Viruses and the DNA Damage Response: Activation and Antagonism

被引:95
|
作者
Luftig, Micah A. [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Ctr Virol, Durham, NC 27710 USA
来源
关键词
DNA damage response; virus replication; DNA repair; cell cycle checkpoints; cancer; viral genomes; DOUBLE-STRAND BREAKS; TIP60 HISTONE ACETYLTRANSFERASE; CHECKPOINT SIGNAL-TRANSDUCTION; TELANGIECTASIA-MUTATED KINASE; PROMOTES GENOMIC INSTABILITY; HUMAN-PAPILLOMAVIRUS TYPE-16; NUCLEAR DOMAIN 10; REACTIVE OXYGEN; REPLICATION COMPARTMENTS; REPAIR PROTEINS;
D O I
10.1146/annurev-virology-031413-085548
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Viruses must interact with their hosts in order to replicate; these interactions often provoke the evolutionarily conserved response to DNA damage, known as the DNA damage response (DDR). The DDR can be activated by incoming viral DNA, during the integration of retroviruses, or in response to the aberrant DNA structures generated upon replication of DNA viruses. Furthermore, DNA and RNA viral proteins can induce the DDR by promoting inappropriate S phase entry, by modifying cellular DDR factors directly, or by unintentionally targeting host DNA. The DDR may be antiviral, although viruses often require proximal DDR activation of repair and recombination factors to facilitate replication as well as downstream DDR signaling suppression to ensure cell survival. An unintended consequence of DDR attenuation during infection is the long-term survival and proliferation of precancerous cells. Therefore, the molecular basis for DDR activation and attenuation by viruses remains an important area of study that will likely provide key insights into how viruses have evolved with their hosts.
引用
收藏
页码:605 / 625
页数:21
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