Pokeweed antiviral protein restores levels of cellular APOBEC3G during HIV-1 infection by depurinating Vif mRNA

被引:5
作者
Krivdova, Gabriela [1 ]
Hudak, Katalin A. [1 ]
机构
[1] York Univ, Dept Biol, Toronto, ON M3J 1P3, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Pokeweed antiviral protein; RNA glycosidase; HIV-1; Vif; APOBEC3G; Ribosome-inactivating protein; VIRUS; DEGRADATION; CEM15;
D O I
10.1016/j.antiviral.2015.08.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Pokeweed antiviral protein (PAP) is an RNA glycosidase that inhibits production of human immunodeficiency virus type 1 (HIV-1) when expressed in human culture cells. Previously, we showed that the expression of PAP reduced the levels of several viral proteins, including virion infectivity factor (Vif). However, the mechanism causing Vif reduction and the consequences of the inhibition were not determined. Here we show that the Vif mRNA is directly depurinated by PAP. Because of depurination at two specific sites within the Vif ORF, Vif levels decrease during infections and the progeny viruses that are generated are similar to 10-fold less infectious and compromised for proviral integration. These results are consistent with PAP activity inhibiting translation of Vif, which in turn reduces the effect of Vif to inactivate the host restriction factor APOBEC3G (apolipoprotein B mRNA-editing enzyme, catalytic polypeptide-like editing complex 3G). Our findings identify Vif mRNA as a new substrate for PAP and demonstrate that derepression of innate immunity against HIV-1 contributes to its antiviral activity. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:51 / 54
页数:4
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