persistence, or exposure, of the component, or of a nucleic acid that encodes the component, in the body, a compartment, tissue or organ.

In certain embodiments, the first pharmacodynamic or pharmacokinetic property, e.g., distribution, persistence or exposure, is more limited than the second pharmacodynamic or pharrnacokinetic property.

In n embodiments, the first mode of delivery is selected to ze, e.g., minimize, a pharmacodynamic or pharrnacokinetic ty, e. g., distribution, persistence or exposure.

In certain embodiments, the second mode of delivery is selected to optimize, e.g., maximize, a pharmacodynamic or pharmacokinetic property, e. g., distribution, persistence or exposure.

In certain embodiments, the first mode of delivery comprises the use of a relatively tent element, e. g., a nucleic acid, e.g., a plasmid or viral vector, e. g., an AAV or lentivirus. As such vectors are relatively tent product transcribed from them would be relatively persistent.

In n ments, the second mode of delivery comprises a relatively transient element, e.g., an RNA or protein.

In certain embodiments, the first component comprises gRNA, and the delivery mode is relatively persistent, e. g, the gRNA is transcribed from a plasmid or viral vector, e. g., an AAV or irus. Transcription of these genes would be of little physiological consequence because the genes do not encode for a protein product, and the gRNAs are incapable of acting in isolation. The second component, a RNA-guided nuclease molecule, is red in a transient manner, for example as mRNA or as n, ensuring that the full RNA-guided nuclease molecule/gRNA complex is only present and active for a short period of time.

Furthermore, the components can be delivered in different lar form or with ent delivery vectors that complement one another to enhance safety and tissue specificity.

Use of differential delivery modes can enhance performance, safety, and/or efficacy, e. g., the likelihood of an eventual off-target modification can be reduced.

Delivery of immunogenic components, e.g., Cas9 molecules, by less persistent modes can reduce immunogenicity, as peptides from the bacterially-derived Cas enzyme are displayed on the surface of the cell by MHC molecules. A two-part ry system can alleviate these drawbacks.

Differential delivery modes can be used to r components to different, but overlapping target regions. The formation active complex is minimized outside the p of the target s. Thus, in certain embodiments, a first component, e. g., a gRNA is delivered by a first delivery mode that results in a first spatial, e.g., , distribution. A second component, e.g., a RNA-gmided nuclease molecule is delivered by a second delivery mode that results in a second spatial, e.g., tissue, distribution. In n embodiments, the first mode comprises a first element selected from a liposome, nanoparticle, e.g., polymeric nanoparticle, and a c acid, e.g., viral vector. The second mode comprises a second t selected from the group. In certain ments, the first mode of delivery comprises a first targeting element, e.g., a cell specific receptor or an antibody, and the second mode of delivery does not include that element. In certain embodiments, the second mode of delivery ses a second targeting element, e.g., a second cell specific receptor or second antibody.

When the RNA-guided nuclease molecule is delivered in a virus delivery vector, a liposome, or polymeric nanoparticle, there is the potential for delivery to and therapeutic activity in multiple tissues, when it may be desirable to only target a single tissue. A two-part delivery system can resolve this challenge and enhance tissue specificity. If the gRNA and the RNA-guided nuclease molecule are packaged in separated ry vehicles with distinct but overlapping tissue tropism, the fully functional complex is only be formed in the tissue that is targeted by both vectors.

Examples The ing Examples are merely illustrative and are not intended to limit the scope or content of the invention in any way.

Example 1 — Self-inactivating design embeds target sites in vector An AAV vector system is engineered such that it contains self-inactivating, universally applicable, tunable modules. These modules include the already-targeted endogenous cellular sequence, obviating the need for any additional gRNAs. In addition, these modules can be tuned based on ons within the viral , choice of gRNA, or PAM sequence.

The self-inactivating design contains DNA sequences that are identical or nearly identical to that of the endogenous target locus. Figure 1A is a diagram illustrating a SaCas9 (S. aureus Cas9)—gRNA complex targets both an endogenous cellular target and a nucleic acid encoding the SaCas9 in a viral vector.

Target sequences in the AAV are variably positioned, at either a site in the viral backbone or one of four regions in the SaCas9 coding sequences, and n either canonical or suboptimal PAMs. Figure 1B is a cartoon diagram depicting a or system in which engineered SaCas9 and gRNAS are encoded on separate viral genomes.

Three types of ary sites in an AAV genome into which heterologous cellular sequences can be engineered are marked by arrows. In type (a), the cellular ce is inserted at a site in the AAV backbone, in type (b), the cellular sequence is inserted at one of four regions (AC1, AC2, AC3, or N—terminal (NT)) in the SaCas9 coding sequence. In certain AAV vectors, the cellular sequences can be inserted at both type (a) and type (b) sites. SaCas9 and gRNAs can also be engineered into a single-vector system.

