[go: up one dir, main page]

WO1997008308A1 - Gene du syndrome de batten-steinert - Google Patents

Gene du syndrome de batten-steinert Download PDF

Info

Publication number
WO1997008308A1
WO1997008308A1 PCT/US1996/013896 US9613896W WO9708308A1 WO 1997008308 A1 WO1997008308 A1 WO 1997008308A1 US 9613896 W US9613896 W US 9613896W WO 9708308 A1 WO9708308 A1 WO 9708308A1
Authority
WO
WIPO (PCT)
Prior art keywords
batten disease
seq
ofthe
polypeptide
leu
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US1996/013896
Other languages
English (en)
Other versions
WO1997008308A9 (fr
Inventor
Terry J. Lerner
Peter E. M. Taschner
Martijn H. Breuning
James F. Gusella
Sara E. Mole
Mark R. Gardiner
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
University College London
Universiteit Leiden
General Hospital Corp
Original Assignee
University College London
Universiteit Leiden
General Hospital Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by University College London, Universiteit Leiden, General Hospital Corp filed Critical University College London
Priority to AU69603/96A priority Critical patent/AU6960396A/en
Publication of WO1997008308A1 publication Critical patent/WO1997008308A1/fr
Publication of WO1997008308A9 publication Critical patent/WO1997008308A9/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Definitions

