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黄病毒RNA复制酶复合体的组织形式。

Organization of the Flavivirus RNA replicase complex.

作者信息

Brand Carolin, Bisaillon Martin, Geiss Brian J

机构信息

Département de Biochimie, Faculté de Médecine et des Sciences de la Santé, Université de Sherbrooke, Sherbrooke, QC, Canada.

Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA.

出版信息

Wiley Interdiscip Rev RNA. 2017 Nov;8(6). doi: 10.1002/wrna.1437. Epub 2017 Aug 16.

Abstract

Flaviviruses, such as dengue, Japanese encephalitis, West Nile, yellow fever, and Zika viruses, are serious human pathogens that cause significant morbidity and mortality globally each year. Flaviviruses are single-stranded, positive-sense RNA viruses, and encode two multidomain proteins, NS3 and NS5, that possess all enzymatic activities required for genome replication and capping. NS3 and NS5 interact within virus-induced replication compartments to form the RNA genome replicase complex. Although the individual enzymatic activities of both proteins have been extensively studied and are well characterized, there are still gaps in our understanding of how they interact to efficiently coordinate their respective activities during positive-strand RNA synthesis and capping. Here, we discuss what is known about the structures and functions of the NS3 and NS5 proteins and propose a preliminary NS3:NS5:RNA interaction model based on a large body of literature about how the viral enzymes function, physical restraints between NS3 and NS5, as well as critical steps in the replication process. WIREs RNA 2017, 8:e1437. doi: 10.1002/wrna.1437 For further resources related to this article, please visit the WIREs website.

摘要

黄病毒,如登革热病毒、日本脑炎病毒、西尼罗河病毒、黄热病病毒和寨卡病毒,都是严重的人类病原体,每年在全球范围内导致大量发病和死亡。黄病毒是单链正义RNA病毒,编码两种多结构域蛋白NS3和NS5,它们拥有基因组复制和加帽所需的所有酶活性。NS3和NS5在病毒诱导的复制区室内相互作用,形成RNA基因组复制酶复合物。尽管这两种蛋白的各自酶活性已得到广泛研究且特征明确,但我们对它们在正链RNA合成和加帽过程中如何相互作用以有效协调各自活性的理解仍存在空白。在此,我们讨论了关于NS3和NS5蛋白的结构和功能的已知信息,并基于大量有关病毒酶如何发挥功能、NS3和NS5之间的物理限制以及复制过程中的关键步骤的文献,提出了一个初步的NS3:NS5:RNA相互作用模型。WIREs RNA 2017, 8:e1437. doi: 10.1002/wrna.1437 有关本文的更多资源,请访问WIREs网站。

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