Lévesque Kathy, Halvorsen Melanie, Abrahamyan Levon, Chatel-Chaix Laurent, Poupon Viviane, Gordon Heather, DesGroseillers Luc, Gatignol Anne, Mouland Andrew J
HIV-1 RNA Trafficking Laboratory, 3755 Côte-Ste-Catherine Road, Montréal, Québec, Canada H3T 1E2.
Traffic. 2006 Sep;7(9):1177-93. doi: 10.1111/j.1600-0854.2006.00461.x.
Few details are known about how the human immunodeficiency virus type 1 (HIV-1) genomic RNA is trafficked in the cytoplasm. Part of this process is controlled by the activity of heterogeneous nuclear ribonucleoprotein A2 (hnRNP A2). The role of hnRNP A2 during the expression of a bona fide provirus in HeLa cells is investigated in this study. Using immunofluorescence and fluorescence in situ hybridization techniques, we show that knockdown of hnRNP A2 expression in HIV-1-expressing cells results in the rapid accumulation of HIV-1 genomic RNA in a distinct, cytoplasmic space that corresponds to the microtubule-organizing center (MTOC). The RNA exits in the nucleus and accumulates at the MTOC region as a result of hnRNP A2 knockdown even during the expression of a provirus harboring mutations in the hnRNP A2-response element (A2RE), the expression of which results in nuclear retention of genomic RNA. We also demonstrate that hnRNP A2 expression is required for downstream trafficking of genomic RNA from the MTOC in the cytoplasm. Genomic RNA localization at the MTOC that was both the result of hnRNP A2 knockdown and the overexpression of Rab7-interacting lysosomal protein had little effect on pr55Gag synthesis but negatively influenced virus production and infectivity. These data indicate that altered HIV-1 genomic RNA localization modulates viral assembly and that the MTOC serves as a central site to which HIV-1 genomic RNA converges following its exit from the nucleus, with the host protein, hnRNP A2, playing a central role in taking it to and from this site in the cell.
关于1型人类免疫缺陷病毒(HIV-1)基因组RNA在细胞质中的运输方式,目前所知细节甚少。这一过程的部分环节受异质性核糖核蛋白A2(hnRNP A2)活性的控制。本研究调查了hnRNP A2在HeLa细胞中真正的原病毒表达过程中的作用。利用免疫荧光和荧光原位杂交技术,我们发现,在表达HIV-1的细胞中敲低hnRNP A2的表达会导致HIV-1基因组RNA在一个与微管组织中心(MTOC)相对应的独特细胞质空间中迅速积累。即使在含有hnRNP A2反应元件(A2RE)突变的原病毒表达过程中,由于hnRNP A2被敲低,RNA仍会从细胞核中排出并在MTOC区域积累,而A2RE的表达会导致基因组RNA滞留于细胞核。我们还证明,hnRNP A2的表达对于基因组RNA从细胞质中的MTOC进行下游运输是必需的。由hnRNP A2敲低和Rab7相互作用溶酶体蛋白过表达导致的基因组RNA在MTOC处的定位,对pr55Gag的合成影响不大,但对病毒产生和感染性有负面影响。这些数据表明,HIV-1基因组RNA定位的改变会调节病毒组装,并且MTOC是HIV-1基因组RNA从细胞核排出后汇聚的中心位点,宿主蛋白hnRNP A2在将其带入和带出细胞内该位点的过程中发挥着核心作用。