中介激酶CDK8和CDK19的调控功能。

IF 3.6 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Transcription-Austin Pub Date : 2019-04-01 Epub Date: 2018-12-26 DOI:10.1080/21541264.2018.1556915
Charli B Fant, Dylan J Taatjes
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引用次数: 72

摘要

介质相关激酶CDK8和CDK19在另外三种蛋白的背景下起作用:CCNC和MED12,它们激活CDK8/CDK19激酶的功能,MED13,使它们能够与介质复合物结合。中介激酶通过磷酸化转录因子和控制中介的结构和功能间接影响RNA聚合酶II (pol II)的转录。在这篇综述中,我们讨论了中介激酶的细胞作用和机制,使其生物学功能。我们专注于序列特异性,dna结合转录因子和其他中介激酶底物,以及CDK8或CDK19如何通过增强子和染色质环实现代谢和转录重编程。我们还总结了中介激酶抑制剂及其治疗潜力。总之,我们注意到酵母和哺乳动物CDK8之间的保守和不同的功能,并强调了激酶模块功能的许多方面仍然是谜,从pol II启动子-近端暂停到液-液相分离的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Regulatory functions of the Mediator kinases CDK8 and CDK19.

Regulatory functions of the Mediator kinases CDK8 and CDK19.

Regulatory functions of the Mediator kinases CDK8 and CDK19.

The Mediator-associated kinases CDK8 and CDK19 function in the context of three additional proteins: CCNC and MED12, which activate CDK8/CDK19 kinase function, and MED13, which enables their association with the Mediator complex. The Mediator kinases affect RNA polymerase II (pol II) transcription indirectly, through phosphorylation of transcription factors and by controlling Mediator structure and function. In this review, we discuss cellular roles of the Mediator kinases and mechanisms that enable their biological functions. We focus on sequence-specific, DNA-binding transcription factors and other Mediator kinase substrates, and how CDK8 or CDK19 may enable metabolic and transcriptional reprogramming through enhancers and chromatin looping. We also summarize Mediator kinase inhibitors and their therapeutic potential. Throughout, we note conserved and divergent functions between yeast and mammalian CDK8, and highlight many aspects of kinase module function that remain enigmatic, ranging from potential roles in pol II promoter-proximal pausing to liquid-liquid phase separation.

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来源期刊
Transcription-Austin
Transcription-Austin BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
6.50
自引率
5.60%
发文量
9
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