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多瘤病毒与DNA损伤反应的相互作用。

Polyomavirus interaction with the DNA damage response.

作者信息

Justice Joshua L, Verhalen Brandy, Jiang Mengxi

机构信息

Department of Microbiology, University of Alabama at Birmingham, Birmingham, 35294, USA.

出版信息

Virol Sin. 2015 Apr;30(2):122-9. doi: 10.1007/s12250-015-3583-6. Epub 2015 Apr 20.

Abstract

Viruses are obligate intracellular parasites that subvert cellular metabolism and pathways to mediate their own replication-normally at the expense of the host cell. Polyomaviruses are a group of small DNA viruses, which have long been studied as a model for eukaryotic DNA replication. Polyomaviruses manipulate host replication proteins, as well as proteins involved in DNA maintenance and repair, to serve as essential cofactors for productive infection. Moreover, evidence suggests that polyomavirus infection poses a unique genotoxic threat to the host cell. In response to any source of DNA damage, cells must initiate an effective DNA damage response (DDR) to maintain genomic integrity, wherein two protein kinases, ataxia telangiectasia mutated (ATM) and ATM- and Rad3-related (ATR), are major regulators of DNA damage recognition and repair. Recent investigation suggests that these essential DDR proteins are required for productive polyomavirus infection. This review will focus on polyomaviruses and their interaction with ATM- and ATR-mediated DNA damage responses and the effect of this interaction on host genomic stability.

摘要

病毒是专性细胞内寄生虫,它们破坏细胞代谢和途径以介导自身复制,通常是以宿主细胞为代价。多瘤病毒是一类小型DNA病毒,长期以来一直被作为真核DNA复制的模型进行研究。多瘤病毒操纵宿主复制蛋白以及参与DNA维持和修复的蛋白,将其作为有效感染的必需辅助因子。此外,有证据表明多瘤病毒感染对宿主细胞构成独特的基因毒性威胁。针对任何DNA损伤来源,细胞必须启动有效的DNA损伤反应(DDR)以维持基因组完整性,其中两种蛋白激酶,即共济失调毛细血管扩张症突变蛋白(ATM)和ATM及Rad3相关蛋白(ATR),是DNA损伤识别和修复的主要调节因子。最近的研究表明,这些必需的DDR蛋白是多瘤病毒有效感染所必需的。本综述将聚焦于多瘤病毒及其与ATM和ATR介导的DNA损伤反应的相互作用,以及这种相互作用对宿主基因组稳定性的影响。

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