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PMID: 10966112 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Initiation of protein synthesis from the A site of the ribosome.

Cell ·Vol. 102 ·No. 4 ·2000-08-18 ·Pages 511-20

Wilson JE, Pestova TV, Hellen CU, Sarnow P

Abstract

Positioning of the translation initiation complex on mRNAs requires interaction between the anticodon of initiator Met-tRNA, associated with eIF2-GTP and 40S ribosomal subunit, and the cognate start codon of the mRNA. We show that an internal ribosome entry site located in the genome of cricket paralysis virus can form 80S ribosomes without initiator Met-tRNA, eIF2, or GTP hydrolysis, with a CCU triplet in the ribosomal P site and a GCU triplet in the A site. P-site mutagenesis revealed that the P site was not decoded, and protein sequence analysis showed that translation initiates at the triplet in the A site. Translational initiation from the A site of the ribosome suggests that the repertoire of translated open reading frames in eukaryotic mRNAs may be greater than anticipated.

MeSH Terms
Animals Anticodon Base Sequence Codon, Terminator Eukaryotic Initiation Factor-2/metabolism Guanosine Triphosphate/metabolism Molecular Sequence Data Mutagenesis, Site-Directed Nucleic Acid Conformation Open Reading Frames Peptide Chain Initiation, Translational Protein Biosynthesis RNA, Messenger/metabolism RNA, Transfer, Met/genetics Rabbits Ribosomes/metabolism
Chemicals
Anticodon Codon, Terminator Eukaryotic Initiation Factor-2 RNA, Messenger RNA, Transfer, Met Guanosine Triphosphate
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Wilson J E
Department of Microbiology and Immunology, Stanford University School of Medicine, California 94305, USA.
Pestova T V
Hellen C U
Sarnow P
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
2000-08-18
Pages
511-20
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NIAID NIH HHS · AI44108 · United States
NIGMS NIH HHS · GM55979 · United States
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