CYCLINg through transcription Posttranslational modifications of P-TEFb regulate transcription elongation

被引:53
|
作者
Cho, Sungyoo [1 ]
Schroeder, Sebastian [1 ]
Ott, Melanie [1 ]
机构
[1] Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94143 USA
关键词
transcription elongation; RNA polymerase II; cyclin T; CDK9; RNA-POLYMERASE-II; BROMODOMAIN PROTEIN BRD4; DEPENDENT KINASE REGULATION; VIRUS TYPE-1 TRANSCRIPTION; 7SK SNRNA; HIV-1; TAT; CELL-CYCLE; T-LOOP; GENE-EXPRESSION; CDK9/CYCLIN T1;
D O I
10.4161/cc.9.9.11346
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The cyclin T/CDK9 complex, also called positive transcription elongation factor b (P-TEFb) phosphorylates the C-terminal domain of the large fragment of the RNA polymerase II. This action is a hallmark of the transition from transcription initiation to elongation. P-TEFb is itself modified by phosphorylation and ubiquitination. Recently, the core components of P-TEFb, cyclin T1 and CDK9, were identified as novel substrates of histone acetyltransferases. Here, we review how posttranslational modifications regulate the activity of the P-TEFb complex and discuss how acetylation of the complex optimizes transcription elongation in the context of other posttranslational modifications.
引用
收藏
页码:1697 / 1705
页数:9
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