User-Friendly Genetic Conditional Knockout Strategies by CRISPR/Cas9

被引:1
|
作者
Chen, Liangliang [1 ]
Ye, Ying [1 ]
Dai, Hongxia [1 ]
Zhang, Heyao [1 ]
Zhang, Xue [1 ]
Wu, Qiang [2 ]
Zhu, Zhexin [3 ]
Spalinskas, Rapolas [4 ]
Ren, Wenyan [1 ]
Zhang, Wensheng [1 ]
机构
[1] Soochow Univ, Cam Su Genom Resource Ctr, Suzhou 215123, Peoples R China
[2] Macau Univ Sci & Technol, State Key Lab Qual Res Chinese Med, Ave Wai Long, Taipa, Macau, Peoples R China
[3] St Jude Childrens Res Hosp, Dept Oncol, 262 Danny Thomas Pl, Memphis, TN 38105 USA
[4] KTH Royal Inst Technol, Div Gene Technol, Sci Life Lab, S-10691 Stockholm, Sweden
关键词
PROTEIN EED; GENERATION;
D O I
10.1155/2018/9576959
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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.
引用
收藏
页数:10
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