Example 2 — Target sites in SaCas9 do not disrupt SaCas9 nuclease ty This e provides systems and methods of engineering of targets sites in SaCas9 coding sequences that do not disrupt SaCas9 nuclease activity. s plasmids were constructed, with different target sites at four ent positions (NT, AC1, AC2, or AC3) in the SaCas9 coding sequence. Figure 4A is a cartoon diagram depicting exemplary ucts with target sites at the four different positions in the SaCas9 coding sequence, as well as a human VEGFA-3 gRNA expression plasmid. The target sites were from mCEP29O (guides 7, 9), hCEP290 s 64, 323, KKH) and SERPINAl (guides 333 and 776).

Self—inactivating or control Cas9 plasmids were transfected into HEK293 cells along with the gRNA expression plasmid targeting VEFGA site 3. mCherry was expressed through a separate promoter and was used to normalize the transfected amount of plasmid. GFP was expressed from the same transcript as SaCas9 and was used to measure the potential differences between transcription and translation rates. Figure 4B shows that self-inactivating SaCas9 mutants exhibited r expression level compared to control SaCas9 (WT) in HEK293 cells. GFP expression in self-inactivating SaCas9 constructs correlated with that of control SaCas9 constructs (WT), indicating unhindered transcription and translation of the self-inactivating SaCas9.

Wild-type control and engineered self-inactivating SaCas9 proteins exhibited similar levels of nuclease activity as shown in Figures 4C-4E. Self-inactivating SaCas9 constructs having c target ces inserted at specific target sites are indicated in each figure. Target sites AC1, AC2, AC3, and NT are in the coding sequence as 2O depicted in Figures 1B and 2. Target sequences m7, m9, a3, a7, 64-1, 64-2, 323-1, 323-2, KKH—l, and KKH—2 refer to sequences in genes mouse CEP290 (guides m7 and m9), human AlATSERPINAl (guides a3 and a7), and human CEP290 (guides 64-1, 64-2, 323-1, 323-2, KKH-l, and KKH-2), which are shown in Table 10 below. Control (labeled as “Standard”) and self-inactivating SaCas9 nuclease activity was ed by a T7E1 assay. The x-axis shows the amount of plasmid transfected into HEK293 cells, and the y-axis shows the % indels in VEGFA-3 as determined by the T7E1 assay.

Table 10 GTGTGCCAGCTGGCGGTATAGG [SEQ ID NO: 18] 64-1 and 64-2 GTCAAAAGCTACCGGTTACCTG [SEQ ID NO: 19] 323-1 and 323-2 TCCTCAGTAAAAGGTA [SEQ ID NO: 20] KKH-l and KKH—2 CAATAGGGATAGGTATGAGATACT [SEQ ID NO: 21] e 3 — Self-inactivating AAVs maintain efficacy at target GFP plasmids while self-inactivating in HEK293 cells This example provides in vitro data demonstrating the feasibility of attaining both robust target ation and self-targeting the pool of AAV DNA at its source.

HEK293 cells were seeded in 24-well plates and transfected with 500 ng/well of GFP expression plasmids ning gRNA target sites embedded in the 5’ end of the GFP coding sequences. The HEK293 cells were transduced the next day with a mixture of gRNA AAV targeting GFP, and either wild-type or self-targeting SaCas9 AAV (as shown in Figure 1B) at a total dose of 200,000 l. Two days later, cells were analyzed by fluorescence—activated cell sorting (FAC S) to determine knockdown of GFP expression. A schematic of the experimental design is shown in Figure 5A. Figure 5B shows GFP expression levels in HEK293 cells with or t wild-type or engineered SaCas9 ns. Control: no SaCas9 protein; WT: ype SaCas9 protein; BB (sub): engineered SaCas9 with target site inserted in the AAV backbone with suboptimal PAM sequence NNGRRA or NNGRRV; BB: engineered SaCas9 with target site inserted in the AAV backbone with canonical PAM sequence; AC1: engineered SaCas9 with target site inserted at the AC1 site of the SaCas9 coding sequence; BB/ACl: engineered SaCas9 with target site inserted both in the AAV backbone and at the AC1 site of the SaCas9 coding sequence. Two ent gRNA constructs (mCEP-7 and mCEP-9) were tested individually with self-inactivating SaCas9 proteins. As shown in Figure 5B, lower left panel, the control SaCas9 uct (WT) and the self-inactivating SaCas9 constructs exhibited similar capacities in knocking down GFP expression.

Protein was also harvested and SaCas9 level was quantified by an alphaLISA assay. Figure 5B, lower right panel shows Cas9 protein levels in HEK293 cells transduced with wild-type or self-inactivating SaCas9 constructs. All cells transduced with self-inactivating SaCas9 constructs ted reduced levels of SaCas9 protein, Engineered SaCas9 constructs with target site inserted at the AC1 site of SaCas9 coding sequence exhibited improved efficacy of self-inactivation compared to SaCas9 ucts with target site inserted in the AAV backbone alone. In addition, gRNA mCEP-9 exhibited stronger self-inactivating capacity than gRNA mCEP-7 . e 4 — Self-inactivating AAVs maintain efficacy at target locus while self- inactivating in retinal explants This example provides tissue t data demonstrating the feasibility of attaining both robust target modification and self-targeting the pool of AAV DNA at its source.

