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When is it time for reverse transcription to start and go?
Upon cell infection by a retrovirus, the viral DNA polymerase, called reverse transcriptase (RT), copies the genomic RNA to generate the proviral DNA flanked by two long terminal repeats (LTR). A discovery twenty years ago demonstrated that the structural viral nucleocapsid protein (NC) encoded by G...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656454/ https://www.ncbi.nlm.nih.gov/pubmed/19261185 http://dx.doi.org/10.1186/1742-4690-6-24 |
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author | Mougel, Marylène Houzet, Laurent Darlix, Jean-Luc |
author_facet | Mougel, Marylène Houzet, Laurent Darlix, Jean-Luc |
author_sort | Mougel, Marylène |
collection | PubMed |
description | Upon cell infection by a retrovirus, the viral DNA polymerase, called reverse transcriptase (RT), copies the genomic RNA to generate the proviral DNA flanked by two long terminal repeats (LTR). A discovery twenty years ago demonstrated that the structural viral nucleocapsid protein (NC) encoded by Gag is an essential cofactor of reverse transcription, chaperoning RT during viral DNA synthesis. However, it is only recently that NC was found to exert a control on the timing of reverse transcription, in a spatio-temporal manner. This brief review summarizes findings on the timing of reverse transcription in wild type HIV-1 and in nucleopcapsid (NC) mutants where virions contain a large amount of newly made viral DNA. This brief review also proposes some explanations of how NC may control late reverse transcription during Gag assembly in virus producer cells. |
format | Text |
id | pubmed-2656454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26564542009-03-17 When is it time for reverse transcription to start and go? Mougel, Marylène Houzet, Laurent Darlix, Jean-Luc Retrovirology Review Upon cell infection by a retrovirus, the viral DNA polymerase, called reverse transcriptase (RT), copies the genomic RNA to generate the proviral DNA flanked by two long terminal repeats (LTR). A discovery twenty years ago demonstrated that the structural viral nucleocapsid protein (NC) encoded by Gag is an essential cofactor of reverse transcription, chaperoning RT during viral DNA synthesis. However, it is only recently that NC was found to exert a control on the timing of reverse transcription, in a spatio-temporal manner. This brief review summarizes findings on the timing of reverse transcription in wild type HIV-1 and in nucleopcapsid (NC) mutants where virions contain a large amount of newly made viral DNA. This brief review also proposes some explanations of how NC may control late reverse transcription during Gag assembly in virus producer cells. BioMed Central 2009-03-04 /pmc/articles/PMC2656454/ /pubmed/19261185 http://dx.doi.org/10.1186/1742-4690-6-24 Text en Copyright © 2009 Mougel 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 Mougel, Marylène Houzet, Laurent Darlix, Jean-Luc When is it time for reverse transcription to start and go? |
title | When is it time for reverse transcription to start and go? |
title_full | When is it time for reverse transcription to start and go? |
title_fullStr | When is it time for reverse transcription to start and go? |
title_full_unstemmed | When is it time for reverse transcription to start and go? |
title_short | When is it time for reverse transcription to start and go? |
title_sort | when is it time for reverse transcription to start and go? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656454/ https://www.ncbi.nlm.nih.gov/pubmed/19261185 http://dx.doi.org/10.1186/1742-4690-6-24 |
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