Howard Hughes Medical Institute, The University of Colorado at Boulder, Boulder, Colorado, USA.
Nat Struct Mol Biol. 2010 Feb;17(2):194-201. doi: 10.1038/nsmb.1752. Epub 2010 Jan 24.
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.
中介复合物允许转录因子和 RNA 聚合酶 II(RNAPII)之间进行通信。细胞周期蛋白依赖性激酶 8(CDK8)是一些中介体变体中发现的激酶,其主要被描述为转录抑制剂。最近,CDK8 被证明是一种有效的癌蛋白。在这里,我们使用人肿瘤细胞系表明,CDK8 是血清反应网络中基因的正调节剂,包括激活蛋白 1 和早期生长反应家族的几个致癌转录因子成员。机制研究表明,CDK8 对于 RNAPII 的募集或启动子逃逸不是必需的。相反,CDK8 的耗竭导致出现携带低磷酸化 RNAPII 的较慢延伸复合物。CDK8-中介复合物调节 RNAPII 延伸复合物组装的精确步骤,包括正转录延伸因子 b 和 BRD4 的募集。此外,CDK8-中介复合物特异性地与正转录延伸因子 b 相互作用。因此,我们发现 CDK8 在转录调节中的作用可能与其致癌作用有关。