Exp Mol Med.  2009 Oct;41(10):746-756. 10.3858/emm.2009.41.10.081.

Comparative study of synonymous codon usage variations between the nucleocapsid and spike genes of coronavirus, and C-type lectin domain genes of human and mouse

Affiliations
  • 1Supercomputing Center, Korea Institute of Science and Technology Information, Daejon 305-806, Korea.
  • 2Laboratory of Computational Biology and Bioinformatics, Institute of Health and Environment, Graduate School of Public Health, Seoul National University, Seoul 110-799, Korea. hss2003@snu.ac.kr
  • 3Interdisciplinary Graduate Program in Bioinformatics, College of Natural Science, Seoul National University, Seoul 151-742, Korea.

Abstract

Coronaviruses (CoVs) are single-stranded RNA viruses which contain the largest RNA genomes, and severe acute respiratory syndrome coronavirus (SARS-CoV), a newly found group 2 CoV, emerged as infectious disease with high mortality rate. In this study, we compared the synonymous codon usage patterns between the nucleocapsid and spike genes of CoVs, and C-type lectin domain (CTLD) genes of human and mouse on the codon basis. Findings indicate that the nucleocapsid genes of CoVs were affected from the synonymous codon usage bias than spike genes, and the CTLDs of human and mouse partially overlapped with the nucleocapsid genes of CoVs. In addition, we observed that CTLDs which showed the similar relative synonymous codon usage (RSCU) patterns with CoVs were commonly derived from the human chromosome 12, and mouse chromosome 6 and 12, suggesting that there might be a specific genomic region or chromosomes which show a more similar synonymous codon usage pattern with viral genes. Our findings contribute to developing the codon-optimization method in DNA vaccines, and further study is needed to determine a specific correlation between the codon usage patterns and the chromosomal locations in higher organisms.

Keyword

coronavirus; host-pathogen interactions; lectins, C-type

MeSH Terms

Animals
Codon/*genetics
Humans
Lectins, C-Type/*genetics
Membrane Glycoproteins/*genetics
Mice
Nucleocapsid/*genetics
Phylogeny
SARS Virus/*genetics/pathogenicity
Severe Acute Respiratory Syndrome/prevention & control
Species Specificity
Vaccines, DNA
Viral Envelope Proteins/*genetics
Virus Attachment
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