An efficient genotyping method for genome-modified animals and human cells generated with CRISPR/Cas9 system

一种针对利用 CRISPR/Cas9 系统生成的基因组编辑动物和人类细胞的高效基因分型方法

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作者:Xiaoxiao Zhu ,Yajie Xu ,Shanshan Yu ,Lu Lu ,Mingqin Ding ,Jing Cheng ,Guoxu Song ,Xing Gao ,Liangming Yao ,Dongdong Fan ,Shu Meng ,Xuewen Zhang ,Shengdi Hu ,Yong Tian

Abstract

The rapid generation of various species and strains of laboratory animals using CRISPR/Cas9 technology has dramatically accelerated the interrogation of gene function in vivo. So far, the dominant approach for genotyping of genome-modified animals has been the T7E1 endonuclease cleavage assay. Here, we present a polyacrylamide gel electrophoresis-based (PAGE) method to genotype mice harboring different types of indel mutations. We developed 6 strains of genome-modified mice using CRISPR/Cas9 system, and utilized this approach to genotype mice from F0 to F2 generation, which included single and multiplexed genome-modified mice. We also determined the maximal detection sensitivity for detecting mosaic DNA using PAGE-based assay as 0.5%. We further applied PAGE-based genotyping approach to detect CRISPR/Cas9-mediated on- and off-target effect in human 293T and induced pluripotent stem cells (iPSCs). Thus, PAGE-based genotyping approach meets the rapidly increasing demand for genotyping of the fast-growing number of genome-modified animals and human cell lines created using CRISPR/Cas9 system or other nuclease systems such as TALEN or ZFN.

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