CBP Regulates Recruitment and Release of Promoter-Proximal RNA Polymerase II

被引:58
作者
Boija, Ann [1 ]
Mahat, Dig Bijay [2 ]
Zare, Aman [3 ,4 ]
Holmqvist, Per-Henrik [1 ]
Philip, Philge [3 ,4 ]
Meyers, David J. [5 ]
Cole, Philip A. [5 ]
Lis, John T. [2 ]
Stenberg, Per [3 ,4 ,6 ]
Mannervik, Mattias [1 ]
机构
[1] Stockholm Univ, Wenner Gren Inst, Dept Mol Biosci, S-10691 Stockholm, Sweden
[2] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14850 USA
[3] Umea Univ, Dept Mol Biol, S-90187 Umea, Sweden
[4] Umea Univ, Computat Life Sci Cluster CLiC, S-90187 Umea, Sweden
[5] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, 725 North Wolfe St, Baltimore, MD 21205 USA
[6] Swedish Def Res Agcy, FOI, Div CBRN Def & Secur, S-90621 Umea, Sweden
基金
瑞典研究理事会;
关键词
GAGA FACTOR; ACETYLTRANSFERASE ACTIVITY; DROSOPHILA-MELANOGASTER; GENE-EXPRESSION; HISTONE H3; TRANSCRIPTION; ACETYLATION; ACTIVATION; P300/CBP; BINDING;
D O I
10.1016/j.molcel.2017.09.031
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
Transcription activation involves RNA polymerase II (Pol II) recruitment and release from the promoter into productive elongation, but how specific chromatin regulators control these steps is unclear. Here, we identify a novel activity of the histone acetyltransferase p300/CREB-binding protein (CBP) in regulating promoter-proximal paused Pol II. We find that Drosophila CBP inhibition results in "dribbling'' of Pol II from the pause site to positions further downstream but impedes transcription through the + 1 nucleosome genome-wide. Promoters strongly occupied by CBP and GAGA factor have high levels of paused Pol II, a unique chromatin signature, and are highly expressed regardless of cell type. Interestingly, CBP activity is rate limiting for Pol II recruitment to these highly paused promoters through an interaction with TFIIB but for transit into elongation by histone acetylation at other genes. Thus, CBP directly stimulates both Pol II recruitment and the ability to traverse the first nucleosome, thereby promoting transcription of most genes.
引用
收藏
页码:491 / +
页数:18
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