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Integrase and integration: biochemical activities of HIV-1 integrase
Integration of retroviral DNA is an obligatory step of retrovirus replication because proviral DNA is the template for productive infection. Integrase, a retroviral enzyme, catalyses integration. The process of integration can be divided into two sequential reactions. The first one, named 3'-pr...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2615046/ https://www.ncbi.nlm.nih.gov/pubmed/19091057 http://dx.doi.org/10.1186/1742-4690-5-114 |
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author | Delelis, Olivier Carayon, Kevin Saïb, Ali Deprez, Eric Mouscadet, Jean-François |
author_facet | Delelis, Olivier Carayon, Kevin Saïb, Ali Deprez, Eric Mouscadet, Jean-François |
author_sort | Delelis, Olivier |
collection | PubMed |
description | Integration of retroviral DNA is an obligatory step of retrovirus replication because proviral DNA is the template for productive infection. Integrase, a retroviral enzyme, catalyses integration. The process of integration can be divided into two sequential reactions. The first one, named 3'-processing, corresponds to a specific endonucleolytic reaction which prepares the viral DNA extremities to be competent for the subsequent covalent insertion, named strand transfer, into the host cell genome by a trans-esterification reaction. Recently, a novel specific activity of the full length integrase was reported, in vitro, by our group for two retroviral integrases (HIV-1 and PFV-1). This activity of internal cleavage occurs at a specific palindromic sequence mimicking the LTR-LTR junction described into the 2-LTR circles which are peculiar viral DNA forms found during viral infection. Moreover, recent studies demonstrated the existence of a weak palindromic consensus found at the integration sites. Taken together, these data underline the propensity of retroviral integrases for binding symmetrical sequences and give perspectives for targeting specific sequences used for gene therapy. |
format | Text |
id | pubmed-2615046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26150462009-01-08 Integrase and integration: biochemical activities of HIV-1 integrase Delelis, Olivier Carayon, Kevin Saïb, Ali Deprez, Eric Mouscadet, Jean-François Retrovirology Review Integration of retroviral DNA is an obligatory step of retrovirus replication because proviral DNA is the template for productive infection. Integrase, a retroviral enzyme, catalyses integration. The process of integration can be divided into two sequential reactions. The first one, named 3'-processing, corresponds to a specific endonucleolytic reaction which prepares the viral DNA extremities to be competent for the subsequent covalent insertion, named strand transfer, into the host cell genome by a trans-esterification reaction. Recently, a novel specific activity of the full length integrase was reported, in vitro, by our group for two retroviral integrases (HIV-1 and PFV-1). This activity of internal cleavage occurs at a specific palindromic sequence mimicking the LTR-LTR junction described into the 2-LTR circles which are peculiar viral DNA forms found during viral infection. Moreover, recent studies demonstrated the existence of a weak palindromic consensus found at the integration sites. Taken together, these data underline the propensity of retroviral integrases for binding symmetrical sequences and give perspectives for targeting specific sequences used for gene therapy. BioMed Central 2008-12-17 /pmc/articles/PMC2615046/ /pubmed/19091057 http://dx.doi.org/10.1186/1742-4690-5-114 Text en Copyright © 2008 Delelis 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 | Review Delelis, Olivier Carayon, Kevin Saïb, Ali Deprez, Eric Mouscadet, Jean-François Integrase and integration: biochemical activities of HIV-1 integrase |
title | Integrase and integration: biochemical activities of HIV-1 integrase |
title_full | Integrase and integration: biochemical activities of HIV-1 integrase |
title_fullStr | Integrase and integration: biochemical activities of HIV-1 integrase |
title_full_unstemmed | Integrase and integration: biochemical activities of HIV-1 integrase |
title_short | Integrase and integration: biochemical activities of HIV-1 integrase |
title_sort | integrase and integration: biochemical activities of hiv-1 integrase |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2615046/ https://www.ncbi.nlm.nih.gov/pubmed/19091057 http://dx.doi.org/10.1186/1742-4690-5-114 |
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