Cdk7:处于转录核心的激酶,也是发现抗癌药物的关键。

IF 3.6 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Transcription-Austin Pub Date : 2019-04-01 Epub Date: 2018-12-06 DOI:10.1080/21541264.2018.1553483
Robert P Fisher
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引用次数: 0

摘要

RNA 聚合酶 II(Pol II)的转录周期由一组细胞周期蛋白依赖性激酶(CDK)调控。与转录起始因子 TFIIH 相关联的 Cdk7 既是一种效应 CDK,可使 Pol II 和转录机制中的其他靶点磷酸化,也是至少一种参与转录的其他基本 CDK 的 CDK 激活激酶(CAK)。最近的研究揭示了 Cdk7 在整个 Pol II 转录周期中的功能,从启动子清除和启动子近端暂停,到基因体内的共转录染色质修饰,再到 mRNA 3 端形成和终止。Cdk7 也已成为小分子抑制剂的靶标,有望用于治疗癌症和炎症。现在的挑战是确定 Cdk7 在转录周期每个步骤中的相关靶点,并了解癌症患者如何对一种重要的 CDK 产生更强的依赖性,以及如何利用这种依赖性进行治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cdk7: a kinase at the core of transcription and in the crosshairs of cancer drug discovery.

Cdk7: a kinase at the core of transcription and in the crosshairs of cancer drug discovery.

Cdk7: a kinase at the core of transcription and in the crosshairs of cancer drug discovery.

The transcription cycle of RNA polymerase II (Pol II) is regulated by a set of cyclin-dependent kinases (CDKs). Cdk7, associated with the transcription initiation factor TFIIH, is both an effector CDK that phosphorylates Pol II and other targets within the transcriptional machinery, and a CDK-activating kinase (CAK) for at least one other essential CDK involved in transcription. Recent studies have illuminated Cdk7 functions that are executed throughout the Pol II transcription cycle, from promoter clearance and promoter-proximal pausing, to co-transcriptional chromatin modification in gene bodies, to mRNA 3´-end formation and termination. Cdk7 has also emerged as a target of small-molecule inhibitors that show promise in the treatment of cancer and inflammation. The challenges now are to identify the relevant targets of Cdk7 at each step of the transcription cycle, and to understand how heightened dependence on an essential CDK emerges in cancer, and might be exploited therapeutically.

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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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