Absence of translationally selected synonymous codon usage bias in Helicobacter pylori

Institute of Genetics 1 , and Division of Gastroenterology, Department of Medicine and Institute of Infections and Immunity 2 , University of Nottingham, Queen’s Medical Centre, Nottingham NG7 2UH, UK Author for correspondence: Paul M. Sharp. Tel: +44 115 970 9263. Fax: +44 115 970 9906. e-mail: pau...

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Published inMicrobiology (Society for General Microbiology) Vol. 146; no. 4; pp. 851 - 860
Main Authors Lafay, Benedicte, Atherton, John C, Sharp, Paul M
Format Journal Article
LanguageEnglish
Published Reading Soc General Microbiol 01.04.2000
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Abstract Institute of Genetics 1 , and Division of Gastroenterology, Department of Medicine and Institute of Infections and Immunity 2 , University of Nottingham, Queen’s Medical Centre, Nottingham NG7 2UH, UK Author for correspondence: Paul M. Sharp. Tel: +44 115 970 9263. Fax: +44 115 970 9906. e-mail: paul{at}evol.nott.ac.uk Synonymous codon usage in the complete genome of Helicobacter pylori was investigated. The moderate A+T-richness of the genome (G+C=39 mol%) is reflected in the overall synonymous codon usage but the frequencies of some codons cannot be explained by simple mutational biases. A low level of heterogeneity among genes was observed, but this does not appear to be due to varying mutational bias or translational selection. Some of the heterogeneity was due to amino acid composition variation among the encoded proteins, and some may be attributable to recent acquisition of genes from other species. Since Hel. pylori codon usage is not dominated by biased mutation patterns, the absence of evidence for translationally mediated selection among synonymous codons is striking. This has implications with regard to the life history of this species, and in particular suggests that Hel. pylori strains are not subject to periods of competitive exponential growth. Despite the lack of selected codon usage, base composition immediately after the translation initiation site is skewed, consistent with selection against secondary structure formation in this region. Keywords: codon usage, Helicobacter pylori , translational selection, cag pathogenicity island, molecular evolution Abbreviations: GC3 s , G+C content at synonymously variable third positions of sense codons; N c , effective number of codons; RSCU, relative synonymous codon usage a Present address: Centre d’Océanologie de Marseille, CNRS-UMR 6540, Station Marine d’Endoume, rue Batterie des Lions, 13007 Marseille, France.
AbstractList Synonymous codon usage in the complete genome of Helicobacter pylori was investigated. The moderate A+T-richness of the genome (G+C=39 mol%) is reflected in the overall synonymous codon usage but the frequencies of some codons cannot be explained by simple mutational biases. A low level of heterogeneity among genes was observed, but this does not appear to be due to varying mutational bias or translational selection. Some of the heterogeneity was due to amino acid composition variation among the encoded proteins, and some may be attributable to recent acquisition of genes from other species. Since Hel. pylori codon usage is not dominated by biased mutation patterns, the absence of evidence for translationally mediated selection among synonymous codons is striking. This has implications with regard to the life history of this species, and in particular suggests that Hel. pylori strains are not subject to periods of competitive exponential growth. Despite the lack of selected codon usage, base composition immediately after the translation initiation site is skewed, consistent with selection against secondary structure formation in this region.
