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Horizontal transfer of BovB and L1 retrotransposons in eukaryotes

BACKGROUND: Transposable elements (TEs) are mobile DNA sequences, colloquially known as jumping genes because of their ability to replicate to new genomic locations. TEs can jump between organisms or species when given a vector of transfer, such as a tick or virus, in a process known as horizontal t...

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Autores principales: Ivancevic, Atma M., Kortschak, R. Daniel, Bertozzi, Terry, Adelson, David L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036668/
https://www.ncbi.nlm.nih.gov/pubmed/29983116
http://dx.doi.org/10.1186/s13059-018-1456-7
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author Ivancevic, Atma M.
Kortschak, R. Daniel
Bertozzi, Terry
Adelson, David L.
author_facet Ivancevic, Atma M.
Kortschak, R. Daniel
Bertozzi, Terry
Adelson, David L.
author_sort Ivancevic, Atma M.
collection PubMed
description BACKGROUND: Transposable elements (TEs) are mobile DNA sequences, colloquially known as jumping genes because of their ability to replicate to new genomic locations. TEs can jump between organisms or species when given a vector of transfer, such as a tick or virus, in a process known as horizontal transfer. Here, we propose that LINE-1 (L1) and Bovine-B (BovB), the two most abundant TE families in mammals, were initially introduced as foreign DNA via ancient horizontal transfer events. RESULTS: Using analyses of 759 plant, fungal and animal genomes, we identify multiple possible L1 horizontal transfer events in eukaryotic species, primarily involving Tx-like L1s in marine eukaryotes. We also extend the BovB paradigm by increasing the number of estimated transfer events compared to previous studies, finding new parasite vectors of transfer such as bed bug, leech and locust, and BovB occurrences in new lineages such as bat and frog. Given that these transposable elements have colonised more than half of the genome sequence in today’s mammals, our results support a role for horizontal transfer in causing long-term genomic change in new host organisms. CONCLUSIONS: We describe extensive horizontal transfer of BovB retrotransposons and provide the first evidence that L1 elements can also undergo horizontal transfer. With the advancement of genome sequencing technologies and bioinformatics tools, we anticipate our study to be a valuable resource for inferring horizontal transfer from large-scale genomic data. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-018-1456-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-60366682018-07-12 Horizontal transfer of BovB and L1 retrotransposons in eukaryotes Ivancevic, Atma M. Kortschak, R. Daniel Bertozzi, Terry Adelson, David L. Genome Biol Research BACKGROUND: Transposable elements (TEs) are mobile DNA sequences, colloquially known as jumping genes because of their ability to replicate to new genomic locations. TEs can jump between organisms or species when given a vector of transfer, such as a tick or virus, in a process known as horizontal transfer. Here, we propose that LINE-1 (L1) and Bovine-B (BovB), the two most abundant TE families in mammals, were initially introduced as foreign DNA via ancient horizontal transfer events. RESULTS: Using analyses of 759 plant, fungal and animal genomes, we identify multiple possible L1 horizontal transfer events in eukaryotic species, primarily involving Tx-like L1s in marine eukaryotes. We also extend the BovB paradigm by increasing the number of estimated transfer events compared to previous studies, finding new parasite vectors of transfer such as bed bug, leech and locust, and BovB occurrences in new lineages such as bat and frog. Given that these transposable elements have colonised more than half of the genome sequence in today’s mammals, our results support a role for horizontal transfer in causing long-term genomic change in new host organisms. CONCLUSIONS: We describe extensive horizontal transfer of BovB retrotransposons and provide the first evidence that L1 elements can also undergo horizontal transfer. With the advancement of genome sequencing technologies and bioinformatics tools, we anticipate our study to be a valuable resource for inferring horizontal transfer from large-scale genomic data. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-018-1456-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-09 /pmc/articles/PMC6036668/ /pubmed/29983116 http://dx.doi.org/10.1186/s13059-018-1456-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Ivancevic, Atma M.
Kortschak, R. Daniel
Bertozzi, Terry
Adelson, David L.
Horizontal transfer of BovB and L1 retrotransposons in eukaryotes
title Horizontal transfer of BovB and L1 retrotransposons in eukaryotes
title_full Horizontal transfer of BovB and L1 retrotransposons in eukaryotes
title_fullStr Horizontal transfer of BovB and L1 retrotransposons in eukaryotes
title_full_unstemmed Horizontal transfer of BovB and L1 retrotransposons in eukaryotes
title_short Horizontal transfer of BovB and L1 retrotransposons in eukaryotes
title_sort horizontal transfer of bovb and l1 retrotransposons in eukaryotes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036668/
https://www.ncbi.nlm.nih.gov/pubmed/29983116
http://dx.doi.org/10.1186/s13059-018-1456-7
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