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Production of single- and multiple-gene-modified mice via maternal SpCas9-based gene editing
Maternally and transiently accumulated SpCas9 (maternal SpCas9) in a zygote derived from a systemically SpCas9-expressing transgenic mouse strain was used to generate single- and multiple-gene-modified mice. Maternal SpCas9-based gene editing allows for high indel and knockin mutation efficiency, lo...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122177/ https://www.ncbi.nlm.nih.gov/pubmed/34027476 http://dx.doi.org/10.1016/j.xpro.2021.100509 |
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author | Sakurai, Takayuki Shindo, Takayuki |
author_facet | Sakurai, Takayuki Shindo, Takayuki |
author_sort | Sakurai, Takayuki |
collection | PubMed |
description | Maternally and transiently accumulated SpCas9 (maternal SpCas9) in a zygote derived from a systemically SpCas9-expressing transgenic mouse strain was used to generate single- and multiple-gene-modified mice. Maternal SpCas9-based gene editing allows for high indel and knockin mutation efficiency, low mosaicism, increased pup delivery rate, and simultaneous induction of mutations at multiple loci in contrast to conventional CRISPR/SpCas9-based gene editing. For complete details on the use and execution of this protocol, please refer to Sakurai et al. (2020). |
format | Online Article Text |
id | pubmed-8122177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-81221772021-05-21 Production of single- and multiple-gene-modified mice via maternal SpCas9-based gene editing Sakurai, Takayuki Shindo, Takayuki STAR Protoc Protocol Maternally and transiently accumulated SpCas9 (maternal SpCas9) in a zygote derived from a systemically SpCas9-expressing transgenic mouse strain was used to generate single- and multiple-gene-modified mice. Maternal SpCas9-based gene editing allows for high indel and knockin mutation efficiency, low mosaicism, increased pup delivery rate, and simultaneous induction of mutations at multiple loci in contrast to conventional CRISPR/SpCas9-based gene editing. For complete details on the use and execution of this protocol, please refer to Sakurai et al. (2020). Elsevier 2021-05-08 /pmc/articles/PMC8122177/ /pubmed/34027476 http://dx.doi.org/10.1016/j.xpro.2021.100509 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Protocol Sakurai, Takayuki Shindo, Takayuki Production of single- and multiple-gene-modified mice via maternal SpCas9-based gene editing |
title | Production of single- and multiple-gene-modified mice via maternal SpCas9-based gene editing |
title_full | Production of single- and multiple-gene-modified mice via maternal SpCas9-based gene editing |
title_fullStr | Production of single- and multiple-gene-modified mice via maternal SpCas9-based gene editing |
title_full_unstemmed | Production of single- and multiple-gene-modified mice via maternal SpCas9-based gene editing |
title_short | Production of single- and multiple-gene-modified mice via maternal SpCas9-based gene editing |
title_sort | production of single- and multiple-gene-modified mice via maternal spcas9-based gene editing |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122177/ https://www.ncbi.nlm.nih.gov/pubmed/34027476 http://dx.doi.org/10.1016/j.xpro.2021.100509 |
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