MX2018001617A - Composiciones de crispr-cas9 diseñados y metodos de uso. - Google Patents
Composiciones de crispr-cas9 diseñados y metodos de uso.Info
- Publication number
- MX2018001617A MX2018001617A MX2018001617A MX2018001617A MX2018001617A MX 2018001617 A MX2018001617 A MX 2018001617A MX 2018001617 A MX2018001617 A MX 2018001617A MX 2018001617 A MX2018001617 A MX 2018001617A MX 2018001617 A MX2018001617 A MX 2018001617A
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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
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- C12N15/102—Mutagenizing nucleic acids
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- C12N15/09—Recombinant DNA-technology
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- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
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- C12N15/09—Recombinant DNA-technology
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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
- C12N15/907—Stable introduction of foreign DNA into chromosome using homologous recombination in mammalian cells
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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 RNAses, DNAses
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- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/96—Stabilising an enzyme by forming an adduct or a composition; Forming enzyme conjugates
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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 [CRISPRs]
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- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/30—Chemical structure
- C12N2310/35—Nature of the modification
- C12N2310/351—Conjugate
- C12N2310/3513—Protein; Peptide
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- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/50—Physical structure
- C12N2310/53—Physical structure partially self-complementary or closed
- C12N2310/531—Stem-loop; Hairpin
Abstract
La presente especificación describe sistemas de polinucleótidos de nexo de división asociados a CRISPR-Cas9 tipo II (sn-casPN), incluyendo sistemas que comprenden tres polinucleótidos de nexo de división (sn1-casPN/sn2-casPN/sn3-casPN) y sistemas que comprenden dos polinucleótidos de nexo de división (sn1-casPN/sn2-casPN). Junto con una proteína Cas9, sn-casPN facilitan modificaciones específicas de sitio, incluyendo corte y mutagénesis, de un polinucleótido objetivo in vitro e in vivo. Adicionalmente, los sistemas de polinucleótidos de nexo de división asociado a CRISR-Cas9 tipo II que comprenden sn-casPN son útiles en métodos para regular la expresión de un ácido nucleico objetivo. Se describen métodos en la presente para la creación de una variedad de sistemas de polinucleótidos de nexo de división asociado a CRISPR-Cas9 tipo II diseñados que comprenden dos o más sn-casPN. Las secuencias de polinucleótidos, casetes de expresión, vectores, composiciones y kits para realizar una variedad de métodos también se describen. Además, la presente especificación proporciona células genéticamente modificadas, composiciones de células modificadas, organismos transgénicos, composiciones farmacéuticas, así como una variedad de composiciones y métodos que involucran los sistemas de polinucleótidos de nexo de división asociados a CRISPR-cas9 tipo II diseñados.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US201562202715P | 2015-08-07 | 2015-08-07 | |
US201562209334P | 2015-08-24 | 2015-08-24 | |
PCT/US2016/045915 WO2017027423A1 (en) | 2015-08-07 | 2016-08-05 | Engineered crispr-cas9 compositions and methods of use |
Publications (1)
Publication Number | Publication Date |
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MX2018001617A true MX2018001617A (es) | 2018-06-06 |
Family
ID=56694254
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2018001617A MX2018001617A (es) | 2015-08-07 | 2016-08-05 | Composiciones de crispr-cas9 diseñados y metodos de uso. |
Country Status (16)
Country | Link |
---|---|
US (5) | US9580727B1 (es) |
EP (2) | EP3320092B1 (es) |
JP (1) | JP6649468B2 (es) |
KR (1) | KR102012382B1 (es) |
CN (1) | CN107922944B (es) |
AU (1) | AU2016304795B2 (es) |
CA (1) | CA2994166C (es) |
DK (1) | DK3320092T3 (es) |
ES (1) | ES2705540T3 (es) |
GB (1) | GB2556276A (es) |
HK (1) | HK1247238B (es) |
IL (1) | IL257307B (es) |
MX (1) | MX2018001617A (es) |
NZ (1) | NZ738689A (es) |
WO (1) | WO2017027423A1 (es) |
ZA (1) | ZA201800330B (es) |
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