MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge CB2 0QH, UK.
MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge CB2 0QH, UK.
Cell. 2014 May 8;157(4):823-31. doi: 10.1016/j.cell.2014.04.015. Epub 2014 May 1.
The cricket paralysis virus internal ribosome entry site (CrPV-IRES) is a folded structure in a viral mRNA that allows initiation of translation in the absence of any host initiation factors. By using recent advances in single-particle electron cryomicroscopy, we have solved the structure of CrPV-IRES bound to the ribosome of the yeast Kluyveromyces lactis in both the canonical and rotated states at overall resolutions of 3.7 and 3.8 Å, respectively. In both states, the pseudoknot PKI of the CrPV-IRES mimics a tRNA/mRNA interaction in the decoding center of the A site of the 40S ribosomal subunit. The structure and accompanying factor-binding data show that CrPV-IRES binding mimics a pretranslocation rather than initiation state of the ribosome. Translocation of the IRES by elongation factor 2 (eEF2) is required to bring the first codon of the mRNA into the A site and to allow the start of translation.
Cricket 麻痹病毒内部核糖体进入位点 (CrPV-IRES) 是病毒 mRNA 中的一种折叠结构,允许在没有任何宿主起始因子的情况下启动翻译。通过使用单颗粒电子 cryomicroscopy 的最新进展,我们分别以 3.7 和 3.8 Å 的整体分辨率解决了与酵母 Kluyveromyces lactis 核糖体结合的 CrPV-IRES 的在规范和旋转状态下的结构。在这两种状态下,CrPV-IRES 的假结 PKI 模拟了 A 位点 40S 核糖体亚基解码中心中的 tRNA/mRNA 相互作用。结构和伴随的因子结合数据表明,CrPV-IRES 结合模拟了核糖体的前移位而不是起始状态。延伸因子 2 (eEF2) 的 IRES 易位需要将 mRNA 的第一个密码子带入 A 位点并允许翻译开始。