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The 5′ and 3′ ends of alphavirus RNAs – Non-coding is not non-functional

The non-coding regions found at the 5′ and 3′ ends of alphavirus genomes regulate viral gene expression, replication, translation and virus–host interactions, which have significant implications for viral evolution, host range, and pathogenesis. The functions of these non-coding regions are mediated...

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Autores principales: Hyde, Jennifer L., Chen, Rubing, Trobaugh, Derek W., Diamond, Michael S., Weaver, Scott C., Klimstra, William B., Wilusz, Jeffrey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4654126/
https://www.ncbi.nlm.nih.gov/pubmed/25630058
http://dx.doi.org/10.1016/j.virusres.2015.01.016
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author Hyde, Jennifer L.
Chen, Rubing
Trobaugh, Derek W.
Diamond, Michael S.
Weaver, Scott C.
Klimstra, William B.
Wilusz, Jeffrey
author_facet Hyde, Jennifer L.
Chen, Rubing
Trobaugh, Derek W.
Diamond, Michael S.
Weaver, Scott C.
Klimstra, William B.
Wilusz, Jeffrey
author_sort Hyde, Jennifer L.
collection PubMed
description The non-coding regions found at the 5′ and 3′ ends of alphavirus genomes regulate viral gene expression, replication, translation and virus–host interactions, which have significant implications for viral evolution, host range, and pathogenesis. The functions of these non-coding regions are mediated by a combination of linear sequence and structural elements. The capped 5′ untranslated region (UTR) contains promoter elements, translational regulatory sequences that modulate dependence on cellular translation factors, and structures that help to avoid innate immune defenses. The polyadenylated 3′ UTR contains highly conserved sequence elements for viral replication, binding sites for cellular miRNAs that determine cell tropism, host range, and pathogenesis, and conserved binding regions for a cellular protein that influences viral RNA stability. Nonetheless, there are additional conserved elements in non-coding regions of the virus (e.g., the repeated sequence elements in the 3′ UTR) whose function remains obscure. Thus, key questions remain as to the function of these short yet influential untranslated segments of alphavirus RNAs.
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spelling pubmed-46541262016-08-03 The 5′ and 3′ ends of alphavirus RNAs – Non-coding is not non-functional Hyde, Jennifer L. Chen, Rubing Trobaugh, Derek W. Diamond, Michael S. Weaver, Scott C. Klimstra, William B. Wilusz, Jeffrey Virus Res Article The non-coding regions found at the 5′ and 3′ ends of alphavirus genomes regulate viral gene expression, replication, translation and virus–host interactions, which have significant implications for viral evolution, host range, and pathogenesis. The functions of these non-coding regions are mediated by a combination of linear sequence and structural elements. The capped 5′ untranslated region (UTR) contains promoter elements, translational regulatory sequences that modulate dependence on cellular translation factors, and structures that help to avoid innate immune defenses. The polyadenylated 3′ UTR contains highly conserved sequence elements for viral replication, binding sites for cellular miRNAs that determine cell tropism, host range, and pathogenesis, and conserved binding regions for a cellular protein that influences viral RNA stability. Nonetheless, there are additional conserved elements in non-coding regions of the virus (e.g., the repeated sequence elements in the 3′ UTR) whose function remains obscure. Thus, key questions remain as to the function of these short yet influential untranslated segments of alphavirus RNAs. Elsevier B.V. 2015-08-03 2015-01-25 /pmc/articles/PMC4654126/ /pubmed/25630058 http://dx.doi.org/10.1016/j.virusres.2015.01.016 Text en Copyright © 2015 Elsevier B.V. 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
Hyde, Jennifer L.
Chen, Rubing
Trobaugh, Derek W.
Diamond, Michael S.
Weaver, Scott C.
Klimstra, William B.
Wilusz, Jeffrey
The 5′ and 3′ ends of alphavirus RNAs – Non-coding is not non-functional
title The 5′ and 3′ ends of alphavirus RNAs – Non-coding is not non-functional
title_full The 5′ and 3′ ends of alphavirus RNAs – Non-coding is not non-functional
title_fullStr The 5′ and 3′ ends of alphavirus RNAs – Non-coding is not non-functional
title_full_unstemmed The 5′ and 3′ ends of alphavirus RNAs – Non-coding is not non-functional
title_short The 5′ and 3′ ends of alphavirus RNAs – Non-coding is not non-functional
title_sort 5′ and 3′ ends of alphavirus rnas – non-coding is not non-functional
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4654126/
https://www.ncbi.nlm.nih.gov/pubmed/25630058
http://dx.doi.org/10.1016/j.virusres.2015.01.016
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