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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 (...

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Autores principales: Boissin-Quillon, Aurélia, Piau, Didier, Leroux, Caroline
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
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.
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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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