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Silencing viruses by RNA interference

Post-transcriptional gene silencing (PTGS) makes possible new approaches for studying the various steps of the viral cycle. Plus-strand RNA viruses appear to be attractive targets for small interfering RNAs (siRNAs), as their genome functions as both mRNA and replication template. PTGS creates an al...

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Detalles Bibliográficos
Autores principales: Colbère-Garapin, Florence, Blondel, Bruno, Saulnier, Aure, Pelletier, Isabelle, Labadie, Karine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier SAS. 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7110879/
https://www.ncbi.nlm.nih.gov/pubmed/15820151
http://dx.doi.org/10.1016/j.micinf.2005.02.003
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author Colbère-Garapin, Florence
Blondel, Bruno
Saulnier, Aure
Pelletier, Isabelle
Labadie, Karine
author_facet Colbère-Garapin, Florence
Blondel, Bruno
Saulnier, Aure
Pelletier, Isabelle
Labadie, Karine
author_sort Colbère-Garapin, Florence
collection PubMed
description Post-transcriptional gene silencing (PTGS) makes possible new approaches for studying the various steps of the viral cycle. Plus-strand RNA viruses appear to be attractive targets for small interfering RNAs (siRNAs), as their genome functions as both mRNA and replication template. PTGS creates an alternative to classic reverse genetics for viruses with either negative-strand or double-stranded RNA genomes and for those with a large genome. PTGS allows modification of the expression of a given cellular gene as a means to elucidate its role in the viral cycle and in virus–host cell interactions, and to investigate cellular pathways involved in viral pathogenesis. It also allows the creation of new animal models of human diseases. In addition, PTGS already appears to be a promising new therapeutic tool to fight viral multiplication and dissemination through the host and to prevent inflammation and virus-induced pathogenesis, including virus-induced tumorigenesis.
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spelling pubmed-71108792020-04-02 Silencing viruses by RNA interference Colbère-Garapin, Florence Blondel, Bruno Saulnier, Aure Pelletier, Isabelle Labadie, Karine Microbes Infect Article Post-transcriptional gene silencing (PTGS) makes possible new approaches for studying the various steps of the viral cycle. Plus-strand RNA viruses appear to be attractive targets for small interfering RNAs (siRNAs), as their genome functions as both mRNA and replication template. PTGS creates an alternative to classic reverse genetics for viruses with either negative-strand or double-stranded RNA genomes and for those with a large genome. PTGS allows modification of the expression of a given cellular gene as a means to elucidate its role in the viral cycle and in virus–host cell interactions, and to investigate cellular pathways involved in viral pathogenesis. It also allows the creation of new animal models of human diseases. In addition, PTGS already appears to be a promising new therapeutic tool to fight viral multiplication and dissemination through the host and to prevent inflammation and virus-induced pathogenesis, including virus-induced tumorigenesis. Elsevier SAS. 2005-04 2005-03-13 /pmc/articles/PMC7110879/ /pubmed/15820151 http://dx.doi.org/10.1016/j.micinf.2005.02.003 Text en Copyright © 2005 Elsevier 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
Colbère-Garapin, Florence
Blondel, Bruno
Saulnier, Aure
Pelletier, Isabelle
Labadie, Karine
Silencing viruses by RNA interference
title Silencing viruses by RNA interference
title_full Silencing viruses by RNA interference
title_fullStr Silencing viruses by RNA interference
title_full_unstemmed Silencing viruses by RNA interference
title_short Silencing viruses by RNA interference
title_sort silencing viruses by rna interference
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7110879/
https://www.ncbi.nlm.nih.gov/pubmed/15820151
http://dx.doi.org/10.1016/j.micinf.2005.02.003
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