Szilvay Anne Marie, Bøe Stig-Ove, Kalland Karl-Henning
Department of Molecular Biology1 and Centre for Research in Virology, Department of Microbiology and Immunology2, The Gade Institute, University of Bergen, HIB, Post-box 7800, N-5020 Bergen, Norway.
J Gen Virol. 1999 Aug;80 ( Pt 8):1965-1974. doi: 10.1099/0022-1317-80-8-1965.
Trans-dominant negative mutants of the human immunodeficiency virus type 1 (HIV-1) regulatory protein Rev inhibit the function of wild-type Rev in a dose-dependent manner. This was previously shown to be caused by nuclear retention of the wild-type protein. In the present work, further analysis of the trans-dominant negative effect was performed using cotransfection experiments with different constructs encoding HIV-1 Rev and viral structural proteins together with a plasmid encoding a trans-dominant negative Rev mutant. Thus, one species of pre-mRNA was transcribed from the reporter plasmids. This pre-mRNA was then either spliced or exported by Rev as unspliced RNA for translation of the HIV structural proteins. An immunofluorescence assay and Western blot analysis were used for analysis of protein expression. In situ hybridization was applied for labelling of unspliced mRNA in transfected cells, and RNase protection analysis was used to determine the relative amount of unspliced versus spliced mRNAs. The experiments confirmed that the transdominant negative mutant inhibited nuclear export of unspliced mRNA. It was, in addition, demonstrated for the first time that the trans-dominant negative mutant also affected a Rev-dependent regulatory step connected with viral pre-mRNA splicing. As a consequence, proteins expressed from unspliced and singly spliced HIV mRNAs decreased while there was an increase in protein products encoded by spliced and alternatively spliced mRNAs.
人类免疫缺陷病毒1型(HIV-1)调节蛋白Rev的反式显性负突变体以剂量依赖的方式抑制野生型Rev的功能。先前已证明这是由野生型蛋白的核滞留引起的。在本研究中,使用不同构建体进行共转染实验,这些构建体编码HIV-1 Rev和病毒结构蛋白,同时还使用了一个编码反式显性负Rev突变体的质粒,对反式显性负效应进行了进一步分析。因此,报告质粒转录出一种前体mRNA。然后,这种前体mRNA要么被剪接,要么由Rev作为未剪接的RNA输出,用于HIV结构蛋白的翻译。免疫荧光测定和蛋白质印迹分析用于分析蛋白质表达。原位杂交用于标记转染细胞中的未剪接mRNA,核糖核酸酶保护分析用于确定未剪接mRNA与剪接mRNA的相对量。实验证实,反式显性负突变体抑制了未剪接mRNA的核输出。此外,首次证明反式显性负突变体还影响了与病毒前体mRNA剪接相关的Rev依赖性调节步骤。结果,未剪接和单剪接的HIV mRNA表达的蛋白质减少,而剪接和可变剪接的mRNA编码的蛋白质产物增加。