MX2021015157A - Construcciones de edicion de genes dirigidas y metodos de uso de las mismas. - Google Patents
Construcciones de edicion de genes dirigidas y metodos de uso de las mismas.Info
- Publication number
- MX2021015157A MX2021015157A MX2021015157A MX2021015157A MX2021015157A MX 2021015157 A MX2021015157 A MX 2021015157A MX 2021015157 A MX2021015157 A MX 2021015157A MX 2021015157 A MX2021015157 A MX 2021015157A MX 2021015157 A MX2021015157 A MX 2021015157A
- Authority
- MX
- Mexico
- Prior art keywords
- nucleic acid
- methods
- same
- gene editing
- targeted gene
- Prior art date
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- 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
- C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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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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- C12N15/00—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
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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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
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/102—Mutagenizing nucleic acids
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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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
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
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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
- C12N15/11—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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- C12N15/00—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
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/62—DNA sequences coding for fusion proteins
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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
- C12N15/63—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
- C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
- C12N15/86—Viral vectors
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- C12N7/00—Viruses; Bacteriophages; Compositions thereof; Preparation or purification thereof
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- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/10—Transferases (2.)
- C12N9/12—Transferases (2.) transferring phosphorus containing groups, e.g. kinases (2.7)
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/10—Transferases (2.)
- C12N9/12—Transferases (2.) transferring phosphorus containing groups, e.g. kinases (2.7)
- C12N9/1241—Nucleotidyltransferases (2.7.7)
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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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2319/00—Fusion polypeptide
- C07K2319/80—Fusion polypeptide containing a DNA binding domain, e.g. Lacl or Tet-repressor
- C07K2319/81—Fusion polypeptide containing a DNA binding domain, e.g. Lacl or Tet-repressor containing a Zn-finger domain for DNA binding
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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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- C12N2740/00—Reverse transcribing RNA viruses
- C12N2740/00011—Details
- C12N2740/10011—Retroviridae
- C12N2740/16011—Human Immunodeficiency Virus, HIV
- C12N2740/16022—New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12N2740/00—Reverse transcribing RNA viruses
- C12N2740/00011—Details
- C12N2740/10011—Retroviridae
- C12N2740/16011—Human Immunodeficiency Virus, HIV
- C12N2740/16041—Use of virus, viral particle or viral elements as a vector
- C12N2740/16043—Use of virus, viral particle or viral elements as a vector viral genome or elements thereof as genetic vector
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12N2800/00—Nucleic acids vectors
- C12N2800/10—Plasmid DNA
- C12N2800/106—Plasmid DNA for vertebrates
- C12N2800/107—Plasmid DNA for vertebrates for mammalian
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- C12N2800/00—Nucleic acids vectors
- C12N2800/80—Vectors containing sites for inducing double-stranded breaks, e.g. meganuclease restriction sites
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12N2800/00—Nucleic acids vectors
- C12N2800/90—Vectors containing a transposable element
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Zoology (AREA)
- Biomedical Technology (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Microbiology (AREA)
- Physics & Mathematics (AREA)
- Plant Pathology (AREA)
- Biophysics (AREA)
- Medicinal Chemistry (AREA)
- Cell Biology (AREA)
- Mycology (AREA)
