Kolobynina Ksenia G, Rapp Alexander, Cardoso M Cristina
Department of Biology, Cell Biology and Epigenetics, Technical University of Darmstadt, Darmstadt, Germany.
Front Cell Dev Biol. 2022 Jul 5;10:928113. doi: 10.3389/fcell.2022.928113. eCollection 2022.
Chromatin is the context for all DNA-based molecular processes taking place in the cell nucleus. The initial chromatin structure at the site of the DNA damage determines both, lesion generation and subsequent activation of the DNA damage response (DDR) pathway. In turn, proceeding DDR changes the chromatin at the damaged site and across large fractions of the genome. Ubiquitination, besides phosphorylation and methylation, was characterized as an important chromatin post-translational modification (PTM) occurring at the DNA damage site and persisting during the duration of the DDR. Ubiquitination appears to function as a highly versatile "signal-response" network involving several types of players performing various functions. Here we discuss how ubiquitin modifiers fine-tune the DNA damage recognition and response and how the interaction with other chromatin modifications ensures cell survival.
染色质是细胞核中所有基于DNA的分子过程发生的背景。DNA损伤部位的初始染色质结构决定了损伤的产生以及随后DNA损伤反应(DDR)途径的激活。反过来,进行中的DDR会改变受损部位以及基因组大部分区域的染色质。除了磷酸化和甲基化外,泛素化被认为是一种重要的染色质翻译后修饰(PTM),它发生在DNA损伤部位并在DDR持续期间持续存在。泛素化似乎作为一个高度通用的“信号-反应”网络发挥作用,涉及执行各种功能的几种类型的参与者。在这里,我们讨论泛素修饰剂如何微调DNA损伤的识别和反应,以及与其他染色质修饰的相互作用如何确保细胞存活。