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首页> 外文期刊>Molecular cell >Regulation of chromatin architecture by the PWWP domain-containing DNA damage-responsive factor EXPAND1/MUM1.
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Regulation of chromatin architecture by the PWWP domain-containing DNA damage-responsive factor EXPAND1/MUM1.

机译:含PWWP域的DNA损伤反应因子EXPAND1 / MUM1对染色质结构的调节。

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摘要

Dynamic changes of chromatin structure facilitate diverse biological events, including DNA replication, repair, recombination, and gene transcription. Recent evidence revealed that DNA damage elicits alterations to the chromatin to facilitate proper checkpoint activation and DNA repair. Here we report the identification of the PWWP domain-containing protein EXPAND1/MUM1 as an architectural component of the chromatin, which in response to DNA damage serves as an accessory factor to promote cell survival. Depletion of EXPAND1/MUM1 or inactivation of its PWWP domain resulted in chromatin compaction. Upon DNA damage, EXPAND1/MUM1 rapidly concentrates at the vicinity of DNA damage sites via its direct interaction with 53BP1. Ablation of this interaction impaired damage-induced chromatin decondensation, which is accompanied by sustained DNA damage and hypersensitivity to genotoxic stress. Collectively, our study uncovers a chromatin-bound factor that serves an accessory role in coupling damage signaling with chromatin changes in response to DNA damage.
机译:染色质结构的动态变化促进了多种生物学事件,包括DNA复制,修复,重组和基因转录。最近的证据表明,DNA损伤引起染色质发生改变,以促进适当的检查点激活和DNA修复。在这里,我们报告鉴定包含PWWP域的蛋白质EXPAND1 / MUM1作为染色质的建筑成分,该染色质在响应DNA损伤时作为促进细胞存活的辅助因子。 EXPAND1 / MUM1的耗尽或PWWP结构域的失活导致染色质紧缩。 DNA受到破坏后,EXPAND1 / MUM1通过与53BP1的直接相互作用迅速集中在DNA破坏位点附近。这种相互作用的消除损害了损伤诱导的染色质的缩聚,这伴随着持续的DNA损伤和对遗传毒性应激的超敏性。总的来说,我们的研究发现了染色质结合因子,该因子在将损伤信号与响应DNA损伤的染色质变化耦合中起辅助作用。

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