APOBEC3G inhibits DNA strand transfer during HIV-1 reverse transcription

被引:131
作者
Li, Xiao-Yu
Guo, Fei
Zhang, Li
Kleiman, Lawrence
Cen, Shan
机构
[1] McGill Univ, Jewish Gen Hosp, Lady Davis Inst Med Res, Montreal, PQ H3T 1E2, Canada
[2] McGill Univ, Jewish Gen Hosp, McGill AIDS Ctr, Montreal, PQ H3T 1E2, Canada
[3] McGill Univ, Dept Med, Montreal, PQ H3T 1E2, Canada
[4] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ H3T 1E2, Canada
[5] Chinese Acad Med Sci, Dept Virol, Inst Med Biotechnol, Beijing 100050, Peoples R China
关键词
D O I
10.1074/jbc.M703423200
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
Human APOBEC3G ( hA3G) has been identified as an anti-HIV-1 host factor. The presence of hA3G in HIV-1 strongly inhibits the ability of the virus to produce new viral DNA upon infection. In this report, we demonstrate that the reduction of late viral DNA synthesis is due to the inhibition by hA3G of the strand transfer steps that occur during reverse transcription. Analysis of viral cDNA intermediates in vivo reveals that hA3G causes an inhibition of the minus and plus strand transfers, without having a significant impact on DNA elongation. Using an in vitro system to measure minus strand transfer similarly shows a dose-dependent reduction of strand transfer by hA3G. This inhibition of strand transfer occurs independently the editing activity of hA3G and is correlated with its ability to prevent RNaseH degradation of the template RNA.
引用
收藏
页码:32065 / 32074
页数:10
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