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GTP-independent tRNA Delivery to the Ribosomal P-site by a Novel Eukaryotic Translation Factor
Authors:Sergey E. Dmitriev  Ilya M. Terenin  Dmitri E. Andreev  Pavel A. Ivanov  Jacov E. Dunaevsky  William C. Merrick  Ivan N. Shatsky
Affiliation:From the Belozersky Institute of Physico-Chemical Biology and ;§Faculty of Biology, Moscow State University, Moscow 119992, Russia and ;the Department of Biochemistry, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106
Abstract: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 tRNAiMet 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.
Keywords:Ribosome Function   RNA   RNA Viruses   Translation Initiation Factors   Translation Regulation   Hepatitis C Virus   SUI1 Domain   eIF2A   eIF2D   Ligatin
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