  • the invention relates to the Batten disease gene. Batten disease polypeptides, and methods using these and other related compounds.
  • NCLs neuronal ceroid lipofuscinoses
  • Inheritance is autosomal recessive for the childhood onset forms which include: infantile (CLNI; Haltia-Santavuori disease, MIM256730), classical late-infantile (CLN2; Jansky-Bielschowsky disease, MIM204500), juvenile (CLN3; Batten or Spielmeyer-Vogt-Sjogren disease, MIM304200), and Finnish variant late-infantile (CLN5; MIM256731).
  • the primary biochemical defects in these disorders are not known. Batten disease, the juvenile onset form of NCL, is the most common neurodegenerative disorder of childhood. Its incidence is estimated at up to 1/25,000 births (Zeman W. (1974) J. Neuropathol. Exp. Neurol.
  • the inventors have identified and cloned the gene responsible for Batten disease, hereafter referred to as "the Batten disease gene.”
  • the gene is located on human chromosome 16pl2.1 and encodes a polypeptide having a predicted 438 amino acid sequence, hereafter referred to as "a Batten disease polypeptide”.
  • the invention features a polypeptide, e.g., a recombinant polypeptide or substantially pure preparation of a polypeptide, the sequence of which includes, or is, the sequence of a Batten disease polypeptide, e.g., the sequence shown in SEQ ID NO: 2 or SEQ ID NO: 19.
  • the invention also features fragments and analogs preferably having at least one biological activity (as defined herein) of a Batten disease polypeptide.
  • polypeptide is a mammalian, e.g., a human or a rodent, e.g., a mouse or a rat, polypeptide.
  • the polypeptide has at least one biological activity, e.g., it reacts with an antibody, or antibody fragment, specific for a Batten disease polypeptide; the polypeptide includes an amino acid sequence at least 60%, 80%, 90%, 95%, 98%, or 99% homologous to an amino acid sequence from SEQ ID NO: 2 or SEQ ID NO: 19; the polypeptide includes an amino acid sequence more than 85% homologous to an amino acid sequence from SEQ ID NO: 2 or SEQ ID NO: 19; the polypeptide includes an amino acid sequence essentially the same as an amino acid sequence in SEQ ID NO: 2 or SEQ ID NO: 19; the polypeptide is at least 5, 10, 20, 50, 100, or 150 amino acids in length; the polypeptide includes at least 5, preferably at least 10, more preferably at least 20.
  • the polypeptide includes an amino acid sequence at least 60%, 80%, 90%, 95%, 98%, or 99% homologous to an amino acid sequence from SEQ ID NO: 2 or SEQ ID NO: 19; the polypeptid
  • the polypeptide is preferably at least 10, but no more than 100, amino acids in length, and contains one, two, three or more phosphorylation sites;
  • the Batten disease polypeptide is either, an agonist or an antagonist, of a biological activity of a naturally occurring Batten disease polypeptide.
  • the Batten disease polypeptide is encoded by the nucleic acid sequence of SEQ ID NO: 1 or SEQ ID NO: 18, or by a nucleic acid having at least 60%, 70%, 80%, 90%, 95%, 98%, or 99% homology with the nucleic acid of SEQ ID NO: 1; the polypeptide is encoded by a nucleic acid having more than 82% homology with the nucleic acid of SEQ ID NO: 1 or SEQ ID NO: 18.
  • the Batten disease polypeptide can be encoded by a nucleic acid sequence which differs from a nucleic acid sequence of SEQ ID NO: 1 or SEQ ID NO: 18 due to degeneracy in the genetic code.
  • the nucleic acid encoding the Batten disease polypeptide is a mammalian, e.g., a human or a rodent, e.g., a mouse or a rat, nucleic acid.
  • the Batten disease polypeptide is an agonist of a naturally-occurring mutant or wild type Batten disease polypeptide (e.g., a polypeptide having an amino acid sequence shown in SEQ ID NO: 2 or SEQ ID NO: 19).
  • the polypeptide is an antagonist which, for example, inhibits an undesired activity of a naturally-occurring Batten disease polypeptide (e.g., a mutant polypeptide).
  • the Batten disease polypeptide includes amino acid residues 155-226 of SEQ ID NO: 2 and/or residues 255-352 of SEQ ID NO: 2.
  • the Batten disease polypeptide differs in amino acid sequence at 1, 2, 3, 5, 10 or more residues, from a sequence in SEQ ID NO: 2 or SEQ ID NO: 19. The differences, however, are such that the Batten disease polypeptide exhibits at least one biological activity of a Batten disease polypeptide, e.g., the Batten disease polypeptide retains a biological activity of a naturally occurring Batten disease polypeptide.
  • the Batten disease polypeptide includes a Batten disease polypeptide sequence, as described herein, as well as other N-terminal and/or C- terminal amino acid sequences.
  • the polypeptide includes all or a fragment of an amino acid sequence from SEQ ID NO: 2 or SEQ ID NO: 19, fused, in reading frame, to additional amino acid residues, preferably to residues encoded by genomic DNA 5' to the genomic DNA which encodes a sequence from SEQ ID NO: 2 or SEQ ID NO: 19.
  • the Batten disease polypeptide is a recombinant fusion protein having a first Batten disease polypeptide portion and a second polypeptide portion having an amino acid sequence unrelated to a Batten disease polypeptide.
  • the second polypeptide portion can be, e.g., any of glutathione-S-transferase, a DNA binding domain, or a polymerase activating domain.
  • the fusion protein can be used in a two-hybrid assay.
  • the Batten disease polypeptide is a fragment or analog of a naturally occurring Batten disease polypeptide which inhibits reactivity with antibodies, or F(ab')2 fragments, specific for a naturally occurring Batten disease polypeptide.
  • the Batten disease polypeptide includes a leader sequence, e.g., an N-terminal sequence responsible for secretion ofthe polypeptide from a cell in which it is expressed, or other sequence which is not present in the mature protein.
  • the Batten disease polypeptide e.g., the polypeptide of SEQ ID NO: 2 or SEQ ID NO: 19, lacks a leader sequence, e.g., an N-terminal sequence responsible for secretion ofthe polypeptide from a cell in which it is expressed, or other sequence which is not present in the mature protein.
  • the Batten Disease polypeptide has a molecular weight of about 48 kDa.
  • Polypeptides ofthe invention include those which arise as a result ofthe existence of multiple genes, alternative transcription events, alternative RNA splicing events, and alternative translational and postranslational events.
  • the invention includes an immunogen which includes an active or inactive Batten disease polypeptide, or an analog or a fragment thereof, in an immunogenic preparation, the immunogen being capable of eliciting an immune response specific for the Batten disease polypeptide, e.g., a humoral response, an antibody response, or a cellular response.
  • the immunogen comprising an antigenic determinant, e.g., a unique determinant, from a protein represented by SEQ ID NO: 2 or SEQ ID NO: 19.
  • the invention also includes an antibody preparation, preferably a monoclonal antibody preparation, specifically reactive with an epitope ofthe Batten disease immunogen or generally of a Batten disease polypeptide.
  • compositions which includes a Batten disease polypeptide (or a nucleic acid which encodes it) and one or more additional components, e.g., a carrier, diluent, or solvent.
  • additional component can be one which renders the composition useful for in vitro, in vivo, pharmaceutical, or veterinary use.
  • the invention provides a substantially pure nucleic acid having, or comprising, a nucleotide sequence which encodes a polypeptide, the amino acid sequence of which includes, or is, the sequence of a Batten disease polypeptide, or analog or fragment thereof.
  • the nucleic acid encodes a polypeptide having one or more ofthe following characteristics: at least one biological activity of a Batten disease polypeptide, e.g., a polypeptide specifically reactive with an antibody, or antibody fragment, directed against a Batten disease polypeptide; an amino acid sequence at least 60%, 80%, 90%, 95%, 98%, or 99% homologous to an amino acid sequence from SEQ ID NO: 2 or SEQ ID NO: 19; an amino acid sequence more than 85% homologous to an amino acid sequence from SEQ ID NO: 2 or SEQ ID NO: 19; an amino acid sequence essentially the same as an amino acid sequence in SEQ ID NO: 2 or SEQ ID NO: 19, the polypeptide is at least 5, 10, 20, 50, 100, or 150 amino acids in length; at least 5, preferably at least 10, more preferably at least 20, most preferably at least 50, 100, or 150 contiguous amino acids from SEQ ID NO: 2 or SEQ ID NO: 19; an amino acid sequence which is preferably at least 10, but no
  • the nucleic acid is or includes the nucleotide sequence of SEQ ID NO:l or SEQ ID NO: 18; the nucleic acid is at least 60%, 70%, 80%, 90%), 95%, 98%, or 99% homologous with a nucleic acid sequence of SEQ ID NO:l or SEQ ID NO: 18; the nucleic acid is more than 82% homologous with a nucleic acid sequence of SEQ ID NO:l or SEQ ID NO: 18; the nucleic acid includes a fragment of SEQ ID NO:l or SEQ ID NO: 18 which is at least 25, 50, 100, 200, 300, 400, 500, or 1,000 bases in length; the nucleic acid differs from the nucleotide sequence of SEQ ID NO: 1 or SEQ ID NO: 18 due to degeneracy in the genetic code.
  • the polypeptide encoded by the nucleic acid is a mammalian, e.g., a human or a rodent, e.g.,
  • the polypeptide encoded by the nucleic acid is an agonist which, for example, is capable of enhancing an activity of a naturally-occurring mutant or wild type Batten disease polypeptide.
  • the encoded polypeptide is an antagonist which, for example, inhibits an undesired activity of a naturally-occurring Batten disease polypeptide (e.g., a polypeptide having an amino acid sequence shown in SEQ ID NO: 2 or SEQ ID NO: 19).
  • the encoded Batten disease polypeptide differs in amino acid sequence at 1. 2, 3, 5, 10 or more residues, from a sequence in SEQ ID NO:2 or SEQ ID NO: 19. The differences, however, are such that the encoded Batten disease polypeptide exhibits at least one biological activity of a naturally occurring Batten disease polypeptide (e.g., the Batten disease polypeptide of SEQ ID NO:2 or SEQ ID NO: 19).
  • a naturally occurring Batten disease polypeptide e.g., the Batten disease polypeptide of SEQ ID NO:2 or SEQ ID NO: 19.
  • the nucleic acid encodes a Batten disease polypeptide which includes a Batten disease polypeptide sequence, as described herein, as well as other N-terminal and/or C-terminal amino acid sequences.
  • the nucleic acid encodes a polypeptide which includes all or a portion of an amino acid sequence shown in SEQ ID NO:2 or SEQ ID NO: 19, fused, in reading frame, to additional amino acid residues, preferably to residues encoded by genomic DNA 5' to the genomic DNA which encodes a sequence from SEQ ID NO:2 or SEQ ID NO:19.
  • the encoded polypeptide is a recombinant fusion protein having a first Batten disease polypeptide portion and a second polypeptide portion having an amino acid sequence unrelated to a Batten disease polypeptide.
  • the second polypeptide portion can be, e.g., any of glutathione-S-transferase; a DNA binding domain; or a polymerase activating domain.
  • the fusion protein can be used in a two-hybrid assay.
  • the encoded polypeptide is a fragment or analog of a naturally occurring Batten disease polypeptide which inhibits reactivity with antibodies, or F(ab')2 fragments, specific for a naturally occurring Batten disease polypeptide.
  • the nucleic acid will include a transcriptional regulatory sequence, e.g. at least one of a transcriptional promoter or transcriptional enhancer sequence, operably linked to the Batten disease gene sequence, e.g., to render the Batten disease gene sequence suitable for use as an expression vector.
  • the nucleic acid ofthe invention hybridizes under stringent conditions to a nucleic acid probe corresponding to at least 12 consecutive nucleotides from SEQ ID NO: 1 or SEQ ID NO: 18, or more preferably to at least 20 consecutive nucleotides from SEQ ID NO:l, or more preferably to at least 40 consecutive nucleotides from SEQ ID NO: 1 or SEQ ID NO: 18.
  • the nucleic acid comprises bases 598-814 of SEQ ID NO: 1.
  • the nucleic acid preferable encodes a Batten disease polypeptide comprising amino acid residues 155-226 of SEQ ID NO: 2.
  • the nucleic acid encodes a mature polypeptide having a molecular weight of about 48 kDa.
  • nucleic acid encodes a Batten disease polypeptide which includes a leader sequence, e.g., an N-terminal sequence responsible for secretion ofthe polypeptide from a cell in which it is expressed, or other sequence which is not present in the mature protein.
  • nucleic acid encodes a Batten disease polypeptide, e.g., the polypeptide of SEQ ID NO: 2 or SEQ ID NO: 19, which lacks a leader sequence, e.g., an N-terminal sequence responsible for secretion ofthe polypeptide from a cell in which it is expressed, or other sequence which is not present in the mature protein.
  • the invention includes: a vector including a nucleic acid which encodes a Batten disease polypeptide, e.g., a Batten disease polypeptide; a host cell transfected with the vector; and a method of producing a recombinant Batten disease -like polypeptide, e.g., a Batten disease polypeptide; including culturing the cell, e.g., in a cell culture medium, and isolating the Batten disease -like polypeptide, e.g., a Batten disease polypeptide, e.g., from the cell or from the cell culture medium.
  • the invention features, a purified recombinant nucleic acid having at least 50%, 60%, 70%, 80%, 90%, 95%, 98%, or 99% homology with a nucleotide sequence shown in SEQ ID NO: 1 or SEQ ID NO: 18, more preferably having more than 82% homology with a nucleotide sequence shown in SEQ ID NO:l or SEQ ID NO: 18.
  • the invention also provides a probe or primer which, e.g., includes or comprises a substantially purified oligonucleotide.
  • the oligonucleotide includes a region of nucleotide sequence which hybridizes under stringent conditions to at least 10 consecutive nucleotides of sense or antisense sequence from SEQ ID NO:l or SEQ ID NO: 18, or naturally occurring mutants thereof.
  • the probe or primer further includes a label group attached thereto.
  • the label group can be, e.g., a radioisotope, a fluorescent compound, an enzyme, and/or an enzyme co-factor.
  • the oligonucleotide is at least 10 or 20 and preferably less than 20, 30, 50, 100, 150 or 500 nucleotides in length.
  • Preferred primers ofthe invention include oligonucleotides having a nucleotide sequence shown in any of SEQ ID NOS: 3-15 and 20-58.
  • the probe or primer is within a deletion, e.g., the 1.02 Kb deletion described herein; the probe or primer is outside a deletion, e.g., the 1.02 Kb deletion described herein; or the probe or primer spans a deletion, e.g., the 1.02 Kb deletion described herein.
  • the probe or primer overlaps one ofthe lesions described herein.
  • the invention involves nucleic acids, e.g., RNA or DNA, encoding a polypeptide ofthe invention.
  • This includes double stranded nucleic acids as well as coding and antisense single strands.
  • the invention features a method of evaluating whether a mammal, for example a primate or a human, is at risk for Batten disease or the misexpression of a Batten disease gene, characterized by, for example, accumulation of autofluorescent lipopigments (ceroid and lipofuscin) in neurons and other cell types leading to progressive loss of vision, seizures and psychomotor disturbances.
  • autofluorescent lipopigments ceroid and lipofuscin
  • the method includes detecting, in a tissue ofthe subject, the presence or absence of a mutation of a Batten disease gene, e.g., a gene encoding a protein represented by SEQ ID NO: 2 ,SEQ ID NO: 19, or a homolog thereof.
  • detecting the mutation includes ascertaining the existence of at least one of: a deletion of one or more nucleotides from the gene; an insertion of one or more nucleotides into the gene, a point mutation, e.g., a substitution of one or more nucleotides ofthe gene, a gross chromosomal rearrangement ofthe gene, e.g., a translocation, inversion, or deletion.
  • detecting the genetic lesion can include: (i) providing a PCR probe, e.g., a radiolabeled PCR probe, amplified from cDNA (e.g., SEQ ID NO: 1 or SEQ ID NO: 18) encoding a Batten disease polypeptide and containing a nucleotide sequence which hybridizes to a sense or antisense sequence from the Batten disease gene (e.g., SEQ ID NO: 1 or SEQ ID NO: 18), or naturally occurring mutants thereof, or 5' or 3' flanking sequences naturally associated with the Batten disease gene; (ii) exposing the probe/primer to nucleic acid ofthe tissue (e.g., genomic DNA) digested with one of many known restriction endonucleases; and (iii) detecting by in situ hybridization ofthe probe/primer to the nucleic acid, the presence or absence ofthe genetic lesion.
