MX384887B - Ensamblaje de adn mediado por nucleasa. - Google Patents

Ensamblaje de adn mediado por nucleasa.

Info

Publication number
MX384887B
MX384887B MX2021000857A MX2021000857A MX384887B MX 384887 B MX384887 B MX 384887B MX 2021000857 A MX2021000857 A MX 2021000857A MX 2021000857 A MX2021000857 A MX 2021000857A MX 384887 B MX384887 B MX 384887B
Authority
MX
Mexico
Prior art keywords
sequences
create
overlapping
complementary
nuclease
Prior art date
Application number
MX2021000857A
Other languages
English (en)
Other versions
MX2021000857A (es
Inventor
Andrew J Murphy
Caitlin Montagna
Chris Schoenherr
Corey Momont
David M Valenzuela
Gregg S Warshaw
John Mcwhirter
Jose F Rojas
Ka-Man Venus Lai
Lynn Macdonald
Original Assignee
Regeneron Pharma
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 Regeneron Pharma filed Critical Regeneron Pharma
Publication of MX2021000857A publication Critical patent/MX2021000857A/es
Publication of MX384887B publication Critical patent/MX384887B/es

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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
    • C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
    • 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
    • C12N15/66—General methods for inserting a gene into a vector to form a recombinant vector using cleavage and ligation; Use of non-functional linkers or adaptors, e.g. linkers containing the sequence for a restriction endonuclease
    • 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
    • C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
    • C12N15/102—Mutagenizing nucleic acids
    • C12N15/1031—Mutagenizing nucleic acids mutagenesis by gene assembly, e.g. assembly by oligonucleotide extension PCR
    • 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
    • C12N15/64—General methods for preparing the vector, for introducing it into the cell or for selecting the vector-containing host

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  • Genetics & Genomics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Biomedical Technology (AREA)
  • Wood Science & Technology (AREA)
  • Biotechnology (AREA)
  • General Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Molecular Biology (AREA)
  • Plant Pathology (AREA)
  • Microbiology (AREA)
  • Biophysics (AREA)
  • Physics & Mathematics (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Cell Biology (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

La presente invención se refiere a métodos para ensamblar al menos dos ácidos nucleicos mediante el uso de un agente nucleasa específico de secuencias (p. ej., un complejo ARNg-Cas) para crear secuencias de extremo que tienen complementariedad y ensamblar posteriormente las secuencias complementarias superpuestas. El agente nucleasa (p. ej., un complejo ARNg-Cas) puede crear rupturas bicatenarias en el ADNbc con el propósito de crear secuencias de extremo superpuestas o puede crear mellas en cada cadena para producir secuencias de extremo salientes complementarias. El ensamblaje mediante el uso del método descrito en la presente descripción puede ensamblar cualquier ácido nucleico que tenga secuencias superpuestas o puede usar un acoplador oligo para ensamblar secuencias sin extremos complementarios.
MX2021000857A 2014-06-23 2015-06-23 Ensamblaje de adn mediado por nucleasa. MX384887B (es)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201462015809P 2014-06-23 2014-06-23
US201462016400P 2014-06-24 2014-06-24
US201462036983P 2014-08-13 2014-08-13
PCT/US2015/037199 WO2015200334A1 (en) 2014-06-23 2015-06-23 Nuclease-mediated dna assembly

Publications (2)

Publication Number Publication Date
MX2021000857A MX2021000857A (es) 2021-07-28
MX384887B true MX384887B (es) 2025-03-14

Family

ID=53525285

Family Applications (2)

Application Number Title Priority Date Filing Date
MX2021000857A MX384887B (es) 2014-06-23 2015-06-23 Ensamblaje de adn mediado por nucleasa.
MX2016016905A MX379237B (es) 2014-06-23 2015-06-23 Ensamblaje de adn mediado por nucleasa.

Family Applications After (1)

Application Number Title Priority Date Filing Date
MX2016016905A MX379237B (es) 2014-06-23 2015-06-23 Ensamblaje de adn mediado por nucleasa.

Country Status (25)

Country Link
US (6) US9738897B2 (es)
EP (3) EP3155099B1 (es)
JP (4) JP6336140B2 (es)
KR (2) KR102237151B1 (es)
CN (2) CN112029787B (es)
AU (3) AU2015280120B2 (es)
BR (1) BR112016030145A8 (es)
CA (1) CA2953499C (es)
CY (2) CY1120520T1 (es)
DK (2) DK3155099T3 (es)
ES (2) ES2666179T3 (es)
HR (1) HRP20200523T1 (es)
HU (1) HUE049405T2 (es)
IL (1) IL249612B (es)
LT (1) LT3354732T (es)
MX (2) MX384887B (es)
NZ (1) NZ765591A (es)
PL (2) PL3155099T3 (es)
PT (2) PT3354732T (es)
RS (1) RS60366B1 (es)
RU (1) RU2707911C2 (es)
SG (2) SG10201803444YA (es)
SI (1) SI3354732T1 (es)
SM (1) SMT202000174T1 (es)
WO (1) WO2015200334A1 (es)

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