生物
乙酰转移酶
乙酰化
抄写(语言学)
细胞生物学
增强子
RNA聚合酶Ⅱ
增强子rna
P300-CBP转录因子
遗传学
基因表达
发起人
转录因子
基因
哲学
组蛋白乙酰转移酶
语言学
作者
Takeo Narita,Shinsuke Ito,Yoshiki Higashijima,Wai Kit Chu,Katrin Neumann,Jonas Walter,Shankha Satpathy,Tim Liebner,William B. Hamilton,Elina Maskey,Gabriela Pruś,Marika Shibata,Vytautas Iešmantavičius,Joshua M. Brickman,Konstantinos Anastassiadis,Haruhiko Koseki,Chunaram Choudhary
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2021-03-24
卷期号:81 (10): 2166-2182.e6
被引量:164
标识
DOI:10.1016/j.molcel.2021.03.008
摘要
The metazoan-specific acetyltransferase p300/CBP is involved in activating signal-induced, enhancer-mediated transcription of cell-type-specific genes. However, the global kinetics and mechanisms of p300/CBP activity-dependent transcription activation remain poorly understood. We performed genome-wide, time-resolved analyses to show that enhancers and super-enhancers are dynamically activated through p300/CBP-catalyzed acetylation, deactivated by the opposing deacetylase activity, and kinetic acetylation directly contributes to maintaining cell identity at very rapid (minutes) timescales. The acetyltransferase activity is dispensable for the recruitment of p300/CBP and transcription factors but essential for promoting the recruitment of TFIID and RNAPII at virtually all enhancers and enhancer-regulated genes. This identifies pre-initiation complex assembly as a dynamically controlled step in the transcription cycle and reveals p300/CBP-catalyzed acetylation as the signal that specifically promotes transcription initiation at enhancer-regulated genes. We propose that p300/CBP activity uses a “recruit-and-release” mechanism to simultaneously promote RNAPII recruitment and pause release and thereby enables kinetic activation of enhancer-mediated transcription.
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