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User-Friendly Genetic Conditional Knockout Strategies by CRISPR/Cas9

Loss-of-function studies are critically important in gene functional analysis of model organisms and cells. However, conditional gene inactivation in diploid cells is difficult to achieve, as it involves laborious vector construction, multifold electroporation, and complicated genotyping. Here, a st...

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Autores principales: Chen, Liangliang, Ye, Ying, Dai, Hongxia, Zhang, Heyao, Zhang, Xue, Wu, Qiang, Zhu, Zhexin, Spalinskas, Rapolas, Ren, Wenyan, Zhang, Wensheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022269/
https://www.ncbi.nlm.nih.gov/pubmed/30013601
http://dx.doi.org/10.1155/2018/9576959
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author Chen, Liangliang
Ye, Ying
Dai, Hongxia
Zhang, Heyao
Zhang, Xue
Wu, Qiang
Zhu, Zhexin
Spalinskas, Rapolas
Ren, Wenyan
Zhang, Wensheng
author_facet Chen, Liangliang
Ye, Ying
Dai, Hongxia
Zhang, Heyao
Zhang, Xue
Wu, Qiang
Zhu, Zhexin
Spalinskas, Rapolas
Ren, Wenyan
Zhang, Wensheng
author_sort Chen, Liangliang
collection PubMed
description Loss-of-function studies are critically important in gene functional analysis of model organisms and cells. However, conditional gene inactivation in diploid cells is difficult to achieve, as it involves laborious vector construction, multifold electroporation, and complicated genotyping. Here, a strategy is presented for generating biallelic conditional gene and DNA regulatory region knockouts in mouse embryonic stem cells by codelivery of CRISPR-Cas9 and short-homology-arm targeting vectors sequentially or simultaneously. Collectively, a simple and rapid method was presented to knock out any DNA element conditionally. This approach will facilitate the functional studies of essential genes and regulatory regions during development.
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spelling pubmed-60222692018-07-16 User-Friendly Genetic Conditional Knockout Strategies by CRISPR/Cas9 Chen, Liangliang Ye, Ying Dai, Hongxia Zhang, Heyao Zhang, Xue Wu, Qiang Zhu, Zhexin Spalinskas, Rapolas Ren, Wenyan Zhang, Wensheng Stem Cells Int Research Article Loss-of-function studies are critically important in gene functional analysis of model organisms and cells. However, conditional gene inactivation in diploid cells is difficult to achieve, as it involves laborious vector construction, multifold electroporation, and complicated genotyping. Here, a strategy is presented for generating biallelic conditional gene and DNA regulatory region knockouts in mouse embryonic stem cells by codelivery of CRISPR-Cas9 and short-homology-arm targeting vectors sequentially or simultaneously. Collectively, a simple and rapid method was presented to knock out any DNA element conditionally. This approach will facilitate the functional studies of essential genes and regulatory regions during development. Hindawi 2018-06-14 /pmc/articles/PMC6022269/ /pubmed/30013601 http://dx.doi.org/10.1155/2018/9576959 Text en Copyright © 2018 Liangliang Chen et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chen, Liangliang
Ye, Ying
Dai, Hongxia
Zhang, Heyao
Zhang, Xue
Wu, Qiang
Zhu, Zhexin
Spalinskas, Rapolas
Ren, Wenyan
Zhang, Wensheng
User-Friendly Genetic Conditional Knockout Strategies by CRISPR/Cas9
title User-Friendly Genetic Conditional Knockout Strategies by CRISPR/Cas9
title_full User-Friendly Genetic Conditional Knockout Strategies by CRISPR/Cas9
title_fullStr User-Friendly Genetic Conditional Knockout Strategies by CRISPR/Cas9
title_full_unstemmed User-Friendly Genetic Conditional Knockout Strategies by CRISPR/Cas9
title_short User-Friendly Genetic Conditional Knockout Strategies by CRISPR/Cas9
title_sort user-friendly genetic conditional knockout strategies by crispr/cas9
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022269/
https://www.ncbi.nlm.nih.gov/pubmed/30013601
http://dx.doi.org/10.1155/2018/9576959
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