RNA-sequence-mediated gene regulation in HIV-1.

Infectious agents and disease Pub Date : 1994-04-01
B R Cullen
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Abstract

The quantity and quality of human immunodeficiency virus type 1 (HIV-1) gene expression is controlled in large part by the action of two small nuclear viral regulatory proteins termed Tat and Rev. Tat is unique among transcriptional trans-activators in that it acts via a structured RNA target sequence, termed TAR, to induce high levels of transcription from the HIV-1 long terminal repeat promoter element. The activity of the viral Rev protein is also unprecedented in that this protein functions to induce the nuclear export of a specific class of viral RNA species that are otherwise sequestered in the nucleus by the action of cellular factors. Like Tat, Rev also interacts with a highly specific cis-acting target sequence termed, in this case, the Rev Response Element. In this review, I provide an outline of our current understanding of the roles and mechanisms of action of these two novel RNA-sequence-dependent regulatory proteins.

rna序列介导的HIV-1基因调控。
人类免疫缺陷病毒1型(HIV-1)基因表达的数量和质量在很大程度上受两种小核病毒调节蛋白Tat和rev的作用控制。Tat在转录反式激活因子中是独一无二的,因为它通过称为TAR的结构化RNA靶序列起作用,诱导HIV-1长末端重复启动子元件的高水平转录。病毒Rev蛋白的活性也是前所未有的,因为这种蛋白的功能是诱导细胞核输出特定类别的病毒RNA物种,否则这些RNA物种会被细胞因子的作用隔离在细胞核中。与Tat一样,Rev也与高度特异性的顺式作用靶序列相互作用,在这种情况下称为Rev响应元件。在这篇综述中,我概述了我们目前对这两种新的rna序列依赖性调节蛋白的作用和作用机制的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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