Anderson Jenny L, Hope Thomas J
Department of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Virology. 2008 May 25;375(1):1-12. doi: 10.1016/j.virol.2008.01.042. Epub 2008 Mar 4.
Cellular APOBEC3G (A3G) protein is packaged into human immunodeficiency virus type 1 (HIV-1) virions in producer cells yet restricts viral replication in target cells. To characterize this restriction in target cells, the effect of A3G on generating various HIV-1 cDNA products was measured by quantitative real-time PCR. A3G decreased cDNA products from Vif-deficient HIV-1, with minor effects on early reverse transcripts and larger declines in late reverse transcripts. However, the greatest decline was typically observed in nuclear 2-LTR circles. Moreover, the magnitude of these declines varied with A3G dose. Adding integration inhibitor did not stop the A3G-mediated loss in 2-LTR circles. Moreover, obstructing HIV-1 nuclear entry using vesicular stomatitis virus matrix protein did not stop the A3G-mediated decline in late reverse transcripts. Collectively, these data suggest that A3G has important restriction activity in the cytoplasm and progressively diminishes viral cytoplasmic and nuclear cDNA forms with increasing magnitude during restriction.
细胞载脂蛋白B mRNA编辑酶催化多肽样蛋白3G(APOBEC3G)在病毒产生细胞中被包装进1型人类免疫缺陷病毒(HIV-1)病毒粒子,但在靶细胞中限制病毒复制。为了在靶细胞中表征这种限制作用,通过定量实时PCR测定了APOBEC3G对产生各种HIV-1 cDNA产物的影响。APOBEC3G减少了来自Vif缺陷型HIV-1的cDNA产物,对早期逆转录产物影响较小,对晚期逆转录产物的减少幅度更大。然而,通常在核内2-LTR环中观察到最大程度的减少。此外,这些减少的程度随APOBEC3G剂量而变化。添加整合抑制剂并不能阻止APOBEC3G介导的2-LTR环的损失。此外,使用水泡性口炎病毒基质蛋白阻碍HIV-1核进入并不能阻止APOBEC3G介导的晚期逆转录产物的减少。总体而言,这些数据表明APOBEC3G在细胞质中具有重要的限制活性,并且在限制过程中随着程度的增加逐渐减少病毒的细胞质和核cDNA形式。