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细胞周期蛋白依赖性激酶7:转录核心的激酶以及癌症药物发现的焦点。

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

作者信息

Fisher Robert P

机构信息

a Department of Oncological Sciences , Icahn School of Medicine at Mount Sinai , New York , NY , USA.

出版信息

Transcription. 2019 Apr;10(2):47-56. doi: 10.1080/21541264.2018.1553483. Epub 2018 Dec 6.

Abstract

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.

摘要

RNA聚合酶II(Pol II)的转录循环受一组细胞周期蛋白依赖性激酶(CDK)调控。与转录起始因子TFIIH相关的Cdk7,既是一种效应CDK,可磷酸化Pol II及转录机制中的其他靶点,也是至少一种参与转录的其他必需CDK的CDK激活激酶(CAK)。最近的研究阐明了Cdk7在整个Pol II转录循环中执行的功能,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点,这些抑制剂在癌症和炎症治疗中显示出前景。现在面临的挑战是确定转录循环每个步骤中Cdk7的相关靶点,并了解癌症中如何出现对必需CDK的高度依赖性,以及如何在治疗中加以利用。

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