Centro de Biología Molecular Severo Ochoa, CSIC-UAM, Madrid, Spain.
FEBS Open Bio. 2022 Jun;12(6):1125-1141. doi: 10.1002/2211-5463.13400. Epub 2022 Mar 30.
The genome of viruses classified as picornaviruses consists of a single monocistronic positive strand RNA. The coding capacity of these RNA viruses is rather limited, and thus, they rely on the cellular machinery for their viral replication cycle. Upon the entry of the virus into susceptible cells, the viral RNA initially competes with cellular mRNAs for access to the protein synthesis machinery. Not surprisingly, picornaviruses have evolved specialized strategies that successfully allow the expression of viral gene products, which we outline in this review. The main feature of all picornavirus genomes is the presence of a heavily structured RNA element on the 5´UTR, referred to as an internal ribosome entry site (IRES) element, which directs viral protein synthesis as well and, consequently, triggers the subsequent steps required for viral replication. Here, we will summarize recent studies showing that picornavirus IRES elements consist of a modular structure, providing sites of interaction for ribosome subunits, eIFs, and a selective group of RNA-binding proteins.
分类为小核糖核酸病毒的病毒基因组由单顺反子单链正 RNA 组成。这些 RNA 病毒的编码能力相当有限,因此它们依赖于细胞机制来完成病毒复制周期。病毒进入易感细胞后,病毒 RNA 最初会与细胞 mRNA 竞争进入蛋白质合成机制的机会。毫不奇怪,小核糖核酸病毒已经进化出专门的策略,成功地允许病毒基因产物的表达,我们在这篇综述中概述了这些策略。所有小核糖核酸病毒基因组的主要特征是在 5'UTR 上存在一个高度结构化的 RNA 元件,称为内部核糖体进入位点(IRES)元件,该元件也可指导病毒蛋白合成,从而触发病毒复制所需的后续步骤。在这里,我们将总结最近的研究表明,小核糖核酸病毒 IRES 元件由模块化结构组成,为核糖体亚基、eIF 和一组选择性的 RNA 结合蛋白提供了相互作用的位点。