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Novel 3′ Proximal Replication Elements in Umbravirus Genomes

The 3′ untranslated regions (UTRs) of positive-strand RNA plant viruses commonly contain elements that promote viral replication and translation. The ~700 nt 3′UTR of umbravirus pea enation mosaic virus 2 (PEMV2) contains three 3′ cap-independent translation enhancers (3′CITEs), including one (PTE)...

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Autores principales: Johnson, Philip Z., Reuning, Hannah M., Bera, Sayanta, Gao, Feng, Du, Zhiyou, Simon, Anne E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9780821/
https://www.ncbi.nlm.nih.gov/pubmed/36560619
http://dx.doi.org/10.3390/v14122615
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author Johnson, Philip Z.
Reuning, Hannah M.
Bera, Sayanta
Gao, Feng
Du, Zhiyou
Simon, Anne E.
author_facet Johnson, Philip Z.
Reuning, Hannah M.
Bera, Sayanta
Gao, Feng
Du, Zhiyou
Simon, Anne E.
author_sort Johnson, Philip Z.
collection PubMed
description The 3′ untranslated regions (UTRs) of positive-strand RNA plant viruses commonly contain elements that promote viral replication and translation. The ~700 nt 3′UTR of umbravirus pea enation mosaic virus 2 (PEMV2) contains three 3′ cap-independent translation enhancers (3′CITEs), including one (PTE) found in members of several genera in the family Tombusviridae and another (the 3′TSS) found in numerous umbraviruses and several carmoviruses. In addition, three 3′ terminal replication elements are found in nearly every umbravirus and carmovirus. For this report, we have identified a set of three hairpins and a putative pseudoknot, collectively termed “Trio”, that are exclusively found in a subset of umbraviruses and are located just upstream of the 3′TSS. Modification of these elements had no impact on viral translation in wheat germ extracts or in translation of luciferase reporter constructs in vivo. In contrast, Trio hairpins were critical for viral RNA accumulation in Arabidopsis thaliana protoplasts and for replication of a non-autonomously replicating replicon using a trans-replication system in Nicotiana benthamiana leaves. Trio and other 3′ terminal elements involved in viral replication are highly conserved in umbraviruses possessing different classes of upstream 3′CITEs, suggesting conservation of replication mechanisms among umbraviruses despite variation in mechanisms for translation enhancement.
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spelling pubmed-97808212022-12-24 Novel 3′ Proximal Replication Elements in Umbravirus Genomes Johnson, Philip Z. Reuning, Hannah M. Bera, Sayanta Gao, Feng Du, Zhiyou Simon, Anne E. Viruses Article The 3′ untranslated regions (UTRs) of positive-strand RNA plant viruses commonly contain elements that promote viral replication and translation. The ~700 nt 3′UTR of umbravirus pea enation mosaic virus 2 (PEMV2) contains three 3′ cap-independent translation enhancers (3′CITEs), including one (PTE) found in members of several genera in the family Tombusviridae and another (the 3′TSS) found in numerous umbraviruses and several carmoviruses. In addition, three 3′ terminal replication elements are found in nearly every umbravirus and carmovirus. For this report, we have identified a set of three hairpins and a putative pseudoknot, collectively termed “Trio”, that are exclusively found in a subset of umbraviruses and are located just upstream of the 3′TSS. Modification of these elements had no impact on viral translation in wheat germ extracts or in translation of luciferase reporter constructs in vivo. In contrast, Trio hairpins were critical for viral RNA accumulation in Arabidopsis thaliana protoplasts and for replication of a non-autonomously replicating replicon using a trans-replication system in Nicotiana benthamiana leaves. Trio and other 3′ terminal elements involved in viral replication are highly conserved in umbraviruses possessing different classes of upstream 3′CITEs, suggesting conservation of replication mechanisms among umbraviruses despite variation in mechanisms for translation enhancement. MDPI 2022-11-23 /pmc/articles/PMC9780821/ /pubmed/36560619 http://dx.doi.org/10.3390/v14122615 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Johnson, Philip Z.
Reuning, Hannah M.
Bera, Sayanta
Gao, Feng
Du, Zhiyou
Simon, Anne E.
Novel 3′ Proximal Replication Elements in Umbravirus Genomes
title Novel 3′ Proximal Replication Elements in Umbravirus Genomes
title_full Novel 3′ Proximal Replication Elements in Umbravirus Genomes
title_fullStr Novel 3′ Proximal Replication Elements in Umbravirus Genomes
title_full_unstemmed Novel 3′ Proximal Replication Elements in Umbravirus Genomes
title_short Novel 3′ Proximal Replication Elements in Umbravirus Genomes
title_sort novel 3′ proximal replication elements in umbravirus genomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9780821/
https://www.ncbi.nlm.nih.gov/pubmed/36560619
http://dx.doi.org/10.3390/v14122615
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