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HIV-1 Replication and the Cellular Eukaryotic Translation Apparatus
Eukaryotic translation is a complex process composed of three main steps: initiation, elongation, and termination. During infections by RNA- and DNA-viruses, the eukaryotic translation machinery is used to assure optimal viral protein synthesis. Human immunodeficiency virus type I (HIV-1) uses sever...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306834/ https://www.ncbi.nlm.nih.gov/pubmed/25606970 http://dx.doi.org/10.3390/v7010199 |
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author | Guerrero, Santiago Batisse, Julien Libre, Camille Bernacchi, Serena Marquet, Roland Paillart, Jean-Christophe |
author_facet | Guerrero, Santiago Batisse, Julien Libre, Camille Bernacchi, Serena Marquet, Roland Paillart, Jean-Christophe |
author_sort | Guerrero, Santiago |
collection | PubMed |
description | Eukaryotic translation is a complex process composed of three main steps: initiation, elongation, and termination. During infections by RNA- and DNA-viruses, the eukaryotic translation machinery is used to assure optimal viral protein synthesis. Human immunodeficiency virus type I (HIV-1) uses several non-canonical pathways to translate its own proteins, such as leaky scanning, frameshifting, shunt, and cap-independent mechanisms. Moreover, HIV-1 modulates the host translation machinery by targeting key translation factors and overcomes different cellular obstacles that affect protein translation. In this review, we describe how HIV-1 proteins target several components of the eukaryotic translation machinery, which consequently improves viral translation and replication. |
format | Online Article Text |
id | pubmed-4306834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-43068342015-02-02 HIV-1 Replication and the Cellular Eukaryotic Translation Apparatus Guerrero, Santiago Batisse, Julien Libre, Camille Bernacchi, Serena Marquet, Roland Paillart, Jean-Christophe Viruses Review Eukaryotic translation is a complex process composed of three main steps: initiation, elongation, and termination. During infections by RNA- and DNA-viruses, the eukaryotic translation machinery is used to assure optimal viral protein synthesis. Human immunodeficiency virus type I (HIV-1) uses several non-canonical pathways to translate its own proteins, such as leaky scanning, frameshifting, shunt, and cap-independent mechanisms. Moreover, HIV-1 modulates the host translation machinery by targeting key translation factors and overcomes different cellular obstacles that affect protein translation. In this review, we describe how HIV-1 proteins target several components of the eukaryotic translation machinery, which consequently improves viral translation and replication. MDPI 2015-01-19 /pmc/articles/PMC4306834/ /pubmed/25606970 http://dx.doi.org/10.3390/v7010199 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Guerrero, Santiago Batisse, Julien Libre, Camille Bernacchi, Serena Marquet, Roland Paillart, Jean-Christophe HIV-1 Replication and the Cellular Eukaryotic Translation Apparatus |
title | HIV-1 Replication and the Cellular Eukaryotic Translation Apparatus |
title_full | HIV-1 Replication and the Cellular Eukaryotic Translation Apparatus |
title_fullStr | HIV-1 Replication and the Cellular Eukaryotic Translation Apparatus |
title_full_unstemmed | HIV-1 Replication and the Cellular Eukaryotic Translation Apparatus |
title_short | HIV-1 Replication and the Cellular Eukaryotic Translation Apparatus |
title_sort | hiv-1 replication and the cellular eukaryotic translation apparatus |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306834/ https://www.ncbi.nlm.nih.gov/pubmed/25606970 http://dx.doi.org/10.3390/v7010199 |
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