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增强子通过 p300/CBP 活性依赖性 PIC 组装、RNAPII 募集和暂停释放来激活。

Enhancers are activated by p300/CBP activity-dependent PIC assembly, RNAPII recruitment, and pause release.

机构信息

Department of Proteomics, The Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, Copenhagen 2200, Denmark.

Laboratory of Developmental Genetics, RIKEN Center for Integrative Medical Sciences, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa 230-0045, Japan.

出版信息

Mol Cell. 2021 May 20;81(10):2166-2182.e6. doi: 10.1016/j.molcel.2021.03.008. Epub 2021 Mar 24.

Abstract

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.

摘要

后生动物特异性乙酰转移酶 p300/CBP 参与激活信号诱导的、增强子介导的细胞类型特异性基因的转录。然而,p300/CBP 活性依赖性转录激活的全局动力学和机制仍知之甚少。我们进行了全基因组、时分辨析,结果表明增强子和超级增强子通过 p300/CBP 催化的乙酰化动态激活,通过相反的去乙酰化酶活性失活,并且动力学乙酰化直接有助于在非常快速(分钟)的时间尺度上维持细胞身份。乙酰转移酶活性对于 p300/CBP 和转录因子的募集不是必需的,但对于促进 TFIID 和 RNAPII 在几乎所有增强子和增强子调控基因上的募集是必需的。这将起始前复合物组装鉴定为转录周期中的一个动态控制步骤,并揭示了 p300/CBP 催化的乙酰化作为专门促进增强子调控基因转录起始的信号。我们提出,p300/CBP 活性使用“招募和释放”机制来同时促进 RNAPII 的募集和暂停释放,从而能够使增强子介导的转录的动力学激活。

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