ES2552535T3 - Sistemas de CRISPR-Cas y métodos para alterar la expresión de productos génicos - Google Patents

Sistemas de CRISPR-Cas y métodos para alterar la expresión de productos génicos Download PDF

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ES2552535T3
ES2552535T3 ES13824232.6T ES13824232T ES2552535T3 ES 2552535 T3 ES2552535 T3 ES 2552535T3 ES 13824232 T ES13824232 T ES 13824232T ES 2552535 T3 ES2552535 T3 ES 2552535T3
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sequence
crispr
target
tracr
cell
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Spanish (es)
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Feng Zhang
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Massachusetts Institute of Technology
Broad Institute Inc
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Massachusetts Institute of Technology
Broad Institute Inc
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    • 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
    • C12N15/87—Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
    • C12N15/90—Stable introduction of foreign DNA into chromosome
    • C12N15/902—Stable introduction of foreign DNA into chromosome using homologous recombination
    • C12N15/907—Stable introduction of foreign DNA into chromosome using homologous recombination in mammalian cells
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    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
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    • C12N15/09—Recombinant DNA-technology
    • C12N15/87—Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
    • C12N15/90—Stable introduction of foreign DNA into chromosome
    • C12N15/902—Stable introduction of foreign DNA into chromosome using homologous recombination
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    • 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]
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    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
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    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
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    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/43—Enzymes; Proenzymes; Derivatives thereof
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    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/43—Enzymes; Proenzymes; Derivatives thereof
    • A61K38/46—Hydrolases (3)
    • A—HUMAN NECESSITIES
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    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/43—Enzymes; Proenzymes; Derivatives thereof
    • A61K38/46—Hydrolases (3)
    • A61K38/47—Hydrolases (3) acting on glycosyl compounds (3.2), e.g. cellulases, lactases
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    • C12N15/09—Recombinant DNA-technology
    • C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
    • C12N15/1034—Isolating an individual clone by screening libraries
    • C12N15/1082—Preparation or screening gene libraries by chromosomal integration of polynucleotide sequences, HR-, site-specific-recombination, transposons, viral vectors
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    • C12N2310/00—Structure or type of the nucleic acid
    • C12N2310/10—Type of nucleic acid
    • C12N2310/20—Type of nucleic acid involving clustered regularly interspaced short palindromic repeats [CRISPR]
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    • C12N2800/00—Nucleic acids vectors
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    • C12N9/14—Hydrolases (3)
    • C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
    • C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
    • C12N9/52—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from bacteria or Archaea

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  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
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  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
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ES13824232.6T 2012-12-12 2013-12-12 Sistemas de CRISPR-Cas y métodos para alterar la expresión de productos génicos Active ES2552535T3 (es)

Applications Claiming Priority (13)

Application Number Priority Date Filing Date Title
US201261736527P 2012-12-12 2012-12-12
US201261736527P 2012-12-12
US201361748427P 2013-01-02 2013-01-02
US201361748427P 2013-01-02
US201361791409P 2013-03-15 2013-03-15
US201361791409P 2013-03-15
US201361835931P 2013-06-17 2013-06-17
US201361835931P 2013-06-17
US201361842322P 2013-07-02 2013-07-02
US201361842322P 2013-07-02
US14/054,414 US8697359B1 (en) 2012-12-12 2013-10-15 CRISPR-Cas systems and methods for altering expression of gene products
US201314054414 2013-10-15
PCT/US2013/074743 WO2014093661A2 (en) 2012-12-12 2013-12-12 Crispr-cas systems and methods for altering expression of gene products

Publications (1)

Publication Number Publication Date
ES2552535T3 true ES2552535T3 (es) 2015-11-30

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ID=50441380

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ES13824232.6T Active ES2552535T3 (es) 2012-12-12 2013-12-12 Sistemas de CRISPR-Cas y métodos para alterar la expresión de productos génicos

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US (8) US8697359B1 (enExample)
EP (2) EP2998400A1 (enExample)
JP (6) JP6545621B2 (enExample)
KR (1) KR20150107739A (enExample)
CN (4) CN106170549B (enExample)
AU (5) AU2013359238B2 (enExample)
BR (1) BR112015013785A2 (enExample)
CA (1) CA2894688A1 (enExample)
DK (1) DK2764103T3 (enExample)
ES (1) ES2552535T3 (enExample)
HK (1) HK1216259A1 (enExample)
PL (1) PL2764103T3 (enExample)
PT (1) PT2764103E (enExample)
RU (1) RU2687451C1 (enExample)
WO (1) WO2014093661A2 (enExample)

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