Retinal explants were extracted from BL6 mice and ed in 24-well plates.

The explants were transduced with a mixture of gRNA AAV and either wild-type or self- targeting SaCas9 AAV (as shown in Figure 1B) at a total dose of IBM vg/retina. At day 14 post extraction, both DNA and RNA were harvested from the explants. The nous target locus (mCEP290) was amplified from extracted DNA by PCR, cloned into TOPO vector, and sequenced. Control (WT) or self-inactivating SaCas9 constructs exhibited similar gene editing rate at the endogenous target locus in mouse retinal explants as shown in Figure 6A.

In addition, cDNA was generated from the extracted RNA. SaCas9 sequence was amplified by PCR, cloned into TOPO vector, and ced. The % indel rates in SaCas9 cDNA are shown in Figure 6B.

Example 5 — Self-inactivating AAVs successfully modified target loci while selfinactivating in vivo This example provides in vivo data demonstrating the feasibility of attaining both efficient target modification and self-targeting the pool of AAV DNA at its source.

AAVs with SaCas9 and gRNAs targeting mCEP29O were injected sub-retinally into 6J mice, and s were harvested 6 weeks later for DNA and cDNA sequencing.

A mixture of gRNA AAV and either wild-type control or self-targeting SaCas9 AAV (as shown in Figure 1B) at a total dose of 1.16 x 1010 AAV per eye were transduced. At 6 weeks post transduction, both DNA and RNA were harvested from the animal . The endogenous target locus was amplified from extracted DNA by PCR and sequenced with Next tion Sequencing methods on a Miseq machine. Self— inactivating SaCas9 constructs exhibited efficient gene editing rates compared to the negative control as shown in Figure 7A, though the gene editing rates of SaCas9 constructs having targeting sites within Cas9 coding ce (AC and BB/AC) were relatively lower compared to the ype control.

In addition, cDNA was generated from the extracted RNA. SaCas9 sequence was amplified by PCR, cloned into TOPO vector, and sequenced. The fold change of specific transcripts of the self-inactivating SaCas9 constructs compared to the wildtype SaCas9 construct are shown in Figure 7B. Transcripts containing SaCas9 coding sequence were significantly reduced in tissues transduced with AC-m9-WT PAM construct (self-inactivating SaCas9 having target site inserted at the AC1 site of the SaCas9 coding sequence) and BB-m7-AC-m9 construct (self-inactivating SaCas9 having target site inserted both in the AAV backbone and at the AC1 site of the SaCas9 coding ce).

INCORPORATION BY NCE All publications, patents, and patent applications mentioned herein are hereby incorporated by nce in their entirety as if each individual publication, patent or patent application was specifically and individually indicated to be incorporated by nce. In case of conflict, the present application, ing any tions herein, will control.

EQUIVALENTS Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments described herein. Such equivalents are intended to be encompassed by the following paragraphs.

Other embodiments of the invention as described herein are defined in the following aphs (corresponding to the PCT claims): 1. An isolated nucleic acid encoding an RNA-guided nuclease comprising a eukaryotic nucleic acid sequence, wherein the eukaryotic nucleic acid sequence is at least 17 nucleotides in length and either comprises or is adjacent to a protospacer adjacent motif (PAM) that is recognized by the RNA-guided nuclease. 2. The isolated nucleic acid of paragraph 1, further encoding a guide RNA (gRNA) comprising a targeting domain that is complementary to a portion of the otic nucleic acid sequence that is adjacent to the PAM. 3. The ed nucleic acid of paragraph 1 or 2, wherein the RNA-guided nuclease is a Cas9 protein. 4. The isolated nucleic acid of any one of paragraphs 1-3, wherein the targeting domain of the gRNA is 16-24 nucleotides in length.

. The isolated c acid of any one of aphs 1-4, wherein the eukaryotic nucleic acid ce is within a Cas9 coding sequence. 6. The isolated nucleic acid of paragraph 5, wherein the eukaryotic nucleic acid sequence encodes a modified portion of the Cas9 protein. 7. The isolated nucleic acid of any one of paragraphs 1-6, wherein the eukaryotic nucleic acid sequence is within a portion of the nucleic acid that includes, at each of its 3’ and 5’ ends, at least one codon for glycine, alanine or valine. 8. The isolated nucleic acid of aph 7, wherein the portion of the nucleic acid sing the eukaryotic nucleic acid ce encodes a polypeptide comprising the sequence of G-(X)6G. 9. The isolated nucleic acid of any one of paragraphs 3-8, wherein the Cas9 protein comprises an amino acid insertion relative to SEQ ID NO: 2 selected from the group consisting of: E271_N272insGX6-10G; L371_N372insGX6-10G; and Q737_A738insGX6-10G.

