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人类免疫缺陷病毒1型基因组5'前导区中的RNA结构与包装信号

RNA structure and packaging signals in the 5' leader region of the human immunodeficiency virus type 1 genome.

作者信息

Clever Jared L, Miranda Daniel, Parslow Tristram G

机构信息

Department of Pathology, University of California, San Francisco, San Francisco, California 94143-0511, USA.

出版信息

J Virol. 2002 Dec;76(23):12381-7. doi: 10.1128/jvi.76.23.12381-12387.2002.

Abstract

The leader region of the human immunodeficiency virus type 1 (HIV-1) genome has a highly folded structure, comprising at least two RNA stem-loops [the transactivation response (TAR) and poly(A) hairpins] near its 5' end and four others (SL1 to SL4) downstream. Each of these stem-loops contributes to the function of the HIV-1 packaging signal, which efficiently targets genomic RNA into nascent virions. The central 140-base region of the leader, which includes the U5 and primer binding site (PBS) sequences, is also believed to adopt a complex structure, but the nature of this structure and its possible role in RNA packaging have not been extensively explored. Here we report a mutational analysis identifying at least three separate loci within the U5-PBS region which, when mutated, impair both HIV-1 packaging specificity and infectivity in a single-round proviral assay. In common with those of all previously described packaging signals in the leader, the function of one of these loci appeared to depend on secondary structure rather than on sequence alone. By contrast, the activity of the other two loci did not correlate with any predicted conformations. Moreover, unlike SL1 to SL4, the TAR, poly(A), and U5-PBS hairpins were not bound with high affinity by the nucleocapsid portion of the HIV-1 Gag protein in vitro, implying that they contribute to packaging through a mechanism distinct from that of SL1 to SL4. Our findings confirm the existence and importance of secondary structure around the PBS and demonstrate that functional packaging signals are distributed across the entire HIV-1 leader.

摘要

人类免疫缺陷病毒1型(HIV-1)基因组的前导区具有高度折叠的结构,在其5'端附近至少包含两个RNA茎环[反式激活应答(TAR)和聚腺苷酸发夹],下游还有另外四个(SL1至SL4)。这些茎环中的每一个都对HIV-1包装信号的功能有贡献,该信号可有效地将基因组RNA靶向新生病毒粒子。前导区的中央140个碱基区域,包括U5和引物结合位点(PBS)序列,也被认为具有复杂的结构,但这种结构的性质及其在RNA包装中可能的作用尚未得到广泛研究。在这里,我们报告了一项突变分析,确定了U5-PBS区域内至少三个独立的位点,当这些位点发生突变时,在单轮前病毒检测中会损害HIV-1的包装特异性和感染性。与前导区中所有先前描述的包装信号一样,这些位点之一的功能似乎取决于二级结构而非仅取决于序列。相比之下,其他两个位点的活性与任何预测的构象均无相关性。此外,与SL1至SL4不同,TAR、聚腺苷酸和U5-PBS发夹在体外与HIV-1 Gag蛋白的核衣壳部分没有高亲和力结合,这意味着它们通过与SL1至SL4不同的机制促进包装。我们的研究结果证实了PBS周围二级结构的存在及其重要性,并表明功能性包装信号分布在整个HIV-1前导区。

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