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Nidovirales: Evolving the largest RNA virus genome

This review focuses on the monophyletic group of animal RNA viruses united in the order Nidovirales. The order includes the distantly related coronaviruses, toroviruses, and roniviruses, which possess the largest known RNA genomes (from 26 to 32 kb) and will therefore be called ‘large’ nidoviruses i...

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Autores principales: Gorbalenya, Alexander E., Enjuanes, Luis, Ziebuhr, John, Snijder, Eric J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114179/
https://www.ncbi.nlm.nih.gov/pubmed/16503362
http://dx.doi.org/10.1016/j.virusres.2006.01.017
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author Gorbalenya, Alexander E.
Enjuanes, Luis
Ziebuhr, John
Snijder, Eric J.
author_facet Gorbalenya, Alexander E.
Enjuanes, Luis
Ziebuhr, John
Snijder, Eric J.
author_sort Gorbalenya, Alexander E.
collection PubMed
description This review focuses on the monophyletic group of animal RNA viruses united in the order Nidovirales. The order includes the distantly related coronaviruses, toroviruses, and roniviruses, which possess the largest known RNA genomes (from 26 to 32 kb) and will therefore be called ‘large’ nidoviruses in this review. They are compared with their arterivirus cousins, which also belong to the Nidovirales despite having a much smaller genome (13–16 kb). Common and unique features that have been identified for either large or all nidoviruses are outlined. These include the nidovirus genetic plan and genome diversity, the composition of the replicase machinery and virus particles, virus-specific accessory genes, the mechanisms of RNA and protein synthesis, and the origin and evolution of nidoviruses with small and large genomes. Nidoviruses employ single-stranded, polycistronic RNA genomes of positive polarity that direct the synthesis of the subunits of the replicative complex, including the RNA-dependent RNA polymerase and helicase. Replicase gene expression is under the principal control of a ribosomal frameshifting signal and a chymotrypsin-like protease, which is assisted by one or more papain-like proteases. A nested set of subgenomic RNAs is synthesized to express the 3′-proximal ORFs that encode most conserved structural proteins and, in some large nidoviruses, also diverse accessory proteins that may promote virus adaptation to specific hosts. The replicase machinery includes a set of RNA-processing enzymes some of which are unique for either all or large nidoviruses. The acquisition of these enzymes may have improved the low fidelity of RNA replication to allow genome expansion and give rise to the ancestors of small and, subsequently, large nidoviruses.
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spelling pubmed-71141792020-04-02 Nidovirales: Evolving the largest RNA virus genome Gorbalenya, Alexander E. Enjuanes, Luis Ziebuhr, John Snijder, Eric J. Virus Res Article This review focuses on the monophyletic group of animal RNA viruses united in the order Nidovirales. The order includes the distantly related coronaviruses, toroviruses, and roniviruses, which possess the largest known RNA genomes (from 26 to 32 kb) and will therefore be called ‘large’ nidoviruses in this review. They are compared with their arterivirus cousins, which also belong to the Nidovirales despite having a much smaller genome (13–16 kb). Common and unique features that have been identified for either large or all nidoviruses are outlined. These include the nidovirus genetic plan and genome diversity, the composition of the replicase machinery and virus particles, virus-specific accessory genes, the mechanisms of RNA and protein synthesis, and the origin and evolution of nidoviruses with small and large genomes. Nidoviruses employ single-stranded, polycistronic RNA genomes of positive polarity that direct the synthesis of the subunits of the replicative complex, including the RNA-dependent RNA polymerase and helicase. Replicase gene expression is under the principal control of a ribosomal frameshifting signal and a chymotrypsin-like protease, which is assisted by one or more papain-like proteases. A nested set of subgenomic RNAs is synthesized to express the 3′-proximal ORFs that encode most conserved structural proteins and, in some large nidoviruses, also diverse accessory proteins that may promote virus adaptation to specific hosts. The replicase machinery includes a set of RNA-processing enzymes some of which are unique for either all or large nidoviruses. The acquisition of these enzymes may have improved the low fidelity of RNA replication to allow genome expansion and give rise to the ancestors of small and, subsequently, large nidoviruses. Elsevier B.V. 2006-04 2006-02-28 /pmc/articles/PMC7114179/ /pubmed/16503362 http://dx.doi.org/10.1016/j.virusres.2006.01.017 Text en Copyright © 2006 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
Gorbalenya, Alexander E.
Enjuanes, Luis
Ziebuhr, John
Snijder, Eric J.
Nidovirales: Evolving the largest RNA virus genome
title Nidovirales: Evolving the largest RNA virus genome
title_full Nidovirales: Evolving the largest RNA virus genome
title_fullStr Nidovirales: Evolving the largest RNA virus genome
title_full_unstemmed Nidovirales: Evolving the largest RNA virus genome
title_short Nidovirales: Evolving the largest RNA virus genome
title_sort nidovirales: evolving the largest rna virus genome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114179/
https://www.ncbi.nlm.nih.gov/pubmed/16503362
http://dx.doi.org/10.1016/j.virusres.2006.01.017
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