  • a PCR probe e.g., a radiolabeled PCR probe, ampl
  • direct PCR analysis using primers specific for a Batten disease gene (e.g., a gene comprising the nucleotide sequence shown in SEQ ID NO: 1 or SEQ ID NO:l 8), can be used to detect the presence or absence of the genetic lesion in genomic DNA from an individual.
  • a Batten disease gene e.g., a gene comprising the nucleotide sequence shown in SEQ ID NO: 1 or SEQ ID NO:l 8
  • sequencing ofthe Batten disease gene or fragments thereof can be used to detect lesions described in Table 3 below.
  • the invention provides a method for detecting in a tissue of a subject, the presence or absence of a lesion, e.g., a deletion, an insertion or a rearrangement, in a Batten disease gene, e.g., a gene encoding a protein represented by SEQ ID NO: 2 ,SEQ ID NO: 19, or a homolog thereof.
  • the method includes: (i) providing a primer which spans the lesion; (ii) amplifying a nucleic acid ofthe tissue (e.g., genomic DNA) with the lesion spanning primer; and (iii) detecting the presence or absence ofthe lesion.
  • the deletion is from about 200 to about 2000 bp in size; the deletion is about 1000 bp in size; the deletion has a core haplotype "56" (based on the size of alleles, D16S299 and D16S298, with which it displays close linkage disequilibrium).
  • the method further includes either or both of amplifying the nucleic acid ofthe tissue with a primer located within the lesion, and a second primer located outside the lesion.
  • primers of SEQ ID NOs:20-28 can be used to detect a frequently occuring 1.02 Kb deletion ofthe Batten disease gene.
  • the lesion can be any of lesions described herein, e.g., a 1.02 Kb deletion or those described in Table 3 below.
  • the invention provides a method of determining if a subject mammal, e.g., a primate, e.g., a human, is at risk for a Batten disease or misexpression of a Batten disease gene, characterized by, for example, accumulation of autofluorescent lipopigments (ceroid and lipofuscin) in neurons and other cell types leading to progressive loss of vision, seizures and psychomotor disturbances.
  • the method includes detecting, in a tissue ofthe subject, misexpression (e.g., a non-wild type level) of a Batten disease polypeptide or Batten disease polypeptide RNA.
  • the method utilizes an antibody, such as a monoclonal antibody, specific for a Batten disease polypeptide, or an analog or fragment of a Batten disease polypeptide, to detect misexpression of a Batten disease polypeptide.
  • the invention features a method of evaluating a compound for the ability to interact with, e.g., bind, a Batten disease polypeptide.
  • the method includes contacting the compound with the Batten disease polypeptide, and evaluating ability ofthe compound to interact with, e.g., to bind or form a complex with the Batten disease polypeptide.
  • This method can be performed in vitro, e.g., in a cell free system, or in vivo, e.g., in a two-hybrid interaction trap assay. This method can be used to identify naturally occurring molecules which interact with Batten disease polypeptides. It can also be used to find natural or synthetic inhibitors of mutant Batten disease polypeptides.
  • a two hybrid assay system allows for detection of protein-protein interactions in yeast cells.
  • the known protein e.g., a Batten disease polypeptide
  • the proteins tested for binding to the bait protein are often referred to as "fish” proteins.
  • the "bait” protein e.g., a Batten disease polypeptide
  • the "bait” protein is fused to the GAL4 DNA binding domain. Potential "fish” proteins are fused to the GAL4 activating domain. If the "bait" protein and a "fish” protein interact, the two GAL4 domains are brought into close proximity, thus rendering the host yeast cell capable of surviving a specific growth selection.
  • the invention features a method of identifying compounds which interact with fragments or analogs of a Batten disease polypeptide.
  • the method includes first identifying compounds which interact with a Batten disease polypeptide, for example, the two hybrid assay described above. These compounds can then be used as "bait" to fish for and identify fragments ofthe Batten disease polypeptide which also interact, bind, or form a complex with these compounds.
  • the invention features a method of evaluating an effect of a treatment, e.g., a treatment used to treat a disorder related to the Batten disease gene, e.g., a disorder characterized by progressive loss of vision, seizures and psychomotor disturbances, e.g., Batten disease.
  • a treatment used to treat a disorder related to the Batten disease gene, e.g., a disorder characterized by progressive loss of vision, seizures and psychomotor disturbances, e.g., Batten disease.
  • the method uses a wild type test cell or organism, or a cell or organism which misexpresses the Batten disease gene or which has a Batten disease transgene, e.g., a transgenic animal.
  • the method includes: administering the treatment to a test cell or organism, e.g., a cultured neural cell, or a mammal, and evaluating the effect ofthe treatment on a parameter related to an aspect of Batten disease, e.g., a neurodegenerative parameter, such as the accumulation of autofluorescent lipopigments in the cultured neural cell or cells ofthe mammal, or on the expression ofthe gene.
  • a parameter related to an aspect of Batten disease e.g., a neurodegenerative parameter, such as the accumulation of autofluorescent lipopigments in the cultured neural cell or cells ofthe mammal, or on the expression ofthe gene.
  • An effect on the parameter indicates an effect ofthe treatment.
  • the invention features a method of making a Batten disease polypeptide having a non-wild type activity, e.g., an antagonist, agonist, or super agonist of a naturally occurring Batten disease polypeptide.
  • the method includes altering the sequence of a Batten disease polypeptide (e.g., SEQ ID NO: 2 or SEQ ID NO: 19) by, for example, substitution or deletion of one or more residues of a non-conserved region, and testing the altered polypeptide for the desired activity.
  • a Batten disease polypeptide e.g., SEQ ID NO: 2 or SEQ ID NO: 19
  • the invention features a method of making a fragment or analog of a Batten disease polypeptide, e.g., a Batten disease polypeptide having at least one biological activity of a naturally occurring Batten disease polypeptide.
  • the method includes altering the sequence, e.g., by substitution or deletion of one or more residues, preferably which are non-conserved residues, of a Batten disease polypeptide, and testing the altered polypeptide for the desired activity.
  • the invention features a method of treating a mammal, e.g., a human, at risk for Batten disease, e.g., a disorder characterized by neurodegeneration, such as progressive loss of vision, seizures and psychomotor disturbances.
  • the method includes administering to the mammal a therapeutically effective amount of a nucleic acid encoding a Batten disease polypeptide.
  • the nucleic acid can encode an agonist or antagonist of a Batten disease polypeptide.
  • the invention features a method of treating a mammal, e.g., a human, at risk for Batten disease, e.g., a disorder characterized by neurodegeneration, such as progressive loss of vision, seizures and psychomotor disturbances.
  • the method includes administering to the mammal a therapeutically effective amount of a Batten disease polypeptide.
  • the polypeptide can be an agonist or antagonist of a Batten disease polypeptide.
  • the invention features, a method of evaluating a compound for the ability to bind a nucleic acid encoding a Batten disease gene regulatory sequence. The method includes: contacting the compound with the nucleic acid; and evaluating ability of the compound to form a complex with the nucleic acid.
  • the Batten disease gene regulatory sequence is functionally linked to a heterologous gene, e.g., a reporter gene.
  • the invention features a human cell, e.g., a neuron, transformed with a nucleic acid which encodes a Batten disease polypeptide.
  • the invention includes: an expression vector containing a nucleic acid encoding a Batten disease polypeptide (e.g., SEQ ID NO: 2 or SEQ ID NO: 19), or an analog or fragment thereof; a cell transformed with an expression vector containing a nucleic acid encoding a Batten disease polypeptide (e.g., SEQ ID NO: 2 or SEQ ID NO: 19), or an analog or fragment thereof; and a Batten disease polypeptide made by culturing a cell transformed with an expression vector containing a nucleic acid encoding a Batten disease polypeptide (e.g., SEQ ID NO: 2 or SEQ ID NO: 19), or an analog or fragment thereof.
  • a Batten disease polypeptide made by culturing a cell transformed with an expression vector containing a nucleic acid encoding a Batten disease polypeptide (e.g., SEQ ID NO: 2 or SEQ ID NO: 19), or an analog or fragment thereof.
  • the invention includes a transgenic animal, preferably a mammal, e.g., a mouse, rat, pig or goat, having a Batten disease transgene, e.g., a Batten disease gene having a deletion of all or a part ofthe wild type Batten disease gene.
  • the transgenic animal can be heterozygous or homozygous for the transgene.
  • Such a transgenic animal can serve as a model for studying disorders which are related to mutated or mis-expressed Batten disease gene alleles or for use in drug screening.
  • the invention includes a method of evaluating the effect ofthe expression or misexpression of a Batten disease gene on a parameter related to Batten disease.
  • the method includes: providing a transgenic animal having a Batten disease transgene, or which otherwise misexpresses a Batten disease gene; contacting the animal with an agent; and evaluating the effect ofthe transgene on the parameter related to Batten disease polypeptide metabolism.
  • a “heterologous promoter”, as used herein is a promoter which is not naturally associated with the Batten disease gene.
  • a “purified preparation” or a “substantially pure preparation” of a Batten disease polypeptide, or a fragment or analog thereof, as used herein means a Batten disease polypeptide. or a fragment or analog thereof, that has been separated from on or more other proteins, lipids, and nucleic acids with which the Batten disease polypeptide naturally occurs.
  • the polypeptide, or a fragment or analog thereof is also separated from substances which are used to purify it, e.g., antibodies or gel matrix, such as polyacrylamide.
  • the polypeptide, or a fragment or analog thereof constitutes at least 10, 20, 50 70, 80 or 95% dry weight ofthe purified preparation.
  • the preparation contains: sufficient polypeptide to allow protein sequencing; at least 1, 10. or 100 ⁇ g ofthe polypeptide; at least 1, 10, or 100 mg ofthe polypeptide.
  • a “purified preparation of cells”, as used herein. refers to, in the case of plant or animal cells, an in vitro preparation of cells and not an entire intact plant or animal. In the case of cultured cells or microbial cells, it consists of a preparation of at least 10% and more preferably 50% ofthe subject cells.
  • a “treatment”, as used herein, includes any therapeutic treatment, e.g., the administration of a therapeutic agent or substance, e.g., a drug.
  • the "metabolism of a substance”, as used herein, means any aspect ofthe. expression, function, action, or regulation ofthe substance.
  • the metabolism of a substance includes modifications, e.g., covalent or non covalent modifications ofthe substance.
  • the metabolism of a substance includes modifications, e.g., covalent or non covalent modification, the substance induces in other substances.
  • the metabolism of a substance also includes changes in the distribution ofthe substance.
  • the metabolism of a substance includes changes the substance induces in the structure or distribution of other substances.
  • Batten disease polypeptide is a nucleic acid which is one or both of: not immediately contiguous with one or both ofthe coding sequences with which it is immediately contiguous (i.e.. one at the 5' end and one at the 3' end) in the naturally-occurring genome ofthe organism from which the nucleic acid is derived; or which is substantially free of a nucleic acid sequence with which it occurs in the organism from which the nucleic acid is derived.
  • the term includes, for example, a recombinant DNA which is incorporated into a vector, e.g., into an autonomously replicating plasmid or virus, or into the genomic DNA of a prokaryote or eukaryote, or which exists as a separate molecule (e.g., a cDNA or a genomic DNA fragment produced by PCR or restriction endonuclease treatment) independent of other DNA sequences.
  • Substantially pure DNA also includes a recombinant DNA which is part of a hybrid gene encoding additional Batten disease sequences.
  • Homologous refers to the sequence similarity between two polypeptide molecules or between two nucleic acid molecules. When a position in both of the two compared sequences is occupied by the same base or amino acid monomer subunit, e.g., if a position in each of two DNA molecules is occupied by adenine, then the molecules are homologous at that position.
  • the percent of homology between two sequences is a function ofthe number of matching or homologous positions shared by the two sequences divided by the number of positions compared x 100. For example, if 6 of 10, ofthe positions in two sequences are matched or homologous then the two sequences are 60% homologous.
  • DNA sequences ATTGCC and TATGGC share 50% homology. Generally, a comparison is made when two sequences are aligned to give maximum homology.
  • peptides amino acids
  • proteins proteins
  • polypeptides are used interchangeably herein.
  • transgene means a nucleic acid sequence (encoding, e.g., one or more Batten disease polypeptides), which is partly or entirely heterologous, i.e., foreign, to the transgenic animal or cell into which it is introduced, or, is homologous to an endogenous gene ofthe transgenic animal or cell into which it is introduced, but which is designed to be inserted, or is inserted, into the animal's genome in such a way as to alter the genome ofthe cell into which it is inserted (e.g., it is inserted at a location which differs from that ofthe natural gene or its insertion results in a knockout).
  • a transgene can include one or more transcriptional regulatory sequences and any other nucleic acid, such as introns, that may be necessary for optimal expression ofthe selected nucleic acid, all operably linked to the selected nucleic acid, and may include an enhancer sequence.
  • transgenic cell refers to a cell containing a transgene.
  • a "transgenic animal” is any animal in which one or more, and preferably essentially all, ofthe cells ofthe animal includes a transgene.
  • the transgene can be introduced into the cell, directly or indirectly by introduction into a precursor ofthe cell, by way of deliberate genetic manipulation, such as by microinjection or by infection with a recombinant virus.
  • This molecule may be integrated within a chromosome, or it may be extrachromosomally replicating DNA.
  • tissue-specific promoter means a DNA sequence that serves as a promoter, i.e., regulates expression of a selected DNA sequence, such as the Batten disease gene, operably linked to the promoter, and which effects expression of the selected DNA sequence in specific cells of a tissue, such as neurons.
  • tissue-specific promoter means a DNA sequence that serves as a promoter, i.e., regulates expression of a selected DNA sequence, such as the Batten disease gene, operably linked to the promoter, and which effects expression of the selected DNA sequence in specific cells of a tissue, such as neurons.
  • the term also covers so-called “leaky” promoters, which regulate expression of a selected DNA primarily in one tissue, but cause expression in other tissues as well.
  • Unrelated to a Batten disease amino acid or nucleic acid sequence means having less than 30% homology, less than 20% homology, or, preferably, less than 10% homology with a Batten disease sequence disclosed herein.
  • a polypeptide has "at least one biological activity of a Batten disease polypeptide” if it has one or more ofthe following properties: (1) the ability to react with an antibody, or antibody fragment, specific for (a) a wild type Batten disease polypeptide, (b) a naturally-occurring mutant Batten disease polypeptide, or (c) a fragment of either (a) or (b); (2) the ability to prevent, treat or correct a disorder associated with Batten disease, including, for example, neurodegenerative disorders characterized by progressive loss of vision, seizures and psychomotor disturbances; or (3) the ability to act as an antagonist or agonist ofthe activities recited in (1) or (2).
