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Identification of conserved lentiviral sequences as landmarks of genomic flexibility
Considering that recombinations produce quasispecies in lentivirus spreading, we identified and localized highly conserved sequences that may play an important role in viral ontology. Comparison of entire genomes, including 237 human, simian and non-primate mammal lentiviruses and 103 negative contr...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Académie des sciences. Published by Elsevier Masson SAS
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172886/ https://www.ncbi.nlm.nih.gov/pubmed/17027636 http://dx.doi.org/10.1016/j.crvi.2006.07.001 |
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author | Moncany, Maurice L.J. Dalet, Karine Courtois, Pascal R.R. |
author_facet | Moncany, Maurice L.J. Dalet, Karine Courtois, Pascal R.R. |
author_sort | Moncany, Maurice L.J. |
collection | PubMed |
description | Considering that recombinations produce quasispecies in lentivirus spreading, we identified and localized highly conserved sequences that may play an important role in viral ontology. Comparison of entire genomes, including 237 human, simian and non-primate mammal lentiviruses and 103 negative control viruses, led to identify 28 Conserved Lentiviral Sequences (CLSs). They were located mainly in the structural genes forming hot spots particularly in the gag and pol genes and to a lesser extent in LTRs and regulatory genes. The CLS pattern was the same throughout the different HIV-1 subtypes, except for some HIV-1-O strains. Only CLS 3 and 4 were detected in both negative control HTLV-1 oncornaviruses and D-particle-forming simian viruses, which are not immunodeficiency inducers and display a genetic stability. CLSs divided the virus genomes into domains allowing us to distinguish sequence families leading to the notion of ‘species self’ besides that of ‘lentiviral self’. Most of acutely localized CLSs in HIV-1s (82%) corresponded to wide recombination segments being currently reported. To cite this article: M.L.J. Moncany et al., C. R. Biologies 329 (2006). |
format | Online Article Text |
id | pubmed-7172886 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Académie des sciences. Published by Elsevier Masson SAS |
record_format | MEDLINE/PubMed |
spelling | pubmed-71728862020-04-22 Identification of conserved lentiviral sequences as landmarks of genomic flexibility Moncany, Maurice L.J. Dalet, Karine Courtois, Pascal R.R. C R Biol Article Considering that recombinations produce quasispecies in lentivirus spreading, we identified and localized highly conserved sequences that may play an important role in viral ontology. Comparison of entire genomes, including 237 human, simian and non-primate mammal lentiviruses and 103 negative control viruses, led to identify 28 Conserved Lentiviral Sequences (CLSs). They were located mainly in the structural genes forming hot spots particularly in the gag and pol genes and to a lesser extent in LTRs and regulatory genes. The CLS pattern was the same throughout the different HIV-1 subtypes, except for some HIV-1-O strains. Only CLS 3 and 4 were detected in both negative control HTLV-1 oncornaviruses and D-particle-forming simian viruses, which are not immunodeficiency inducers and display a genetic stability. CLSs divided the virus genomes into domains allowing us to distinguish sequence families leading to the notion of ‘species self’ besides that of ‘lentiviral self’. Most of acutely localized CLSs in HIV-1s (82%) corresponded to wide recombination segments being currently reported. To cite this article: M.L.J. Moncany et al., C. R. Biologies 329 (2006). Académie des sciences. Published by Elsevier Masson SAS 2006-10 2006-08-08 /pmc/articles/PMC7172886/ /pubmed/17027636 http://dx.doi.org/10.1016/j.crvi.2006.07.001 Text en Copyright © 2006 Académie des sciences. Published by Elsevier Masson SAS All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Moncany, Maurice L.J. Dalet, Karine Courtois, Pascal R.R. Identification of conserved lentiviral sequences as landmarks of genomic flexibility |
title | Identification of conserved lentiviral sequences as landmarks of genomic flexibility |
title_full | Identification of conserved lentiviral sequences as landmarks of genomic flexibility |
title_fullStr | Identification of conserved lentiviral sequences as landmarks of genomic flexibility |
title_full_unstemmed | Identification of conserved lentiviral sequences as landmarks of genomic flexibility |
title_short | Identification of conserved lentiviral sequences as landmarks of genomic flexibility |
title_sort | identification of conserved lentiviral sequences as landmarks of genomic flexibility |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172886/ https://www.ncbi.nlm.nih.gov/pubmed/17027636 http://dx.doi.org/10.1016/j.crvi.2006.07.001 |
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