Changing the ubiquitin landscape during viral manipulation of the DNA damage response

被引:17
|
作者
Weitzman, Matthew D. [1 ]
Lilley, Caroline E. [1 ]
Chaurushiya, Mira S. [1 ,2 ]
机构
[1] Salk Inst Biol Studies, Genet Lab, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, Grad Program, Div Biol, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
Ubiquitin; Ubiquitin ligase; DNA damage; DNA repair; Virus infection; ANAPHASE-PROMOTING-COMPLEX; PAPILLOMAVIRUS TYPE-16 E7; REGULATORY PROTEIN ICP0; RETINOBLASTOMA TUMOR-SUPPRESSOR; HUMAN CYTOMEGALOVIRUS-INFECTION; E1B 55-KILODALTON PROTEIN; SIMPLEX-VIRUS GENOME; DOUBLE-STRAND BREAKS; EPSTEIN-BARR-VIRUS; ADENOVIRUS E4 34K;
D O I
10.1016/j.febslet.2011.04.049
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Viruses often induce signaling through the same cellular cascades that are activated by damage to the cellular genome. Signaling triggered by viral proteins or exogenous DNA delivered by viruses can be beneficial or detrimental to viral infection. Viruses have therefore evolved to dissect the cellular DNA damage response pathway during infection, often marking key cellular regulators with ubiquitin to induce their degradation or change their function. Signaling controlled by ubiquitin or ubiquitin-like proteins has recently emerged as key regulator of the cellular DNA damage response. Situated at the interface between DNA damage signaling and the ubiquitin system, viruses can reveal key convergence points in this important cellular pathway. In this review, we examine how viruses harness the diversity of the cellular ubiquitin system to modulate the DNA damage signaling pathway. We discuss the implications of viral infiltration of this pathway for both the transcriptional program of the virus and for the cellular response to DNA damage. (C) 2011 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2897 / 2906
页数:10
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