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PMID: 3051379 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

tRNAi(met) functions in directing the scanning ribosome to the start site of translation.

Science (New York, N.Y.) ·Vol. 242 ·No. 4875 ·1988-10-07 ·Pages 93-7

Cigan AM, Feng L, Donahue TF

Abstract

The mechanism by which the scanning ribosome recognizes the first AUG codon nearest the 5' end of eukaryotic messenger RNA has not been established. To investigate this an anticodon change (3'-UCC-5') was introduced into one of the four methionine initiator (tRNAi(met) genes of Saccharomyces cerevisiae. The ability of the mutant transfer RNA to restore growth properties to his4 initiator codon mutant yeast strains in the absence of histidine was then assayed. Only the complementary codon, AGG, at the his4 initiator region supported His+ growth. The mutant transfer RNA also directed the ribosome to initiate at an AGG placed in the upstream region of the his4 message. Initiation at this upstream AGG precluded initiation at a downstream AGG in accordance with the "scanning" model. Therefore, an anticodon: codon interaction between tRNAi(met) as part of the scanning ribosome and the first AUG must function in directing the ribosome to the eukaryotic initiator region.

MeSH Terms
Anticodon Base Sequence Codon Genes, Fungal Molecular Sequence Data Mutation Peptide Chain Initiation, Translational RNA, Transfer, Amino Acid-Specific/genetics RNA, Transfer, Met/genetics Ribosomes/metabolism Saccharomyces cerevisiae/genetics
Chemicals
Anticodon Codon RNA, Transfer, Amino Acid-Specific RNA, Transfer, Met
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Cigan A M
Department of Molecular Biology, Northwestern University Medical School, Chicago, IL 60611.
Feng L
Donahue T F
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1988-10-07
Pages
93-7
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIGMS NIH HHS · GM32263 · United States
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