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Robust and efficient knock-in in embryonic stem cells and early-stage embryos of the common marmoset using the CRISPR-Cas9 system

Genome editing technology greatly facilitates the genetic modification of various cells and animals. The common marmoset (Callithrix jacchus), a small non-human primate which exhibits high reproductive efficiency, is a widely used animal model in biomedical research. Developing genome editing techni...

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Autores principales: Yoshimatsu, Sho, Okahara, Junko, Sone, Takefumi, Takeda, Yuta, Nakamura, Mari, Sasaki, Erika, Kishi, Noriyuki, Shiozawa, Seiji, Okano, Hideyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365532/
https://www.ncbi.nlm.nih.gov/pubmed/30728412
http://dx.doi.org/10.1038/s41598-018-37990-w
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author Yoshimatsu, Sho
Okahara, Junko
Sone, Takefumi
Takeda, Yuta
Nakamura, Mari
Sasaki, Erika
Kishi, Noriyuki
Shiozawa, Seiji
Okano, Hideyuki
author_facet Yoshimatsu, Sho
Okahara, Junko
Sone, Takefumi
Takeda, Yuta
Nakamura, Mari
Sasaki, Erika
Kishi, Noriyuki
Shiozawa, Seiji
Okano, Hideyuki
author_sort Yoshimatsu, Sho
collection PubMed
description Genome editing technology greatly facilitates the genetic modification of various cells and animals. The common marmoset (Callithrix jacchus), a small non-human primate which exhibits high reproductive efficiency, is a widely used animal model in biomedical research. Developing genome editing techniques in the common marmoset will further enhance its utility. Here, we report the successful establishment of a knock-in (KI) method for marmoset embryonic stem cells (ESCs), which is based on the CRISPR-Cas9 system. The use of CRISPR-Cas9, mediated by homologous recombination (HR), enhanced the KI efficiency in marmoset ESCs. Furthermore, we succeeded in performing KI in early-stage marmoset embryos. In the course of the experiments, we found that HR in the marmoset ESCs is innately highly efficient. This suggested that the marmoset possesses a repair mechanism for DNA double-strand breaks. The current study will facilitate the generation of genetically modified marmosets and gene function analysis in the marmoset.
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spelling pubmed-63655322019-02-08 Robust and efficient knock-in in embryonic stem cells and early-stage embryos of the common marmoset using the CRISPR-Cas9 system Yoshimatsu, Sho Okahara, Junko Sone, Takefumi Takeda, Yuta Nakamura, Mari Sasaki, Erika Kishi, Noriyuki Shiozawa, Seiji Okano, Hideyuki Sci Rep Article Genome editing technology greatly facilitates the genetic modification of various cells and animals. The common marmoset (Callithrix jacchus), a small non-human primate which exhibits high reproductive efficiency, is a widely used animal model in biomedical research. Developing genome editing techniques in the common marmoset will further enhance its utility. Here, we report the successful establishment of a knock-in (KI) method for marmoset embryonic stem cells (ESCs), which is based on the CRISPR-Cas9 system. The use of CRISPR-Cas9, mediated by homologous recombination (HR), enhanced the KI efficiency in marmoset ESCs. Furthermore, we succeeded in performing KI in early-stage marmoset embryos. In the course of the experiments, we found that HR in the marmoset ESCs is innately highly efficient. This suggested that the marmoset possesses a repair mechanism for DNA double-strand breaks. The current study will facilitate the generation of genetically modified marmosets and gene function analysis in the marmoset. Nature Publishing Group UK 2019-02-06 /pmc/articles/PMC6365532/ /pubmed/30728412 http://dx.doi.org/10.1038/s41598-018-37990-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yoshimatsu, Sho
Okahara, Junko
Sone, Takefumi
Takeda, Yuta
Nakamura, Mari
Sasaki, Erika
Kishi, Noriyuki
Shiozawa, Seiji
Okano, Hideyuki
Robust and efficient knock-in in embryonic stem cells and early-stage embryos of the common marmoset using the CRISPR-Cas9 system
title Robust and efficient knock-in in embryonic stem cells and early-stage embryos of the common marmoset using the CRISPR-Cas9 system
title_full Robust and efficient knock-in in embryonic stem cells and early-stage embryos of the common marmoset using the CRISPR-Cas9 system
title_fullStr Robust and efficient knock-in in embryonic stem cells and early-stage embryos of the common marmoset using the CRISPR-Cas9 system
title_full_unstemmed Robust and efficient knock-in in embryonic stem cells and early-stage embryos of the common marmoset using the CRISPR-Cas9 system
title_short Robust and efficient knock-in in embryonic stem cells and early-stage embryos of the common marmoset using the CRISPR-Cas9 system
title_sort robust and efficient knock-in in embryonic stem cells and early-stage embryos of the common marmoset using the crispr-cas9 system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365532/
https://www.ncbi.nlm.nih.gov/pubmed/30728412
http://dx.doi.org/10.1038/s41598-018-37990-w
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