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RNA structure analysis of alphacoronavirus terminal genome regions

Coronavirus genome replication is mediated by a multi-subunit protein complex that is comprised of more than a dozen virally encoded and several cellular proteins. Interactions of the viral replicase complex with cis-acting RNA elements located in the 5′ and 3′-terminal genome regions ensure the spe...

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Autores principales: Madhugiri, Ramakanth, Fricke, Markus, Marz, Manja, Ziebuhr, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114417/
https://www.ncbi.nlm.nih.gov/pubmed/25307890
http://dx.doi.org/10.1016/j.virusres.2014.10.001
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author Madhugiri, Ramakanth
Fricke, Markus
Marz, Manja
Ziebuhr, John
author_facet Madhugiri, Ramakanth
Fricke, Markus
Marz, Manja
Ziebuhr, John
author_sort Madhugiri, Ramakanth
collection PubMed
description Coronavirus genome replication is mediated by a multi-subunit protein complex that is comprised of more than a dozen virally encoded and several cellular proteins. Interactions of the viral replicase complex with cis-acting RNA elements located in the 5′ and 3′-terminal genome regions ensure the specific replication of viral RNA. Over the past years, boundaries and structures of cis-acting RNA elements required for coronavirus genome replication have been extensively characterized in betacoronaviruses and, to a lesser extent, other coronavirus genera. Here, we review our current understanding of coronavirus cis-acting elements located in the terminal genome regions and use a combination of bioinformatic and RNA structure probing studies to identify and characterize putative cis-acting RNA elements in alphacoronaviruses. The study suggests significant RNA structure conservation among members of the genus Alphacoronavirus but also across genus boundaries. Overall, the conservation pattern identified for 5′ and 3′-terminal RNA structural elements in the genomes of alpha- and betacoronaviruses is in agreement with the widely used replicase polyprotein-based classification of the Coronavirinae, suggesting co-evolution of the coronavirus replication machinery with cognate cis-acting RNA elements.
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spelling pubmed-71144172020-04-02 RNA structure analysis of alphacoronavirus terminal genome regions Madhugiri, Ramakanth Fricke, Markus Marz, Manja Ziebuhr, John Virus Res Article Coronavirus genome replication is mediated by a multi-subunit protein complex that is comprised of more than a dozen virally encoded and several cellular proteins. Interactions of the viral replicase complex with cis-acting RNA elements located in the 5′ and 3′-terminal genome regions ensure the specific replication of viral RNA. Over the past years, boundaries and structures of cis-acting RNA elements required for coronavirus genome replication have been extensively characterized in betacoronaviruses and, to a lesser extent, other coronavirus genera. Here, we review our current understanding of coronavirus cis-acting elements located in the terminal genome regions and use a combination of bioinformatic and RNA structure probing studies to identify and characterize putative cis-acting RNA elements in alphacoronaviruses. The study suggests significant RNA structure conservation among members of the genus Alphacoronavirus but also across genus boundaries. Overall, the conservation pattern identified for 5′ and 3′-terminal RNA structural elements in the genomes of alpha- and betacoronaviruses is in agreement with the widely used replicase polyprotein-based classification of the Coronavirinae, suggesting co-evolution of the coronavirus replication machinery with cognate cis-acting RNA elements. Elsevier B.V. 2014-12-19 2014-10-13 /pmc/articles/PMC7114417/ /pubmed/25307890 http://dx.doi.org/10.1016/j.virusres.2014.10.001 Text en Copyright © 2014 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
Madhugiri, Ramakanth
Fricke, Markus
Marz, Manja
Ziebuhr, John
RNA structure analysis of alphacoronavirus terminal genome regions
title RNA structure analysis of alphacoronavirus terminal genome regions
title_full RNA structure analysis of alphacoronavirus terminal genome regions
title_fullStr RNA structure analysis of alphacoronavirus terminal genome regions
title_full_unstemmed RNA structure analysis of alphacoronavirus terminal genome regions
title_short RNA structure analysis of alphacoronavirus terminal genome regions
title_sort rna structure analysis of alphacoronavirus terminal genome regions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114417/
https://www.ncbi.nlm.nih.gov/pubmed/25307890
http://dx.doi.org/10.1016/j.virusres.2014.10.001
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