MX2016016905A - Ensamblaje de adn mediado por nucleasa. - Google Patents
Ensamblaje de adn mediado por nucleasa.Info
- Publication number
- MX2016016905A MX2016016905A MX2016016905A MX2016016905A MX2016016905A MX 2016016905 A MX2016016905 A MX 2016016905A MX 2016016905 A MX2016016905 A MX 2016016905A MX 2016016905 A MX2016016905 A MX 2016016905A MX 2016016905 A MX2016016905 A MX 2016016905A
- Authority
- MX
- Mexico
- Prior art keywords
- sequences
- assemble
- overlapping
- create
- complementary
- Prior art date
Links
- 101710163270 Nuclease Proteins 0.000 title abstract 3
- 230000001404 mediated effect Effects 0.000 title 1
- 230000000295 complement effect Effects 0.000 abstract 3
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 150000007523 nucleic acids Chemical class 0.000 abstract 2
- 102000039446 nucleic acids Human genes 0.000 abstract 2
- 108020004707 nucleic acids Proteins 0.000 abstract 2
- 239000002299 complementary DNA Substances 0.000 abstract 1
Classifications
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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
- C12N15/10—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
Landscapes
- Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Zoology (AREA)
- Biomedical Technology (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Molecular Biology (AREA)
- Physics & Mathematics (AREA)
- Microbiology (AREA)
- Plant Pathology (AREA)
- Biophysics (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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
En la presente invención se proporcionan métodos para ensamblar al menos dos ácidos nucleicos mediante el uso de un agente nucleasa específico de secuencia (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 ARNgA-Cas) puede crear rupturas bicatenarias en el ADNbc con el propósito de crear secuencias de extremos superpuestas o puede crear mellas en cada cadena para producir secuencias de extremo salientes complementarias. El ensamblaje mediante el uso del método descrito en el presente descripción puede ensamblar cualquier ácido nucleico que tenga secuencias superpuestas o puede usar un acoplador oligo para ensamblar secuencias sin extremos complementarios.
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 |
|---|---|
| MX2016016905A true MX2016016905A (es) | 2017-08-10 |
| MX379237B MX379237B (es) | 2025-03-10 |
Family
ID=53525285
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2016016905A MX379237B (es) | 2014-06-23 | 2015-06-23 | Ensamblaje de adn mediado por nucleasa. |
| MX2021000857A MX384887B (es) | 2014-06-23 | 2015-06-23 | Ensamblaje de adn mediado por nucleasa. |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2021000857A MX384887B (es) | 2014-06-23 | 2015-06-23 | Ensamblaje de adn mediado por nucleasa. |
Country Status (25)
| Country | Link |
|---|---|
| US (6) | US9738897B2 (es) |
| EP (3) | EP3354732B1 (es) |
| JP (4) | JP6336140B2 (es) |
| KR (2) | KR101822902B1 (es) |
| CN (2) | CN106715694B (es) |
| AU (3) | AU2015280120B2 (es) |
| BR (1) | BR112016030145A8 (es) |
| CA (1) | CA2953499C (es) |
| CY (2) | CY1120520T1 (es) |
| DK (2) | DK3354732T3 (es) |
| ES (2) | ES2781323T3 (es) |
| HR (1) | HRP20200523T1 (es) |
| HU (1) | HUE049405T2 (es) |
| IL (1) | IL249612B (es) |
| LT (1) | LT3354732T (es) |
| MX (2) | MX379237B (es) |
| NZ (1) | NZ765591A (es) |
| PL (2) | PL3354732T3 (es) |
| PT (2) | PT3155099T (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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