A conserved RNA structure within the HCVIRES eIF3-binding site

被引:89
作者
Collier, AJ
Gallego, J
Klinck, R
Cole, PT
Harris, SJ
Harrison, GP
Aboul-ela, F
Varani, G
Walker, S
机构
[1] RiboTargets Ltd, Cambridge CB1 6GB, England
[2] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
基金
英国医学研究理事会;
关键词
D O I
10.1038/nsb785
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The hepatitis C virus (HCV) internal ribosome entry site (IRES) is recognized specifically by the small ribosomal subunit and eukaryotic initiation factor 3 (eIF3) before viral translation initiation. Using extensive mutagenesis and structure probing analysis, we show that the eIF3-binding domain of the HCV IRES contains an internal loop structure (loop IIIb) and an adjacent mismatched helix that are important for IRES-dependent initiation of translation. NMR studies reveal a unique three-dimensional structure for this internal loop that is conserved between viral isolates of varying primary sequence in this region. These data indicate that internal loop IIIb may be an attractive target for structure-based design of new antiviral agents.
引用
收藏
页码:375 / 380
页数:6
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