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正链 RNA 病毒基因组复制细胞器:结构、组装、调控。

Positive-strand RNA virus genome replication organelles: structure, assembly, control.

机构信息

Rowe Center for Virology, Morgridge Institute for Research, Madison, WI, USA; Institute for Molecular Virology, University of Wisconsin-Madison, Madison, WI; McArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI.

Rowe Center for Virology, Morgridge Institute for Research, Madison, WI, USA; Institute for Molecular Virology, University of Wisconsin-Madison, Madison, WI; McArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI.

出版信息

Trends Genet. 2024 Aug;40(8):681-693. doi: 10.1016/j.tig.2024.04.003. Epub 2024 May 8.

Abstract

Positive-strand RNA [(+)RNA] viruses include pandemic SARS-CoV-2, tumor-inducing hepatitis C virus, debilitating chikungunya virus (CHIKV), lethal encephalitis viruses, and many other major pathogens. (+)RNA viruses replicate their RNA genomes in virus-induced replication organelles (ROs) that also evolve new viral species and variants by recombination and mutation and are crucial virus control targets. Recent cryo-electron microscopy (cryo-EM) reveals that viral RNA replication proteins form striking ringed 'crowns' at RO vesicle junctions with the cytosol. These crowns direct RO vesicle formation, viral (-)RNA and (+)RNA synthesis and capping, innate immune escape, and transfer of progeny (+)RNA genomes into translation and encapsidation. Ongoing studies are illuminating crown assembly, sequential functions, host factor interactions, etc., with significant implications for control and beneficial uses of viruses.

摘要

正链 RNA[(+)RNA]病毒包括引发大流行的 SARS-CoV-2、致肿瘤的丙型肝炎病毒、使人虚弱的基孔肯雅热病毒(CHIKV)、致命性脑炎病毒以及许多其他主要病原体。(+)RNA 病毒在病毒诱导的复制细胞器(RO)中复制其 RNA 基因组,这些细胞器还通过重组和突变产生新的病毒物种和变体,是病毒控制的关键目标。最近的冷冻电镜(cryo-EM)揭示,病毒 RNA 复制蛋白在 RO 囊泡与细胞质的连接处形成引人注目的环状“冠”。这些冠引导 RO 囊泡的形成、病毒(-)RNA 和(+)RNA 的合成和加帽、先天免疫逃避以及子代(+)RNA 基因组转移到翻译和封装。正在进行的研究阐明了冠的组装、顺序功能、宿主因子相互作用等,这对病毒的控制和有益利用具有重要意义。

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