. The isolated nucleic acid of any one of paragraphs 3-8, wherein the Cas9 protein comprises an amino acid insertion relative to SEQ ID NO: 2 at or near the N- terminus of the Cas9 protein. 11. The isolated c acid of any one of paragraphs 3-10, wherein the Cas9 protein comprises an amino acid sequence having at least 95% sequence identity to a sequence selected from the group consisting of SEQ ID NOS: 3-5 and 10. 12. The isolated nucleic acid of any one of paragraphs 3-8, comprising an insertion, ve to SEQ ID NO:6, ed from the group consisting of: 814insN24-36; c.1113_1114insN24-36; and c.2211_2212insN24-36. 13. The isolated nucleic acid of any one of paragraphs 3-8, comprising an insertion, relative to SEQ ID NO:6 at or near the N-terminus of a Cas9 protein coding sequence. 14. The isolated nucleic acid of any one of aphs 3-13, comprising a nucleic acid sequence having at least 95% sequence identity to a sequence selected from the group consisting of SEQ ID NOS: 7-9 and 11.

. The isolated nucleic acid of any one of paragraphs 1-14, wherein the nucleic acid comprises a sequence having at least about 80% sequence identity to SEQ ID NO:1 and comprising an insertion of c.157insN19-36. 16. A transiently-active genome editing system comprising an RNA-guided nuclease d by the isolated c acid of any of paragraphs 1-15. 17. The transiently-active genome editing system of paragraph 16, wherein the system alters both a cellular endogenous target gene and the RNA-guided nuclease expression. 18. The ently-active genome editing system of paragraph 16 or 17, n the RNA-guided nuclease has at least about 80% nuclease activity of a wild-type RNA-guided nuclease protein. 19. The transiently-active genome g system of any of paragraphs 16-18, wherein the RNA-guided nuclease is a Cas9 protein. 20. A viral vector comprising the isolated nucleic acid of any one of paragraphs 1-15. 21. The viral vector of paragraph 20, wherein the viral vector is used to alter both a cellular endogenous target gene and the RNA-guided nuclease expression. 22. The vector of aph 20 or 21, wherein the vector is an associated virus (AAV) vector. 23. The vector of any one of paragraphs 20-22, wherein a target site for the gRNA is within the vector backbone. 24. The vector of paragraph 22 or 23, comprising a nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 1.

. A transiently active genome editing system, comprising: a guide RNA (gRNA) comprising a targeting domain that is complementary to a eukaryotic nucleic acid sequence; and an engineered RNA-guided nuclease encoded by a nucleic acid comprising the eukaryotic nucleotide sequence and a protospacer adjacent motif (PAM), wherein the PAM is recognized by the RNA-guided nuclease and is within or adjacent to the eukaryotic nucleotide sequence. 26. The transiently active genome editing system of paragraph 25, wherein the RNA- guided nuclease is a Cas9 protein. 27. The transiently active genome editing system of paragraph 26, wherein the engineered Cas9 protein and the gRNA form a Cas9/gRNA complex. 28. The ently active genome editing system of aph 27, wherein the gRNA/Cas9 complex is adapted to cleave the nucleic acid. 29. The ently active genome editing system of any one of paragraphs 26-28, wherein the engineered Cas9 protein comprises an amino acid insertion or substitution that is at least partially d by the eukaryotic nucleotide sequence.

