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PMID: 2298214 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Selection of the 5'-proximal translation initiation site is influenced by mRNA and eIF-2 concentrations.

European journal of biochemistry ·Vol. 187 ·No. 2 ·1990-01-26 ·Pages 361-71

Dasso MC, Milburn SC, Hershey JW, Jackson RJ

Abstract

A cDNA clone of the influenza virus NS (non-structural protein) gene in a vector carrying a bacteriophage T7 RNA polymerase promoter was manipulated so as to reiterate the initiation site to give two in-frame AUG codons 57 nucleotide residues apart. Each initiation site was in either a preferred context (...AUAAUGG...) or a less favourable context (...UUUAUGG...) and the four possible permutations were constructed. When capped mRNA transcripts of these clones were translated in the rabbit reticulocyte lysate system, products from initiation at both AUG codons were observed. At low RNA concentrations the frequency of initiation at the 5'-proximal AUG codon rather than the second was higher when the first AUG codon was in the preferred context, in qualitative agreement with the scanning ribosome model. However, a completely unexpected finding was that the ratio of initiation at the first AUG codon to initiation at the second decreased with increasing mRNA concentration, irrespective of the particular context involved. Several lines of evidence indicated that the increased frequency of initiation at the second AUG codon was not due solely to the lower density of ribosome loading per mRNA at high RNA concentrations, and may therefore be the result of high RNA concentrations out-titring the capacity of endogenous reticulocyte factors responsible for preferential initiation at the 5'-proximal AUG codon. The effect of supplementing the system with purified initiation factors was examined. Only eIF-2 was capable of decreasing the frequency of initiation at the second AUG codon and promoting use of the first AUG at high mRNA concentrations; eIF-3, 4A, 4B, 4C + 4D, 4F and 5 were inactive.

MeSH Terms
Animals Binding Sites/drug effects Codon/drug effects DNA/analysis DNA-Directed RNA Polymerases/metabolism Dose-Response Relationship, Drug Eukaryotic Initiation Factor-2/pharmacology Genetic Vectors Molecular Sequence Data Orthomyxoviridae/enzymology,genetics Peptide Initiation Factors/pharmacology Promoter Regions, Genetic/drug effects Protein Biosynthesis/drug effects RNA, Messenger/drug effects,pharmacology Rabbits Reticulocytes/metabolism Sequence Homology, Nucleic Acid T-Phages/enzymology Viral Proteins/genetics
Chemicals
Codon Eukaryotic Initiation Factor-2 Peptide Initiation Factors RNA, Messenger Viral Proteins DNA DNA-Directed RNA Polymerases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Dasso M C
Department of Biochemistry, University of Cambridge, England.
Milburn S C
Hershey J W
Jackson R J
Article Info
Journal
European journal of biochemistry
Abbr.
Eur J Biochem
ISSN
0014-2956
Published
1990-01-26
Pages
361-71
Language
English
Region
England
NLM ID
0107600
Subset
IM
Grants
NIGMS NIH HHS · GM22135 · United States
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