清脆的
基因敲除
条件基因敲除
Cas9
电穿孔
生物
计算生物学
基因
基因组编辑
遗传学
基因敲除
基因靶向
表型
作者
Liangliang Chen,Ying Ye,Hongxia Dai,Heyao Zhang,Xue Zhang,Qiang Wu,Zhexin Zhu,Rapolas Spalinskas,Wenyan Ren,Wensheng Zhang
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.
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