Brd4 and JMJD6-Associated Anti-Pause Enhancers in Regulation of Transcriptional Pause Release

被引:314
作者
Liu, Wen [1 ,2 ]
Ma, Qi [1 ,3 ]
Wong, Kaki [1 ]
Li, Wenbo [1 ]
Ohgi, Kenny [1 ]
Zhang, Jie [1 ]
Aggarwal, Aneel K. [4 ]
Rosenfeld, Michael G. [1 ]
机构
[1] Univ Calif San Diego, Sch Med, Howard Hughes Med Inst, Dept Med, La Jolla, CA 92093 USA
[2] Xiamen Univ, Sch Pharmaceut Sci, Xiamen 361102, Fujian, Peoples R China
[3] Univ Calif San Diego, Grad Program Bioinformat & Syst Biol, La Jolla, CA 92093 USA
[4] Mt Sinai Sch Med, Dept Struct & Chem Biol, New York, NY 10029 USA
关键词
RNA-POLYMERASE-II; BROMODOMAIN PROTEIN BRD4; GENE-EXPRESSION; PHOSPHATIDYLSERINE RECEPTOR; P-TEFB; DEPENDENT TRANSCRIPTION; SELECTIVE-INHIBITION; BET BROMODOMAINS; APOPTOTIC CELLS; C-MYC;
D O I
10.1016/j.cell.2013.10.056
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
Distal enhancers characterized by the H3K4me(1) mark play critical roles in developmental and transcriptional programs. However, potential roles of specific distal regulatory elements in regulating RNA polymerase II (Pol II) promoter-proximal pause release remain poorly investigated. Here, we report that a unique cohort of jumonji C-domain-containing protein 6 (JMJD6) and bromodomain-containing protein 4 (Brd4) cobound distal enhancers, termed antipause enhancers (A-PEs), regulate promoter-proximal pause release of a large subset of transcription units via long-range interactions. Brd4-dependent JMJD6 recruitment on A-PEs mediates erasure of H4R3me 2(s), which is directly read by 7SK snRNA, and decapping/demethylation of 7SK snRNA, ensuring the dismissal of the 7SK snRNA/HEXIM inhibitory complex. The interactions of both JMJD6 and Brd4 with the P-TEFb complex permit its activation and pause release of regulated coding genes. The functions of JMJD6/Brd4-associated dual histone and RNA demethylase activity on anti-pause enhancers have intriguing implications for these proteins in development, homeostasis, and disease.
引用
收藏
页码:1581 / 1595
页数:15
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