生物
染色质
核小体
增强子
嘉雅宠物
重编程
基因组
组蛋白
二价染色质
遗传学
转录因子
组蛋白密码
先锋因素
支架/基质附着区域
斑马鱼
背景(考古学)
基因
染色质重塑
细胞生物学
计算生物学
古生物学
作者
Liyun Miao,Yin Tang,Ashley R. Bonneau,Shun Wan Chan,Mina L Kojima,Mark E. Pownall,Charles E. Vejnar,Feng Gao,Smita Krishnaswamy,Caroline E Hendry,Antonio J. Giraldez
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2022-03-01
卷期号:82 (5): 986-1002.e9
被引量:22
标识
DOI:10.1016/j.molcel.2022.01.024
摘要
Upon fertilization, embryos undergo chromatin reprogramming and genome activation; however, the mechanisms that regulate these processes are poorly understood. Here, we generated a triple mutant for Nanog, Pou5f3, and Sox19b (NPS) in zebrafish and found that NPS pioneer chromatin opening at >50% of active enhancers. NPS regulate acetylation across core histones at enhancers and promoters, and their function in gene activation can be bypassed by recruiting histone acetyltransferase to individual genes. NPS pioneer chromatin opening individually, redundantly, or additively depending on sequence context, and we show that high nucleosome occupancy facilitates NPS pioneering activity. Nucleosome position varies based on the input of different transcription factors (TFs), providing a flexible platform to modulate pioneering activity. Altogether, our results illuminate the sequence of events during genome activation and offer a conceptual framework to understand how pioneer factors interpret the genome and integrate different TF inputs across cell types and developmental transitions.
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