  • “Misexpression”, as used herein, refers to a non- wild type pattern of Batten disease gene expression. It includes: expression at non-wild type levels, i.e., over or under expression; a pattern of expression that differs from wild type in terms ofthe time or stage at which the gene is expressed, e.g., increased or decreased expression (as compared with wild type) at a predetermined developmental period or stage; a pattern of expression that differs from wild type in terms of decreased expression (as compared with wild type) in a predetermined cell type or tissue type; a pattern of expression that differs from wild type in terms ofthe splicing, size, amino acid sequence, post-transitional modification, stability, or biological activity ofthe expressed Batten disease polypeptide; a pattern of expression that differs from wild type in terms ofthe effect of an environmental stimulus or extracellular stimulus on expression ofthe Batten disease gene, e.g., a pattern of increased or decreased expression (as compared with wild type) in the presence of an increase or decrease in the strength
  • nucleic acid As described herein, one aspect ofthe invention features a pure (or recombinant) nucleic acid which includes a nucleotide sequence encoding a Batten disease polypeptide, and/or equivalents of such nucleic acids.
  • nucleic acid can include fragments and equivalents.
  • equivalent refers to nucleotide sequences encoding functionally equivalent polypeptides or functionally equivalent polypeptides which, for example, retain the ability to react with an antibody specific for a Batten disease polypeptide.
  • Equivalent nucleotide sequences will include sequences that differ by one or more nucleotide substitutions, additions or deletions, such as allelic variants, and will, therefore, include sequences that differ from the nucleotide sequence of Batten disease shown in SEQ ID NO: 1 due to the degeneracy ofthe genetic code.
  • the Batten disease gene and polypeptide ofthe present invention are useful for studying, diagnosing and/or treating Batten disease.
  • the gene (or fragment thereof) can be used to detect and study genetic mutations or gene transcripts commonly associated with Batten disease, as described in detail below.
  • the gene (or fragment thereof) can be used in gene replacement therapy to correct the absence of a wild type Batten disease gene (e.g., to reconstitute the function of, enhance the function of, or alternatively, antagonize the function of a Batten disease polypeptide in a cell in which the polypeptide is misexpressed).
  • the gene (or fragment thereof) can be used to prepare antisense constructs capable of inhibiting expression of a mutant or wild type Batten disease gene encoding a polypeptide having an undesirable function.
  • a Batten disease polypeptide can be used to raise antibodies capable of detecting proteins or protein levels associated with Batten disease.
  • a Batten disease polypeptide can be administered to a patient afflicted with Batten disease to correct the absence of a wild type Batten disease polypeptide, or as an agonist to enhance the activity of a wild type Batten disease polypeptide.
  • Figure 1 is a schematic representation ofthe CLN3 candidate region on chromosome 16p 12.1. The positions of selected DNA microsatellites used for linkage and haplotype analysis are indicated. Individual cosmids (NL1 IA, NL60D3) of cosmid contig CNL/343.1, which contains D16S298 and D16S48, and cosmid contig C182, which contains D16S299, are indicated by horizontal lines. Three YACs (Cy21Bl 1, Cy302G12, Cy85D3) that form part of a 980 kb contig spanning the candidate region are also indicated by horizontal lines.
  • Figure 2 is a restriction map of cosmid NL1 IA.
  • the genomic extent of cDNA2-3 is shown below the map (arrow indicating the direction of transcription).
  • the position of the 3.12 STS, the microsatellite marker DI6S298, and the overlapping cosmid NL60D3 are shown above the restriction map.
  • Figure 3 is the nucleotide sequence of cDNA2-3.
  • the predicted protein is shown below the DNA sequence, assuming that translation begins at the first in-frame methionine ofthe long open reading frame.
  • Four potential N-linked glycosylation sites are indicated by a dashed line at residues 49, 71, 85, and 310.
  • Two potential glycosaminoglycan sites are indicated by the dotted lines at residues 162 and 186.
  • Potential N-myristoylation sites are indicated by(#). Serine and threonine residues that are potentially phosphorylated by cAMP- and cGMP-dependent protein kinases (%), or protein kinase C (*), or casein kinase 2 ( ⁇ ) are indicated.
  • the polyadenylation site at base 1666 is indicated by the $.
  • cDNA sequence deleted in the "56" deletion (bases 598-814) is boxed.
  • Figure 4 is a Mendelian inheritance diagram showing segregation ofthe "56" haplotype (deletion) in a two-generation Batten Disease family.
  • Figure 5 is a diagram showing the 1.02 kb genomic deletion in disease chromosomes bearing the "56" haplotype. The sequences bordering the deletion are shown. The deletion covers two exons and flanking intronic sequence and leads to the deletion of 217 bp of coding sequence. The two flanking exons are spliced together to read
  • CCTGTGTGCTATTTC SEQ ID NO: 17
  • Position of primers used to delineate the deletion are also indicated. Hatched boxes represent exons. The boxes indicate the positions of Alu-Sx sequences. The deletion breakpoints are shown by the arrows, and deleted sequences are shown in italics.
  • Figure 6 is a schematic representation ofthe genomic deletions ofthe 2-3 gene. Position of primers used to delineate the deletions are indicated.
  • Figure 7 is a schematic representation of a direct detection ofthe major deletion ofthe CLN3 gene. Normal and deletion alleles of CLN3. Primer 2.3LR3 is located within the deleted region whereas primer CLN3mut756R is spanning the deletion junction. The allele-specific PCR products are indicated.
  • Figure 8 is a schematic representation ofthe location of mutations in CLN3.
  • the mutations are shown in relation to their position in the exons ofthe cDNA.
  • Those above the cDNA are point mutations in the ORF, those below deletions, insertions or point mutations in introns.
  • Those in bold are missense mutations.
  • Those in italics are mutations in introns.
  • Figure 9 is a schematic representation ofthe predicted structure of CLN3 protein. The location ofthe six missense mutations is shown.
  • Figure 10 is a cromatograph depicting direct sequence analysis of exon 7 in an unaffected control (lower panel) and patient L29 (upper panel). The * indicates the point mutation (C619G).
  • the invention provides the sequence of a gene responsible for Batten disease, hereafter referred to as CLN3, or as the Batten disease gene.
  • CLN3 gene possesses an open reading frame of 1314 bp (SEQ ID NO: 1) encoding a polypeptide having a predicted length of 438 amino acids (SEQ ID NO: 2) and a predicted molecular weight of about 48 kDa (mature protein), with no significant similarity to previously described proteins.
  • the gene is disrupted by a small (1.02 kb) deletion on all Batten disease chromosomes with a core haplotype "56" (based on the size of alleles, D16S299 and D16S298, with which it displays close linkage disequilibrium), and by independent deletion in theixie patient described below.
  • a cosmid (NL1 IA) which encompasses the D16S298 allele (known to be closely linked to CLN3) was targeted.
  • Exon amplification was used to isolate a 180 bp exon from NL1 IA. This exon was then used to screen a fetal brain cDNA library (Stratagene), yielding a 1.7 kb cDNA clone (CDNA2-3) (SEQ ID NO: 1).
  • Northem blot analysis using cDNA2-3 as a probe revealed a 1.7 kb transcript in polyA-mRNA isolated from a wide variety of human tissues including heart, brain, placenta, lung, liver, skeletal muscle, kidney, and pancreas. This result was consistent with the cDNA clone likely being full-length. The transcript was not detected in cultured lymphoblasts and fibroblasts by Northem blot analysis, but was detectable by RT-PCR analysis of polyA-mRNA isolated from such cell lines. A "zoo" blot containing genomic DNAs from several animal species showed that this gene is conserved in mammals. Strong signals were obtained from mouse, sheep, dog, cow, and pig.
  • Figure 3 shows the nucleotide sequence of cDNA2-3 (SEQ ID NO: 1) which contains 1,689 base pairs (bp) and has a 47 base polyA tail.
  • the cDNA clone has a predicted open reading frame of 1314 bp begins with a potential initiator ATG codon at base 138 and ends with a TGA termination codon at base 1452.
  • An in-frame stop codon is located 36 bases upstream ofthe initiator site and a consensus polyadenylation site is located at base 1666.
  • the predicted product ofthe cDNA is a protein of 438 amino acids (SEQ ID NO: 2) with a molecular weight of about 48 kDa.
  • Table 1 lists the sequences and locations of PCR primers derived from this cDNA sequence and used in the studies described below.
  • F2 (SEQ ID NO: 4) 552 TTCGTCCTGGTTGCCTTT
  • F4 (SEQ ID NO: 5) 676 TGATCTCCTGGTGGTCCTCA
  • F5 (SEQ ID NO: 6) 778 TGTCCATGCTGGGTATCCCT
  • P2 (SEQ ID NO: 7) 860 GAAGAAGAAGCAGAGAGCGC
  • F9 (SEQ ID NO: 8) 888 CAGCCCCTCATAAGAACCGA
  • GFl (SEQ ID NO: 9) 1470 GGACGCAGGTCACATTCA
  • Rl (SEQ ID NO: 10) 656 AGTGAGGGAGAGGAAGGTGA
  • R5 (SEQ ID NO: 12) 1246 CTTGGCAGAAAGCCGAAC
  • R3 (SEQ ID NO: 13) 1612 CCCCTGCAAGGAAACAAG
  • GR1 (SEQ ID NO: 14) 1661 GGCATGATGCCAGGAAAGA
  • the Batten disease cDNA sequence (SEQ ID NO: 1) was compared against GenBank and dbEST databases using BLASTN (Altschul et al. (1990) J. Mol. Biol. 215:403- 410) and FASTA (Pearson et al. (1988) Proc. Natl. Acad. Sci. usa 85:2444-2448) sequence alignment algorithms. These searches revealed no significant similarities to genes of known function.
  • the predicted protein sequence (SEQ ID NO: 2) ofthe polypeptide encoded by cDNA2-3 (SEQ ID NO: 1) was compared against the Swiss-Prot database using BLASTP and Smith- Waterman (Smith et al. (1981) J. Mol. Biol. l41: ⁇ 95-l91) sequence alignment algorithms and against the predicted translation products of GenBank database using BLASTP and Smith- Waterman (Smith et al. (1981) J. Mol. Biol. l41: ⁇ 95-l91) sequence alignment algorithms and against the predicted translation products of GenBank database using
  • Figure 4 illustrates the Mendelian inheritance of this deletion in a two- generation Batten Disease family segregating the "56" haplotype.
  • the chromosomes segregating in this pedigree have been distinguished by extensive typing with polymorphic markers in 16pl2.1-11.2.
  • RT-cDNA was prepared from cytoplasmic RNA isolated from the peripheral blood lymphocytes of 6 normal controls, the fibroblasts of 1 normal control, and the fibroblasts from 4 patients homozygous for the "56" haplotype. PCR products were fractionated on 1-1.5% gels and transferred to Hybond N+ (Amersham) membranes. Blots were hybridized with the radiolabeled PCR fragments amplified from the cDNA2-3 clone.
  • the P1-P3 primer pair (SEQ ID NOS: 3 and 11) yielded a novel product, ⁇ 200 bp smaller than that predicted from the cDNA sequence and found in all non- "56" normal controls, and RT-PCR amplification with the P2-P5 primer pair yielded identical -800 bp products in affected and controls.
  • DNA sequence analysis ofthe P1-P3 product from 5 homozygous "56" patients showed in all cases a 217 bp deletion, from base 598 to base 814 (SEQ ID NO: 16) ofthe cDNA (SEQ ID NO: 1) ( Figure 3).
  • the DNA sequence ofthe RT-cDNA from 4 control individuals revealed no evidence of deletion, matching the cDNA2-3 sequence. Deletion of these 217 bases of coding sequence (SEQ ID NO: 16) produces a frameshift, generating a TAA termination codon 84 bp downstream ofthe deletion junction.
  • the predicted translation product is a truncated protein of 181 amino acids consisting ofthe first 153 residues ofthe protein followed by 28 novel amino acids before the stop codon.
  • Genomic PCR was carried out using primer pair F2-P3 (SEQ ID NOS: 4 and 11) at bases 553 and 880 , respectively, ofthe cDNA2-3 sequence (SEQ ID NO: 1; Fig. 3). PCR amplification was carried out as described below in the Experimental Methods.
  • PCR analysis of patient DNA using the intron primer intR14 (5'- aggaaggaggctggaggata-3'XSEQ ID NO:58) and cDNA primer F9 (SEQ ID NO:8) confirmed an ⁇ 3 kb deletion, including the entire 1.3 kb PstI fragment containing D16S298.
  • RT-cDNA from this second mutant allele was selectively amplified using primer R5 (SEQ ID NO: 12) and primer F5 (SEQ ID NO:6) which is deleted on the "56" chromosome.
  • the amplified product revealed the absence of 266 bp of coding sequence between bases 928-1193 ofthe cDNA, generating a TGA termination codon 84 bp downstream ofthe deletion junction.
  • the predicted translation product is a truncated protein of 291 amino acids consisting ofthe first 263 amino acids ofthe protein followed by 28 novel amino acids before the stop codon. Partial DNA sequence analysis ofthe genomic fragment containing this ⁇ 3 kb deletion has confirmed the loss of bases 928-1193 ofthe cDNA. The sequences bordering this deletion have not yet been defined.
  • SSCP Single stranded conformation polymorphism
  • the Batten disease gene mutation associated with D16S299ID16S298 "56" haplotype is a 1.02 kb deletion that implicates cDNA2-3 as the product of CLN3.
  • This deletion involves the 3' end of two Alu-Sx elements and the following GA4 sequence and may therefore have arisen by recombination involving bordering Alu sequences, a mechanism for which other examples exist in human disease (e.g., Rudiger et al. (1995) Nucleic Acids Res. 23:256-60).
  • the deletion mutation is found on all "56" affected chromosomes examined to date, and on several chromosomes with related haplotypes, accounting for 81% of Batten disease chromosomes.
  • the presence of several potential phosphorylation sites suggests that the protein may undergo phosphorylation as a prerequisite for binding additional protein(s).
  • the PSORT program (version 6.3; Nakai et al. (1992) Genomics 14:897-911) for prediction of protein localization sites indicates that the CLN3 protein may be a membrane spanning protein having 6 transmembrane segments (Heijne et al. (1988) Euro. J. Biochem. 114:611- 678), a possibility supported by hydropathy calculations that suggest the presence of several hydrophobic domains and by numerous potential N-glycosylation and N-myristoylation site.
  • the deletions identified to date are predicted to remove over 100 amino acids from the C-terminal portion ofthe Batten disease polypeptide, suggesting that its normal function would be severely compromised in the disease.
  • the disease phenotype may involve abnormal accumulation of truncated Batten disease polypeptide products rather than, or in addition to, direct loss of protein function.
  • the CLN3 gene is expressed not only in the brain, the site of massive neuronal cell death in Batten patients, but also in a wide range of tissues. Consistent with this, inclusion bodies have been found in many Batten disease tissues in addition to the brain. In addition, Palmer et al (1992) Am. J. Med. Genet.
  • the identification and isolation ofthe Batten disease gene provided by the present invention is the first step toward understanding the pathology underlying this complex disorder.
  • the cDNA clone, cDNA2-3, will provide the basis for analyzing the role ofthe CLN3 polypeptide in both normal and disease cells and a starting point for the design of rational therapies.
  • the availability of cDNA2-3 will allow the study of Batten disease polypeptides encoded by CLN3, and may reveal the underlying cause ofthe other ceroid lipofuscinoses and provide new insights into the mechanisms involved in other neurodegenerative disorders.
  • a murine teratocarcinoma cDNA library (Stratagene) was screened by plaque hybridization with the human Batten disease cDNA clone 2-3 as probe, yielding a 1639-bp cDNA, clone mtc7 (SEQ ID NO:l 8). Clone mtc7 was sequenced manually by the dideoxy method on both strands. The DNA sequence analysis revealed 82% identity between the mouse (SEQ ID NO: 18) and the human cDNA coding sequences (SEQ ID NO:l).
  • clone mtc7 contains a predicted open reading frame (ORF) of 1314 bp, beginning with a potential initiator ATG codon at base 142 and ending with a TGA termination codon at base 1456.
  • An in-frame stop codon is located 54 bases upstream ofthe initiator ATG.
  • the cDNA has a consensus polyadenylation site (AAT AAA) located at bases 1617-1622 and a 19-base poly(A) tail.
