Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, British Columbia V6T 1Z3, Canada; email:
Department of Microbiology and New York University Cancer Institute, New York University School of Medicine, New York, NY 10016; email:
Annu Rev Virol. 2016 Sep 29;3(1):283-307. doi: 10.1146/annurev-virology-100114-055014. Epub 2016 Aug 3.
Although viruses require cellular functions to replicate, their absolute dependence upon the host translation machinery to produce polypeptides indispensable for their reproduction is most conspicuous. Despite their incredible diversity, the mRNAs produced by all viruses must engage cellular ribosomes. This has proven to be anything but a passive process and has revealed a remarkable array of tactics for rapidly subverting control over and dominating cellular regulatory pathways that influence translation initiation, elongation, and termination. Besides enforcing viral mRNA translation, these processes profoundly impact host cell-intrinsic immune defenses at the ready to deny foreign mRNA access to ribosomes and block protein synthesis. Finally, genome size constraints have driven the evolution of resourceful strategies for maximizing viral coding capacity. Here, we review the amazing strategies that work to regulate translation in virus-infected cells, highlighting both virus-specific tactics and the tremendous insight they provide into fundamental translational control mechanisms in health and disease.
虽然病毒复制需要细胞功能,但它们绝对依赖宿主翻译机制来产生对其繁殖必不可少的多肽,这一点最为明显。尽管它们具有令人难以置信的多样性,但所有病毒产生的 mRNA 都必须与细胞核糖体结合。事实证明,这绝不是一个被动的过程,而是揭示了一系列惊人的策略,这些策略迅速颠覆了对影响翻译起始、延伸和终止的细胞调控途径的控制,并对其进行了主导。除了强制翻译病毒 mRNA 之外,这些过程还深刻地影响了宿主细胞固有的免疫防御系统,使其能够阻止外来 mRNA 进入核糖体并阻断蛋白质合成。最后,基因组大小的限制促使病毒进化出了富有创意的策略,以最大限度地提高病毒的编码能力。在这里,我们回顾了调节病毒感染细胞中翻译的惊人策略,重点介绍了病毒特异性策略以及它们为健康和疾病中的基本翻译控制机制提供的巨大见解。