Cited by 191RNA and protein synthesis mechanismsGenomics and Phylogenetic StudiesRNA Research and Splicing

Sequence analysis suggests that tetra-nucleotides signal the termination of protein synthesis in eukaryotes

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Brown, Chris M., Stockwell, P.A., Trotman, C.N.A., Tate, W.P.·1990·Nucleic Acids Research

Abstract

An increasing number of cases where tri-nucleotide stop codons do not signal the termination of protein synthesis are being reported. In order to identify what constitutes an efficient stop signal, we analysed the region around natural stop codons in genes from a wide variety of eukaryotic species and gene families. Certain stop codons and nucleotides following stop codons are over-represented, and this pattern is accentuated in highly expressed genes. For example, the preferred signal for Saccharomyces cerevisiae and Drosophila melanogaster highly expressed genes is UAAG, and generally the signals UAA(A/G) and UGA(A/G) are preferred in eukaryotes. The GC% of the organism or DNA region can affect whether there is A or G in the second or fourth positions. We suggest therefore, that the stop codon and the nucleotide following it comprise a tetra-nucleotide stop signal. A model is proposed in which the polypeptide chain release factor, a protein, recognises this sequence, but will tolerate some substitution, particularly A to G in the second or third positions.

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Crossref · 10.1093/nar/18.21.6339

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1 of 1 references verified0 citation errors · 0 not checkable

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  • The translation termination signal is more than a stop codon, including the downstream +4 site (tetranucleotide stop signal).

    “It has long been recognized that the translation termination signal is more than a stop codon [86,87], leading to an early proposal of tetranucleotide stop signal including the downstream +4 site [63,65,87,88].”

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Authors
Brown, C. M., Stockwell, P. A., Trotman, C. N. A., & Tate, W. P.
Affiliations
University of Otago (NZ)
Corresponding author
Brown, Chris M.
Venue
Nucleic Acids Research
Published
1990
Volume
18
Issue
21
Pages
6339-6345
ISSN
  • 0305-1048 (ISSN-L)
  • 1362-4962
OpenAlex
W2049734985
Cited by
191
References
1
Citations by year
2026: 2 · 2025: 3 · 2024: 3 · 2023: 4 · 2022: 6 · 2021: 6 · 2020: 7 · 2019: 6 · 2018: 16 · 2017: 4 · 2016: 5 · 2015: 6 · 2014: 1 · 2013: 2 · 2012: 4
FWCI
2.88
Type
journal article
Language
en
Open access
Locations
  • Nucleic Acids Research (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
Medical Research Council
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
Keywords
stop codon, translation termination, unnatural amino acids, UGA, UAG, GC content, highly expressed genes, release factors, Saccharomyces cerevisiae, Drosophila melanogaster
MeSH terms
Animals, Base Sequence, Codon, Drosophila melanogaster, Escherichia coli, Multigene Family, Humans, Models, Genetic, Molecular Sequence Data, Peptide Chain Termination, Translational, Saccharomyces cerevisiae

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