Jan Eric
Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Virus Res. 2006 Jul;119(1):16-28. doi: 10.1016/j.virusres.2005.10.011. Epub 2005 Nov 22.
Viruses have evolved unique strategies and mechanisms to recruit ribosomes to ensure continued translation of their viral RNA during infection. The Dicistroviridae family of invertebrate viruses contains an unusual internal ribosome entry site (IRES), which can directly recruit ribosomes in the absence of initiation factors. Moreover, this IRES initiates translation at a non-AUG codon independent of an initiator Met-tRNA. Recent studies have shown that the IRES mimicks a tRNA to interact with and manipulate the ribosome. The presence of this divergent IRES likely allows translation of the dicistroviral RNA during infection when host translation is compromised. This review will explore the unique properties of this unprecedented mechanism of gene expression. Specific topics will examine structural components of the IRES, the mechanism of initiating translation at non-AUG codons and the regulation of this IRES in vivo. The existence of this mechanism suggests that the repertoire of open reading frames in our genome may be greater than anticipated.
病毒已经进化出独特的策略和机制来招募核糖体,以确保在感染期间其病毒RNA能够持续翻译。无脊椎动物病毒的双顺反子病毒科含有一个不同寻常的内部核糖体进入位点(IRES),它可以在没有起始因子的情况下直接招募核糖体。此外,这个IRES在一个非AUG密码子处起始翻译,且不依赖于起始甲硫氨酰-tRNA。最近的研究表明,该IRES模拟tRNA与核糖体相互作用并对其进行操控。当宿主翻译受到损害时,这种不同寻常的IRES的存在可能使得双顺反子病毒RNA在感染期间能够进行翻译。本综述将探讨这种前所未有的基因表达机制的独特特性。具体主题将研究IRES的结构组成部分、在非AUG密码子处起始翻译的机制以及该IRES在体内的调控。这种机制的存在表明我们基因组中开放阅读框的种类可能比预期的更多。