Kieft Jeffrey S
Department of Biochemistry and Molecular Genetics, University of Colorado Denver School of Medicine, Mail Stop 8101, PO Box 6511, Aurora, CO 80045, USA.
Virus Res. 2009 Feb;139(2):148-56. doi: 10.1016/j.virusres.2008.07.007. Epub 2008 Aug 15.
The intergenic region (IGR) internal ribosome entry site (IRES) RNAs do not require any of the canonical translation initiation factors to recruit the ribosome to the viral RNA, they eliminate the need for initiator tRNA, and they begin translation from the A-site. The function of these IRESs depends on a specific three-dimensional folded RNA structure. Thus, a complete understanding of the mechanisms of action of these IRESs requires that we understand their structure in detail. Recently, the structures of both domains of the IGR IRES RNAs were solved by X-ray crystallography, providing the first glimpse into an entire IRES RNA structure. Here, I present an analysis of these structures, emphasizing how the structures explain many aspects of IGR IRES function, discussing how these structures have similarities to motifs found in other viral RNAs, and illustrating how these structures give rise to new mechanistic hypotheses.
基因间区域(IGR)内部核糖体进入位点(IRES)RNA不需要任何典型的翻译起始因子就能将核糖体招募到病毒RNA上,它们无需起始tRNA,并从A位点开始翻译。这些IRES的功能取决于特定的三维折叠RNA结构。因此,要全面了解这些IRES的作用机制,就需要我们详细了解它们的结构。最近,通过X射线晶体学解析了IGR IRES RNA两个结构域的结构,首次让我们得以一窥完整的IRES RNA结构。在此,我对这些结构进行分析,着重阐述这些结构如何解释IGR IRES功能的诸多方面,讨论这些结构与其他病毒RNA中发现的基序有何相似之处,并说明这些结构如何引发新的作用机制假说。