Department of Molecular and Medical Virology, Ruhr University Bochum, Universitätsstraße 150, D-44780 Bochum, Germany.
J Gen Virol. 2010 Aug;91(Pt 8):1893-1897. doi: 10.1099/vir.0.022509-0. Epub 2010 Jun 9.
The Rev protein of human immunodeficiency viruses (HIV) has long been recognized to be essential for the late phase of the virus replication cycle, due to its strong enhancement of expression of viral structural proteins. Surprisingly, a number of recent papers have demonstrated that Rev can also interfere with integration of the reverse-transcribed cDNA into the host-cell genome. This seems to be due to Rev's binding to integrase and LEDGF/p75, an important cellular cofactor of HIV-1 integration. As Rev is presumably expressed at sufficiently high levels only after the encoding genome has already integrated, the main function of Rev during the early phase might be to reduce genotoxicity due to excessive integration events after superinfection of the same cell by subsequent viruses. Other potential consequences for HIV-1 replication and evolution after co-infection of the same cell with two viruses are discussed.
人类免疫缺陷病毒(HIV)的 Rev 蛋白因其能强烈增强病毒结构蛋白的表达,长期以来一直被认为是病毒复制周期晚期所必需的。令人惊讶的是,最近有一些论文表明 Rev 还可以干扰逆转录 cDNA 整合到宿主细胞基因组中。这似乎是由于 Rev 与整合酶和 LEDGF/p75 的结合,后者是 HIV-1 整合的一个重要的细胞辅助因子。由于 Rev 大概只在编码基因组已经整合后才以足够高的水平表达,因此在同一细胞被随后的病毒超感染后,Rev 在早期阶段的主要功能可能是减少由于过多的整合事件而导致的遗传毒性。讨论了同一细胞被两种病毒共同感染后对 HIV-1 复制和进化的其他潜在影响。