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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2015
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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. |
format | Online Article Text |
id | pubmed-4654126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
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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