Generation of a SMO homozygous knockout human embryonic stem cell line WAe001-A-16 by CRISPR/Cas9 editing

通过 CRISPR/Cas9 编辑生成 SMO 纯合敲除人类胚胎干细胞系 WAe001-A-16

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作者:Feima Wu, Ge Gao, Tingcai Pan, Zhen Yang, Guosheng Xu, Nasir Abbas, Yanli Liu, Yan Chen, Shenglin Tan, Kai You, Xinrong Ke, Yuanqi Zhuang, Xianhua Lin, Fan Yang, Yin-Xiong Li

Abstract

The human SMO protein encoded by the smoothened (SMO) gene acts as a positive mediator for Hedgehog signaling. This pathway regulates many cellular activities, developmental morphogenesis, and tumorigenesis. Using CRISPR/Cas9 to edit human embryonic stem cell line WA01 (H1), we established a SMO mutant cell line (WAe001-A-16). This cell line has a 40bp homozygous deletion in exon 2 of SMO leading to a shift in the open reading frame and early termination at amino acid position 287. WAe001-A-16 maintains a normal karyotype, parental cell morphology, pluripotency markers, and the capacity to differentiate into all three germline layers.

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