Literature DB >> 3128715

Codon contexts in enterobacterial and coliphage genes.

M Gouy1.   

Abstract

This investigation of the codon context of enterobacteria, plasmid, and phage protein genes was based on a search for correlations between the presence of one base type at codon position III and the presence of another base type at some other position in adjacent codons. Enterobacterial genes were compared with eukaryotic sequences for codon context effects. In enterobacterial genes, base usage at codon position III is correlated with the third position of the upstream adjacent codon and with all three positions of the downstream codon. Plasmid genes are free of context biases. Phage genes are heterogeneous: MS2 codons have no biased context, whereas lambda genes partly follow the trends of the host bacterium, and T7 genes have biased codon contexts that differ from those of the host. It has been reported that two successive third-codon positions tend to be occupied by two purines or two pyrimidines in Escherichia coli genes of low expression level. Here, the extent to which highly expressed protein genes can modulate base usage at two successive codon positions III, given the constraints on codon usage and protein sequence that act on them, was quantified. This demonstrates that the above-mentioned favored patterns are not a characteristic of weakly expressed genes but occur in all genes in which codon context can vary appreciably. The correlation between successive third-codon positions is a distinct feature of enterobacteria and of some phages, one that may result from adaptation of gene structure to translational efficiency. Conversely, codon context in yeast and human genes is biased--but for reasons unrelated to translation.

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Year:  1987        PMID: 3128715     DOI: 10.1093/oxfordjournals.molbev.a040450

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  22 in total

1.  Regularities of context-dependent codon bias in eukaryotic genes.

Authors:  Alexei Fedorov; Serge Saxonov; Walter Gilbert
Journal:  Nucleic Acids Res       Date:  2002-03-01       Impact factor: 16.971

2.  Gradients in nucleotide and codon usage along Escherichia coli genes.

Authors:  S D Hooper; O G Berg
Journal:  Nucleic Acids Res       Date:  2000-09-15       Impact factor: 16.971

Review 3.  Codon context.

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

4.  Codon bias is a major factor explaining phage evolution in translationally biased hosts.

Authors:  Alessandra Carbone
Journal:  J Mol Evol       Date:  2008-02-20       Impact factor: 2.395

Review 5.  You're one in a googol: optimizing genes for protein expression.

Authors:  Mark Welch; Alan Villalobos; Claes Gustafsson; Jeremy Minshull
Journal:  J R Soc Interface       Date:  2009-03-11       Impact factor: 4.118

6.  Doublet preference and gene evolution.

Authors:  R Hanai; A Wada
Journal:  J Mol Evol       Date:  1990-02       Impact factor: 2.395

7.  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

8.  On concerted origin of transfer RNAs with complementary anticodons.

Authors:  S Rodin; S Ohno; A Rodin
Journal:  Orig Life Evol Biosph       Date:  1993-12       Impact factor: 1.950

9.  The effect of context on synonymous codon usage in genes with low codon usage bias.

Authors:  M Bulmer
Journal:  Nucleic Acids Res       Date:  1990-05-25       Impact factor: 16.971

10.  Mammalian gene evolution: nucleotide sequence divergence between mouse and rat.

Authors:  K H Wolfe; P M Sharp
Journal:  J Mol Evol       Date:  1993-10       Impact factor: 2.395

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