SOX2
增强子
生物
胚胎干细胞
同源盒蛋白纳米
细胞命运测定
转录因子
细胞生物学
染色质
内细胞团
遗传学
胚胎
计算生物学
诱导多能干细胞
胚胎发生
基因
胚泡
作者
Lijia Li,Fang-Nong Lai,Xiaoyu Hu,Bofeng Liu,Xukun Lu,Zili Lin,Ling Liu,Yunlong Xiang,Tristan Frum,Michael A. Halbisen,Fengling Chen,Qiang Fan,Amy Ralston,Wei Xie
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2023-12-14
卷期号:382 (6676)
被引量:12
标识
DOI:10.1126/science.adi5516
摘要
Pioneer transcription factors (TFs), such as OCT4 and SOX2, play crucial roles in pluripotency regulation. However, the master TF-governed pluripotency regulatory circuitry was largely inferred from cultured cells. In this work, we investigated SOX2 binding from embryonic day 3.5 (E3.5) to E7.5 in the mouse. In E3.5 inner cell mass (ICM), SOX2 regulates the ICM-trophectoderm program but is dispensable for opening global enhancers. Instead, SOX2 occupies preaccessible enhancers in part opened by early-stage expressing TFs TFAP2C and NR5A2. SOX2 then widely redistributes when cells adopt naive and formative pluripotency by opening enhancers or poising them for rapid future activation. Hence, multifaceted pioneer TF-enhancer interaction underpins pluripotency progression in embryos, including a distinctive state in E3.5 ICM that bridges totipotency and pluripotency.
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