Epigenetic Regulation of Viral Biological Processes

被引:44
作者
Balakrishnan, Lata [1 ]
Milavetz, Barry [2 ]
机构
[1] Indiana Univ Purdue Univ, Dept Biol, Indianapolis, IN 46202 USA
[2] Univ North Dakota, Dept Biomed Sci, Sch Med & Hlth Sci, Grand Forks, ND 58203 USA
来源
VIRUSES-BASEL | 2017年 / 9卷 / 11期
基金
美国国家卫生研究院;
关键词
epigenetic; DNA virus; regulation; gene expression; histone modifications; nucleosomes; DNA methylation; ChIP-Seq; latency; RNA-POLYMERASE-II; SARCOMA-ASSOCIATED HERPESVIRUS; VIRUS X PROTEIN; SV40; MINICHROMOSOMES; HISTONE ACETYLATION; TRANSCRIPTIONAL REPRESSION; HUMAN PAPILLOMAVIRUSES; LYSINE-9; METHYLATION; POLYOMAVIRUS JC; DNA METHYLATION;
D O I
10.3390/v9110346
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
It is increasingly clear that DNA viruses exploit cellular epigenetic processes to control their life cycles during infection. This review will address epigenetic regulation in members of the polyomaviruses, adenoviruses, human papillomaviruses, hepatitis B, and herpes viruses. For each type of virus, what is known about the roles of DNA methylation, histone modifications, nucleosome positioning, and regulatory RNA in epigenetic regulation of the virus infection will be discussed. The mechanisms used by certain viruses to dysregulate the host cell through manipulation of epigenetic processes and the role of cellular cofactors such as BRD4 that are known to be involved in epigenetic regulation of host cell pathways will also be covered. Specifically, this review will focus on the role of epigenetic regulation in maintaining viral episomes through the generation of chromatin, temporally controlling transcription from viral genes during the course of an infection, regulating latency and the switch to a lytic infection, and global dysregulation of cellular function.
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页数:14
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