Department of Biological Sciences, University at Albany, Albany, New York, USA.
The RNA Institute, University at Albany, Albany, New York, USA.
Wiley Interdiscip Rev RNA. 2021 Mar;12(2):e1613. doi: 10.1002/wrna.1613. Epub 2020 Jul 12.
Upon viral infection of a host cell, each virus starts a program to generate many progeny viruses. Although viruses interact with the host cell in numerous ways, one critical step in the virus life cycle is the expression of viral proteins, which are synthesized by the host ribosomes in conjunction with host translation factors. Here we review different mechanisms viruses have evolved to effectively seize host cell ribosomes, the roles of specific ribosomal proteins and their posttranslational modifications on viral RNA translation, or the cellular response to infection. We further highlight ribosomal proteins with extra-ribosomal function during viral infection and put the knowledge of ribosomal proteins during viral infection into the larger context of ribosome-related diseases, known as ribosomopathies. This article is categorized under: Translation > Translation Mechanisms Translation > Translation Regulation.
当宿主细胞被病毒感染时,每个病毒都会启动一个程序来产生许多子代病毒。尽管病毒与宿主细胞以多种方式相互作用,但病毒生命周期中的一个关键步骤是病毒蛋白的表达,这些蛋白是由宿主核糖体与宿主翻译因子共同合成的。在这里,我们综述了病毒进化出的不同机制来有效地劫持宿主细胞核糖体,特定核糖体蛋白的作用及其对病毒 RNA 翻译的翻译后修饰,或细胞对感染的反应。我们进一步强调了在病毒感染过程中具有核糖体外功能的核糖体蛋白,并将病毒感染过程中核糖体蛋白的知识置于核糖体相关疾病(称为核糖体病)的更大背景下。本文属于以下分类:翻译 > 翻译机制 翻译 > 翻译调控