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非分段负义 RNA 病毒——结构数据为核衣壳组装带来新的见解。

Nonsegmented Negative-Sense RNA Viruses-Structural Data Bring New Insights Into Nucleocapsid Assembly.

机构信息

Institut de Biologie Structurale (IBS), CEA, CNRS, University Grenoble Alpes, Grenoble, France.

Institut de Biologie Structurale (IBS), CEA, CNRS, University Grenoble Alpes, Grenoble, France.

出版信息

Adv Virus Res. 2017;97:143-185. doi: 10.1016/bs.aivir.2016.09.001. Epub 2016 Oct 5.

DOI:10.1016/bs.aivir.2016.09.001
PMID:28057258
Abstract

Viruses with a nonsegmented negative-sense RNA genome (NNVs) include important human pathogens as well as life-threatening zoonotic viruses. These viruses share a common RNA replication complex, including the genomic RNA and three proteins, the nucleoprotein (N), the phosphoprotein (P), and the RNA-dependent RNA polymerase (L). During genome replication, the RNA polymerase complex first synthesizes positive-sense antigenomes, which in turn serve as template for the production of negative-sense progeny genomes. These newly synthesized antigenomic and genomic RNAs must be encapsidated by N, and the source of soluble, RNA-free N, competent for the encapsidation is a complex between N and P, named the N-P complex. In this review, we summarize recent progress made in the structural characterization of the different components of this peculiar RNA polymerase machinery. We discuss common features and replication strategies and highlight idiosyncrasies encountered in different viruses, along with the key role of the dual ordered/disordered architecture of protein components and the dynamics of the viral polymerase machinery. In particular, we focus on the N-P complex and its role in the nucleocapsid assembly process. These new results provide evidence that the mechanism of NC assembly is conserved between the different families and thus support a divergent evolution from a common ancestor. In addition, the successful inhibition of infection due to different NNVs by peptides derived from P suggests that the mechanism of NC assembly is a potential target for antiviral development.

摘要

具有不分节负义 RNA 基因组(NNV)的病毒包括重要的人类病原体以及危及生命的人畜共患病病毒。这些病毒共享一个共同的 RNA 复制复合物,包括基因组 RNA 和三种蛋白质,核蛋白(N)、磷蛋白(P)和 RNA 依赖性 RNA 聚合酶(L)。在基因组复制过程中,RNA 聚合酶复合物首先合成正义抗原基因组,然后作为负义亲代基因组产生的模板。这些新合成的抗原和基因组 RNA 必须由 N 包裹,并且能够用于包装的可溶性、无 RNA 的 N 的来源是 N 和 P 之间的复合物,称为 N-P 复合物。在这篇综述中,我们总结了最近在这个特殊 RNA 聚合酶机制的不同成分的结构特征方面取得的进展。我们讨论了常见的特征和复制策略,并强调了不同病毒中遇到的特殊性,以及蛋白质成分的双重有序/无序结构和病毒聚合酶机制的动态的关键作用。特别是,我们重点介绍了 N-P 复合物及其在核衣壳组装过程中的作用。这些新结果提供了证据,表明 NC 组装的机制在不同家族之间是保守的,因此支持从共同祖先的分歧进化。此外,由于来自 P 的肽,不同 NNV 对感染的成功抑制表明 NC 组装的机制是抗病毒开发的潜在靶点。

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