. The transiently active genome editing system of any one of paragraphs 26-29, wherein the ered Cas9 n has at least about 80% nuclease activity of a wild-type Cas9 n. 31. The transiently active genome editing system of paragraph 29 or 30, comprising an amino acid insertion having a ce of G-(X)6G. 32. The transiently active genome editing system of paragraph 31, wherein the amino acid insertion, relative to SEQ ID NO: 2, is selected from the group consisting of: E271_N272insGX6-10G; L371_N372insGX6-10G; and Q737_A738insGX6-10G. 33. The transiently active genome editing system of paragraph 32, wherein the amino acid ion, ve to SEQ ID NO: 2, is at or near the N-terminus of a Cas9 protein. 34. The transiently active genome editing system of any one of paragraphs 26-33, wherein the engineered Cas9 protein comprises an amino acid sequence having at least 95% sequence ty to a sequence selected from the group consisting of SEQ ID NOS: 3-5 and 10. 35. The transiently active genome editing system of any of paragraphs 26-34, wherein the engineered Cas9 protein is encoded by a nucleic acid comprising an insertion, relative to SEQ ID NO: 6, selected from the group consisting of: c.813_814insN24-36; c.1113_1114insN24-36; and c.2211_2212insN24-36. 36. The transiently active genome editing system of any of paragraphs 26-35, n the engineered Cas9 protein is encoded by a nucleic acid comprising an insertion, ve to SEQ ID NO: 6, at or near the N-terminus of a Cas9 protein coding sequence. 37. The transiently active genome editing system of any one of paragraphs 26-36, wherein the engineered Cas9 protein is encoded by a nucleic acid comprising a sequence having at least 95% sequence ty to a sequence selected from the group consisting of SEQ ID NOS: 7-9 and 11. 38. The transiently active genome editing system of any one of paragraphs 26-37, wherein the engineered Cas9 protein is an engineered S. aureus Cas9. 39. A transiently active genome editing system for altering both a cellular endogenous target gene and an RNA-guided nuclease sion, comprising: a guide RNA (gRNA) comprising a targeting domain that is complementary to a eukaryotic nucleic acid sequence; and an engineered RNA-guided se d by a nucleic acid sing the eukaryotic nucleotide sequence and a protospacer adjacent motif (PAM), n the PAM is recognized by the RNA-guided nuclease and is within or adjacent to the eukaryotic nucleotide sequence. 40. The transiently active genome editing system of paragraph 39, wherein the RNA- guided nuclease is a Cas9 protein. 41. The transiently active genome g system of paragraph 40, wherein the engineered Cas9 protein and the gRNA form a Cas9/gRNA complex. 42. The transiently active genome editing system of paragraph 41, wherein the Cas9/gRNA complex is adapted to cleave both the nucleic acid ng the engineered Cas9 n and a nucleic acid encoding the cellular endogenous target gene. 43. The transiently active genome editing system of any one of paragraphs 40-42, wherein the engineered Cas9 protein comprises an amino acid insertion or substitution that is at least partially encoded by the eukaryotic nucleotide ce. 44. The transiently active genome editing system of any one of paragraphs 40-43, wherein the engineered Cas9 protein has at least about 80% nuclease activity of a wild-type Cas9 protein. 45. The transiently active genome editing system of paragraph 43 or 44, comprising an amino acid insertion having a sequence of G-(X)6G. 46. The transiently active genome editing system of paragraph 45, n the amino acid insertion, relative to SEQ ID NO: 2, is selected from the group consisting of: E271_N272insGX6-10G; L371_N372insGX6-10G; and Q737_A738insGX6-10G. 47. The ently active genome g system of paragraph 45, wherein the amino acid insertion, ve to SEQ ID NO: 2, is at or near the N-terminus of the Cas9 protein. 48. The transiently active genome editing system of any one of paragraphs 40-47, wherein the engineered Cas9 protein comprises an amino acid sequence having at least 95% sequence identity to a sequence selected from the group ting of SEQ ID NOS: 3-5, 10. 49. The transiently active genome editing system of any one of paragraphs 40-48, wherein the engineered Cas9 protein is encoded by a nucleic acid comprising an insertion, relative to SEQ ID NO: 6, selected from the group consisting of: 814insN24-36; c.1113_1114insN24-36; and c.2211_2212insN24-36. 50. The transiently active genome editing system of any one of aphs 40-48, wherein the engineered Cas9 protein is encoded by a nucleic acid comprising an insertion, relative to SEQ ID NO: 6, at or near the N-terminus of a Cas9 protein coding sequence. 51. The transiently active genome editing system of any one of paragraphs 40-50, wherein the engineered Cas9 protein is encoded by a nucleic acid comprising a sequence having at least 95% sequence identity to a sequence selected from the group consisting of SEQ ID NOS: 7-9 and 11. 52. The transiently active genome editing system of any one of paragraphs 40-51, wherein the engineered Cas9 protein is an ered S. aureus Cas9. 53. An RNA-guided nuclease protein comprising an amino acid insertion or substitution at least partially encoded by a eukaryotic nucleic acid sequence of at least 17 nucleotides in length. 54. The ided nuclease of paragraph 53, wherein the RNA-guided nuclease has at least about 80% nuclease activity of a ype RNA-guided nuclease. 