CDK8 is a positive regulator of transcriptional elongation within the serum response network

被引:272
作者
Donner, Aaron J. [1 ,2 ]
Ebmeier, Christopher C. [3 ]
Taatjes, Dylan J. [3 ]
Espinosa, Joaquin M. [1 ,2 ]
机构
[1] Univ Colorado, Howard Hughes Med Inst, Boulder, CO 80309 USA
[2] Univ Colorado, Dept Mol Cellular & Dev Biol, Boulder, CO 80309 USA
[3] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
RNA-POLYMERASE-II; CARBOXYL-TERMINAL DOMAIN; BROMODOMAIN PROTEIN BRD4; P-TEFB; MESSENGER-RNA; PREINITIATION COMPLEX; MEDIATOR INTERACTIONS; GENE-EXPRESSION; CAPPING ENZYME; REPEAT DOMAIN;
D O I
10.1038/nsmb.1752
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 Mediator complex allows communication between transcription factors and RNA polymerase II (RNAPII). Cyclin-dependent kinase 8 (CDK8), the kinase found in some variants of Mediator, has been characterized mostly as a transcriptional repressor. Recently, CDK8 was demonstrated to be a potent oncoprotein. Here we show, using a human tumor cell line, that CDK8 is a positive regulator of genes within the serum response network, including several members of the activator protein 1 and early growth response family of oncogenic transcription factors. Mechanistic studies show that CDK8 is not required for RNAPII recruitment or promoter escape. Instead, CDK8 depletion leads to the appearance of slower elongation complexes carrying hypophosphorylated RNAPII. CDK8-Mediator regulates precise steps in the assembly of the RNAPII elongation complex, including the recruitment of positive transcription elongation factor b and BRD4. Furthermore, CDK8-Mediator specifically interacts with positive transcription elongation factor b. Thus, we have uncovered a role for CDK8 in transcriptional regulation that may contribute to its oncogenic effects.
引用
收藏
页码:194 / U9
页数:9
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