  • the ORF encodes a predicted protein product of 438 amino acids (SEQ ID NO: 19) with a high degree of similarity (85% identity) to the human CLN3 protein (SEQ ID NO:2).
  • mtc7 cDNA was used as a probe to map CLN3 genetically in the mouse.
  • the map location of Cln3 was determined by segregation analysis of a mouse interspecific backcross DNA mapping panel derived from matings of (C57BL/6J x SPRET/Ei) Fl females with SPRET/Ei males and designated MMR-BSS.
  • the MMR-BSS panel consists of 144 individuals that have been typed for more than 300 different polymorphic loci (Johnson et al., Mamm.
  • Mnd mutation has been mapped to mouse Chromosome 8 (Messer et al., Genomics 18:797-802, 1992). On the basis ofthe mapping results presented herein, it has been concluded that Mnd and Cln3 are unique loci.
  • the degree of identity between the human and mouse CLN3 coding sequences indicates that the protein most likely serves the same function in the mouse as in humans. Isolation and characterization ofthe mouse Cln3 gene will allow for construction of vectors for targeted disruption by homologous recombination in embryonic stem cells. Generation of - / - mice should allow for study ofthe detailed pathogenesis of Batten disease.
  • the major Battens disease mutation is a 1 kb deletion, which is found in 81% of affected chromosomes.
  • Direct gene analysis with PCR primers which flank the deletion can be used for prenatal diagnosis (Munroe et al., Lancet 347: 1014-15, 1996) This often results in preferential amplification ofthe deletion allele compared to the normal due to the large difference in size between the products and may give false positive results. Therefore, an allele-specific PCR test which allows the simultaneous detection of normal and major deletion alleles of CLN3 was designed.
  • the test uses one primer spanning the deletion junction in combination with a second primer within the deletion and a third primer outside the deletion to follow the segregation ofthe major deletion within the family of a Batten's disease patient (Fig. 7).
  • PCR analysis was carried out on 50 ng genomic DNA in a total volume of
  • the allele-specific PCR test allows early confirmation ofthe clinical diagnosis in the majority ofthe Batten patients which is important for correct prognosis and genetic counseling, and may help to prevent the birth of additional patients.
  • this test can be used to detect carriers ofthe major deletion in the general population which is important for unrelated partners of proven carriers.
  • the Finnish patient L198Pa had an uneventful birth and early childhood. Since the age of 7, she has experienced progressive visual failure. At age 9, she showed abnormal MRI. Vacuolated lymphocytes were repeatedly observed and electronmicroscopy of a rectal biopsy specimen showed inclusions typical for Batten Disease. She has been on sodium valproate medication since the age of 9, when she experienced her only seizure. Recent examination at the age of 13 showed that her motor status is good but that her mental decline has been relatively fast.
  • Exon amplification was carried out using the pSPL3 vector as described by Church et al 1994.
  • a human fetal brain cDNA library in lambdaZAPII (Stratagene) was screened by standard methods using exon probes.
  • cDNA clones and trapped exons were sequenced manually (Sanger et al (1977) Proc. Natl. Acad. Sci. USA 74:5463-5467) with Sequenase T7 DNA polymerase (U.S. Biochemicals).
  • the polymerase chain reaction was carried out using Taq polymerase, following the recommendations ofthe manufacturer.
  • the oligonucleotide primers used in the experiments are described in Table 1.
  • the assay for the "56" deletion was carried out on 100 ng of genomic DNA using primers F2 (SEQ ID NO: 4) and P3 (SEQ ID NO: 11) (Table 1) in a reaction including 0.2 ⁇ M each primer, 0.2mM each dNTP, 1.5 mM MgCl2 and 0.5-1 ⁇ l AmpliTaq (Perkins Elmer).
  • the reaction was supplemented with 5 units TaqExtender (Stratagene) which was found to enhance the amplification. Annealing temperatures ranging between 55°C and 62°C were used successfully. Samples were fractionated on an 0.8% agarose gel.
  • Genomic DNA from a normal control and the somatic cell hybrid CY101 which carries a single copy of chromosome 16 derived from a patient homozygous for the "56" haplotype was PCR amplified with primers P1-P3 (SEQ ID NOS: 3 and 11) (Table 1). The resulting PCR products were digested with Taql. A 1.5 kb fragment was detected in the control and a 0.5 kb fragment was detected in CY101. These two fragments were subcloned into pUC19 and sequenced with an ABI 373 A automated sequencer. In an independent study, the sequence spanning the "56" deletion was generated by PCR sequencing ofthe subcloned 3.8 kb PstI fragment using an ABI 373 A automated sequencer.
  • a PCR-based assay was used to screen for the 1.02 Kb deletion in the pooled Batten disease patient resource of 194 families. Fourteen individuals did not have the 1.02 Kb deletion whilst 41 were found to be heterozygous and 139 homozygous for this mutation. Thus, 55 individuals in our resource possessed other mutations, including three which have been described above.
  • PCR primers for amplification of CLN3 exons are: Exon 1 - (5'-aaaggtacaggcctcagggt-3')(SEQ ID NO:28) and (5' - agctctcattcccctcaggt-3')(SEQ ID NO:29); Exon 2 - (5'-acctgagggaatgagagct-3')(SEQ ID NO:30) and (5*-tgggttcagctcctttgc-3')(SEQ ID NO:31); Exon 3 - (5'-attgaagggcataggtaaga- 3'XSEQ ID NO:32) and (5'-actttaccccaccttgtccc-3')(SEQ ID NO:33); Exon 4 - (5
  • Primers to amplify each exon and the surrounding intron sequence were designed fiom genomic DNA sequence of CLN3. PCR was performed in a final volume of 100 ⁇ l using 100 ng of genomic DNA, 0.2 ⁇ M of each primer, 0.25 mM of each dNTP, 1.5 mM MgC-2 and 0.3 ⁇ l of AmpliTaq (Perkin-Elmer). A 'hot' start was performed followed by 1 min at 94°C, 1 min at 60°C, 1 min at 72°C (30 cycles), and 10 min at 72°C (1 cycle) using a Hybaid OmniGene. The resulting products were electrophoresed in 1% agarose gels and were visualized after ethidium bromide staining with a UV transilluminator.
  • SSCP single strand conformational polymorphisms
  • RNA extraction and analysis were desalted/concentrated using a Microcon-100 column (Amicon). Sequencing was carried out with the same primers used for exon amplification using the Taq FS Dye Terminator Cycle sequencing kit (Perkin-Elmer) and automated analysis was done with the ABI 373 A sequencer. Sequence comparisons were performed using Sequence Navigator software (Perkin-Elmer). The exons were sequenced manually with Sequenase T7 DNA polymerase (United States Biochemicals). RNA extraction and analysis
  • Primers 6972 and 6700 (5'-gcgctctctgcttcttcttcttc-3') were used to amplify the RNA-cDNA duplex from patient L121/BB. All products were subcloned and sequenced.
  • Amplified exon products were digested according to the manufacturer's recommendations. Samples were electrophoresed in 1% agarose gels and were visualized after ethidium bromide staining with a UV transilluminator.
  • CLN3 homologs e.g., CLN3 genes from different species.
  • degenerate oligonucleotide primers can be synthesized from the regions of homology shared by human and mouse CLN3 genes. The degree of degeneracy ofthe primers will depend on the degeneracy ofthe genetic code for that particular amino acid sequence used.
  • the degenerate primers should also contain restriction endonuclease sites at the 5' end to facilitate subsequent cloning.
  • Total mRNA can be obtained from cells, e.g., brain cells, and reverse transcribed using Superscript Reverse Transcriptase Kit.
  • oligo(dT) primer supplied with the kit
  • cDNA obtained can than be subjected to a PCR amplification using above described degenerate oligonucleotides.
  • PCR conditions should be optimized for the annealing temperature, Mg " ⁇ concentration and cycle duration. Once the fragment of appropriate size is amplified, it should be Klenow filled, cut with appropriate restriction enzymes and gel purified.
  • Such fragment can tiian be cloned into a vector, e.g., a Bluescript vector.
  • Clones with inserts of appropriate size can be digested with restriction enzymes to compare generated fragments with those of other CLN3 genes, e.g., hauman and mouse CLN3 genes. Those clones with distinct digestion profiles can be sequenced.
  • antibodies can be made to the conserved regions ofthe human and/or mouse CLN3 genes and used to screen expression libraries.
  • the gene constmcts ofthe invention can also be used as a part of a gene therapy protocol to deliver nucleic acids encoding either an agonistic or antagonistic form of a Batten disease polypeptide.
  • the invention features expression vectors for in vivo transfection and expression of a Batten disease polypeptide in particular cell types (e.g., neural cells) so as to reconstitute the function of, enhance the function of, or altematively, antagonize the function of a Batten disease polypeptide in a cell in which the polypeptide is misexpressed.
  • Expression constmcts of Batten disease polypeptides may be administered in any biologically effective carrier, e.g. any formulation or composition capable of effectively delivering the Batten disease gene to cells in vivo.
  • Approaches include insertion ofthe subject gene into viral vectors including recombinant retroviruses, adenovims, adeno- associated vims, and herpes simplex virus- 1, or recombinant bacterial or eukaryotic plasmids.
  • Viral vectors transfect cells directly; plasmid DNA can be delivered with the help of, for example, cationic liposomes (lipofectin) or derivatized (e.g. antibody conjugated), polylysine conjugates, gramacidin S, artificial viral envelopes or other such intracellular carriers, as well as direct injection ofthe gene constmct or CaPO4 precipitation carried out in vivo.
  • a preferred approach for in vivo introduction of nucleic acid into a cell is by use of a viral vector containing nucleic acid, e.g. a cDNA encoding a Batten disease polypeptide.
  • a viral vector containing nucleic acid e.g. a cDNA encoding a Batten disease polypeptide.
  • Infection of cells with a viral vector has the advantage that a large proportion of d e targeted cells can receive the nucleic acid.
  • molecules encoded within the viral vector e.g., by a cDNA contained in the viral vector, are expressed efficiently in cells which have taken up viral vector nucleic acid.
  • Retrovims vectors and adeno-associated vims vectors can be used as a recombinant gene delivery system for the transfer of exogenous genes in vivo, particularly into humans. These vectors provide efficient delivery of genes into cells, and the transferred nucleic acids are stably integrated into the chromosomal DNA of d e host.
  • the development of specialized cell lines (termed "packaging cells") which produce only replication-defective retroviruses has increased the utility of retrovimses for gene therapy, and defective retrovimses are characterized for use in gene transfer for gene therapy purposes (for a review see Miller. A.D. (1990) Blood 76:271).
  • a replication defective retrovims can be packaged into virions which can be used to infect a target cell through the use of a helper virus by standard techniques. Protocols for producing recombinant retrovimses and for infecting cells in vitro or in vivo with such vimses can be found in Current Protocols in Molecular Biology. Ausubel, F.M. et al. (eds.) Greene Publishing Associates, (1989), Sections 9.10-9.14 and odier standard laboratory manuals. Examples of suitable retrovimses include pLJ, pZIP, pWE and pEM which are known to those skilled in d e art.
  • Suitable packaging vims lines for preparing both ecotropic and amphotropic retroviral systems include ⁇ Crip, ⁇ Cre, ⁇ 2 and ⁇ Am. Retrovimses have been used to introduce a variety of genes into " many different cell types, including epithelial cells, in vitro and/or in vivo (see for example Eglitis, et al. (1985) Science 230:1395-1398; Danos and Mulligan (1988) Proc. Natl. Acad. Sci. USA 85:6460-6464; Wilson et al. (1988) Proc. Natl. Acad. Sci. USA 85:3014-3018; Armentano et al. (1990) Proc. Natl. Acad. Sci.
  • Another viral gene delivery system useful in the present invention utilizes adeno vims-derived vectors.
  • the genome of an adenovims can be manipulated such that it encodes and expresses a gene product of interest but is inactivated in terms of its ability to replicate in a normal lytic viral life cycle. See, for example, Berkner et al. (1988) BioTechniques 6:616; Rosenfeld et al. (1991) Science 252:431-434; and Rosenfeld et al. (1992) Cell 68:143-155.
  • adenoviral vectors derived from the adenovims strain Ad type 5 dl324 or other strains of adenovims are known to those skilled in the art.
  • Recombinant adenovimses can be advantageous in certain circumstances in that they are not capable of infecting nondividing cells and can be used to infect a wide variety of cell types, including epithelial cells (Rosenfeld et al. (1992) cited supra).
  • the vims particle is relatively stable and amenable to purification and concentration, and as above, can be modified so as to affect the spectrum of infectivity.
  • introduced adenoviral DNA (and foreign DNA contained therein) is not integrated into the genome of a host cell but remains episomal, thereby avoiding potential problems that can occur as a result of insertional mutagenesis in situations where introduced DNA becomes integrated into the host genome (e.g., retroviral DNA).
  • the carrying capacity ofthe adenoviral genome for foreign DNA is large (up to 8 kilobases) relative to other gene delivery vectors (Berkner et al. cited supra; Haj-Ahmand and Graham (1986) J Virol. 57:267).
  • Adeno-associated vims is a naturally occurring defective vims that requires another vims, such as an adenovims or a herpes vims, as a helper vims for efficient replication and a productive life cycle.
  • An AAV vector such as that described in Tratschin et al. (1985) Mol. Cell. Biol. 5:3251-3260 can be used to introduce DNA into cells.
  • a variety of nucleic acids have been introduced into different cell types using AAV vectors (see for example Hermonat et al. (1984) Proc. Natl. Acad. Sci. USA 81:6466-6470; Tratschin et al. (1985) Mol. Cell. Biol. 4:2072-2081; Wondisford et al. (1988) Mol. Endocrinol. 2:32-39; Tratschin et al. (1984) J. Virol. 51:611- 619; and Flotte et al. (1993) J. Biol. Chem.
  • non- viral methods can also be employed to cause expression of a Batten disease polypeptide in the tissue of a mammal, such as a human.
  • Most nonviral methods of gene transfer rely on normal mechanisms used by mammalian cells for the uptake and intracellular transport of macromolecules.
  • non- viral gene delivery systems ofthe present invention rely on endocytic pathways for the uptake ofthe subject Batten disease gene by the targeted cell.
  • Exemplary gene delivery systems of diis type include liposomal derived systems, poly-lysine conjugates, and artificial viral envelopes.
  • a gene encoding a Batten disease polypeptide can be entrapped in liposomes bearing positive charges on dieir surface (e.g., lipofectins) and (optionally) which are tagged with antibodies against cell surface antigens ofthe target tissue (Mizuno et al. (1992) No Shinkei Geha 20:547-551; PCT publication WO91/06309; Japanese patent application 1047381; and European patent publication EP-A-43075).
  • dieir surface e.g., lipofectins
  • the gene delivery systems for the therapeutic Batten disease gene can be introduced into a patient by any of a number of mediods, each of which is familiar in the art.
  • a pharmaceutical preparation ofthe gene delivery system can be introduced systemically, e.g. by intravenous injection, and specific transduction ofthe protein in the target cells occurs predominantly from specificity of transfection provided by d e gene delivery vehicle, cell-type or tissue-type expression due to the transcriptional regulatory sequences controlling expression ofthe receptor gene, or a combination thereof.
  • initial delivery ofthe recombinant gene is more limited with introduction into die animal being quite localized.
  • the gene delivery vehicle can be introduced by catheter (see U.S.
  • the Batten disease gene is targeted to neural cells.
  • the pharmaceutical preparation ofthe gene therapy constmct can consist essentially ofthe gene delivery system in an acceptable diluent, or can comprise a slow release matrix in which the gene delivery vehicle is imbedded. Altematively, where the complete gene delivery system can be produced in tact from recombinant cells, e.g. retroviral vectors, die pharmaceutical preparation can comprise one or more cells which produce the gene delivery system.
