Multiple APOBEC3 Restriction Factors for HIV-1 and One Vif to Rule Them All

被引:162
作者
Desimmie, Belete A. [1 ]
Delviks-Frankenberrry, Krista A. [1 ]
Burdick, Ryan C. [1 ]
Qi, DongFei [1 ]
Izumi, Taisuke [1 ]
Pathak, Vinay K. [1 ]
机构
[1] NCI, Viral Mutat Sect, HIV Drug Resistance Program, Frederick, MD 21702 USA
关键词
APOBEC3G; APOBEC3F; APOBEC3H; Vif; restriction factor; HUMAN-IMMUNODEFICIENCY-VIRUS; SINGLE AMINO-ACID; RNA-EDITING ENZYME; CD4(+) T-CELLS; ACTIVATION-INDUCED DEAMINASE; APOBEC3G-CATALYZED PROCESSIVE DEAMINATION; ANTIVIRAL PROTEIN APOBEC3G; VIRAL INFECTIVITY FACTOR; DNA CYTIDINE DEAMINASE; MURINE LEUKEMIA-VIRUS;
D O I
10.1016/j.jmb.2013.10.033
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
Several members of the APOBEC3 family of cellular restriction factors provide intrinsic immunity to the host against viral infection. Specifically, APOBEC3DE, APOBEC3F, APOBEC3G, and APOBEC3H haplotypes II, V, and VII provide protection against HIV-1 Delta vif through hypermutation of the viral genome, inhibition of reverse transcription, and inhibition of viral DNA integration into the host genome. HIV-1 counteracts APOBEC3 proteins by encoding the viral protein Vif, which contains distinct domains that specifically interact with these APOBEC3 proteins to ensure their proteasomal degradation, allowing virus replication to proceed. Here, we review our current understanding of APOBEC3 structure, editing and non-editing mechanisms of APOBEC3-mediated restriction, Vif-APOBEC3 interactions that trigger APOBEC3 degradation, and the contribution of APOBEC3 proteins to restriction and control of HIV-1 replication in infected patients. Published by Elsevier Ltd.
引用
收藏
页码:1220 / 1245
页数:26
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