Literature DB >> 2186375

The signal for the termination of protein synthesis in procaryotes.

C M Brown1, P A Stockwell, C N Trotman, W P Tate.   

Abstract

The sequences around the stop codons of 862 Escherichia coli genes have been analysed to identify any additional features which contribute to the signal for the termination of protein synthesis. Highly significant deviations from the expected nucleotide distribution were observed, both before and after the stop codon. Immediately prior to UAA stop codons in E. coli there is a preference for codons of the form NAR (any base, adenine, purine), and in particular those that code for glutamine or the basic amino acids. In contrast, codons for threonine or branched nonpolar amino acids were under-represented. Uridine was over-represented in the nucleotide position immediately following all three stop codons, whereas adenine and cytosine were under-represented. This pattern is accentuated in highly expressed genes, but is not as marked in either lowly expressed genes or those that terminate in UAG, the codon specifically recognised by polypeptide chain release factor-1. These observations suggest that for the efficient termination of protein synthesis in E. coli, the 'stop signal' may be a tetranucleotide, rather than simply a tri-nucleotide codon, and that polypeptide chain release factor-2 recognises this extended signal. The sequence following stop codons was analysed in genes from several other procaryotes and bacteriophages. Salmonella typhimurium, Bacillus subtilis, bacteriophages and the methanogenic archaebacteria showed a similar bias to E. coli.

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Year:  1990        PMID: 2186375      PMCID: PMC330686          DOI: 10.1093/nar/18.8.2079

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  32 in total

1.  Effects of release factor context at UAA codons in Escherichia coli.

Authors:  R Martin; M Weiner; J Gallant
Journal:  J Bacteriol       Date:  1988-10       Impact factor: 3.490

2.  The influence of the reading context upon the suppression of nonsense codons.

Authors:  W Salser
Journal:  Mol Gen Genet       Date:  1969-10-13

3.  Context effects: translation of UAG codon by suppressor tRNA is affected by the sequence following UAG in the message.

Authors:  L Bossi
Journal:  J Mol Biol       Date:  1983-02-15       Impact factor: 5.469

4.  Effects of surrounding sequence on the suppression of nonsense codons.

Authors:  J H Miller; A M Albertini
Journal:  J Mol Biol       Date:  1983-02-15       Impact factor: 5.469

5.  A temperature-sensitive mutant of Escherichia coli that shows enhanced misreading of UAG/A and increased efficiency for some tRNA nonsense suppressors.

Authors:  S M Rydén; L A Isaksson
Journal:  Mol Gen Genet       Date:  1984

6.  Codon usage in bacteria: correlation with gene expressivity.

Authors:  M Gouy; C Gautier
Journal:  Nucleic Acids Res       Date:  1982-11-25       Impact factor: 16.971

7.  UGA suppression by normal tRNA Trp in Escherichia coli: codon context effects.

Authors:  H Engelberg-Kulka
Journal:  Nucleic Acids Res       Date:  1981-02-25       Impact factor: 16.971

8.  Usage of the three termination codons: compilation and analysis of the known eukaryotic and prokaryotic translation termination sequences.

Authors:  J Kohli; H Grosjean
Journal:  Mol Gen Genet       Date:  1981

9.  The influence of codon context on genetic code translation.

Authors:  L Bossi; J R Roth
Journal:  Nature       Date:  1980-07-10       Impact factor: 49.962

10.  Mechanism of ribosome frameshifting during translation of the genetic code.

Authors:  R Weiss; J Gallant
Journal:  Nature       Date:  1983 Mar 31-Apr 6       Impact factor: 49.962

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  46 in total

Review 1.  Misreading of termination codons in eukaryotes by natural nonsense suppressor tRNAs.

Authors:  H Beier; M Grimm
Journal:  Nucleic Acids Res       Date:  2001-12-01       Impact factor: 16.971

2.  Mutations in eukaryotic release factors 1 and 3 act as general nonsense suppressors in Drosophila.

Authors:  Anna T Chao; Herman A Dierick; Tracie M Addy; Amy Bejsovec
Journal:  Genetics       Date:  2003-10       Impact factor: 4.562

3.  Mutations in E.coli 16s rRNA that enhance and decrease the activity of a suppressor tRNA.

Authors:  C D Prescott; H C Kornau
Journal:  Nucleic Acids Res       Date:  1992-04-11       Impact factor: 16.971

Review 4.  Codon context.

Authors:  R H Buckingham
Journal:  Experientia       Date:  1990-12-01

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

Authors:  C M Brown; P A Stockwell; C N Trotman; W P Tate
Journal:  Nucleic Acids Res       Date:  1990-11-11       Impact factor: 16.971

Review 6.  Recent evidence for evolution of the genetic code.

Authors:  S Osawa; T H Jukes; K Watanabe; A Muto
Journal:  Microbiol Rev       Date:  1992-03

7.  Eukaryotic start and stop translation sites.

Authors:  D R Cavener; S C Ray
Journal:  Nucleic Acids Res       Date:  1991-06-25       Impact factor: 16.971

8.  Decoding with the A:I wobble pair is inefficient.

Authors:  J F Curran
Journal:  Nucleic Acids Res       Date:  1995-02-25       Impact factor: 16.971

Review 9.  Termination of protein synthesis.

Authors:  M F Tuite; I Stansfield
Journal:  Mol Biol Rep       Date:  1994-05       Impact factor: 2.316

10.  Ribosome-mediated translational pause and protein domain organization.

Authors:  T A Thanaraj; P Argos
Journal:  Protein Sci       Date:  1996-08       Impact factor: 6.725

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