Everett Roger D
MRC Virology Unit, Church Street, Glasgow G11 5JR, Scotland, UK.
Cell Microbiol. 2006 Mar;8(3):365-74. doi: 10.1111/j.1462-5822.2005.00677.x.
ND10 are small nuclear substructures that are defined by the presence the promyelocytic leukaemia protein PML. Many other proteins have been detected within ND10, a complexity that is reflected in reports of their involvement in multiple cellular pathways that include the regulation of gene expression, chromatin dynamics, protein modification, apoptosis, p53 function, senescence, DNA repair, the interferon response and viral infection. This review summarizes recent evidence of similarities between the behaviour of ND10 components and DNA repair pathway proteins in response to viral infection and DNA damage. ND10 structures become associated with the parental genomes and early replication compartments of many DNA viruses, and DNA repair pathway proteins are also recruited to these sites. Similarly, PML and DNA repair proteins are recruited to sites of DNA damage. The mechanisms by which these events might occur, and the implications for ND10 function in DNA virus infection and chromatin metabolism, are discussed.
核点(ND10)是由早幼粒细胞白血病蛋白PML的存在所定义的小核亚结构。在核点内已检测到许多其他蛋白质,这种复杂性反映在有关它们参与多种细胞途径的报道中,这些途径包括基因表达调控、染色质动力学、蛋白质修饰、细胞凋亡、p53功能、衰老、DNA修复、干扰素反应和病毒感染。本综述总结了核点成分与DNA修复途径蛋白在应对病毒感染和DNA损伤时行为相似性的最新证据。核点结构与许多DNA病毒的亲本基因组和早期复制区室相关联,并且DNA修复途径蛋白也被招募到这些位点。同样,PML和DNA修复蛋白也被招募到DNA损伤位点。本文讨论了这些事件可能发生的机制,以及它们对核点在DNA病毒感染和染色质代谢中的功能的影响。