Zapp M L, Green M R
Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, Massachusetts 02138.
Nature. 1989 Dec 7;342(6250):714-6. doi: 10.1038/342714a0.
The human immunodeficiency virus type 1 (HIV-1) Rev protein acts post-transcriptionally to increase the amounts of the viral gag-pol and env messenger RNAs in the cytoplasm of infected cells. The mechanism of Rev action is uncertain. Possibilities include an accelerating effect on the rate of export of its mRNA targets from the nucleus and/or modulation of the splicing of pre-mRNAs. Both the gag-pol and env mRNAs contain a sequence that is required for responsiveness to Rev--the Rev responsive element, RRE. Here we show that Rev is a sequence-specific binding protein, whose binding site is the RRE. This information should help to clarify the mechanism by which Rev acts.
1型人类免疫缺陷病毒(HIV-1)的Rev蛋白在转录后发挥作用,增加受感染细胞胞质中病毒gag-pol和env信使核糖核酸(mRNA)的量。Rev作用的机制尚不清楚。可能的机制包括对其mRNA靶标从细胞核输出速率的加速作用和/或对前体mRNA剪接的调节。gag-pol和env mRNA都含有一个对Rev反应所必需的序列——Rev反应元件(RRE)。我们在此表明,Rev是一种序列特异性结合蛋白,其结合位点是RRE。这一信息应有助于阐明Rev发挥作用的机制。