The Cap-Binding Translation Initiation Factor, elF4E, Binds a Pseudoknot in a Viral Cap-Independent Translation Element

被引:53
|
作者
Wang, Zhaohui [1 ,2 ]
Parisien, Marc [3 ]
Scheets, Kay [4 ]
Miller, W. Allen [1 ,2 ]
机构
[1] Iowa State Univ, Dept Plant Pathol, Ames, IA 50011 USA
[2] Iowa State Univ, Biochem Biophys & Mol Biol Dept, Ames, IA 50011 USA
[3] Univ Chicago, Dept Biochem & Mol Biol, Chicago, IL 60637 USA
[4] Oklahoma State Univ, Dept Bot, Stillwater, OK 74078 USA
关键词
MESSENGER-RNA CAP; 3'-UNTRANSLATED REGION; PROTEIN EIF4E; VIRUS BINDS; MECHANISM; ENHANCER; RECOGNITION; RESISTANCE; EXTENSION; SECONDARY;
D O I
10.1016/j.str.2011.03.013
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
Eukaryotic initiation factor elF4E performs a key early step in translation by specifically recognizing the m 7 GpppN cap structure at the 5' end of cellular mRNAs. Many viral mRNAs lack a 5' cap and thus bypass elF4E. In contrast, we reported a cap-independent translation element (PTE) in Pea enation mosaic virus RNA2 that binds and requires elF4E for translation initiation. To understand how this uncapped RNA is bound tightly by elF4E, we employ SHAPE probing, phylogenetic comparisons with new PTEs discovered in panico- and carmoviruses, footprinting of the elF4E binding site, and 3D RNA modeling using NAST, MC-Fold, and MC-Sym to predict a compact, 3D structure of the RNA. We propose that the cap-binding pocket of elF4E clamps around a pseudoknot, placing a highly SHAPE-reactive guanosine in the pocket in place of the normal m 7 GpppN cap. This reveals a new mechanism of mRNA recognition by elF4E.
引用
收藏
页码:868 / 880
页数:13
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