Weichselbraun I, Farrington G K, Rusche J R, Böhnlein E, Hauber J
SANDOZ Research Institute, Vienna, Austria.
J Virol. 1992 Apr;66(4):2583-7. doi: 10.1128/JVI.66.4.2583-2587.1992.
The human retroviruses human immunodeficiency virus type 1 (HIV-1) and human T-cell leukemia virus type I (HTLV-I) are characterized by complex regulation of gene expression. Each virus encodes a posttranscriptional regulator, the 19-kDa HIV-1 Rev protein and the 27-kDa HTLV-I Rex protein, which is required for viral replication. Expression of these trans activators results in the cytoplasmic accumulation of unspliced or singly spliced viral mRNA which encode the gag, pol, and env gene products. The finding that the HTLV-I Rex protein is able to functionally substitute for the Rev protein of HIV-1 indicates that HIV-1 Rev and HTLV-I Rex may interact with the same component of a cellular pathway involved in either mRNA splicing or transport. In this study, we have generated functional Rev/Rex hybrid proteins by domain exchange. We have defined, using in vivo and in vitro analyses, the activation domains of Rev and Rex which are the putative targets of a common host cell factor(s) required for Rev and Rex function.
人类逆转录病毒1型人类免疫缺陷病毒(HIV-1)和1型人类T细胞白血病病毒(HTLV-I)的特征在于基因表达的复杂调控。每种病毒都编码一种转录后调节因子,即19 kDa的HIV-1 Rev蛋白和27 kDa的HTLV-I Rex蛋白,它们是病毒复制所必需的。这些反式激活因子的表达导致未剪接或单剪接的病毒mRNA在细胞质中积累,这些mRNA编码gag、pol和env基因产物。HTLV-I Rex蛋白能够在功能上替代HIV-1的Rev蛋白这一发现表明,HIV-1 Rev和HTLV-I Rex可能与参与mRNA剪接或转运的细胞途径的同一成分相互作用。在本研究中,我们通过结构域交换产生了功能性Rev/Rex杂交蛋白。我们利用体内和体外分析确定了Rev和Rex的激活结构域,它们是Rev和Rex功能所需的共同宿主细胞因子的假定靶点。