Functional Association of Gdown1 with RNA Polymerase II Poised on Human Genes

被引:115
作者
Cheng, Bo [1 ]
Li, Tiandao [2 ]
Rahl, Peter B. [3 ]
Adamson, Todd E. [2 ]
Loudas, Nicholas B. [2 ]
Guo, Jiannan [2 ]
Varzavand, Katayoun [2 ]
Cooper, Jeffrey J. [2 ]
Hu, Xiaopeng [4 ,5 ]
Gnatt, Averell [4 ]
Young, Richard A. [3 ]
Price, David H. [1 ,2 ]
机构
[1] Univ Iowa, Mol & Cellular Biol Program, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Biochem, Iowa City, IA 52242 USA
[3] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[4] Univ Maryland, Sch Med, Dept Pharmacol & Expt Therapeut, Baltimore, MD 21201 USA
[5] Sun Yat Sen Univ, Sch Pharmaceut Sci, High Educ Mega Ctr, Guangzhou 510006, Guangdong, Peoples R China
基金
美国国家卫生研究院;
关键词
P-TEFB; TRANSCRIPTION ELONGATION; PRODUCTIVE ELONGATION; DROSOPHILA EMBRYO; IN-VIVO; POL-II; COMPLEXES; EXPRESSION; INITIATION; PROMOTERS;
D O I
10.1016/j.molcel.2011.10.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Most human genes are loaded with promoter-proximally paused RNA polymerase II (Pol II) molecules that are poised for release into productive elongation by P-TEFb. We present evidence that Gdown1, the product of the POLR2M gene that renders Pot II responsive to Mediator, is involved in Pol II elongation control. During in vitro transcription, Gdown1 specifically blocked elongation stimulation by TFIIF, inhibited the termination activity of TTF2, and influenced pausing factors NELF and DSIF, but did not affect the function of TFIIS or the mRNA capping enzyme. Without P-TEFb, Gdown1 led to the production of stably paused polymerases in the presence of nuclear extract. Supporting these mechanistic insights, ChIP-Seq demonstrated that Gdown1 mapped over essentially all poised polymerases across the human genome. Our results establish that Gdown1 stabilizes poised polymerases while maintaining their responsiveness to P-TEFb and suggest that Mediator overcomes a Gdown1-mediated block of initiation by allowing TFIIF function.
引用
收藏
页码:38 / 50
页数:13
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