GTP-independent tRNA Delivery to the Ribosomal P-site by a Novel Eukaryotic Translation Factor

被引:126
|
作者
Dmitriev, Sergey E.
Terenin, Ilya M.
Andreev, Dmitri E.
Ivanov, Pavel A. [2 ]
Dunaevsky, Jacov E.
Merrick, William C. [3 ]
Shatsky, Ivan N. [1 ]
机构
[1] Moscow MV Lomonosov State Univ, Belozersky Inst Physicochem Biol, Moscow 119992, Russia
[2] Moscow MV Lomonosov State Univ, Fac Biol, Moscow 119992, Russia
[3] Case Western Reserve Univ, Sch Med, Dept Biochem, Cleveland, OH 44106 USA
基金
俄罗斯基础研究基金会;
关键词
INITIATION-FACTOR EIF1; MESSENGER-RNA; START CODON; MEMBRANE PROTEINS; GENE-EXPRESSION; IDENTIFICATION; BINDING; CELL; RECOGNITION; COMPLEXES;
D O I
10.1074/jbc.M110.119693
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
During translation, aminoacyl-tRNAs are delivered to the ribosome by specialized GTPases called translation factors. Here, we report the tRNA binding to the P-site of 40 S ribosomes by a novel GTP-independent factor eIF2D isolated from mammalian cells. The binding of tRNA(i)(Met) occurs after the AUG codon finds its position in the P-site of 40 S ribosomes, the situation that takes place during initiation complex formation on the hepatitis C virus internal ribosome entry site or on some other specific RNAs (leaderless mRNA and A-rich mRNAs with relaxed scanning dependence). Its activity in tRNA binding with 40 S subunits does not require the presence of the aminoacyl moiety. Moreover, the factor possesses the unique ability to deliver non-Met (elongator) tRNAs into the P-site of the 40 S subunit. The corresponding gene is found in all eukaryotes and includes an SUI1 domain present also in translation initiation factor eIF1. The versatility of translation initiation strategies in eukaryotes is discussed.
引用
收藏
页码:26779 / 26787
页数:9
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