生物
基因组编辑
多路复用
计算生物学
基因组
基因靶向
基因
克隆(编程)
遗传学
合成生物学
基因组工程
工具箱
人类基因组
基因组学
脱甲基酶
限制
突变
报告基因
作者
Jian Cao,Lizhen Wu,Shang‐Min Zhang,Min Lu,William K.C. Cheung,Wesley L. Cai,Molly Gale,Qi Xu,Qin Yan
摘要
The CRISPR/Cas9 system is a powerful genome editing tool and has been widely used for biomedical research. However, many challenges, such as off-target effects and lack of easy solutions for multiplex targeting, are still limiting its applications. To overcome these challenges, we first developed a highly efficient doxycycline-inducible Cas9-EGFP vector. This vector allowed us to track the cells for uniform temporal control and efficient gene disruption, even in a polyclonal setting. Furthermore, the inducible CRISPR/Cas9 system dramatically decreased off-target effects with a pulse exposure of the genome to the Cas9/sgRNA complex. To target multiple genes simultaneously, we established simple one-step cloning approaches for expression of multiple sgRNAs with improved vectors. By combining our inducible and multiplex genome editing approaches, we were able to simultaneously delete Lysine Demethylase (KDM) 5A, 5B and 5C efficiently in vitro and in vivo This user friendly and highly efficient toolbox provides a solution for easy genome editing with tight temporal control, minimal off-target effects and multiplex targeting.
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