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Relationship of SARS-CoV to other pathogenic RNA viruses explored by tetranucleotide usage profiling
BACKGROUND: The exact origin of the cause of the Severe Acute Respiratory Syndrome (SARS) is still an open question. The genomic sequence relationship of SARS-CoV with 30 different single-stranded RNA (ssRNA) viruses of various families was studied using two non-standard approaches. Both approaches...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2003
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC222961/ https://www.ncbi.nlm.nih.gov/pubmed/14499005 http://dx.doi.org/10.1186/1471-2105-4-43 |
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author | Yap, Yee Leng Zhang, Xue Wu Danchin, Antoine |
author_facet | Yap, Yee Leng Zhang, Xue Wu Danchin, Antoine |
author_sort | Yap, Yee Leng |
collection | PubMed |
description | BACKGROUND: The exact origin of the cause of the Severe Acute Respiratory Syndrome (SARS) is still an open question. The genomic sequence relationship of SARS-CoV with 30 different single-stranded RNA (ssRNA) viruses of various families was studied using two non-standard approaches. Both approaches began with the vectorial profiling of the tetra-nucleotide usage pattern V for each virus. In approach one, a distance measure of a vector V, based on correlation coefficient was devised to construct a relationship tree by the neighbor-joining algorithm. In approach two, a multivariate factor analysis was performed to derive the embedded tetra-nucleotide usage patterns. These patterns were subsequently used to classify the selected viruses. RESULTS: Both approaches yielded relationship outcomes that are consistent with the known virus classification. They also indicated that the genome of RNA viruses from the same family conform to a specific pattern of word usage. Based on the correlation of the overall tetra-nucleotide usage patterns, the Transmissible Gastroenteritis Virus (TGV) and the Feline CoronaVirus (FCoV) are closest to SARS-CoV. Surprisingly also, the RNA viruses that do not go through a DNA stage displayed a remarkable discrimination against the CpG and UpA di-nucleotide (z = -77.31, -52.48 respectively) and selection for UpG and CpA (z = 65.79,49.99 respectively). Potential factors influencing these biases are discussed. CONCLUSION: The study of genomic word usage is a powerful method to classify RNA viruses. The congruence of the relationship outcomes with the known classification indicates that there exist phylogenetic signals in the tetra-nucleotide usage patterns, that is most prominent in the replicase open reading frames. |
format | Text |
id | pubmed-222961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-2229612003-10-24 Relationship of SARS-CoV to other pathogenic RNA viruses explored by tetranucleotide usage profiling Yap, Yee Leng Zhang, Xue Wu Danchin, Antoine BMC Bioinformatics Research Article BACKGROUND: The exact origin of the cause of the Severe Acute Respiratory Syndrome (SARS) is still an open question. The genomic sequence relationship of SARS-CoV with 30 different single-stranded RNA (ssRNA) viruses of various families was studied using two non-standard approaches. Both approaches began with the vectorial profiling of the tetra-nucleotide usage pattern V for each virus. In approach one, a distance measure of a vector V, based on correlation coefficient was devised to construct a relationship tree by the neighbor-joining algorithm. In approach two, a multivariate factor analysis was performed to derive the embedded tetra-nucleotide usage patterns. These patterns were subsequently used to classify the selected viruses. RESULTS: Both approaches yielded relationship outcomes that are consistent with the known virus classification. They also indicated that the genome of RNA viruses from the same family conform to a specific pattern of word usage. Based on the correlation of the overall tetra-nucleotide usage patterns, the Transmissible Gastroenteritis Virus (TGV) and the Feline CoronaVirus (FCoV) are closest to SARS-CoV. Surprisingly also, the RNA viruses that do not go through a DNA stage displayed a remarkable discrimination against the CpG and UpA di-nucleotide (z = -77.31, -52.48 respectively) and selection for UpG and CpA (z = 65.79,49.99 respectively). Potential factors influencing these biases are discussed. CONCLUSION: The study of genomic word usage is a powerful method to classify RNA viruses. The congruence of the relationship outcomes with the known classification indicates that there exist phylogenetic signals in the tetra-nucleotide usage patterns, that is most prominent in the replicase open reading frames. BioMed Central 2003-09-20 /pmc/articles/PMC222961/ /pubmed/14499005 http://dx.doi.org/10.1186/1471-2105-4-43 Text en Copyright © 2003 Yap et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research Article Yap, Yee Leng Zhang, Xue Wu Danchin, Antoine Relationship of SARS-CoV to other pathogenic RNA viruses explored by tetranucleotide usage profiling |
title | Relationship of SARS-CoV to other pathogenic RNA viruses explored by tetranucleotide usage profiling |
title_full | Relationship of SARS-CoV to other pathogenic RNA viruses explored by tetranucleotide usage profiling |
title_fullStr | Relationship of SARS-CoV to other pathogenic RNA viruses explored by tetranucleotide usage profiling |
title_full_unstemmed | Relationship of SARS-CoV to other pathogenic RNA viruses explored by tetranucleotide usage profiling |
title_short | Relationship of SARS-CoV to other pathogenic RNA viruses explored by tetranucleotide usage profiling |
title_sort | relationship of sars-cov to other pathogenic rna viruses explored by tetranucleotide usage profiling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC222961/ https://www.ncbi.nlm.nih.gov/pubmed/14499005 http://dx.doi.org/10.1186/1471-2105-4-43 |
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