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The impact of RNA structure on picornavirus IRES activity

Internal ribosome entry site (IRES) elements consist of cis-acting regions that recruit the translation machinery to an internal position in the mRNA. The biological relevance of RNA structure-mediated mechanisms involved in internal ribosome recruitment is now emerging from the structural and funct...

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Detalles Bibliográficos
Autor principal: Martínez-Salas, Encarnación
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172834/
https://www.ncbi.nlm.nih.gov/pubmed/18420413
http://dx.doi.org/10.1016/j.tim.2008.01.013
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author Martínez-Salas, Encarnación
author_facet Martínez-Salas, Encarnación
author_sort Martínez-Salas, Encarnación
collection PubMed
description Internal ribosome entry site (IRES) elements consist of cis-acting regions that recruit the translation machinery to an internal position in the mRNA. The biological relevance of RNA structure-mediated mechanisms involved in internal ribosome recruitment is now emerging from the structural and functional analysis of viral IRES elements. However, because IRES elements found in genetically distant mRNAs seem to be organized in different RNA structures, the definition of the structural requirements for IRES activity is challenging and demands multidisciplinary approaches. This review discusses the latest reports that establish a relationship between RNA structure and IRES function in picornavirus genomes, the first RNAs described to contain these specialized regulatory elements.
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spelling pubmed-71728342020-04-22 The impact of RNA structure on picornavirus IRES activity Martínez-Salas, Encarnación Trends Microbiol Article Internal ribosome entry site (IRES) elements consist of cis-acting regions that recruit the translation machinery to an internal position in the mRNA. The biological relevance of RNA structure-mediated mechanisms involved in internal ribosome recruitment is now emerging from the structural and functional analysis of viral IRES elements. However, because IRES elements found in genetically distant mRNAs seem to be organized in different RNA structures, the definition of the structural requirements for IRES activity is challenging and demands multidisciplinary approaches. This review discusses the latest reports that establish a relationship between RNA structure and IRES function in picornavirus genomes, the first RNAs described to contain these specialized regulatory elements. Elsevier Ltd. 2008-05 2008-04-15 /pmc/articles/PMC7172834/ /pubmed/18420413 http://dx.doi.org/10.1016/j.tim.2008.01.013 Text en Copyright © 2008 Elsevier Ltd. 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
Martínez-Salas, Encarnación
The impact of RNA structure on picornavirus IRES activity
title The impact of RNA structure on picornavirus IRES activity
title_full The impact of RNA structure on picornavirus IRES activity
title_fullStr The impact of RNA structure on picornavirus IRES activity
title_full_unstemmed The impact of RNA structure on picornavirus IRES activity
title_short The impact of RNA structure on picornavirus IRES activity
title_sort impact of rna structure on picornavirus ires activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172834/
https://www.ncbi.nlm.nih.gov/pubmed/18420413
http://dx.doi.org/10.1016/j.tim.2008.01.013
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