- Virology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Immunology (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Peptides Or Proteins (AREA)
- Enzymes And Modification Thereof (AREA)
Abstract
La presente divulgación proporciona las construcciones de ácidos nucleicos para usarse en la mejora de la inserción específica del sitio de un ácido nucleico exógeno en un genoma. En algunos aspectos, la construcción del ácido nucleico comprende una primera secuencia de polinucleótidos que codifica una proteína de enlace al ADN que se diseña de una forma tal como para que se enlace a una secuencia de ADN genómico específica, un segundo polinucleótido que comprende una integrasa modificada o una transposasa modificada que permite que se haga la inserción del ácido nucleico exógeno en el genoma, y una secuencia de ácido nucleico que codifica un enlazador entre los dos nucleótidos. En algunas modalidades, la construcción de ácido nucleico codifica una proteína de fusión, por ejemplo, una proteína de fusión para su suministro a una célula por medio de una partícula lentiviral.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201962860186P | 2019-06-11 | 2019-06-11 | |
PCT/IB2020/055507 WO2020250181A1 (en) | 2019-06-11 | 2020-06-11 | Targeted gene editing constructs and methods of using the same |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2021015157A true MX2021015157A (es) | 2022-03-17 |
Family
ID=72178837
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2021015157A MX2021015157A (es) | 2019-06-11 | 2020-06-11 | Construcciones de edicion de genes dirigidas y metodos de uso de las mismas. |
Country Status (11)
Country | Link |
---|---|
US (1) | US20220235379A1 (es) |
EP (1) | EP3983541A1 (es) |
JP (1) | JP2022540318A (es) |
KR (1) | KR20220019794A (es) |
CN (1) | CN114026240A (es) |
AU (1) | AU2020290790A1 (es) |
BR (1) | BR112021024828A2 (es) |
CA (1) | CA3141422A1 (es) |
IL (1) | IL288794A (es) |
MX (1) | MX2021015157A (es) |
WO (1) | WO2020250181A1 (es) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2022129438A1 (en) | 2020-12-16 | 2022-06-23 | Universitat Pompeu Fabra | Programmable transposases and uses thereof |
EP4263818A1 (en) * | 2020-12-16 | 2023-10-25 | Universitat Pompeu Fabra | Therapeutic lama2 payload for treatment of congenital muscular dystrophy |
EP4341392A1 (en) * | 2021-05-14 | 2024-03-27 | Becton Dickinson and Company | Multiplexed unbiased nucleic acid amplification method |
KR20240099249A (ko) * | 2021-10-04 | 2024-06-28 | 포세이다 테라퓨틱스, 인크. | 트랜스포사제 및 이의 용도 |
IL313824A (en) * | 2021-12-30 | 2024-08-01 | Regel Therapeutics Inc | Compounds for modulating expression of sodium channel alpha subunit 1 and uses thereof |
WO2023141504A2 (en) * | 2022-01-19 | 2023-07-27 | Genomeminer, Inc. (Formally Tupac Bio, Inc.) | Dcas9-integrase for targeted genome editing |
CN118185901A (zh) * | 2022-12-12 | 2024-06-14 | 上海精缮生物科技有限责任公司 | 一种PBase蛋白、融合蛋白、核酸和基因整合系统及应用 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004009792A2 (en) * | 2002-07-24 | 2004-01-29 | Vanderbilt University | Transposon-based vectors and methods of nucleic acid integration |
EP3277805A1 (en) * | 2015-03-31 | 2018-02-07 | Exeligen Scientific, Inc. | Cas 9 retroviral integrase and cas 9 recombinase systems for targeted incorporation of a dna sequence into a genome of a cell or organism |
WO2018175872A1 (en) * | 2017-03-24 | 2018-09-27 | President And Fellows Of Harvard College | Methods of genome engineering by nuclease-transposase fusion proteins |
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2020
- 2020-06-11 AU AU2020290790A patent/AU2020290790A1/en active Pending
- 2020-06-11 CN CN202080043025.3A patent/CN114026240A/zh active Pending
- 2020-06-11 WO PCT/IB2020/055507 patent/WO2020250181A1/en unknown
- 2020-06-11 MX MX2021015157A patent/MX2021015157A/es unknown
- 2020-06-11 KR KR1020227000857A patent/KR20220019794A/ko unknown
- 2020-06-11 CA CA3141422A patent/CA3141422A1/en active Pending
- 2020-06-11 BR BR112021024828A patent/BR112021024828A2/pt unknown
- 2020-06-11 EP EP20760532.0A patent/EP3983541A1/en active Pending
- 2020-06-11 JP JP2021574234A patent/JP2022540318A/ja active Pending
- 2020-06-11 US US17/617,252 patent/US20220235379A1/en active Pending
-
2021
- 2021-12-08 IL IL288794A patent/IL288794A/en unknown
Also Published As
Publication number | Publication date |
---|---|
US20220235379A1 (en) | 2022-07-28 |
CN114026240A (zh) | 2022-02-08 |
IL288794A (en) | 2022-02-01 |
JP2022540318A (ja) | 2022-09-15 |
CA3141422A1 (en) | 2020-12-17 |
KR20220019794A (ko) | 2022-02-17 |
WO2020250181A1 (en) | 2020-12-17 |
AU2020290790A1 (en) | 2022-01-27 |
BR112021024828A2 (pt) | 2022-01-25 |
EP3983541A1 (en) | 2022-04-20 |
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