55. The RNA-guided nuclease of paragraph 54, wherein the eukaryotic nucleic acid sequence is a mammalian sequence. 56. The RNA-guided nuclease protein of any one of paragraphs 53-55, wherein the eukaryotic nucleic acid sequence ses or is adjacent to a protospacer adjacent motif (PAM) that is recognized by the engineered RNA-guided nuclease protein. 57. The RNA-guided se of aph 56, wherein the eukaryotic nucleic acid sequence comprises at least 17 nucleotides adjacent to the PAM. 58. The RNA-guided se of any of paragraphs 53-57, wherein the RNA-guided nuclease is a Cas9 protein. 59. The Cas9 protein of paragraph 58, comprising an insertion having a sequence of G-(X)6G. 60. The Cas9 protein of paragraph 58 or 59, comprising an ion selected from the group consisting of: E271_N272insGX6-10G; L371_N372insGX6-10G; and Q737_A738insGX6-10G. 61. The Cas9 protein of paragraph 58 or 59, comprising an insertion at or near the N- terminus of the Cas9 protein. 62. The Cas9 protein of any one of paragraphs 58-61, comprising an amino acid sequence of at least 95% sequence identity relative to a sequence selected from the group consisting of SEQ ID NOS: 3-5 and 10. 63. An isolated c acid encoding the ided nuclease of any one of aphs 53-62. 64. A method of altering a target site in a cell comprising delivering to the cell a ently active genome editing system, the transiently expressed genome editing system comprising: a guide RNA (gRNA) comprising a targeting domain that is mentary to a eukaryotic nucleic acid sequence; and an ered RNA-guided nuclease encoded by the nucleic acid comprising the otic nucleotide ce and a protospacer adjacent motif (PAM), wherein the PAM is recognized by the RNA-guided nuclease and is within or adjacent to the eukaryotic nucleotide sequence. 65. The method of paragraph 64, wherein the RNA-guided nuclease is a Cas9 protein. 66. The method of paragraph 65, wherein the engineered Cas9 protein and the gRNA form a Cas9/gRNA complex. 67. The method of paragraph 66, wherein the gRNA/Cas9 complex is adapted to cleave the nucleic acid encoding the engineered Cas9 protein. 68. The method of paragraph 65, wherein the gRNA/Cas9 complex is adapted to cleave both the nucleic acid encoding the engineered Cas9 protein and the target site in the cell. 69. The method of any one of paragraphs 65-68, wherein the engineered Cas9 n comprises an amino acid insertion or substitution that is at least lly encoded by the eukaryotic nucleotide ce. 70. The method of any one of paragraphs 65-69, wherein the engineered Cas9 protein has at least about 80% nuclease activity of a wild-type Cas9 protein. 71. The method of any one of paragraphs 65-70, wherein the engineered Cas9 protein comprises an amino acid ion having a sequence of G-(X)6G. 72. The method of any one of paragraphs 65-71, n the amino acid insertion, relative to SEQ ID NO: 2, is selected from the group consisting of: E271_N272insGX6-10G; L371_N372insGX6-10G; and Q737_A738insGX6-10G. 73. The method of any one of paragraphs 65-71, wherein the amino acid insertion, relative to SEQ ID NO: 2, is at or near the N-terminus of the Cas9 protein. 74. The method of any one of paragraphs 65-73, wherein the engineered Cas9 protein comprises an amino acid ce having at least 95% ce identity to a sequence selected from the group consisting of SEQ ID NOS: 3-5 and 10. 75. The method of any one of paragraphs 65-74, wherein the nucleic acid encoding the engineered Cas9 protein comprises an insertion, relative to SEQ ID NO: 6, selected from the group consisting of: c.813_814insN24-36; c.1113_1114insN24-36; and c.2211_2212insN24-36. 76. The method of any one of paragraphs 65-74, wherein the nucleic acid encoding the engineered Cas9 protein comprises an ion, relative to SEQ ID NO: 6, at or near the N-terminus of a Cas9 protein coding sequence. 77. The method of any one of paragraphs 65-76, wherein the nucleic acid encoding the engineered Cas9 protein comprises a sequence having at least 95% sequence identity to a sequence selected from the group consisting of SEQ ID NOS: 7-9 and 11. 78. The method of any of paragraphs 65-77, wherein the Cas9 is an S. aureus Cas9. 79. An isolated nucleic acid encoding a Cpf1 RNA-guided nuclease comprising a eukaryotic nucleic acid sequence, wherein the eukaryotic nucleic acid sequence is at least 17 tides in length and either ses or is adjacent to a protospacer nt motif (PAM) that is recognized by the RNA-guided nuclease. 80. The isolated nucleic acid of paragraph 79, further encoding a guide RNA (gRNA) comprising a targeting domain that is complementary to a portion of the nucleic acid sequence that is adjacent to the PAM. 81. The isolated nucleic acid of any one of paragraphs 79-80, wherein the targeting domain of the gRNA is 16-24 tides in length. 82. The isolated nucleic acid of any one of paragraphs 79-81, wherein the eukaryotic nucleic acid ce is within a Cpf1 coding sequence. 83. The isolated nucleic acid of paragraph 82, wherein the eukaryotic nucleic acid sequence encodes a modified portion of the Cpf1 protein. 84. The isolated nucleic acid of any one of paragraphs 79-83, wherein the otic nucleic acid sequence is within a n of the nucleic acid that includes, at each of its 3’ and 5’ ends, at least one codon for glycine. 