Babaylova Elena, Graifer Dmitri, Malygin Alexey, Stahl Joachim, Shatsky Ivan, Karpova Galina
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, 630090, Russia.
Nucleic Acids Res. 2009 Mar;37(4):1141-51. doi: 10.1093/nar/gkn1026. Epub 2009 Jan 7.
The 5'-untranslated region of the hepatitis C virus (HCV) RNA contains a highly structured motif called IRES (Internal Ribosome Entry Site) responsible for the cap-independent initiation of the viral RNA translation. At first, the IRES binds to the 40S subunit without any initiation factors so that the initiation AUG codon falls into the P site. Here using an original site-directed cross-linking strategy, we identified 40S subunit components neighboring subdomain IIId, which is critical for HCV IRES binding to the subunit, and apical loop of domain II, which was suggested to contact the 40S subunit from data on cryo-electron microscopy of ribosomal complexes containing the HCV IRES. HCV IRES derivatives that bear a photoactivatable group at nucleotide A275 or at G263 in subdomain IIId cross-link to ribosomal proteins S3a, S14 and S16, and HCV IRES derivatized at the C83 in the apex of domain II cross-link to proteins S14 and S16.
丙型肝炎病毒(HCV)RNA的5'非翻译区包含一个高度结构化的基序,称为内部核糖体进入位点(IRES),它负责病毒RNA翻译的不依赖帽子结构的起始。起初,IRES在没有任何起始因子的情况下与40S亚基结合,使得起始AUG密码子落入P位点。在这里,我们使用一种原创的定点交联策略,鉴定了与IIId亚结构域相邻的40S亚基成分,IIId亚结构域对于HCV IRES与该亚基的结合至关重要,还鉴定了结构域II的顶端环,根据含有HCV IRES的核糖体复合物的冷冻电镜数据,该顶端环被认为与40S亚基接触。在IIId亚结构域的核苷酸A275或G263处带有光活化基团的HCV IRES衍生物与核糖体蛋白S3a、S14和S16交联,而在结构域II顶端的C83处衍生化的HCV IRES与蛋白S14和S16交联。