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对脊髓灰质炎病毒的全球 RNA 结构分析鉴定出一个参与病毒复制和感染性的保守 RNA 结构。

Global RNA structure analysis of poliovirus identifies a conserved RNA structure involved in viral replication and infectivity.

机构信息

Tetrad Graduate Program, University of California, San Francisco, California, USA.

出版信息

J Virol. 2013 Nov;87(21):11670-83. doi: 10.1128/JVI.01560-13. Epub 2013 Aug 21.

Abstract

The genomes of RNA viruses often contain RNA structures that are crucial for translation and RNA replication and may play additional, uncharacterized roles during the viral replication cycle. For the picornavirus family member poliovirus, a number of functional RNA structures have been identified, but much of its genome, especially the open reading frame, has remained uncharacterized. We have now generated a global RNA structure map of the poliovirus genome using a chemical probing approach that interrogates RNA structure with single-nucleotide resolution. In combination with orthogonal evolutionary analyses, we uncover several conserved RNA structures in the open reading frame of the viral genome. To validate the ability of our global analyses to identify functionally important RNA structures, we further characterized one of the newly identified structures, located in the region encoding the RNA-dependent RNA polymerase, 3D(pol), by site-directed mutagenesis. Our results reveal that the structure is required for viral replication and infectivity, since synonymous mutants are defective in these processes. Furthermore, these defects can be partially suppressed by mutations in the viral protein 3C(pro), which suggests the existence of a novel functional interaction between an RNA structure in the 3D(pol)-coding region and the viral protein(s) 3C(pro) and/or its precursor 3CD(pro).

摘要

RNA 病毒的基因组通常包含对翻译和 RNA 复制至关重要的 RNA 结构,并且在病毒复制周期中可能发挥其他尚未确定的作用。对于小核糖核酸病毒科成员脊髓灰质炎病毒,已经鉴定出许多具有功能的 RNA 结构,但它的大部分基因组,特别是开放阅读框,仍然没有特征。我们现在使用化学探测方法生成了脊髓灰质炎病毒基因组的全局 RNA 结构图谱,该方法使用单核苷酸分辨率探测 RNA 结构。结合正交进化分析,我们在病毒基因组的开放阅读框中发现了几个保守的 RNA 结构。为了验证我们的全局分析识别功能重要的 RNA 结构的能力,我们进一步通过定点诱变对新鉴定的结构之一进行了表征,该结构位于编码 RNA 依赖性 RNA 聚合酶 3D(pol)的区域。我们的结果表明,该结构对于病毒复制和感染性是必需的,因为同义突变体在这些过程中存在缺陷。此外,这些缺陷可以部分被病毒蛋白 3C(pro)的突变所抑制,这表明在 3D(pol)编码区域中的 RNA 结构和病毒蛋白 3C(pro)及其前体 3CD(pro)之间存在新的功能相互作用。

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