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PMID: 8127650 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

On the relationship between preferred termination codon contexts and nonsense suppression in human cells.

Nucleic acids research ·Vol. 22 ·No. 1 ·1994-01-11 ·Pages 15-9

Martin R

Abstract

The nucleotide sequences 3' to the translational termination codons in a collection of human genes have been analysed for evidence of a preferred 3' context for natural UAG codons. The aim was to see whether human UAG contexts can be related to the recent demonstration of the effects of 3' context on nonsense suppression in human cells. Since mammalian genomes are known to consist of a patchwork of blocks of sequences or 'isochores' with different G+C contents, the collection of genes was split into 5 classes containing genes with similar frequencies of G+C at the 3rd position of synonymous codons. This analysis revealed that the frequency of bases 3' to UAG varies with the G+C frequency of the gene, and that these changes were mirrored by changes in the patterns of bases in GN and AGN strings. The identity of the next 3' base appears therefore to be determined by genome wide changes in G+C composition, rather than selection to maintain a particular tetranucleotide stop signal. These findings argue strongly that the failure to find bias in the patterns of bases used in human coding sequences is an insensitive guide for the existence of codon usage or codon context effects during translation in human cells.

MeSH Terms
Base Composition Codon Gene Expression Genes, Suppressor Humans Peptide Chain Termination, Translational Point Mutation Structure-Activity Relationship
Chemicals
Codon
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Martin R
Krebs Institute for Biomolecular Research, University of Sheffield, Western Bank, UK.
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26 references, click to expand
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1994-01-11
Pages
15-9
Language
English
Region
England
NLM ID
0411011
PMCID
PMC307739
Subset
IM
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