EIF4E公司
真核翻译
假结
翻译(生物学)
真核起始因子
核糖核酸
起始因子
EIF4G系列
生物
内部核糖体进入位点
真核生物γ翻译起始因子4
信使核糖核酸
细胞生物学
遗传学
基因
作者
Zhaohui Wang,Marc Parisien,Kay Scheets,Warner A. Miller
出处
期刊:Structure
[Elsevier BV]
日期:2011-06-08
卷期号:19 (6): 868-880
被引量:64
标识
DOI:10.1016/j.str.2011.03.013
摘要
Eukaryotic initiation factor eIF4E performs a key early step in translation by specifically recognizing the m⁷GpppN cap structure at the 5' end of cellular mRNAs. Many viral mRNAs lack a 5' cap and thus bypass eIF4E. In contrast, we reported a cap-independent translation element (PTE) in Pea enation mosaic virus RNA2 that binds and requires eIF4E for translation initiation. To understand how this uncapped RNA is bound tightly by eIF4E, we employ SHAPE probing, phylogenetic comparisons with new PTEs discovered in panico- and carmoviruses, footprinting of the eIF4E 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 eIF4E clamps around a pseudoknot, placing a highly SHAPE-reactive guanosine in the pocket in place of the normal m⁷GpppN cap. This reveals a new mechanism of mRNA recognition by eIF4E.
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