Synonymous codon usage in the complete genome of Helicobacter pylori was investigated. The moderate A+T-richness of the genome (G+C=39 mol%) is reflected in the overall synonymous codon usage but the frequencies of some codons cannot be explained by simple mutational biases. A low level of heterogeneity among genes was observed, but this does not appear to be due to varying mutational bias or translational selection. Some of the heterogeneity was due to amino acid composition variation among the encoded proteins, and some may be attributable to recent acquisition of genes from other species. Since Hel. pylori codon usage is not dominated by biased mutation patterns, the absence of evidence for translationally mediated selection among synonymous codons is striking. This has implications with regard to the life history of this species, and in particular suggests that Hel. pylori strains are not subject to periods of competitive exponential growth. Despite the lack of selected codon usage, base composition immediately after the translation initiation site is skewed, consistent with selection against secondary structure formation in this region.Synonymous codon usage in the complete genome of Helicobacter pylori was investigated. The moderate A+T-richness of the genome (G+C=39 mol%) is reflected in the overall synonymous codon usage but the frequencies of some codons cannot be explained by simple mutational biases. A low level of heterogeneity among genes was observed, but this does not appear to be due to varying mutational bias or translational selection. Some of the heterogeneity was due to amino acid composition variation among the encoded proteins, and some may be attributable to recent acquisition of genes from other species. Since Hel. pylori codon usage is not dominated by biased mutation patterns, the absence of evidence for translationally mediated selection among synonymous codons is striking. This has implications with regard to the life history of this species, and in particular suggests that Hel. pylori strains are not subject to periods of competitive exponential growth. Despite the lack of selected codon usage, base composition immediately after the translation initiation site is skewed, consistent with selection against secondary structure formation in this region.
Institute of Genetics 1 , and Division of Gastroenterology, Department of Medicine and Institute of Infections and Immunity 2 , University of Nottingham, Queen’s Medical Centre, Nottingham NG7 2UH, UK Author for correspondence: Paul M. Sharp. Tel: +44 115 970 9263. Fax: +44 115 970 9906. e-mail: paul{at}evol.nott.ac.uk Synonymous codon usage in the complete genome of Helicobacter pylori was investigated. The moderate A+T-richness of the genome (G+C=39 mol%) is reflected in the overall synonymous codon usage but the frequencies of some codons cannot be explained by simple mutational biases. A low level of heterogeneity among genes was observed, but this does not appear to be due to varying mutational bias or translational selection. Some of the heterogeneity was due to amino acid composition variation among the encoded proteins, and some may be attributable to recent acquisition of genes from other species. Since Hel. pylori codon usage is not dominated by biased mutation patterns, the absence of evidence for translationally mediated selection among synonymous codons is striking. This has implications with regard to the life history of this species, and in particular suggests that Hel. pylori strains are not subject to periods of competitive exponential growth. Despite the lack of selected codon usage, base composition immediately after the translation initiation site is skewed, consistent with selection against secondary structure formation in this region. Keywords: codon usage, Helicobacter pylori , translational selection, cag pathogenicity island, molecular evolution Abbreviations: GC3 s , G+C content at synonymously variable third positions of sense codons; N c , effective number of codons; RSCU, relative synonymous codon usage a Present address: Centre d’Océanologie de Marseille, CNRS-UMR 6540, Station Marine d’Endoume, rue Batterie des Lions, 13007 Marseille, France.
Author Sharp, Paul M
Lafay, Benedicte
Atherton, John C
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Issue 4
Keywords Genetic variability
Spirillales
Synonymy
Use
Spirillaceae
Genetical translation
Gene expression
Genetic code
Molecular evolution
Nucleic base
Codon
Helicobacter pylori
DNA
Bacteria
Chemical composition
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Snippet Institute of Genetics 1 , and Division of Gastroenterology, Department of Medicine and Institute of Infections and Immunity 2 , University of Nottingham,...
Synonymous codon usage in the complete genome of Helicobacter pylori was investigated. The moderate A+T-richness of the genome (G+C=39 mol%) is reflected in...
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SubjectTerms Bacteriology
Biodiversity
Bioinformatics
Biological and medical sciences
Codon
Computer Science
Fundamental and applied biological sciences. Psychology
Genetics
Genome, Bacterial
Helicobacter pylori
Helicobacter pylori - genetics
Life Sciences
Microbiology
Populations and Evolution
Protein Biosynthesis
Quantitative Methods
synonymous codon usage
translation initiation
Title Absence of translationally selected synonymous codon usage bias in Helicobacter pylori
URI http://mic.sgmjournals.org/cgi/content/abstract/146/4/851
https://www.ncbi.nlm.nih.gov/pubmed/10784043
https://www.proquest.com/docview/17753953
https://www.proquest.com/docview/71071537
https://hal.science/hal-00412908
Volume 146
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