  • Antisense Therapy Another aspect ofthe invention relates to the use ofthe isolated nucleic acid in
  • antisense therapy refers to administration or in situ generation of oligonucleotides or dieir derivatives which specifically hybridize (e.g. bind) under cellular conditions, with the cellular mRNA and/or genomic DNA encoding a Batten disease polypeptide, or mutant thereof, so as to inhibit expression ofthe encoded protein, e.g. by inhibiting transcription and/or translation.
  • the binding may be by conventional base pair complementarity, or, for example, in die case of binding to DNA duplexes, through specific interactions in the major groove ofthe double helix.
  • antisense therapy refers to the range of techniques generally employed in the art, and includes any therapy which relies on specific binding to oligonucleotide sequences.
  • the antisense constmct binds to a naturally-occurring sequence of a Batten disease gene which, for example, is involved in expression ofthe gene. These sequences include, for example, start codons, stop codons, and RNA primer binding sites.
  • the antisense construct binds to a nucleotide sequence which is not present in the wild type gene.
  • the antisense constmct can bind to a region of a Batten disease gene which contains an insertion of an exogenous, non- wild type sequence.
  • d e antisense constmct can bind to a region of a Batten disease gene which has undergone a deletion, tiiereby bringing two regions ofthe gene togedier which are not normally positioned together and which, together, create a non-wild type sequence.
  • antisense constmcts When administered in vivo to a subject, antisense constmcts which bind to non- wild type sequences provide the advantage of inhibiting the expression of mutant Batten disease genes (e.g., which encode polypeptides which are unstable, have an undesirable activity, or otherwise give rise to disorders associated with Batten disease), without inhibiting expression of any wild type Batten disease gene
  • An antisense constmct ofthe present invention can be delivered, for example, as an expression plasmid which, when transcribed in the cell, produces RNA which is complementary to at least a unique portion ofthe cellular mRNA which encodes a Batten disease polypeptide.
  • the antisense constmct is an oligonucleotide probe which is generated ex vivo and which, when introduced into die cell causes inhibition of expression by hybridizing with the mRNA and or genomic sequences of a Batten disease gene.
  • oligonucleotide probes are preferably modified oligonucleotide which are resistant to endogenous nucleases, e.g. exonucleases and or endonucleases, and is therefore stable in vivo.
  • Exemplary nucleic acid molecules for use as antisense oligonucleotides are phosphoramidate, phosphothioate and mediylphosphonate analogs of DNA (see " also U.S.
  • Patents 5,176,996; 5,264,564; and 5,256,775) are reviewed, for example, by Van der Krol et al. (1988) Biotechnigues 6:958-976; and Stein et al. (1988) Cancer Res 48:2659- 2668.
  • the modified oligomers ofthe invention are useful in therapeutic, diagnostic, and research contexts.
  • the oligomers are utilized in a manner appropriate for antisense therapy in general.
  • the oligomers ofthe invention can be formulated for a variety of loads of administration, including systemic and topical or localized administration.
  • systemic administration injection is preferred, including intramuscular, intravenous, intraperitoneal, and subcutaneous for injection
  • the oligomers ofthe invention can be formulated in liquid solutions, preferably in physiologically compatible buffers such as Hank's solution or Ringer's solution.
  • the oligomers may be formulated in solid form and redissolved or suspended immediately prior to use. Lyophilized forms are also included in the invention.
  • the compounds can be administered orally, or by transmucosal or transdermal means.
  • penetrants appropriate to the barrier to be permeated are used in the formulation.
  • penetrants include, for example, for transmucosal administration bile salts and fusidic acid derivatives, and detergents.
  • Transmucosal administration may be through nasal sprays or using suppositories.
  • the oligomers are formulated into conventional oral administration forms such as capsules, tablets, and tonics.
  • the oligomers ofthe invention are formulated into ointments, salves, gels, or creams as known in the art.
  • die oligomers ofthe invention may be used as diagnostic reagents to detect the presence or absence ofthe target DNA or RNA sequences to which they specifically bind.
  • the antisense constmcts ofthe present invention by antagonizing the expression of a Batten disease gene, can be used in the manipulation of tissue, both in vivo and in ex vivo tissue cultures.
  • the invention includes transgenic animals which include cells (of that animal) which contain a Batten disease transgene and which preferably (though optionally) express (or misexpress) an endogenous or exogenous Batten disease gene in one or more cells in the animal.
  • the Batten disease transgene can encode a mutant Batten disease polypeptide, thereby creating an animal model for Batten disease. Such animals can be used as disease models or can be used to screen for agents effective at treating Batten disease.
  • the Batten disease transgene can encode the wild-type form ofthe protein, or can encode homologs thereof, including both agonists and antagonists, as well as antisense constmcts.
  • the expression ofthe transgene is restricted to specific subsets of cells, or tissues utilizing, for example, cis-acting sequences that control expression in the desired pattem. Tissue-specific regulatory sequences and conditional regulatory sequences can be used to control expression ofthe transgene in certain spatial pattems.
  • Temporal pattems of expression can be provided by, for example, conditional recombination systems or prokaryotic transcriptional regulatory sequences.
  • the transgenic animal carries a "knockout" Batten disease gene, i.e., a deletion of all or a part ofthe gene.
  • Genetic techniques which allow for the expression of transgenes, that are regulated in vivo via site-specific genetic manipulation, are known to those skilled in the art. For example, genetic systems are available which allow for the regulated expression of a recombinase that catalyzes the genetic recombination a target sequence.
  • target sequence refers to a nucleotide sequence that is genetically recombined by a recombinase.
  • the target sequence is flanked by recombinase recognition sequences and is generally either excised or inverted in cells expressing recombinase activity.
  • Recombinase catalyzed recombination events can be designed such that recombination ofthe target sequence results in either the activation or repression of expression ofthe subject Batten disease gene.
  • excision of a target sequence which interferes with the expression of a recombinant Batten disease gene such as one which encodes an agonistic homolog, can be designed to activate expression of that gene.
  • This interference with expression ofthe protein can result from a variety of mechanisms, such as spatial separation of die Batten disease gene from the promoter element or an intemal stop codon.
  • the transgene can be made so mat the coding sequence of die gene is flanked with recombinase recognition sequences and is initially transfected into cells in a 3' to 5' orientation with respect to the promoter element.
  • inversion ofthe target sequence will reorient the subject gene by placing the 5' end ofthe coding sequence in an orientation with respect to the promoter element which allow for promoter driven transcriptional activation. See e.g., descriptions of d e crelloxP recombinase system of bacteriophage Pl (Lakso et al.
  • This regulated control will result in genetic recombination ofthe target sequence only in cells where recombinase expression is mediated by the promoter element.
  • the activation expression ofthe recombinant Batten disease gene can be regulated via control of recombinase expression.
  • conditional transgenes can be provided using prokaryotic promoter sequences which require prokaryotic proteins to be simultaneous expressed in order to facilitate expression ofthe transgene.
  • Exemplary promoters and the corresponding trans ⁇ activating prokaryotic proteins are given in U.S. Patent No. 4,833,080.
  • expression ofthe conditional transgenes can be induced by gene tiierapy-like methods wherein a gene encoding the trans-activating protein, e.g. a recombinase or a prokaryotic protein, is delivered to the tissue and caused to be expressed, such as in a cell-type specific manner. By this method, die Batten disease transgene could remain silent into adulthood until "turned on" by the introduction ofthe trans-activator.
  • the inventor has provided the primary amino acid stmcture of a Batten disease polypeptide.
  • a Batten disease polypeptide Once an example of this core stmcture has been provided, one skilled in die art can alter the disclosed stmcture by producing fragments or analogs, and testing the newly produced stmctures for activity. Examples of prior art methods which allow die production and testing of fragments and analogs are discussed below.
  • These, or analogous mediods can be used to make and screen fragments and analogs of a Batten disease polypeptide having at least one biological activity e.g., which react with an antibody (e.g., a monoclonal antibody) specific for a Batten disease polypeptide.
  • Fragments of a protein can be produced in several ways, e.g., recombinantly, by proteolytic digestion, or by chemical synthesis.
  • Intemal or terminal fragments of a polypeptide can be generated by removing one or more nucleotides from one end (for a terminal fragment) or both ends (for an intemal fragment) of a nucleic acid which encodes the polypeptide.
  • Expression ofthe mutagenized DNA produces polypeptide fragments. Digestion with "end-nibbling" endonucleases can thus generate DNA's which encode an array of fragments.
  • DNA's which encode fragments of a protein can also be generated by random shearing, restriction digestion or a combination ofthe above-discussed methods.
  • Fragments can also be chemically synthesized using techniques known in the art such as conventional Merrifield solid phase f-Moc or t-Boc chemistry.
  • peptides ofthe present invention may be arbitrarily divided into fragments of desired length with no overlap ofthe fragments, or divided into overlapping fragments of a desired length.
  • Production of Altered DNA and Peptide Sequences Random Methods Amino acid sequence variants of a protein can be prepared by random mutagenesis of DNA which encodes a protein or a particular domain or region of a protein.
  • Useful methods include PCR mutagenesis and saturation mutagenesis.
  • a library of random amino acid sequence variants can also be generated by the syndiesis of a set of degenerate oligonucleotide sequences. (Methods for screening proteins in a library of variants are elsewhere herein.)
  • PCR Mutagenesis In PCR mutagenesis, reduced Taq polymerase fidelity is used to introduce random mutations into a cloned fragment of DNA (Leung et al., 1989, Technique 1:11-15). This is a very powerful and relatively rapid method of introducing random mutations.
  • the DNA region to be mutagenized is amplified using the polymerase chain reaction (PCR) under conditions that reduce the fidelity of DNA synthesis by Taq DNA polymerase, e.g., by using a dGTP/dATP ratio of five and adding Mn 2+ to the PCR reaction.
  • the pool of amplified DNA fragments are inserted into appropriate cloning vectors to provide random mutant libraries.
  • Saturation mutagenesis allows for the rapid introduction of a large number of single base substitutions into cloned DNA fragments (Mayers et al., 1985, Science 229:242). This technique includes generation of mutations, e.g., by chemical treatment or irradiation of single-stranded DNA in vitro, and synthesis of a complementary DNA strand.
  • the mutation frequency can be modulated by modulating the severity ofthe treatment, and essentially all possible base substitutions can be obtained. Because this procedure does not involve a genetic selection for mutant fragments both neutral substitutions, as well as those that alter function, are obtained. The distribution of point mutations is not biased toward conserved sequence elements.
  • a library of homologs can also be generated from a set of degenerate oligonucleotide sequences. Chemical synthesis of a degenerate sequences can be carried out in an automatic DNA synthesizer, and the synthetic genes then ligated into an appropriate expression vector. The synthesis of degenerate oligonucleotides is known in the art (see for example, Narang, SA (1983) Tetrahedron 39:3; Itakura et al. (1981) Recombinant DNA,
  • Non-random or directed, mutagenesis techniques can be used to provide specific sequences or mutations in specific regions. These techniques can be used to create variants which include, e.g., deletions, insertions, or substitutions, of residues of die known amino acid sequence of a protein.
  • the sites for mutation can be modified individually or in series, e.g., by (1) substituting first with conserved amino acids and then with more radical choices depending upon results achieved, (2) deleting the target residue, or (3) inserting residues ofthe same or a different class adjacent to the located site, or combinations of options 1-3.
  • Alanine scanning mutagenesis is a useful method for identification of certain residues or regions ofthe desired protein that are preferred locations or domains for mutagenesis, Cunningham and Wells (Science 244:1081-1085, 1989).
  • a residue or group of target residues are identified (e.g., charged residues such as Arg, Asp, His, Lys, and Glu) and replaced by a neutral or negatively charged amino acid (most preferably alanine or polyalanine).
  • Replacement of an amino acid can affect the interaction ofthe amino acids with die surrounding aqueous environment in or outside die cell.
  • Those domains demonstrating functional sensitivity to the substitutions are then refined by introducing further or other variants at or for the sites of substitution.
  • d e nature ofthe mutation per se need not be predetermined.
  • alanine scanning or random mutagenesis may be conducted at the target codon or region and the expressed desired protein subunit variants are screened for the optimal combination of desired activity.
  • Oligonucleotide-mediated mutagenesis is a useful method for preparing substitution, deletion, and insertion variants of DNA, see, e.g., Adelman et al., (DNA 2:183, 1983). Briefly, the desired DNA is altered by hybridizing an oligonucleotide encoding a mutation to a DNA template, where the template is the single-stranded form of a plasmid or bacteriophage containing the unaltered or native DNA sequence ofthe desired protein. After hybridization, a DNA polymerase is used to syntiiesize an entire second complementary strand ofthe template that will thus incorporate the oligonucleotide primer.
  • oligonucleotides of at least 25 nucleotides in length are used.
  • An optimal oligonucleotide will have 12 to 15 nucleotides diat are completely complementary to the template on either side ofthe nucleotide(s) coding for the mutation. This ensures that the oligonucleotide will hybridize properly to the single- stranded DNA template molecule.
  • the oligonucleotides are readily synthesized using techniques known in the art such as that described by Crea et al. (Proc. Natl. Acad. Sci. USA, 75: 5765[1978]).
  • preferred oligonucleotide primers have a nucleotide sequence shown in SEQ ID NOS: 3-15.
  • the starting material is a plasmid (or other vector) which includes the protein subunit DNA to be mutated.
  • the codon(s) in the protein subunit DNA to be mutated are identified.
  • a double-stranded oligonucleotide encoding the sequence of die DNA between the restriction sites but containing the desired mutation(s) is synthesized using standard procedures. The two strands are synthesized separately and then hybridized together using standard techniques.
  • This double-stranded oligonucleotide is referred to as the cassette.
  • This cassette is designed to have 3' and 5' ends diat are comparable with the ends of die linearized plasmid. such diat it can be directly ligated to the plasmid.
  • This plasmid now contains the mutated desired protein subunit DNA sequence.
  • Combinatorial mutagenesis can also be used to generate mutants, e.g., a library of variants which is generated by combinatorial mutagenesis at the nucleic acid level, and is encoded by a variegated gene library.
