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甲型流感病毒生成的小 RNA 调节转录到复制的转换。

Influenza A virus-generated small RNAs regulate the switch from transcription to replication.

机构信息

Microbiology Graduate School Training Program, Department of Microbiology, Mount Sinai School of Medicine, New York, NY 10029, USA.

出版信息

Proc Natl Acad Sci U S A. 2010 Jun 22;107(25):11525-30. doi: 10.1073/pnas.1001984107. Epub 2010 Jun 1.

Abstract

The discovery of regulatory small RNAs continues to reshape paradigms in both molecular biology and virology. Here we describe examples of influenza A virus-derived small viral RNAs (svRNAs). svRNAs are 22-27 nt in length and correspond to the 5' end of each of the viral genomic RNA (vRNA) segments. Expression of svRNA correlates with the accumulation of vRNA and a bias in RNA-dependent RNA polymerase (RdRp) activity from transcription toward genome replication. Synthesis of svRNA requires the RdRp, nucleoprotein and the nuclear export protein NS2. In addition, svRNA is detectable during replication of various influenza A virus subtypes across multiple host species and associates physically with the RdRp. We demonstrate that depletion of svRNA has a minimal impact on mRNA and complementary vRNA (cRNA) but results in a dramatic loss of vRNA in a segment-specific manner. We propose that svRNA triggers the viral switch from transcription to replication through interactions with the viral polymerase machinery. Taken together, the discovery of svRNA redefines the mechanistic switch of influenza virus transcription/replication and provides a potential target for broad-range, anti-influenza virus-based therapeutics.

摘要

调控小 RNA 的发现不断改变分子生物学和病毒学的范式。在这里,我们描述了甲型流感病毒衍生的小病毒 RNA(svRNA)的例子。svRNA 的长度为 22-27 个核苷酸,与每个病毒基因组 RNA(vRNA)片段的 5'端相对应。svRNA 的表达与 vRNA 的积累以及 RNA 依赖性 RNA 聚合酶(RdRp)活性从转录向基因组复制的偏向相关。svRNA 的合成需要 RdRp、核蛋白和核输出蛋白 NS2。此外,svRNA 在多种宿主物种中各种甲型流感病毒亚型的复制过程中均可检测到,并与 RdRp 物理结合。我们证明,svRNA 的耗竭对 mRNA 和互补 vRNA(cRNA)的影响很小,但会导致 vRNA 以特定片段的方式显著丢失。我们提出,svRNA 通过与病毒聚合酶机制相互作用触发病毒从转录到复制的转变。总之,svRNA 的发现重新定义了流感病毒转录/复制的机制开关,并为广谱抗流感病毒治疗提供了一个潜在的靶点。

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