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Positioning of subdomain IIId and apical loop of domain II of the hepatitis C IRES on the human 40S ribosome

机译:丙型肝炎IRES的IIId亚域和II区顶端环在人40S核糖体上的定位

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摘要

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.
机译: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IRES(内部核糖体进入位点),负责病毒RNA翻译的帽独立性启动。首先,IRES没有任何起始因子就与40S亚基结合,因此起始AUG密码子落入P位点。在这里使用原始的定点交联策略,我们确定了邻近亚结构域IIId的40S亚基成分,这对于HCV IRES与亚基的结合至关重要,并且还发现了结构域II的根尖环,建议从数据上联系40S亚基。包含HCV IRES的核糖体复合物的冷冻电子显微镜检查。 HCV IRES衍生物在亚结构域IIId的核苷酸A275或G263处具有可光激活的基团,与核糖体蛋白S3a,S14和S16交联,而HCV IRES在结构域II的顶点C83处衍生,与蛋白S14和S16交联。

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