  • a mixture of synthetic oligonucleotides can be enzymatically ligated into gene sequences such that the degenerate set of potential sequences are expressible as individual peptides, or altematively, as a set of larger fusion proteins containing the set of degenerate sequences.
  • Techniques for screening large gene libraries often include cloning d e gene library into replicable expression vectors, transforming appropriate cells with the resulting library of vectors, and expressing die genes under conditions in which detection of a desired activity, e.g., in diis case, binding to an antibody specific for a Batten disease polypeptide.
  • detection of a desired activity e.g., in diis case, binding to an antibody specific for a Batten disease polypeptide.
  • Each of the techniques described below is amenable to high through-put analysis for screening large numbers of sequences created, e.g., by random mutagenesis techniques.
  • the candidate peptides are displayed on the surface of a cell or viral particle, and die ability of particular cells or viral particles to bind an appropriate receptor protein via the displayed product is detected in a "panning assay".
  • the gene library can be cloned into the gene for a surface membrane protein of a bacterial cell, and die resulting fusion protein detected by panning (Ladner et al., WO 88/06630; Fuchs et al. (1991) Bio/Technology 9:1370-1371; and Goward et al. (1992) TIBS 18:136-140).
  • a detectably labeled ligand can be used to score for potentially functional peptide homologs.
  • Fluorescentiy labeled ligands e.g., receptors
  • fluorescentiy labeled ligands allows cells to be visually inspected and separated under a fluorescence microscope, or, where the mo ⁇ hology ofthe cell permits, to be separated by a fluorescence- activated cell sorter.
  • a gene library can be expressed as a fusion protein on the surface of a viral particle.
  • foreign peptide sequences can be expressed on the surface of infectious phage, thereby conferring two significant benefits.
  • coli filamentous phages Ml 3, fd., and fl are most often used in phage display libraries. Either ofthe phage gill or gVIII coat proteins can be used to generate fusion proteins without dismpting die ultimate packaging ofthe viral particle.
  • Foreign epitopes can be expressed at the NH 2 -terminal end of pill and phage bearing such epitopes recovered from a large excess of phage lacking this epitope (Ladner et al. PCT publication WO 90/02909; Ganard et al., PCT publication WO 92/09690; Marks et al. (1992) J. Biol. Chem. 267:16007-16010; Griffiths et al.
  • Examples include the Staphylococcus protein A and the outer membrane protease IgA of Neisseria (Hansson et al. (1992) J. Bacteriol. 174, 4239-4245 and Klauser et al. (1990) EMBOJ. 9, 1991-1999).
  • the physical link between the peptide and its encoding DNA occurs by die containment ofthe DNA within a particle (cell or phage) that carries the peptide on its surface. Capturing the peptide captures the particle and the DNA within.
  • An altemative scheme uses the DNA- binding protein Lad to form a link between peptide and DNA (Cull et al.
  • the plasmids in each cell contain only a single oligonucleotide sequence and each cell expresses only a single peptide sequence, the peptides become specifically and stably associated widi the DNA sequence that directed its synthesis.
  • the cells ofthe library are gently lysed and the peptide-DNA complexes are exposed to a matrix of immobilized receptor to recover the complexes containing active peptides.
  • the associated plasmid DNA is then reintroduced into cells for amplification and DNA sequencing to determine the identity ofthe peptide ligands.
  • peptides-on-plasmids differs in two important ways from die phage display methods.
  • the peptides are attached to die C- terminus of die fusion protein, resulting in the display of die library members as peptides having free carboxy termini.
  • Both ofthe filamentous phage coat proteins, pill and pVIII are anchored to the phage dirough their C-termini, and the guest peptides are placed into die outward-extending N-terminal domains.
  • the phage-displayed peptides are presented right at die amino terminus ofthe fusion protein.
  • a second difference is the set of biological biases affecting the population of peptides actually present in the libraries.
  • the Lad fusion molecules are confined to the cytoplasm of die host cells.
  • the phage coat fusions are exposed briefly to the cytoplasm during translation but are rapidly secreted through the inner membrane into the periplasmic compartment, remaining anchored in the membrane by their C-terminal hydrophobic domains, with die N-termini, containing the peptides, protmding into die periplasm while awaiting assembly into phage particles.
  • the peptides in die Lad and phage libraries may differ significantly as a result of their exposure to different proteolytic activities.
  • phage coat proteins require transport across the inner membrane and signal peptidase processing as a prelude to incorporation into phage.
  • Certain peptides exert a deleterious effect on diese processes and are underrepresented in the libraries (Gallop et aL (1994) J. Med. Chem. 37(9):1233-1251). These particular biases are not a factor in the Lad display system.
  • RNA from the bound complexes is recovered, converted to cDNA, and amplified by PCR to produce a template for the next round of syndiesis and screening.
  • the polysome display method can be coupled to the phage display system.
  • cDNA from the enriched pool of polysomes was cloned into a phagemid vector.
  • This vector serves as both a peptide expression vector, displaying peptides fused to the coat proteins, and as a DNA sequencing vector for peptide identification.
  • a DNA sequencing vector for peptide identification.
  • Secondary Screens The high through-put assays described above can be followed by secondary screens in order to identify further biological activities which will, e.g., allow one skilled in the art to differentiate agonists from antagonists.
  • the type of a secondary screen used will depend on the desired activity that needs to be tested.
  • an assay can be developed in which the ability to inhibit an interaction between a protein of interest and its respective ligand can be used to identify antagonists from a group of peptide fragments isolated tiiough one ofthe primary screens described above.
  • the invention also includes antibodies specifically reactive with a subject Batten disease polypeptide.
  • Anti-protein/anti-peptide antisera or monoclonal antibodies can be made by standard protocols (See, for example, Antibodies: A Laboratory Manual ed. by Harlow and Lane (Cold Spring Harbor Press: 1988)).
  • a mammal such as a mouse, a hamster or rabbit can be immunized with an immunogenic form ofthe peptide.
  • Techniques for confening immunogenicity on a protein or peptide include conjugation to carriers or other techniques well known in the art.
  • An immunogenic portion ofthe subject Batten disease polypeptide can be administered in the presence of adjuvant. The progress of immunization can be monitored by detection of antibody titers in plasma or serum.
  • Standard ELISA or other immunoassays can be used widi die immunogen as antigen to assess the levels of antibodies.
  • the subject antibodies are immunospecific for antigenic determinants ofthe Batten disease polypeptide of die invention, e.g. antigenic determinants of a polypeptide of SEQ ID NO: 2.
  • antibody intended to include fragments diereof which are also specifically reactive with a Batten disease polypeptide.
  • Antibodies can be fragmented using conventional techniques and the fragments screened for utility in the same manner as described above for whole antibodies. For example, F(ab')2 fragments can be generated by treating antibody with pepsin. The resulting F(ab')2 fragment can be treated to reduce disulfide bridges to produce Fab' fragments.
  • the antibody ofthe present invention is further intended to include bispecific and chimeric molecules having an anti-Batten disease polypeptide portion.
  • Bodi monoclonal and polyclonal antibodies directed against Batten disease polypeptides, or fragments or analogs diereof, and antibody fragments such as Fab " and F(ab ' )2, can be used to block die action of a Batten disease polypeptide and allow the study of the role of a Batten disease polypeptide of the present invention.
  • Antibodies which specifically bind Batten disease polypeptide epitopes can also be used in immunohistochemical staining of tissue samples in order to evaluate the abundance and pattem of expression of Batten disease polypeptide.
  • Anti-Batten disease polypeptide antibodies can be used diagnostically in immuno-precipitation and immuno- blotting to detect and evaluate wild type or mutant Batten disease polypeptide levels in tissue or bodily fluid as part of a clinical testing procedure.
  • the ability to monitor Batten disease polypeptide levels in an individual can allow determination ofthe efficacy of a given treatment regimen for an individual afflicted with disorders associated with Batten disease.
  • the level of a Batten disease polypeptide can be measured in cells found in bodily fluid, such as in samples of cerebral spinal fluid, or can be measured in tissue, such as produced by biopsy.
  • Diagnostic assays using anti-Batten disease polypeptide antibodies can include. for example, immunoassays designed to aid in early diagnosis of Batten disease polypeptide- mediated disorders, e.g., to detect cells in which a mutation of die Batten disease gene has occuned.
  • Anodier application of anti-Batten disease antibodies ofthe present invention is in the immunological screening of cDNA libraries constmcted in expression vectors such as ⁇ gtl 1, ⁇ gtl 8-23, ⁇ ZAP, and ⁇ ORF8.
  • Messenger libraries of this type having coding sequences inserted in the conect reading frame and orientation, can produce fusion proteins.
  • ⁇ gtl 1 will produce fusion proteins whose amino termini consist of ⁇ - galactosidase amino acid sequences and whose carboxy termini consist of a foreign polypeptide.
  • Antigenic epitopes of a subject Batten disease polypeptide can then be detected with antibodies, as, for example, reacting nitrocellulose filters lifted from infected plates with anti-Batten disease polypeptide antibodies. Phage, scored by this assay, can then be isolated from the infected plate.
  • Batten disease homologs can be detected and cloned from other animals, andretemate isoforms (including splicing variants) can be detected and cloned from human sources.
  • the present invention provides assays which can be used to screen for dmgs which are either agonists or antagonists ofthe normal cellular function, in this case, ofthe subject Batten disease polypeptide.
  • die assay evaluates the ability of a compound to modulate binding between a Batten disease polypeptide and a naturally occurring ligand, e.g., an antibody specific for a Batten disease polypeptide.
  • a naturally occurring ligand e.g., an antibody specific for a Batten disease polypeptide.
  • the effects of cellular toxicity and or bioavailability ofthe test compound can be generally ignored in die in vitro system, the assay instead being focused primarily on the effect ofthe dmg on the molecular target as may be manifest in an alteration of binding affinity with other proteins or change in enzymatic properties ofthe molecular target.
  • allelic variations include allelic variations; natural mutants; induced mutants; proteins encoded by DNA that hybridizes under high or low stringency conditions to a nucleic acid which encodes a polypeptide of SEQ ID NO:2 (for definitions of high and low stringency see Cunent Protocols in Molecular Biology, John Wiley & Sons, New York, 1989, 6.3.1 - 6.3.6, hereby incorporated by reference); and, polypeptides specifically bound by antisera to a Batten disease polypeptide.
  • the invention also includes fragments, preferably biologically active fragments, or analogs of a Batten disease polypeptide.
  • a biologically active fragment or analog is one having any in vivo or in vitro activity which is characteristic ofthe Batten disease polypeptide shown in SEQ ID NO:2, or of other naturally occu ing Batten disease polypeptides, e.g., one or more ofthe biological activities described above.
  • fragments which exist in vivo e.g., fragments which arise from post transcriptional processing or which arise from translation of altematively spliced RNA's.
  • Fragments include diose expressed in native or endogenous cells, e.g., as a result bf post- translational processing, e.g., as the result ofthe removal of an amino-terminal signal sequence, as well as those made in expression systems, e.g., in CHO cells.
  • a useful Batten disease polypeptide fragment or Batten disease polypeptide analog is one which exhibits a biological activity in any biological assay for Batten disease polypeptide activity.
  • the fragment or analog possesses 10%, preferably 40%, or at least 90% ofthe activity of a Batten disease polypeptide (SEQ ID NO: 2), in any in vivo or in vitro Batten disease polypeptide activity assay.
  • Analogs can differ from a naturally occuning Batten disease polypeptide in amino acid sequence or in ways that do not involve sequence, or both.
  • Non-sequence modifications include in vivo or in vitro chemical derivatization of a Batten disease polypeptide.
  • Non-sequence modifications include changes in acetylation, methylation, phosphorylation, carboxylation, or glycosylation.
  • Prefened analogs include a Batten disease polypeptide (or biologically active fragments thereof) whose sequences differ from the wild-type sequence by one or more conservative amino acid substitutions or by one or more non-conservative amino acid substitutions, deletions, or insertions which do not abolish die Batten disease polypeptide biological activity.
  • Conservative substitutions typically include the substitution of one amino acid for another with similar characteristics, e.g., substitutions widiin the following groups: valine, glycine; glycine, alanine; valine, isoleucine, leucine; aspartic acid, glutamic acid; asparagine, glutamine; serine, threonine; lysine, arginine; and phenylalanine, tyrosine. Other conservative substitutions can be taken from the table below.
  • Arginine R D-Arg, Lys, D-Lys, homo- Arg, D- homo-Arg, Met, Ile, D-Met, D-Ile, Orn, D-Orn
  • Glutamic Acid E D-Glu, D-Asp, Asp, Asn, D-Asn, Gin, D-Gln
  • Lysine K D-Lys, Arg, D-Arg, homo-Arg, D- homo-Arg, Met, D-Met, Ile, D-Ile, Orn. D-Orn
  • Phenylalanine F D-Phe, Tyr, D-Thr, L-Dopa, His, D- His, T ⁇ , D-Trp, Trans-3,4, or 5- phenylproline, cis-3,4, or 5-phenylproline
  • Tyrosine Y D-Tyr Phe, D-Phe, L-Dopa, His, D- His
  • analogs within the invention are those with modifications which increase peptide stability; such analogs may contain, for example, one or more non-peptide bonds (which replace the peptide bonds) in the peptide sequence. Also included are: analogs that include residues other than naturally occurring L-amino acids, e.g., D-amin ⁇ acids or non-naturally occurring or synthetic amino acids, e.g., ⁇ or ⁇ amino acids; and cyclic analogs.
  • fragment as applied to a Batten disease polypeptide analog, will ordinarily be at least about 20 residues, more typically at least about 40 residues, preferably at least about 60 residues in length. Fragments of a Batten disease polypeptide can be generated by mediods known to those skilled in the art. The ability of a candidate fragment to exhibit a biological activity of a Batten disease polypeptide can be assessed by mediods known to diose skilled in d e art, as described herein. Also included are Batten disease polypeptides containing residues diat are not required for biological activity of the peptide or that result from altemative mRNA splicing or altemative protein processing events.
  • a Batten disease polypeptide-encoding DNA can be introduced into an expression vector, the vector introduced into a cell suitable for expression ofthe desired protein, and the peptide recovered and purified, by prior art mediods.
  • Antibodies to the peptides an proteins can be made by immunizing an animal, e.g., a rabbit or mouse, and recovering anti-Batten disease polypeptide antibodies by prior art methods.
  • AGC CTC TCC CTT CGG GAA AGG TGG ACA GTA TTC AAG GGT CTG CTG TGG 986 Ser Leu Ser Leu Arg Glu Arg Trp Thr Val Phe Lys Gly Leu Leu Trp 270 275 280
  • MOLECULE TYPE protein
  • MOLECULE TYPE cDNA
  • MOLECULE TYPE other nucleic acid
  • SEQUENCE DESCRIPTION SEQ ID NO:20: GGGGGAGGAC AAGCACTG 18 (2) INFORMATION FOR SEQ ID NO:21:
  • MOLECULE TYPE other nucleic acid
  • SEQUENCE DESCRIPTION SEQ ID NO:49:

