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Small RNAs: Emerging key players in DNA double-strand break repair

机译:小RNA:DNA双链断裂修复中的新兴关键参与者

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DNA double-strand break (DSB) is the most deleterious form of DNA damage and poses great threat to genome stability. Eukaryotes have evolved complex mechanisms to repair DSBs through coordinated actions of protein sensors, transducers, and effectors. DSB-induced small RNAs (diRNAs) or Dicer/Drosha-dependent RNAs (DDRNAs) have been recently discovered in plants and vertebrates, adding an unsuspected RNA component into the DSB repair pathway. DiRNAs/DDRNAs control DNA damage response (DDR) activation by affecting DDR foci formation and cell cycle checkpoint enforcement and are required for efficient DSB repair. Here, we summarize the findings of diRNAs/DDRNAs and discuss the possible mechanisms through which they act to facilitate DSB repair.
机译:DNA双链断裂(DSB)是DNA损害的最有害形式,对基因组稳定性构成极大威胁。真核生物已经进化出了复杂的机制,可以通过蛋白质传感器,传感器和效应子的协同作用来修复DSB。最近在植物和脊椎动物中发现了DSB诱导的小RNA(diRNA)或Dicer / Drosha依赖的RNA(DDRNA),这在DSB修复途径中增加了不可怀疑的RNA成分。 DiRNA / DDRNA通过影响DDR灶的形成和细胞周期检查点的执行来控制DNA损伤反应(DDR)的激活,这是有效DSB修复所必需的。在这里,我们总结了diRNAs / DDRNAs的发现,并讨论了它们通过作用促进DSB修复的可能机制。

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