Lukavsky P J, Otto G A, Lancaster A M, Sarnow P, Puglisi J D
Department of Structural Biology, Stanford University School of Medicine, Stanford, California 94305-5126, USA.
Nat Struct Biol. 2000 Dec;7(12):1105-10. doi: 10.1038/81951.
Translation of the hepatitis C virus (HCV) polyprotein is initiated at an internal ribosome entry site (IRES) element in the 5' untranslated region of HCV RNA. The HCV IRES element interacts directly with the 40S subunit, and biochemical experiments have implicated RNA elements near the AUG start codon as required for IRES-40S subunit complex formation. The data we present here show that two RNA stem loops, domains IIId and IIIe, are involved in IRES-40S subunit interaction. The structures of the two RNA domains were solved by NMR spectroscopy and reveal structural features that may explain their role in IRES function.
丙型肝炎病毒(HCV)多聚蛋白的翻译起始于HCV RNA 5'非翻译区的一个内部核糖体进入位点(IRES)元件。HCV IRES元件直接与40S亚基相互作用,生化实验表明AUG起始密码子附近的RNA元件是IRES - 40S亚基复合物形成所必需的。我们在此展示的数据表明,两个RNA茎环结构域IIId和IIIe参与了IRES - 40S亚基的相互作用。通过核磁共振光谱法解析了这两个RNA结构域的结构,并揭示了可能解释它们在IRES功能中作用的结构特征。