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

被引:50
作者
Babaylova, Elena [1 ]
Graifer, Dmitri [1 ]
Malygin, Alexey [1 ]
Stahl, Joachim [2 ]
Shatsky, Ivan [3 ]
Karpova, Galina [1 ]
机构
[1] Russian Acad Sci, Inst Chem Biol & Fundamental Med, Siberian Branch, Novosibirsk 630090, Russia
[2] Max Delbruck Ctr Mol Med, D-13092 Berlin, Germany
[3] Moscow MV Lomonosov State Univ, Belozersky Inst Physicohem Biol, Moscow 119899, Russia
基金
俄罗斯基础研究基金会;
关键词
TRANSLATION INITIATION-COMPLEXES; MESSENGER-RNA CODONS; HUMAN 80S RIBOSOME; ENTRY SITE; VIRUS-RNA; RAT-LIVER; PROTEINS; SUBUNIT; HCVIRES; BINDING;
D O I
10.1093/nar/gkn1026
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 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.
引用
收藏
页码:1141 / 1151
页数:11
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