Adam Salomé, Dabin Juliette, Polo Sophie E
Epigenome Integrity Group, UMR 7216 CNRS/Paris Diderot University, 35 rue Helene Brion, 75013 Paris, France; Chromatin Dynamics Group, UMR 3664 CNRS/Institut Curie Research Center, 26 rue d'Ulm 75005 Paris, France.
Epigenome Integrity Group, UMR 7216 CNRS/Paris Diderot University, 35 rue Helene Brion, 75013 Paris, France.
DNA Repair (Amst). 2015 Aug;32:120-126. doi: 10.1016/j.dnarep.2015.04.022. Epub 2015 May 1.
DNA damage poses a major threat to cell function and viability by compromising both genome and epigenome integrity. The DNA damage response indeed operates in the context of chromatin and relies on dynamic changes in chromatin organization. Here, we review the molecular bases of chromatin alterations in response to DNA damage, focusing on core histone mobilization in mammalian cells. Building on our current view of nucleosome dynamics in response to DNA damage, we highlight open challenges and avenues for future development. In particular, we discuss the different levels of regulation of chromatin plasticity during the DNA damage response and their potential impact on cell function and epigenome maintenance.
DNA损伤通过损害基因组和表观基因组的完整性,对细胞功能和生存能力构成重大威胁。DNA损伤反应确实在染色质的背景下发挥作用,并依赖于染色质组织的动态变化。在这里,我们回顾了DNA损伤反应中染色质改变的分子基础,重点关注哺乳动物细胞中核心组蛋白的动员。基于我们目前对DNA损伤反应中核小体动力学的认识,我们强调了未来发展面临的挑战和途径。特别是,我们讨论了DNA损伤反应过程中染色质可塑性的不同调控水平及其对细胞功能和表观基因组维持的潜在影响。