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PMID: 3053704 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Site-directed mutagenesis of the tryptophan residues in yeast eukaryotic initiation factor 4E. Effects on cap binding activity.

The Journal of biological chemistry ·Vol. 263 ·No. 33 ·1988-11-25 ·Pages 17229-32

Altmann M, Edery I, Trachsel H, Sonenberg N

Abstract

Initiation factor 4E is a 24-kilodalton polypeptide that binds specifically to the 5' cap structure of eukaryotic mRNAs. Sequence analysis of cDNA clones of initiation factor 4E from several species revealed a high tryptophan content (8 residues). Strikingly, all tryptophans are conserved evolutionarily in number and position between yeast and mammals. Here we show, using site-directed mutagenesis, that two of the tryptophans (those referred to as numbers 1 and 8) are absolutely required for the cap binding activity of an Escherichia coli expressed initiation factor 4E.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Escherichia coli/genetics Eukaryotic Initiation Factor-4E Genes Genes, Fungal Humans Mice Molecular Sequence Data Mutation Oligonucleotide Probes Peptide Initiation Factors/genetics,metabolism RNA Caps/metabolism Saccharomyces cerevisiae/genetics Sequence Homology, Nucleic Acid Species Specificity Transcription, Genetic Tryptophan
Chemicals
Eukaryotic Initiation Factor-4E Oligonucleotide Probes Peptide Initiation Factors RNA Caps Tryptophan
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Altmann M
Department of Biochemistry, McGill University, Montreal, Canada.
Edery I
Trachsel H
Sonenberg N
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1988-11-25
Pages
17229-32
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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