Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2007 Dec;35(3):767-76.
doi: 10.1007/s11262-007-0159-z. Epub 2007 Sep 1.

Mutation pressure shapes codon usage in the GC-Rich genome of foot-and-mouth disease virus

Affiliations

Mutation pressure shapes codon usage in the GC-Rich genome of foot-and-mouth disease virus

Jincheng Zhong et al. Virus Genes. 2007 Dec.

Abstract

Foot-and-mouth disease (FMD) is economically the most important viral-induced livestock disease worldwide. In this study, we report the results of a survey of codon usage bias of FMD virus (FMDV) representing all seven serotypes (A, O, C, Asia 1, SAT 1, SAT 2, and SAT 3). Correspondence analysis, a commonly used multivariate statistical approach, was carried out to analyze synonymous codon usage bias. The analysis showed that the overall extent of codon usage bias in FMDV is low. Furthermore, the good correlation between the frequency of G + C at the synonymous third position of sense codons (GC3S) content at silent sites of each sequence and codon usage bias suggested that mutation pressure rather than natural (translational) selection is the most important determinant of the codon bias observed. In addition, other factors, such as the lengths of open reading frame (ORF) and the hydrophobicity of genes also influence the codon usage variation among the genomes of FMDV in a minor way. The result of phylogenetic analyses based on the relative synonymous codon usage (RSCU) values indicated a few obvious phylogenetic incongruities, which suggest that more FMDV genome diversity may exist in nature than is currently indicated. Our work might give some clues to the features of FMDV genome and some evolutionary information of this virus.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Correlation between GC content at first and second codon positions (GC12) with that at synonymous third codon positions (GC3S). ORF, open reading frame
Fig. 2
Fig. 2
Distribution of the codon usage index, ENC, and GC content at synonymous third codon positions (GC3S). The curve indicates the expected codon usage if GC compositional constraints alone account for codon usage bias. ENC: effective number of codons; ORF, open reading frame
Fig. 3
Fig. 3
Correlation between the first (A), second axis (B) values in COA and GC3S values of each FMDV strains. COA: Correspondence analysis; GC3S: the frequency of the nucleotide G + C at the synonymous third codon position (excluding Met, Trp and the termination codons); ORF, open reading frame
Fig. 4
Fig. 4
Cluster tree based on the relative synonymous codon usage (RSCU) values of 40 FMDV strains examined. The cluster tree was generated by using Hierarchical cluster method

Similar articles

Cited by

References

    1. Grantham R., Gautier C., Gouy M. Nucl Acids Res. 1980;8:1893–1912. doi: 10.1093/nar/8.9.1893. - DOI - PMC - PubMed
    1. Bulmer M. J. Evol. Biol. 1988;1:15–26. doi: 10.1046/j.1420-9101.1988.1010015.x. - DOI
    1. Shields D.C., Sharp P.M., Higgins D.G., Wright F. Mol. Biol. Evol. 1988;5:704–716. - PubMed
    1. Stenico M., Lloyd A.T., Sharp P.M. Nucleic Acids Res. 1994;22:2437–2446. doi: 10.1093/nar/22.13.2437. - DOI - PMC - PubMed
    1. Karlin S., Mrazek J. J. Mol. Biol. 1996;262:459–472. doi: 10.1006/jmbi.1996.0528. - DOI - PubMed

Publication types