Retroviral integration: Site matters: Mechanisms and consequences of retroviral integration site selection

被引:49
|
作者
Demeulemeester, Jonas [1 ,2 ,3 ]
De Rijck, Jan [1 ]
Gijsbers, Rik [2 ]
Debyser, Zeger [1 ]
机构
[1] KU Leuven Univ Leuven, Dept Pharmaceut & Pharmacol Sci, Lab Mol Virol & Drug Discovery, Leuven, Belgium
[2] KU Leuven Univ Leuven, Dept Pharmaceut & Pharmacol Sci, Lab Viral Vector Technol & Gene Therapy, Leuven, Belgium
[3] KU Leuven Univ Leuven, Dept Chem, Lab Biomol Modeling, Leuven, Belgium
基金
比利时弗兰德研究基金会;
关键词
cofactor; HIV-1; integration; latency; MLV; retrovirus; viral vector; HUMAN-IMMUNODEFICIENCY-VIRUS; HIV-1 PREINTEGRATION COMPLEXES; TRANSCRIPTION START SITES; HUMAN GENOME; NUCLEAR-PORE; STRUCTURAL BASIS; DNA INTEGRATION; GENE-EXPRESSION; CHROMATIN BINDING; CLONAL EXPANSION;
D O I
10.1002/bies.201500051
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
Here, we review genomic target site selection during retroviral integration as a multistep process in which specific biases are introduced at each level. The first asymmetries are introduced when the virus takes a specific route into the nucleus. Next, by co-opting distinct host cofactors, the integration machinery is guided to particular chromatin contexts. As the viral integrase captures a local target nucleosome, specific contacts introduce fine-grained biases in the integration site distribution. In vivo, the established population of proviruses is subject to both positive and negative selection, thereby continuously reshaping the integration site distribution. By affecting stochastic proviral expression as well as the mutagenic potential of the virus, integration site choice may be an inherent part of the evolutionary strategies used by different retroviruses to maximise reproductive success.
引用
收藏
页码:1202 / 1214
页数:13
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