Mougel Marylène, Houzet Laurent, Darlix Jean-Luc
LaboRetro, Unité de virologie humaine INSERM U758, IFR128, ENS, 46 allée d'Italie, Lyon, France.
Retrovirology. 2009 Mar 4;6:24. doi: 10.1186/1742-4690-6-24.
Upon cell infection by a retrovirus, the viral DNA polymerase, called reverse transcriptase (RT), copies the genomic RNA to generate the proviral DNA flanked by two long terminal repeats (LTR). A discovery twenty years ago demonstrated that the structural viral nucleocapsid protein (NC) encoded by Gag is an essential cofactor of reverse transcription, chaperoning RT during viral DNA synthesis. However, it is only recently that NC was found to exert a control on the timing of reverse transcription, in a spatio-temporal manner. This brief review summarizes findings on the timing of reverse transcription in wild type HIV-1 and in nucleopcapsid (NC) mutants where virions contain a large amount of newly made viral DNA. This brief review also proposes some explanations of how NC may control late reverse transcription during Gag assembly in virus producer cells.
当细胞被逆转录病毒感染时,被称为逆转录酶(RT)的病毒DNA聚合酶会将基因组RNA进行复制,以生成两侧带有两个长末端重复序列(LTR)的前病毒DNA。二十年前的一项发现表明,由Gag编码的病毒结构核衣壳蛋白(NC)是逆转录过程中必不可少的辅助因子,在病毒DNA合成过程中陪伴逆转录酶。然而,直到最近才发现NC以时空方式对逆转录的时间进行控制。这篇简短的综述总结了关于野生型HIV-1和核衣壳(NC)突变体中逆转录时间的研究结果,在这些突变体中,病毒粒子含有大量新合成的病毒DNA。这篇简短的综述还对NC在病毒产生细胞中Gag组装过程中如何控制晚期逆转录提出了一些解释。