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人类免疫缺陷病毒2型Tat反式激活因子的功能分析。

Functional analysis of the Tat trans activator of human immunodeficiency virus type 2.

作者信息

Fenrick R, Malim M H, Hauber J, Le S Y, Maizel J, Cullen B R

机构信息

Howard Hughes Medical Institute, Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710.

出版信息

J Virol. 1989 Dec;63(12):5006-12. doi: 10.1128/JVI.63.12.5006-5012.1989.

Abstract

The trans-activator (Tat) proteins of the related but distinct type 1 and type 2 human immunodeficiency viruses (HIV-1 and HIV-2) display incomplete functional reciprocity. One possible explanation of this observation, suggested by computer analysis of potential RNA secondary structures within the viral trans-activation response (TAR) elements, is that HIV-2 Tat requires the presentation of two viral RNA stem-loop sequences for full activity whereas HIV-1 Tat is maximally active upon presentation of a single stem-loop structure. Here, we demonstrate that the HIV-2 long terminal repeat indeed contains two functionally independent TAR elements. However, the second (3') TAR element of HIV-2 is significantly less active than the 5' TAR element and is functionally masked in the context of an intact HIV-2 long terminal repeat. Evidence is presented suggesting that the activities of these two HIV-2 TAR elements reflect, at least in part, their relative distances from the site of transcription initiation. Although the HIV-2 TAR element proximal to the viral mRNA cap site appears to be sufficient for effective trans activation by HIV-2 Tat in vitro, this functional redundancy may nevertheless serve to enhance HIV-2 replication in infected cells in vivo.

摘要

密切相关但又有所不同的1型和2型人类免疫缺陷病毒(HIV-1和HIV-2)的反式激活蛋白(Tat)表现出不完全的功能对等性。对病毒反式激活应答(TAR)元件内潜在RNA二级结构进行计算机分析后提出的这一观察结果的一种可能解释是,HIV-2 Tat需要呈现两个病毒RNA茎环序列才能完全发挥活性,而HIV-1 Tat在呈现单个茎环结构时活性最高。在此,我们证明HIV-2长末端重复序列确实包含两个功能独立的TAR元件。然而,HIV-2的第二个(3')TAR元件的活性明显低于5' TAR元件,并且在完整的HIV-2长末端重复序列背景下其功能被掩盖。有证据表明,这两个HIV-2 TAR元件的活性至少部分反映了它们与转录起始位点的相对距离。尽管靠近病毒mRNA帽位点的HIV-2 TAR元件在体外似乎足以被HIV-2 Tat有效反式激活,但这种功能冗余可能仍有助于增强HIV-2在体内感染细胞中的复制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c7f/251160/cfdc51149758/jvirol00079-0030-a.jpg

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