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Tracheophyte genomes keep track of the deep evolution of the Caulimoviridae

Endogenous viral elements (EVEs) are viral sequences that are integrated in the nuclear genomes of their hosts and are signatures of viral infections that may have occurred millions of years ago. The study of EVEs, coined paleovirology, provides important insights into virus evolution. The Caulimovi...

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Autores principales: Diop, Seydina Issa, Geering, Andrew D. W., Alfama-Depauw, Françoise, Loaec, Mikaël, Teycheney, Pierre-Yves, Maumus, Florian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766536/
https://www.ncbi.nlm.nih.gov/pubmed/29330451
http://dx.doi.org/10.1038/s41598-017-16399-x
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author Diop, Seydina Issa
Geering, Andrew D. W.
Alfama-Depauw, Françoise
Loaec, Mikaël
Teycheney, Pierre-Yves
Maumus, Florian
author_facet Diop, Seydina Issa
Geering, Andrew D. W.
Alfama-Depauw, Françoise
Loaec, Mikaël
Teycheney, Pierre-Yves
Maumus, Florian
author_sort Diop, Seydina Issa
collection PubMed
description Endogenous viral elements (EVEs) are viral sequences that are integrated in the nuclear genomes of their hosts and are signatures of viral infections that may have occurred millions of years ago. The study of EVEs, coined paleovirology, provides important insights into virus evolution. The Caulimoviridae is the most common group of EVEs in plants, although their presence has often been overlooked in plant genome studies. We have refined methods for the identification of caulimovirid EVEs and interrogated the genomes of a broad diversity of plant taxa, from algae to advanced flowering plants. Evidence is provided that almost every vascular plant (tracheophyte), including the most primitive taxa (clubmosses, ferns and gymnosperms) contains caulimovirid EVEs, many of which represent previously unrecognized evolutionary branches. In angiosperms, EVEs from at least one and as many as five different caulimovirid genera were frequently detected, and florendoviruses were the most widely distributed, followed by petuviruses. From the analysis of the distribution of different caulimovirid genera within different plant species, we propose a working evolutionary scenario in which this family of viruses emerged at latest during Devonian era (approx. 320 million years ago) followed by vertical transmission and by several cross-division host swaps.
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spelling pubmed-57665362018-01-17 Tracheophyte genomes keep track of the deep evolution of the Caulimoviridae Diop, Seydina Issa Geering, Andrew D. W. Alfama-Depauw, Françoise Loaec, Mikaël Teycheney, Pierre-Yves Maumus, Florian Sci Rep Article Endogenous viral elements (EVEs) are viral sequences that are integrated in the nuclear genomes of their hosts and are signatures of viral infections that may have occurred millions of years ago. The study of EVEs, coined paleovirology, provides important insights into virus evolution. The Caulimoviridae is the most common group of EVEs in plants, although their presence has often been overlooked in plant genome studies. We have refined methods for the identification of caulimovirid EVEs and interrogated the genomes of a broad diversity of plant taxa, from algae to advanced flowering plants. Evidence is provided that almost every vascular plant (tracheophyte), including the most primitive taxa (clubmosses, ferns and gymnosperms) contains caulimovirid EVEs, many of which represent previously unrecognized evolutionary branches. In angiosperms, EVEs from at least one and as many as five different caulimovirid genera were frequently detected, and florendoviruses were the most widely distributed, followed by petuviruses. From the analysis of the distribution of different caulimovirid genera within different plant species, we propose a working evolutionary scenario in which this family of viruses emerged at latest during Devonian era (approx. 320 million years ago) followed by vertical transmission and by several cross-division host swaps. Nature Publishing Group UK 2018-01-12 /pmc/articles/PMC5766536/ /pubmed/29330451 http://dx.doi.org/10.1038/s41598-017-16399-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Diop, Seydina Issa
Geering, Andrew D. W.
Alfama-Depauw, Françoise
Loaec, Mikaël
Teycheney, Pierre-Yves
Maumus, Florian
Tracheophyte genomes keep track of the deep evolution of the Caulimoviridae
title Tracheophyte genomes keep track of the deep evolution of the Caulimoviridae
title_full Tracheophyte genomes keep track of the deep evolution of the Caulimoviridae
title_fullStr Tracheophyte genomes keep track of the deep evolution of the Caulimoviridae
title_full_unstemmed Tracheophyte genomes keep track of the deep evolution of the Caulimoviridae
title_short Tracheophyte genomes keep track of the deep evolution of the Caulimoviridae
title_sort tracheophyte genomes keep track of the deep evolution of the caulimoviridae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766536/
https://www.ncbi.nlm.nih.gov/pubmed/29330451
http://dx.doi.org/10.1038/s41598-017-16399-x
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