85. The isolated nucleic acid of paragraph 84, wherein the portion of the c acid comprising the eukaryotic nucleic acid sequence encodes a polypeptide comprising the sequence of G-(X)6G. 86. The isolated nucleic acid of any one of aphs 79-85, wherein the Cpf1 protein comprises an amino acid insertion, ve to SEQ ID NO: 13, at a position selected from the group consisting of between amino acid positions 147 and 148, anywhere between amino acid positions 484 and 492, anywhere between amino acid positions 568 and 590, anywhere between amino acid positions 795 and 855, anywhere between amino acid positions 1131 and 1140, and anywhere between amino acid positions 1160 and 1173. 87. The ed nucleic acid of any one of paragraphs 79-85, wherein the Cpf1 protein comprises an amino acid ion relative to SEQ ID NO: 13 at or near the N-terminus of the Cpf1 protein. 88. The isolated nucleic acid of any one of paragraphs 79-87, wherein the Cpf1 protein comprises an amino acid sequence having at least 95% sequence identity to SEQ ID NO: 13. 89. The isolated nucleic acid of any one of aphs 79-85, comprising an insertion, relative to SEQ ID NO: 14, at a position selected from the group consisting of: between nucleic acid positions 441 and 442, anywhere n nucleic acid positions 1452 and 1474, anywhere between c acid positions 1704 and 1768, anywhere between nucleic acid positions 2385 and 2563, anywhere between nucleic acid positions 3393 and 3418, and re between nucleic acid positions 3480 and 3517, wherein the insertion does not alter the g frame of the isolated nucleic acid. 90. The isolated nucleic acid of any one of paragraphs 79-85, sing an insertion, relative to SEQ ID NO: 14 at or near the N-terminus of a Cpf1 protein coding sequence. 91. The isolated nucleic acid of any one of paragraphs 79-90, comprising a nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 14. 92. A transiently-active genome editing system comprising an RNA-guided se encoded by the isolated nucleic acid of any of paragraphs 79-91. 93. The transiently-active genome editing system of paragraph 92, n the system alters both a cellular endogenous target gene and the RNA-guided nuclease expression. 94. The transiently-active genome editing system of paragraph 91 or 92, wherein the RNA-guided nuclease has at least about 80% nuclease activity of a wild-type RNA-guided se protein. 95. A viral vector comprising the isolated nucleic acid of any one of paragraphs 79- 91. 96. A method of altering a target site in a cell comprising delivering to the cell a transiently active genome editing system, the transiently sed genome editing system comprising: a guide RNA (gRNA) comprising a targeting domain that is complementary to a eukaryotic nucleic acid sequence; and an engineered Cpf1 RNA-guided nuclease encoded by the nucleic acid comprising the eukaryotic nucleotide sequence and a protospacer adjacent motif (PAM), wherein the PAM is recognized by the CpF1 RNA-guided nuclease and is within or nt to the eukaryotic nucleotide sequence. 97. The method of paragraph 96, wherein the engineered Cpf1 protein and the gRNA form a RNA complex. 98. The method of paragraph 97, wherein the RNA complex is adapted to cleave the nucleic acid encoding the engineered Cpf1 protein. 99. The method of paragraph 96, wherein the Cpf1/gRNA complex is adapted to cleave both the c acid encoding the engineered Cpf1 protein and the target site in the cell. 100. The method of any one of paragraphs 96-99, wherein the engineered Cpf1 protein ses an amino acid insertion or substitution that is at least partially encoded by the otic nucleotide sequence. 101. The method of any one of paragraphs 96-100, wherein the engineered Cpf1 protein has at least about 80% nuclease activity of a wild-type Cpf1 protein. 102. The method of any one of paragraphs 96-101, wherein the n of the nucleic acid comprising the eukaryotic nucleic acid sequence encodes a polypeptide sing the sequence of G-(X)6G. 103. The method of any one of paragraphs 96-102, wherein the Cpf1 protein comprises an amino acid insertion, relative to SEQ ID NO: 13, at a position selected from the group consisting of between amino acid positions 147 and 148, anywhere between amino acid positions 484 and 492, anywhere between amino acid positions 568 and 590, anywhere between amino acid positions 795 and 855, anywhere between amino acid positions 1131 and 1140, and anywhere between amino acid positions 1160 and 1173. 104. The method of any one of paragraphs , wherein the Cpf1 protein ses an amino acid insertion relative to SEQ ID NO: 13 at or near the N- terminus of the Cpf1 protein. 105. The isolated nucleic acid of any one of paragraphs 79-87, wherein the Cpf1 protein comprises an amino acid sequence having at least 95% sequence identity to SEQ ID NO: 13. 106. The method of any one of paragraphs 96-102, comprising an insertion, relative to SEQ ID NO: 14, at a position selected from the group consisting of: between nucleic acid positions 441 and 442, anywhere n c acid positions 1452 and 1474, re between nucleic acid positions 1704 and 1768, anywhere between nucleic acid positions 2385 and 2563, anywhere between c acid positions 3393 and 3418, and anywhere between nucleic acid ons 3480 and 3517, wherein the insertion does not alter the g frame of the isolated nucleic acid. 107. The method of any one of paragraphs 96-102, comprising an insertion, relative to SEQ ID NO: 14 at or near the N-terminus of a Cpf1 protein coding sequence. 108. The method of any one of paragraphs 96-102, comprising a nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 14.

