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CL2012002007A1 - Método para eliminar una región de adn en una planta, que comprende proporcionar una planta que comprende dicha región de adn en su genoma, la cual expresa una nucleasa de ‘dedo de zinc’ diseñada para disociar el adn genómico en una secuencia de reconocimiento; ácido nucleico aislado que comprende un gen de interés flanqueado por dos secuencias de reconocimiento para una nucleasa de dedo de zinc. - Google Patents

Método para eliminar una región de adn en una planta, que comprende proporcionar una planta que comprende dicha región de adn en su genoma, la cual expresa una nucleasa de ‘dedo de zinc’ diseñada para disociar el adn genómico en una secuencia de reconocimiento; ácido nucleico aislado que comprende un gen de interés flanqueado por dos secuencias de reconocimiento para una nucleasa de dedo de zinc.

Info

Publication number
CL2012002007A1
CL2012002007A1 CL2012002007A CL2012002007A CL2012002007A1 CL 2012002007 A1 CL2012002007 A1 CL 2012002007A1 CL 2012002007 A CL2012002007 A CL 2012002007A CL 2012002007 A CL2012002007 A CL 2012002007A CL 2012002007 A1 CL2012002007 A1 CL 2012002007A1
Authority
CL
Chile
Prior art keywords
dna
plant
region
zinc finger
nuclease
Prior art date
Application number
CL2012002007A
Other languages
English (en)
Inventor
Sean Russel
Joseph F Petolino
Original Assignee
Dow Agrosciences Llc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=44307617&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CL2012002007(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Dow Agrosciences Llc filed Critical Dow Agrosciences Llc
Publication of CL2012002007A1 publication Critical patent/CL2012002007A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8201—Methods for introducing genetic material into plant cells, e.g. DNA, RNA, stable or transient incorporation, tissue culture methods adapted for transformation
    • C12N15/8213—Targeted insertion of genes into the plant genome by homologous recombination
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8241—Phenotypically and genetically modified plants via recombinant DNA technology
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8241—Phenotypically and genetically modified plants via recombinant DNA technology
    • C12N15/8261—Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield
    • C12N15/8262—Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield involving plant development
    • C12N15/8265—Transgene containment, e.g. gene dispersal
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/16—Hydrolases (3) acting on ester bonds (3.1)
    • C12N9/22—Ribonucleases [RNase]; Deoxyribonucleases [DNase]

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Biomedical Technology (AREA)
  • Biotechnology (AREA)
  • Zoology (AREA)
  • Organic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Wood Science & Technology (AREA)
  • Molecular Biology (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Microbiology (AREA)
  • Cell Biology (AREA)
  • Physics & Mathematics (AREA)
  • Biophysics (AREA)
  • Plant Pathology (AREA)
  • Medicinal Chemistry (AREA)
  • Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Botany (AREA)
  • Developmental Biology & Embryology (AREA)
  • Environmental Sciences (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Cultivation Of Plants (AREA)

Abstract

Método para eliminar una región de ADN en una planta, que comprende proporcionar una planta que comprende dicha región de ADN en su genoma, la cual expresa una nucleasa de ""Dedo de Zinc"" diseñada para disociar el ADN genómico en una secuencia de reconocimiento; ácido nucleico aislado que comprende un gen de interés flanqueado por dos secuencias de reconocimiento para una nucleasa de dedo de zinc.
CL2012002007A 2010-01-22 2012-07-19 Método para eliminar una región de adn en una planta, que comprende proporcionar una planta que comprende dicha región de adn en su genoma, la cual expresa una nucleasa de ‘dedo de zinc’ diseñada para disociar el adn genómico en una secuencia de reconocimiento; ácido nucleico aislado que comprende un gen de interés flanqueado por dos secuencias de reconocimiento para una nucleasa de dedo de zinc. CL2012002007A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US29762810P 2010-01-22 2010-01-22

Publications (1)

Publication Number Publication Date
CL2012002007A1 true CL2012002007A1 (es) 2012-10-19

Family

ID=44307617

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2012002007A CL2012002007A1 (es) 2010-01-22 2012-07-19 Método para eliminar una región de adn en una planta, que comprende proporcionar una planta que comprende dicha región de adn en su genoma, la cual expresa una nucleasa de ‘dedo de zinc’ diseñada para disociar el adn genómico en una secuencia de reconocimiento; ácido nucleico aislado que comprende un gen de interés flanqueado por dos secuencias de reconocimiento para una nucleasa de dedo de zinc.

Country Status (20)

Country Link
US (3) US9695432B2 (es)
EP (1) EP2525649B1 (es)
JP (2) JP2013517774A (es)
KR (1) KR101951489B1 (es)
CN (1) CN102843904B (es)
AR (1) AR079968A1 (es)
AU (3) AU2011207387B2 (es)
BR (1) BR112012017896A2 (es)
CA (1) CA2787674C (es)
CL (1) CL2012002007A1 (es)
CO (1) CO6592070A2 (es)
EA (1) EA031356B1 (es)
GE (1) GEP201606544B (es)
IL (2) IL220870A (es)
MX (1) MX2012008485A (es)
NZ (1) NZ600546A (es)
PH (1) PH12012501467B1 (es)
UA (1) UA113493C2 (es)
WO (1) WO2011091311A2 (es)
ZA (1) ZA201204519B (es)

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