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Chromatin Dynamics during Nucleotide Excision Repair: Histones on the Move

机译:核苷酸切除修复过程中的染色质动力学:移动中的组蛋白

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It has been a long-standing question how DNA damage repair proceeds in a nuclear environment where DNA is packaged into chromatin. Several decades of analysis combining in vitro and in vivo studies in various model organisms ranging from yeast to human have markedly increased our understanding of the mechanisms underlying chromatin disorganization upon damage detection and re-assembly after repair. Here, we review the methods that have been developed over the years to delineate chromatin alterations in response to DNA damage by focusing on the well-characterized Nucleotide Excision Repair (NER) pathway. We also highlight how these methods have provided key mechanistic insight into histone dynamics coupled to repair in mammals, raising new issues about the maintenance of chromatin integrity. In particular, we discuss how NER factors and central players in chromatin dynamics such as histone modifiers, nucleosome remodeling factors, and histone chaperones function to mobilize histones during repair.
机译:一个长期的问题是,在将DNA包装到染色质中的核环境中,如何进行DNA损伤修复。数十年的分析相结合,在从酵母到人类的各种模式生物中进行了体外和体内研究,这大大提高了我们对损伤检测和修复后重新组装后染色质分解的潜在机制的理解。在这里,我们回顾了多年来开发的方法,通过侧重于特征明确的核苷酸切除修复(NER)途径来描述对DNA损伤的染色质变化。我们还将重点介绍这些方法如何为与哺乳动物修复相关的组蛋白动力学提供关键的机械见解,从而引发有关染色质完整性维持的新问题。特别是,我们讨论了NER因子和染色质动力学中的中心参与者(例如组蛋白修饰剂,核小体重塑因子和组蛋白伴侣)如何在修复过程中动员组蛋白。

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