Multidisciplinary Center for Infectious Diseases, University of Bern, Bern, Switzerland.
Department of Chemistry and Biochemistry, University of Bern, Bern, Switzerland.
EMBO J. 2024 Jan;43(2):151-167. doi: 10.1038/s44318-023-00019-8. Epub 2024 Jan 10.
Coronaviruses are a group of related RNA viruses that cause respiratory diseases in humans and animals. Understanding the mechanisms of translation regulation during coronaviral infections is critical for developing antiviral therapies and preventing viral spread. Translation of the viral single-stranded RNA genome in the host cell cytoplasm is an essential step in the life cycle of coronaviruses, which affects the cellular mRNA translation landscape in many ways. Here we discuss various viral strategies of translation control, including how members of the Betacoronavirus genus shut down host cell translation and suppress host innate immune functions, as well as the role of the viral non-structural protein 1 (Nsp1) in the process. We also outline the fate of viral RNA, considering stress response mechanisms triggered in infected cells, and describe how unique viral RNA features contribute to programmed ribosomal -1 frameshifting, RNA editing, and translation shutdown evasion.
冠状病毒是一组相关的 RNA 病毒,可引起人类和动物的呼吸道疾病。了解冠状病毒感染过程中翻译调控的机制对于开发抗病毒疗法和阻止病毒传播至关重要。在冠状病毒的生命周期中,病毒单链 RNA 基因组在宿主细胞质中的翻译是一个关键步骤,它以多种方式影响细胞 mRNA 翻译图谱。在这里,我们讨论了各种病毒的翻译调控策略,包括β属冠状病毒如何关闭宿主细胞翻译并抑制宿主固有免疫功能,以及病毒非结构蛋白 1(Nsp1)在这一过程中的作用。我们还概述了病毒 RNA 的命运,考虑到受感染细胞中触发的应激反应机制,并描述了独特的病毒 RNA 特征如何有助于有规律的核糖体-1 移码、RNA 编辑和翻译关闭逃逸。