Still further embodiments are within the scope of the ing claims.

Claims (26)

1. An isolated nucleic acid encoding a Cpf1 RNA-guided nuclease comprising a eukaryotic nucleic acid sequence, wherein the eukaryotic nucleic acid sequence is at least 17 nucleotides in length and either comprises or is adjacent to a protospacer adjacent motif (PAM) that is recognized by the RNA-guided nuclease.

2. The isolated nucleic acid of claim 1, further encoding a guide RNA (gRNA) comprising a targeting domain that is complementary to a portion of the c acid sequence that is adjacent to the PAM.

3. The ed nucleic acid of claim 1 or 2, wherein the ing domain of the gRNA is 16-24 nucleotides in length.

4. The isolated nucleic acid of any one of claims 1-3, wherein the eukaryotic nucleic acid ce is within a Cpf1 coding sequence.

5. The isolated nucleic acid of claim 4, wherein the eukaryotic nucleic acid sequence encodes a modified portion of the Cpf1 protein.

6. The isolated nucleic acid of any one of claims 1-5, wherein the eukaryotic nucleic acid sequence is within a portion of the nucleic acid that includes, at each of its 3’ and 5’ ends, at least one codon for glycine.

7. The isolated nucleic acid of claim 6, wherein the portion of the nucleic acid comprising the otic nucleic acid sequence encodes a polypeptide comprising the ce of G-(X)6G.

8. The isolated nucleic acid of any one of claims 1-7, wherein the Cpf1 protein comprises an amino acid insertion, relative to SEQ ID NO: 13, at a position ed from the group consisting of between amino acid positions 147 and 148, anywhere between amino acid positions 484 and 492, anywhere between amino acid positions 568 and 590, re between amino acid positions 795 and 855, anywhere between amino acid ons 1131 and 1140, and anywhere between amino acid positions 1160 and 1173.

9. The isolated nucleic acid of any one of claims 1-8, wherein the Cpf1 protein comprises an amino acid insertion relative to SEQ ID NO: 13 at or near the inus of the Cpf1 protein.

10. The isolated nucleic acid of any one of claims 1-9, wherein the Cpf1 n comprises an amino acid sequence having at least 95% sequence identity to the amino acid ce set forth in SEQ ID NO: 13.

11. The isolated nucleic acid of any one of claims 1-10, comprising an insertion, relative to SEQ ID NO: 14, at a position selected from the group consisting of: between nucleic acid positions 441 and 442, anywhere between c acid positions 1452 and 1474, anywhere between nucleic acid positions 1704 and 1768, re between nucleic acid positions 2385 and 2563, anywhere between nucleic acid positions 3393 and 3418, and anywhere between nucleic acid positions 3480 and 3517, wherein the insertion does not alter the reading frame of the isolated nucleic acid.

12. The isolated nucleic acid of any one of claims 1-11, comprising an insertion, relative to SEQ ID NO: 14 at or near the N-terminus of a Cpf1 protein coding sequence.

13. The isolated nucleic acid of any one of claims 1-12, sing a c acid sequence having at least 95% ce ty to the nucleic acid sequence set forth in SEQ ID NO: 14.

14. A transiently-active genome editing system comprising a Cpf1 ided nuclease encoded by the isolated nucleic acid of any of claims 1-13.

15. The transiently-active genome editing system of claim 14, wherein the system alters both a cellular endogenous target gene and the Cpf1 RNA-guided nuclease expression.

16. The transiently-active genome editing system of claim 14 or 15, wherein the Cpf1 RNA- guided nuclease has at least about 80% nuclease activity of a wild-type Cpf1 RNA- guided se protein.

17. A viral vector comprising the isolated nucleic acid of any one of claims 1-13.

18. A method of altering a target site in a cell comprising delivering to the cell a transiently active genome editing system, the transiently expressed genome editing system comprising: a guide RNA (gRNA) comprising a targeting domain that is complementary to a eukaryotic c acid sequence; and an engineered Cpf1 RNA-guided nuclease encoded by the nucleic acid comprising the eukaryotic tide sequence and a protospacer adjacent motif (PAM), wherein the PAM is recognized by the Cpf1 RNA-guided nuclease and is within or adjacent to the eukaryotic nucleotide sequence.

19. The method of claim 18, wherein the engineered Cpf1 protein and the gRNA form a Cpf1/gRNA x.

20. The method of claim 19, n the Cpf1/gRNA complex is adapted to cleave the nucleic acid encoding the engineered Cpf1 protein.

21. The method of claim 18, wherein the Cpf1/gRNA complex is adapted to cleave both the nucleic acid encoding the engineered Cpf1 protein and the target site in the cell.

22. The method of any one of claims 18-21, wherein the engineered Cpf1 protein comprises an amino acid insertion or tution that is at least partially encoded by the eukaryotic nucleotide sequence.

23. The method of any one of claims 18-22, wherein the engineered Cpf1 protein has at least about 80% nuclease activity of a wild-type Cpf1 protein.

24. The method of any one of claims 18-23, n the portion of the c acid comprising the eukaryotic nucleic acid sequence encodes a polypeptide comprising the sequence of G-(X)6G.

25. The method of any one of claims 18-24, wherein the Cpf1 protein comprises an amino acid insertion, relative to SEQ ID NO: 13, at a position selected from the group consisting of between amino acid positions 147 and 148, re between amino acid positions 484 and 492, re between amino acid positions 568 and 590, anywhere between amino acid positions 795 and 855, anywhere between amino acid positions 1131 and 1140, and anywhere n amino acid positions 1160 and 1173.

26. The method of any one of claims 18-25, wherein the Cpf1 protein comprises an amino acid insertion relative to SEQ ID NO: 13 at or near the N-terminus of the Cpf1 protein.