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

被引:107
|
作者
Narita, Takeo [1 ]
Ito, Shinsuke [2 ]
Higashijima, Yoshiki [1 ]
Chu, Wai Kit [1 ,6 ]
Neumann, Katrin [3 ,7 ]
Walter, Jonas [1 ]
Satpathy, Shankha [1 ,8 ]
Liebner, Tim [1 ]
Hamilton, William B. [4 ]
Maskey, Elina [1 ]
Prus, Gabriela [1 ]
Shibata, Marika [2 ]
Iesmantavicius, Vytautas [1 ]
Brickman, Joshua M. [4 ]
Anastassiadis, Konstantinos [3 ]
Koseki, Haruhiko [2 ,5 ]
Choudhary, Chunaram [1 ]
机构
[1] Univ Copenhagen, Fac Hlth & Med Sci, Ctr Prot Res, Dept Prote,Novo Nordisk Fdn, Blegdamsvej 3B, DK-2200 Copenhagen, Denmark
[2] RIKEN Ctr Integrat Med Sci, Lab Dev Genet, Tsurumi Ku, 1-7-22 Suehiro Cho, Yokohama, Kanagawa 2300045, Japan
[3] Tech Univ Dresden, Ctr Mol & Cellular Bioengn, Biotechnol Ctr, Stem Cell Engn, D-01307 Dresden, Germany
[4] Univ Copenhagen, Novo Nordisk Fdn, Fac Hlth & Med Sci, Ctr Stem Cell Biol DanStem, Blegdamsvej 3B, DK-2200 Copenhagen, Denmark
[5] Chiba Univ, Grad Sch Med, Immune Regulat,Adv Res Dept, Chuo Ku, 1-8-1 Inohana, Chiba 2608670, Japan
[6] Chinese Univ Hong Kong, Dept Ophthalmol & Visual Sci, Hong Kong, Peoples R China
[7] Tech Univ Dresden, Ctr Mol & Cellular Bioengn CMCB, Stem Cell Engn Facil, Technol Platform, D-01307 Dresden, Germany
[8] Broad Inst Massachusetts Inst Technol & Harvard, Cambridge, MA 02142 USA
基金
新加坡国家研究基金会;
关键词
R/BIOCONDUCTOR PACKAGE; STRUCTURAL BASIS; TRANSCRIPTION; CBP; VISUALIZATION; ACETYLATION; COMPLEX; INHIBITION; EXPRESSION; DATABASE;
D O I
10.1016/j.molcel.2021.03.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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.
引用
收藏
页码:2166 / +
页数:23
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