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Zoology (AREA)
  • Genetics & Genomics (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Toxicology (AREA)
  • Peptides Or Proteins (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La présente invention concerne un acide nucléique sensiblement pur qui encode un polypeptide du syndrome de Batten-Steinert.
PCT/US1996/013896 1995-08-31 1996-08-30 Gene du syndrome de batten-steinert Ceased WO1997008308A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU69603/96A AU6960396A (en) 1995-08-31 1996-08-30 Batten disease gene

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US303095P 1995-08-31 1995-08-31
US60/003,030 1995-08-31

Publications (2)

Publication Number Publication Date
WO1997008308A1 true WO1997008308A1 (fr) 1997-03-06
WO1997008308A9 WO1997008308A9 (fr) 1997-05-15

Family

ID=21703757

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1996/013896 Ceased WO1997008308A1 (fr) 1995-08-31 1996-08-30 Gene du syndrome de batten-steinert

Country Status (2)

Country Link
AU (1) AU6960396A (fr)
WO (1) WO1997008308A1 (fr)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7608394B2 (en) 2004-03-26 2009-10-27 Sequenom, Inc. Methods and compositions for phenotype identification based on nucleic acid methylation
US9249456B2 (en) 2004-03-26 2016-02-02 Agena Bioscience, Inc. Base specific cleavage of methylation-specific amplification products in combination with mass analysis
WO2016100575A1 (fr) * 2014-12-16 2016-06-23 Board Of Regents Of The University Of Nebraska Thérapie génique pour la maladie de steinert juvénile
US9394565B2 (en) 2003-09-05 2016-07-19 Agena Bioscience, Inc. Allele-specific sequence variation analysis
EP3077510B1 (fr) * 2013-12-02 2020-05-06 Ionis Pharmaceuticals, Inc. Composés antisens et leurs utilisations
US11040116B2 (en) 2012-08-01 2021-06-22 Nationwide Children's Hospital Intrathecal delivery of recombinant adeno-associated virus 9
US11219696B2 (en) 2008-12-19 2022-01-11 Nationwide Children's Hospital Delivery of polynucleotides using recombinant AAV9
US11590210B2 (en) 2011-06-08 2023-02-28 Nationwide Children's Hospital, Inc. Methods for delivery of polynucleotides by adeno-associated virus for lysosomal storage disorders

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030190644A1 (en) 1999-10-13 2003-10-09 Andreas Braun Methods for generating databases and databases for identifying polymorphic genetic markers

Non-Patent Citations (7)

* Cited by examiner, † Cited by third party
Title
AMERICAN JOURNAL OF HUMAN GENETICS, 18-22 October 1994, Vol. 55, No. 3, LERNER et al., "Isolation of Candidate Genes from the Batten Disease (JNCL) Region Using Exon Amplification", pages A263, Abstract No. 1541. *
AMERICAN JOURNAL OF HUMAN GENETICS, 1994, Vol. 54, LERNER et al., "Linkage Disequilibrium Between the Juvenile Neuronal Ceroid Lipofuscinosis Gene and Marker Loci on Chromosome 16p12.1", pages 88-94. *
AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, Vol. 57, JARVELA et al., "Physical Map of the Region Containing the Gene for Batten Disease (CLN3)", pages 316-319. *
AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, Vol. 57, LERNER et al., "Isolation of Genes From the Batten Candidate Region Using Exon Amplification", pages 320-323. *
AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, Vol. 57, MITCHISON et al., "Refined Localization of the Batten Disease Gene (CLN3) by Haplotype and Linkage Disequilibrium Mapping to D16S288-D16S383 and Exclusion from this Region of a Variant Form of Batten Disease with Granular Osmiophilic Deposits", pages 312-315. *
CELL, 22 September 1995, Vol. 82, LERNER et al., "Isolation of a Novel Gene Underlying Batten Disease, CLN3", pages 949-957. *
GENOMICS, 1994, Vol. 22, MITCHISON et al., "Genetic Mapping of the Batten Disease Locus (CLN3) to the Interval D16S88-D16S83 by Analysis of Haplotypes and Allelic Association", pages 465-468. *

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9394565B2 (en) 2003-09-05 2016-07-19 Agena Bioscience, Inc. Allele-specific sequence variation analysis
US9249456B2 (en) 2004-03-26 2016-02-02 Agena Bioscience, Inc. Base specific cleavage of methylation-specific amplification products in combination with mass analysis
US7608394B2 (en) 2004-03-26 2009-10-27 Sequenom, Inc. Methods and compositions for phenotype identification based on nucleic acid methylation
US11219696B2 (en) 2008-12-19 2022-01-11 Nationwide Children's Hospital Delivery of polynucleotides using recombinant AAV9
US12324829B2 (en) 2011-06-08 2025-06-10 Nationwide Children's Hospital, Inc. Methods for delivery of polynucleotides by adeno-associated virus for lysosomal storage disorders
US11590210B2 (en) 2011-06-08 2023-02-28 Nationwide Children's Hospital, Inc. Methods for delivery of polynucleotides by adeno-associated virus for lysosomal storage disorders
US11738094B2 (en) 2012-08-01 2023-08-29 Nationwide Children's Hospital Intrathecal delivery of recombinant adeno-associated virus 9
US11730829B2 (en) 2012-08-01 2023-08-22 Nationwide Children's Hospital Intrathecal delivery of recombinant adeno-associated virus 9
US11040116B2 (en) 2012-08-01 2021-06-22 Nationwide Children's Hospital Intrathecal delivery of recombinant adeno-associated virus 9
US12208144B2 (en) 2012-08-01 2025-01-28 Nationwide Children's Hospital Intrathecal delivery of recombinant adeno-associated virus 9
US11413357B2 (en) 2012-08-01 2022-08-16 Nationwide Children's Hospital Intrathecal delivery of recombinant adeno-associated virus 9
US11311634B2 (en) 2012-08-01 2022-04-26 Nationwide Children's Hospital Intrathecal delivery of recombinant Adeno-associated virus 9
EP3077510B1 (fr) * 2013-12-02 2020-05-06 Ionis Pharmaceuticals, Inc. Composés antisens et leurs utilisations
JP2018500311A (ja) * 2014-12-16 2018-01-11 ボード オブ リージェンツ オブ ザ ユニバーシティ オブ ネブラスカ 若年型バッテン病のための遺伝子療法
US20220049272A1 (en) * 2014-12-16 2022-02-17 Board Of Regents Of The University Of Nebraska Gene therapy for juvenile batten disease
AU2015364636B9 (en) * 2014-12-16 2021-12-02 Board Of Regents Of The University Of Nebraska Gene therapy for Juvenile Batten Disease
AU2015364636B2 (en) * 2014-12-16 2021-11-04 Board Of Regents Of The University Of Nebraska Gene therapy for Juvenile Batten Disease
CN107249646B (zh) * 2014-12-16 2021-06-29 内布拉斯加大学董事会 用于青少年巴滕病的基因疗法
US10876134B2 (en) 2014-12-16 2020-12-29 Board Of Regents Of The University Of Nebraska Gene therapy for juvenile batten disease
US20190032078A1 (en) * 2014-12-16 2019-01-31 Board Of Regents Of The University Of Nebraska Gene therapy for juvenile batten disease
CN107249646A (zh) * 2014-12-16 2017-10-13 内布拉斯加大学董事会 用于青少年巴滕病的基因疗法
US12297447B2 (en) * 2014-12-16 2025-05-13 Board Of Regents Of The University Of Nebraska Gene therapy for juvenile Batten disease
WO2016100575A1 (fr) * 2014-12-16 2016-06-23 Board Of Regents Of The University Of Nebraska Thérapie génique pour la maladie de steinert juvénile

Also Published As

Publication number Publication date
AU6960396A (en) 1997-03-19

Similar Documents

Publication Publication Date Title
JP5328603B2 (ja) 良性の家族性新生児痙攣（ｂｆｎｃ）および他の癲癇において突然変異されたｋｃｎｑ２およびｋｃｎｑ３−カリウムチャンネル遺伝子
US5849708A (en) Promotion of eating behavior
US8288096B2 (en) Diagnostic method for epilepsy
JP4204317B2 (ja) 熱性痙攣プラスを伴う全般てんかんのニューロン遺伝子のナトリウムチャネルα１サブユニットおよびそのポリペプチドの変異およびその治療
WO1997008308A1 (fr) Gene du syndrome de batten-steinert
WO1997008308A9 (fr) Gene du syndrome de batten-steinert
US7244577B2 (en) Method of screening for modulator of LRP5 activity
JP2005501536A (ja) イオンチャネルにおける変異
US7282336B2 (en) Method of diagnosing epilepsy
JPH09512166A (ja) 哺乳類スルホニル尿素受容体をコードする配列および新生児期の持続性高インシュリン血症性低血糖の検知法
US6683165B1 (en) Human gene relating to respiratory diseases and obesity
US6528634B1 (en) Aiolos gene
US5656438A (en) CAIP-like gene family
US5641748A (en) Caip-like gene family
US7709225B2 (en) Nucleic acids encoding mutations in sodium channels related to epilepsy
US5837844A (en) CAIP-like gene family
US20040191791A1 (en) Novel mutation
US6818214B2 (en) Two novel genes from psoriatic epidermis: psoriastatin type I and psoriastatin type II
US6423824B1 (en) CAIP-like gene family
WO1997049808A1 (fr) Famille de genes du type caip
AU2002252833A1 (en) Novel mutation

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AU CA IS JP NO

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LU MC NL PT SE

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
COP Corrected version of pamphlet

Free format text: PAGES 1/11-11/11,DRAWINGS,REPLACED BY NEW PAGES 1/9-9/9;DUE TO LATE TRANSMITTAL BY THE RECEIVING OFFICE

121 Ep: the epo has been informed by wipo that ep was designated in this application
122 Ep: pct application non-entry in european phase
NENP Non-entry into the national phase

Ref country code: CA