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In silico segmentations of lentivirus envelope sequences
BACKGROUND: The gene encoding the envelope of lentiviruses exhibits a considerable plasticity, particularly the region which encodes the surface (SU) glycoprotein. Interestingly, mutations do not appear uniformly along the sequence of SU, but they are clustered in restricted areas, called variable (...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1847453/ https://www.ncbi.nlm.nih.gov/pubmed/17376229 http://dx.doi.org/10.1186/1471-2105-8-99 |
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author | Boissin-Quillon, Aurélia Piau, Didier Leroux, Caroline |
author_facet | Boissin-Quillon, Aurélia Piau, Didier Leroux, Caroline |
author_sort | Boissin-Quillon, Aurélia |
collection | PubMed |
description | BACKGROUND: The gene encoding the envelope of lentiviruses exhibits a considerable plasticity, particularly the region which encodes the surface (SU) glycoprotein. Interestingly, mutations do not appear uniformly along the sequence of SU, but they are clustered in restricted areas, called variable (V) regions, which are interspersed with relatively more stable regions, called constant (C) regions. We look for specific signatures of C/V regions, using hidden Markov models constructed with SU sequences of the equine, human, small ruminant and simian lentiviruses. RESULTS: Our models yield clear and accurate delimitations of the C/V regions, when the test set and the training set were made up of sequences of the same lentivirus, but also when they were made up of sequences of different lentiviruses. Interestingly, the models predicted the different regions of lentiviruses such as the bovine and feline lentiviruses, not used in the training set. Models based on composite training sets produce accurate segmentations of sequences of all these lentiviruses. CONCLUSION: Our results suggest that each C/V region has a specific statistical oligonucleotide composition, and that the C (respectively V) regions of one of these lentiviruses are statistically more similar to the C (respectively V) regions of the other lentiviruses, than to the V (respectively C) regions of the same lentivirus. |
format | Text |
id | pubmed-1847453 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18474532007-04-04 In silico segmentations of lentivirus envelope sequences Boissin-Quillon, Aurélia Piau, Didier Leroux, Caroline BMC Bioinformatics Research Article BACKGROUND: The gene encoding the envelope of lentiviruses exhibits a considerable plasticity, particularly the region which encodes the surface (SU) glycoprotein. Interestingly, mutations do not appear uniformly along the sequence of SU, but they are clustered in restricted areas, called variable (V) regions, which are interspersed with relatively more stable regions, called constant (C) regions. We look for specific signatures of C/V regions, using hidden Markov models constructed with SU sequences of the equine, human, small ruminant and simian lentiviruses. RESULTS: Our models yield clear and accurate delimitations of the C/V regions, when the test set and the training set were made up of sequences of the same lentivirus, but also when they were made up of sequences of different lentiviruses. Interestingly, the models predicted the different regions of lentiviruses such as the bovine and feline lentiviruses, not used in the training set. Models based on composite training sets produce accurate segmentations of sequences of all these lentiviruses. CONCLUSION: Our results suggest that each C/V region has a specific statistical oligonucleotide composition, and that the C (respectively V) regions of one of these lentiviruses are statistically more similar to the C (respectively V) regions of the other lentiviruses, than to the V (respectively C) regions of the same lentivirus. BioMed Central 2007-03-21 /pmc/articles/PMC1847453/ /pubmed/17376229 http://dx.doi.org/10.1186/1471-2105-8-99 Text en Copyright © 2007 Boissin-Quillon et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Boissin-Quillon, Aurélia Piau, Didier Leroux, Caroline In silico segmentations of lentivirus envelope sequences |
title | In silico segmentations of lentivirus envelope sequences |
title_full | In silico segmentations of lentivirus envelope sequences |
title_fullStr | In silico segmentations of lentivirus envelope sequences |
title_full_unstemmed | In silico segmentations of lentivirus envelope sequences |
title_short | In silico segmentations of lentivirus envelope sequences |
title_sort | in silico segmentations of lentivirus envelope sequences |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1847453/ https://www.ncbi.nlm.nih.gov/pubmed/17376229 http://dx.doi.org/10.1186/1471-2105-8-99 |
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