The Eukaryotic Translation Initiation Factors eIF1 and eIF1A Induce an Open Conformation of the 40S Ribosome

• Published in: Molecular cell Vol. 26; no. 1; pp. 41 - 50
• Main Authors: Passmore, Lori A., Schmeing, T. Martin, Maag, David, Applefield, Drew J., Acker, Michael G., Algire, Mikkel A., Lorsch, Jon R., Ramakrishnan, V.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 13.04.2007
• Subjects: Binding Sites; Cryoelectron Microscopy; Eukaryotic Initiation Factor-1 - chemistry; Eukaryotic Initiation Factor-1 - genetics; Eukaryotic Initiation Factor-1 - metabolism; Models, Genetic; Molecular Conformation; Protein Binding; Protein Biosynthesis; Ribosomal Proteins - chemistry; Ribosomes - chemistry; Ribosomes - genetics; Ribosomes - metabolism; RNA; RNA, Messenger - chemistry; RNA, Ribosomal - chemistry; Saccharomyces cerevisiae - chemistry; Saccharomyces cerevisiae - genetics; Saccharomyces cerevisiae Proteins - chemistry; Saccharomyces cerevisiae Proteins - genetics; Saccharomyces cerevisiae Proteins - metabolism; Structure-Activity Relationship; RNA
• ISSN: 1097-2765; 1097-4164
• DOI: 10.1016/j.molcel.2007.03.018

Initiation of translation is the process by which initiator tRNA and the start codon of mRNA are positioned in the ribosomal P site. In eukaryotes, one of the first steps involves the binding of two small factors, eIF1 and eIF1A, to the small (40S) ribosomal subunit. This facilitates tRNA binding, allows scanning of mRNA, and maintains fidelity of start codon recognition. Using cryo-EM, we have obtained 3D reconstructions of 40S bound to both eIF1 and eIF1A, and with each factor alone. These structures reveal that together, eIF1 and eIF1A stabilize a conformational change that opens the mRNA binding channel. Biochemical data reveal that both factors accelerate the rate of ternary complex (eIF2•GTP•Met-tRNAiMet) binding to 40S but only eIF1A stabilizes this interaction. Our results suggest that eIF1 and eIF1A promote an open, scanning-competent preinitiation complex that closes upon start codon recognition and eIF1 release to stabilize ternary complex binding and clamp down on mRNA.