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Population genomics supports baculoviruses as vectors of horizontal transfer of insect transposons
Horizontal transfer (HT) of DNA is an important factor shaping eukaryote evolution. Although several hundreds of eukaryote-to-eukaryote HTs of transposable elements (TEs) have been reported, the vectors underlying these transfers remain elusive. Here, we show that multiple copies of two TEs from the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3948050/ https://www.ncbi.nlm.nih.gov/pubmed/24556639 http://dx.doi.org/10.1038/ncomms4348 |
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author | Gilbert, Clément Chateigner, Aurélien Ernenwein, Lise Barbe, Valérie Bézier, Annie Herniou, Elisabeth A. Cordaux, Richard |
author_facet | Gilbert, Clément Chateigner, Aurélien Ernenwein, Lise Barbe, Valérie Bézier, Annie Herniou, Elisabeth A. Cordaux, Richard |
author_sort | Gilbert, Clément |
collection | PubMed |
description | Horizontal transfer (HT) of DNA is an important factor shaping eukaryote evolution. Although several hundreds of eukaryote-to-eukaryote HTs of transposable elements (TEs) have been reported, the vectors underlying these transfers remain elusive. Here, we show that multiple copies of two TEs from the cabbage looper (Trichoplusia ni) transposed in vivo into genomes of the baculovirus Autographa californica multiple nucleopolyhedrovirus (AcMNPV) during caterpillar infection. We further demonstrate that both TEs underwent recent HT between several sympatric moth species (T. ni, Manduca sexta, Helicoverpa spp.) showing different degrees of susceptibility to AcMNPV. Based on two independent population genomics data sets (reaching a total coverage >330,000X), we report a frequency of one moth TE in ~8,500 AcMNPV genomes. Together, our results provide strong support for the role of viruses as vectors of TE HT between animals, and they call for a systematic evaluation of the frequency and impact of virus-mediated HT on the evolution of host genomes. |
format | Online Article Text |
id | pubmed-3948050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-39480502014-03-10 Population genomics supports baculoviruses as vectors of horizontal transfer of insect transposons Gilbert, Clément Chateigner, Aurélien Ernenwein, Lise Barbe, Valérie Bézier, Annie Herniou, Elisabeth A. Cordaux, Richard Nat Commun Article Horizontal transfer (HT) of DNA is an important factor shaping eukaryote evolution. Although several hundreds of eukaryote-to-eukaryote HTs of transposable elements (TEs) have been reported, the vectors underlying these transfers remain elusive. Here, we show that multiple copies of two TEs from the cabbage looper (Trichoplusia ni) transposed in vivo into genomes of the baculovirus Autographa californica multiple nucleopolyhedrovirus (AcMNPV) during caterpillar infection. We further demonstrate that both TEs underwent recent HT between several sympatric moth species (T. ni, Manduca sexta, Helicoverpa spp.) showing different degrees of susceptibility to AcMNPV. Based on two independent population genomics data sets (reaching a total coverage >330,000X), we report a frequency of one moth TE in ~8,500 AcMNPV genomes. Together, our results provide strong support for the role of viruses as vectors of TE HT between animals, and they call for a systematic evaluation of the frequency and impact of virus-mediated HT on the evolution of host genomes. Nature Pub. Group 2014-02-21 /pmc/articles/PMC3948050/ /pubmed/24556639 http://dx.doi.org/10.1038/ncomms4348 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Article Gilbert, Clément Chateigner, Aurélien Ernenwein, Lise Barbe, Valérie Bézier, Annie Herniou, Elisabeth A. Cordaux, Richard Population genomics supports baculoviruses as vectors of horizontal transfer of insect transposons |
title | Population genomics supports baculoviruses as vectors of horizontal transfer of insect transposons |
title_full | Population genomics supports baculoviruses as vectors of horizontal transfer of insect transposons |
title_fullStr | Population genomics supports baculoviruses as vectors of horizontal transfer of insect transposons |
title_full_unstemmed | Population genomics supports baculoviruses as vectors of horizontal transfer of insect transposons |
title_short | Population genomics supports baculoviruses as vectors of horizontal transfer of insect transposons |
title_sort | population genomics supports baculoviruses as vectors of horizontal transfer of insect transposons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3948050/ https://www.ncbi.nlm.nih.gov/pubmed/24556639 http://dx.doi.org/10.1038/ncomms4348 |
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