Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel.
Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel.
Mol Cell. 2023 Feb 2;83(3):481-495. doi: 10.1016/j.molcel.2022.10.012. Epub 2022 Nov 4.
Viral reproduction is contingent on viral protein synthesis that relies on the host ribosomes. As such, viruses have evolved remarkable strategies to hijack the host translational apparatus in order to favor viral protein production and to interfere with cellular innate defenses. Here, we describe the approaches viruses use to exploit the translation machinery, focusing on commonalities across diverse viral families, and discuss the functional relevance of this process. We illustrate the complementary strategies host cells utilize to block viral protein production and consider how cells ensure an efficient antiviral response that relies on translation during this tug of war over the ribosome. Finally, we highlight potential roles mRNA modifications and ribosome quality control play in translational regulation and innate immunity. We address these topics in the context of the COVID-19 pandemic and focus on the gaps in our current knowledge of these mechanisms, specifically in viruses with pandemic potential.
病毒的繁殖依赖于病毒蛋白的合成,而病毒蛋白的合成依赖于宿主核糖体。因此,病毒进化出了显著的策略来劫持宿主的翻译装置,以利于病毒蛋白的产生,并干扰细胞固有防御。在这里,我们描述了病毒利用翻译机制的方法,重点介绍了不同病毒家族之间的共同特征,并讨论了这一过程的功能相关性。我们举例说明了宿主细胞用来阻止病毒蛋白产生的互补策略,并考虑了细胞如何在这场核糖体争夺战中确保有效的抗病毒反应,而这种反应依赖于翻译。最后,我们强调了 mRNA 修饰和核糖体质量控制在翻译调控和先天免疫中的潜在作用。我们在 COVID-19 大流行的背景下讨论这些问题,并关注我们目前对这些机制的认识差距,特别是在具有大流行潜力的病毒中。