中介激酶模块调节DNA损伤后的细胞周期再进入和转录反应。

Gönen Memişoğlu, Stefan Bohn, Nevan J Krogan, James E Haber, Alexander J Ruthenburg
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引用次数: 0

摘要

Cdk8激酶模块(CKM)是转录介质的非专性和可解离亚复合物,是RNA聚合酶II (RNAPII)的关键调节因子。通过酵母的遗传筛选,我们发现了中介CKM在DNA损伤反应(DDR)和有丝分裂再进入中的令人惊讶的作用。值得注意的是,我们发现单个DNA断裂足以导致ckm依赖性的全局转录衰减。在DDR激活后,CKM的激酶活性拮抗RNAPII与核心介质的结合,从而减少转录参与的RNAPII库。这种转录衰减对DDR失活至关重要,并限制了ψ-H2AX向基因体的传播。此外,CKM定位于DNA断裂以阻止RNAPII的结合。重要的是,我们证明了从酵母到哺乳动物,CKM对DDR和转录衰减的作用是保守的,建立了CKM在dna损伤反应的转录调节中的多方面和基本功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Mediator Kinase Module regulates cell cycle re-entry and transcriptional responses following DNA damage.

The Cdk8 kinase module (CKM) is a non-obligate and dissociable subcomplex of Mediator of transcription, a key regulator of RNA polymerase II (RNAPII). Through a genetic screen in yeast, we discovered a surprising role for Mediator CKM in the DNA damage response (DDR) and mitotic re-entry. Remarkably, we find that a single DNA break is sufficient for CKM-dependent global transcriptional attenuation. Upon DDR activation, the kinase activity of CKM antagonizes RNAPII binding to core Mediator, thereby reducing the transcriptionally-engaged RNAPII pool. This transcriptional attenuation is essential for DDR inactivation and limits the spreading of γ-H2AX into gene bodies. Furthermore, CKM localizes to DNA breaks to impede RNAPII binding. Importantly, we demonstrate that the role of CKM on DDR and transcriptional attenuation is conserved from yeast to mammals, establishing a multifaceted and essential function for CKM in transcriptional regulation of DNA-damage response.

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