Epigenetic regulation of HIV-1 transcription

被引:1
作者
Tripathy, Manoj Kumar [1 ]
Abbas, Wasim [1 ]
Herbein, Georges [1 ]
机构
[1] Univ Franche Comte, Dept Virol, CHU Besancon, EA4266,INSERM IFR133, F-25030 Besancon, France
关键词
HIV; latency; transcription; IMMUNODEFICIENCY-VIRUS TYPE-1; NF-KAPPA-B; RNA-POLYMERASE-II; LONG TERMINAL REPEAT; HISTONE LYSINE METHYLATION; CHROMATIN-MODIFYING ENZYMES; DOMAIN-CONTAINING PROTEINS; T-CELL-ACTIVATION; HUMAN-FACTORS YY1; GENE-EXPRESSION;
D O I
10.2217/EPI.11.61
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
After entry into the target cell and reverse transcription, HIV-1 genes are integrated into the host genome. It is now well established that the viral promoter activity is directly governed by its chromatin environment. Nuc-1, a nucleosome located immediately downstream of the HIV-1 transcriptional initiation site directly impedes long-terminal repeat (LTR) activity. Epigenetic modifications and disruption of Nuc-1 are a prerequisite to the activation of LTR-driven transcription and viral expression. The compaction of chromatin and its permissiveness for transcription are directly dependent on the post-translational modifications of histones such as acetylation, methylation, phosphorylation and ubiquitination. Understanding the molecular mechanisms underlying HIV-1 transcriptional silencing and activation is thus a major challenge in the fight against AIDS and will certainly lead to new therapeutic tools.
引用
收藏
页码:487 / 502
页数:16
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