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功能转录启动子在 DNA 双链断裂处介导 RNA 驱动的损伤反应因子相分离。

Functional transcription promoters at DNA double-strand breaks mediate RNA-driven phase separation of damage-response factors.

机构信息

IFOM, The FIRC Institute of Molecular Oncology, Milan, Italy.

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale, Università degli Studi di Milano, Segrate, Italy.

出版信息

Nat Cell Biol. 2019 Oct;21(10):1286-1299. doi: 10.1038/s41556-019-0392-4. Epub 2019 Sep 30.

Abstract

Damage-induced long non-coding RNAs (dilncRNA) synthesized at DNA double-strand breaks (DSBs) by RNA polymerase II are necessary for DNA-damage-response (DDR) focus formation. We demonstrate that induction of DSBs results in the assembly of functional promoters that include a complete RNA polymerase II preinitiation complex, MED1 and CDK9. Absence or inactivation of these factors causes a reduction in DDR foci both in vivo and in an in vitro system that reconstitutes DDR events on nucleosomes. We also show that dilncRNAs drive molecular crowding of DDR proteins, such as 53BP1, into foci that exhibit liquid-liquid phase-separation condensate properties. We propose that the assembly of DSB-induced transcriptional promoters drives RNA synthesis, which stimulates phase separation of DDR factors in the shape of foci.

摘要

DNA 双链断裂 (DSBs) 诱导的长非编码 RNA(dilncRNA) 由 RNA 聚合酶 II 合成,对于 DNA 损伤反应 (DDR) 焦点的形成是必要的。我们证明,DSB 的诱导导致功能性启动子的组装,该启动子包括完整的 RNA 聚合酶 II 起始复合物、MED1 和 CDK9。这些因子的缺失或失活会导致体内和体外系统中 DDR 焦点的减少,体外系统在核小体上重建 DDR 事件。我们还表明,dilncRNA 将 DDR 蛋白(如 53BP1)驱动到焦点中,焦点表现出液-液相分离凝聚物的性质。我们提出,DSB 诱导的转录启动子的组装驱动 RNA 合成,从而刺激 DDR 因子在焦点中的相分离。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c41/6859070/3beec7b383a4/EMS84124-f001.jpg

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