HK1254126A1 - 三組分crispr/cas複合系統及其用途 - Google Patents

三組分crispr/cas複合系統及其用途

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Publication number
HK1254126A1
HK1254126A1 HK18113197.4A HK18113197A HK1254126A1 HK 1254126 A1 HK1254126 A1 HK 1254126A1 HK 18113197 A HK18113197 A HK 18113197A HK 1254126 A1 HK1254126 A1 HK 1254126A1
Authority
HK
Hong Kong
Prior art keywords
complex system
cas complex
component crispr
crispr
component
Prior art date
Application number
HK18113197.4A
Other languages
English (en)
Inventor
王皓毅
A‧程
N‧吉勒特
Original Assignee
杰克遜實驗室
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 杰克遜實驗室 filed Critical 杰克遜實驗室
Publication of HK1254126A1 publication Critical patent/HK1254126A1/zh

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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/10Processes for the isolation, preparation or purification of DNA or RNA
    • C12N15/102Mutagenizing nucleic acids
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/111General methods applicable to biologically active non-coding nucleic acids
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/87Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
    • C12N15/90Stable introduction of foreign DNA into chromosome
    • C12N15/902Stable introduction of foreign DNA into chromosome using homologous recombination
    • C12N15/907Stable introduction of foreign DNA into chromosome using homologous recombination in mammalian cells
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14Hydrolases (3)
    • C12N9/16Hydrolases (3) acting on ester bonds (3.1)
    • C12N9/22Ribonucleases RNAses, DNAses
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2319/00Fusion polypeptide
    • C07K2319/01Fusion polypeptide containing a localisation/targetting motif
    • C07K2319/09Fusion polypeptide containing a localisation/targetting motif containing a nuclear localisation signal
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2319/00Fusion polypeptide
    • C07K2319/85Fusion polypeptide containing an RNA binding domain
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/10Type of nucleic acid
    • C12N2310/20Type of nucleic acid involving clustered regularly interspaced short palindromic repeats [CRISPRs]
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/30Chemical structure
    • C12N2310/35Nature of the modification
    • C12N2310/351Conjugate
    • C12N2310/3519Fusion with another nucleic acid
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/50Physical structure
    • C12N2310/53Physical structure partially self-complementary or closed
    • C12N2310/531Stem-loop; Hairpin
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2800/00Nucleic acids vectors
    • C12N2800/80Vectors containing sites for inducing double-stranded breaks, e.g. meganuclease restriction sites
HK18113197.4A 2015-03-13 2018-10-15 三組分crispr/cas複合系統及其用途 HK1254126A1 (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201562132644P 2015-03-13 2015-03-13
US201562221249P 2015-09-21 2015-09-21
PCT/US2016/021491 WO2016148994A1 (en) 2015-03-13 2016-03-09 A three-component crispr/cas complex system and uses thereof

Publications (1)

Publication Number Publication Date
HK1254126A1 true HK1254126A1 (zh) 2019-07-12

Family

ID=55642857

Family Applications (2)

Application Number Title Priority Date Filing Date
HK18108993.0A HK1249545A1 (zh) 2015-03-13 2018-07-11 三組分crispr/cas複合系統及其用途
HK18113197.4A HK1254126A1 (zh) 2015-03-13 2018-10-15 三組分crispr/cas複合系統及其用途

Family Applications Before (1)

Application Number Title Priority Date Filing Date
HK18108993.0A HK1249545A1 (zh) 2015-03-13 2018-07-11 三組分crispr/cas複合系統及其用途

Country Status (12)

Country Link
US (2) US11434484B2 (zh)
EP (2) EP3858992A1 (zh)
JP (3) JP6588995B2 (zh)
KR (1) KR102004076B1 (zh)
CN (1) CN107922942B (zh)
AU (2) AU2016233648B2 (zh)
CA (2) CA3091771A1 (zh)
ES (1) ES2886901T3 (zh)
HK (2) HK1249545A1 (zh)
IL (2) IL254428B (zh)
SG (2) SG10202008443UA (zh)
WO (1) WO2016148994A1 (zh)

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US9526784B2 (en) 2013-09-06 2016-12-27 President And Fellows Of Harvard College Delivery system for functional nucleases
US9388430B2 (en) 2013-09-06 2016-07-12 President And Fellows Of Harvard College Cas9-recombinase fusion proteins and uses thereof
US9840699B2 (en) 2013-12-12 2017-12-12 President And Fellows Of Harvard College Methods for nucleic acid editing
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AU2017308889B2 (en) 2016-08-09 2023-11-09 President And Fellows Of Harvard College Programmable Cas9-recombinase fusion proteins and uses thereof
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EP3592777A1 (en) 2017-03-10 2020-01-15 President and Fellows of Harvard College Cytosine to guanine base editor
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WO2019183630A2 (en) * 2018-03-23 2019-09-26 The Trustees Of Columbia University In The City Of New York Gene editing for autosomal dominant diseases
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CN109055375B (zh) * 2018-07-26 2021-11-12 东南大学 一种crispr辅助反式增强子激活基因表达的方法及其应用
WO2020041172A1 (en) * 2018-08-21 2020-02-27 The Jackson Laboratory Methods and compositions for recruiting dna repair proteins
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CN114555826A (zh) * 2019-08-16 2022-05-27 杰克逊实验室 非重复基因组基因座的活细胞成像
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Publication number Publication date
JP6588995B2 (ja) 2019-10-09
CN107922942B (zh) 2021-08-31
IL276894A (en) 2020-10-29
KR102004076B1 (ko) 2019-07-25
CA2979567A1 (en) 2016-09-22
KR20170124601A (ko) 2017-11-10
IL276894B (en) 2022-12-01
US11434484B2 (en) 2022-09-06
WO2016148994A1 (en) 2016-09-22
EP3268472A1 (en) 2018-01-17
US20180094257A1 (en) 2018-04-05
IL276894B2 (en) 2023-04-01
EP3268472B1 (en) 2021-05-05
AU2016233648B2 (en) 2019-11-07
CA2979567C (en) 2020-10-13
AU2020200256B2 (en) 2022-03-31
HK1249545A1 (zh) 2018-11-02
AU2016233648A1 (en) 2017-10-05
JP2019176877A (ja) 2019-10-17
CA3091771A1 (en) 2016-09-22
IL254428A0 (en) 2017-11-30
JP2021036899A (ja) 2021-03-11
IL254428B (en) 2020-08-31
CN107922942A (zh) 2018-04-17
SG10202008443UA (en) 2020-10-29
WO2016148994A8 (en) 2016-11-03
ES2886901T3 (es) 2021-12-21
EP3858992A1 (en) 2021-08-04
SG11201707393SA (en) 2017-10-30
US20230071712A1 (en) 2023-03-09
JP2018507713A (ja) 2018-03-22
AU2020200256A1 (en) 2020-02-06
JP6867440B2 (ja) 2021-04-28

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