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人类免疫缺陷病毒1型Tat依赖的对停滞的RNA聚合酶II延伸复合物的激活。

Human immunodeficiency virus type 1 Tat-dependent activation of an arrested RNA polymerase II elongation complex.

作者信息

Liu Y, Suñé C, Garcia-Blanco M A

机构信息

Levine Science Research Center, Duke University Medical Center, Durham, North Carolina, 27710, USA.

出版信息

Virology. 1999 Mar 15;255(2):337-46. doi: 10.1006/viro.1998.9585.

Abstract

The human immunodeficiency virus type 1 (HIV-1) Tat protein is a transcriptional activator that is essential for efficient viral gene expression and replication. Tat increases the level of full-length transcripts from the HIV-1 promoter by dramatically enhancing the elongation efficiency of the RNA polymerase II complexes assembled on this promoter. Tat could potentially activate the transcription machinery during initiation, elongation, or both. We used an immobilized HIV-1 promoter template with a reversible lac repressor (LacR) elongation block inserted downstream to dissect the stages in transcription affected by Tat. Transcription complexes assembled in the absence of Tat and blocked by LacR cannot be activated by incubation with Tat alone. These complexes can, however, be activated if Tat is added in combination with cellular factors. In this system, Tat also promoted the assembly of preinitiation complexes capable of elongating efficiently, suggesting that Tat can associate with transcription complex at an early stage. These data indicate that Tat can activate elongation of RNA polymerase by modifying an already elongating transcription complex. The data also suggest the possibility that Tat can interact with initiation complexes.

摘要

人类免疫缺陷病毒1型(HIV-1)反式激活因子(Tat)蛋白是一种转录激活因子,对有效的病毒基因表达和复制至关重要。Tat通过显著提高组装在该启动子上的RNA聚合酶II复合物的延伸效率,增加了HIV-1启动子全长转录本的水平。Tat可能在起始、延伸或两者过程中激活转录机制。我们使用了一个固定化的HIV-1启动子模板,在其下游插入了一个可逆的乳糖阻遏蛋白(LacR)延伸阻断序列,以剖析受Tat影响的转录阶段。在没有Tat的情况下组装并被LacR阻断的转录复合物,仅与Tat孵育不能被激活。然而,如果将Tat与细胞因子一起添加,这些复合物可以被激活。在这个系统中,Tat还促进了能够有效延伸的起始前复合物的组装,这表明Tat可以在早期阶段与转录复合物结合。这些数据表明,Tat可以通过修饰已经在延伸的转录复合物来激活RNA聚合酶的延伸。数据还提示Tat可能与起始复合物相互作用的可能性。

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