胚胎干细胞
细胞命运测定
内细胞团
卵裂球
基因敲除
胚胎
细胞
SOX2
胚胎发生
生物
细胞分化
细胞生物学
遗传学
基因
胚泡
转录因子
作者
Yingmei Wang,Xiaoman Zheng,Rui Cheng,Jing Han,Xing Ma,Wenjun Xu,Lu Gao,Anmin Lei,Jun Liu,Fusheng Quan,Yong Zhang,Xu Liu
标识
DOI:10.1096/fj.202101196r
摘要
The goal of preimplantation development is to establish the fates of the embryonic and extra-embryonic cells. However, when and how cell fates are determined during early mammalian embryonic development remains unclear. We report that the high mobility group (HMG) protein family member HMGA1 was distributed differentially in mouse two-cell blastomeres. Knockdown of Hmga1 expression in one of the two cells reduced the number of cells contributing to the inner cell mass (ICM), suggesting that differential distribution of HMGA1 in the blastomeres in two-cell mouse embryos affected the selection of embryonic cell lineages. Mechanistically, HMGA1 promotes the expression of the ICM-specific gene Sox2. The results of this study show that mouse embryos demonstrate heterogeneity as early as the two-cell stage, and that these differences are related to cell-fate differentiation in early mouse embryos.
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