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