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Genomic landscape and evolutionary dynamics of mariner transposable elements within the Drosophila genus

BACKGROUND: The mariner family of transposable elements is one of the most widespread in the Metazoa. It is subdivided into several subfamilies that do not mirror the phylogeny of these species, suggesting an ancient diversification. Previous hybridization and PCR studies allowed a partial survey of...

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Autores principales: Wallau, Gabriel Luz, Capy, Pierre, Loreto, Elgion, Hua-Van, Aurélie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4161770/
https://www.ncbi.nlm.nih.gov/pubmed/25163909
http://dx.doi.org/10.1186/1471-2164-15-727
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author Wallau, Gabriel Luz
Capy, Pierre
Loreto, Elgion
Hua-Van, Aurélie
author_facet Wallau, Gabriel Luz
Capy, Pierre
Loreto, Elgion
Hua-Van, Aurélie
author_sort Wallau, Gabriel Luz
collection PubMed
description BACKGROUND: The mariner family of transposable elements is one of the most widespread in the Metazoa. It is subdivided into several subfamilies that do not mirror the phylogeny of these species, suggesting an ancient diversification. Previous hybridization and PCR studies allowed a partial survey of mariner diversity in the Metazoa. In this work, we used a comparative genomics approach to access the genus-wide diversity and evolution of mariner transposable elements in twenty Drosophila sequenced genomes. RESULTS: We identified 36 different mariner lineages belonging to six distinct subfamilies, including a subfamily not described previously. Wide variation in lineage abundance and copy number were observed among species and among mariner lineages, suggesting continuous turn-over. Most mariner lineages are inactive and contain a high proportion of damaged copies. We showed that, in addition to substitutions that rapidly inactivate copies, internal deletion is a major mechanism contributing to element decay and the generation of non-autonomous sublineages. Hence, 23% of copies correspond to several Miniature Inverted-repeat Transposable Elements (MITE) sublineages, the first ever described in Drosophila for mariner. In the most successful MITEs, internal deletion is often associated with internal rearrangement, which sheds light on the process of MITE origin. The estimation of the transposition rates over time revealed that all lineages followed a similar progression consisting of a rapid amplification burst followed by a rapid decrease in transposition. We detected some instances of multiple or ongoing transposition bursts. Different amplification times were observed for mariner lineages shared by different species, a finding best explained by either horizontal transmission or a reactivation process. Different lineages within one species have also amplified at different times, corresponding to successive invasions. Finally, we detected a preference for insertion into short TA-rich regions, which appears to be specific to some subfamilies. CONCLUSIONS: This analysis is the first comprehensive survey of this family of transposable elements at a genus scale. It provides precise measures of the different evolutionary processes that were hypothesized previously for this family based on PCR data analysis. mariner lineages were observed at almost all “life cycle” stages: recent amplification, subsequent decay and potential (re)-invasion or invasion of genomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-727) contains supplementary material, which is available to authorized users.
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spelling pubmed-41617702014-09-19 Genomic landscape and evolutionary dynamics of mariner transposable elements within the Drosophila genus Wallau, Gabriel Luz Capy, Pierre Loreto, Elgion Hua-Van, Aurélie BMC Genomics Research Article BACKGROUND: The mariner family of transposable elements is one of the most widespread in the Metazoa. It is subdivided into several subfamilies that do not mirror the phylogeny of these species, suggesting an ancient diversification. Previous hybridization and PCR studies allowed a partial survey of mariner diversity in the Metazoa. In this work, we used a comparative genomics approach to access the genus-wide diversity and evolution of mariner transposable elements in twenty Drosophila sequenced genomes. RESULTS: We identified 36 different mariner lineages belonging to six distinct subfamilies, including a subfamily not described previously. Wide variation in lineage abundance and copy number were observed among species and among mariner lineages, suggesting continuous turn-over. Most mariner lineages are inactive and contain a high proportion of damaged copies. We showed that, in addition to substitutions that rapidly inactivate copies, internal deletion is a major mechanism contributing to element decay and the generation of non-autonomous sublineages. Hence, 23% of copies correspond to several Miniature Inverted-repeat Transposable Elements (MITE) sublineages, the first ever described in Drosophila for mariner. In the most successful MITEs, internal deletion is often associated with internal rearrangement, which sheds light on the process of MITE origin. The estimation of the transposition rates over time revealed that all lineages followed a similar progression consisting of a rapid amplification burst followed by a rapid decrease in transposition. We detected some instances of multiple or ongoing transposition bursts. Different amplification times were observed for mariner lineages shared by different species, a finding best explained by either horizontal transmission or a reactivation process. Different lineages within one species have also amplified at different times, corresponding to successive invasions. Finally, we detected a preference for insertion into short TA-rich regions, which appears to be specific to some subfamilies. CONCLUSIONS: This analysis is the first comprehensive survey of this family of transposable elements at a genus scale. It provides precise measures of the different evolutionary processes that were hypothesized previously for this family based on PCR data analysis. mariner lineages were observed at almost all “life cycle” stages: recent amplification, subsequent decay and potential (re)-invasion or invasion of genomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-727) contains supplementary material, which is available to authorized users. BioMed Central 2014-08-27 /pmc/articles/PMC4161770/ /pubmed/25163909 http://dx.doi.org/10.1186/1471-2164-15-727 Text en © Wallau et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Article
Wallau, Gabriel Luz
Capy, Pierre
Loreto, Elgion
Hua-Van, Aurélie
Genomic landscape and evolutionary dynamics of mariner transposable elements within the Drosophila genus
title Genomic landscape and evolutionary dynamics of mariner transposable elements within the Drosophila genus
title_full Genomic landscape and evolutionary dynamics of mariner transposable elements within the Drosophila genus
title_fullStr Genomic landscape and evolutionary dynamics of mariner transposable elements within the Drosophila genus
title_full_unstemmed Genomic landscape and evolutionary dynamics of mariner transposable elements within the Drosophila genus
title_short Genomic landscape and evolutionary dynamics of mariner transposable elements within the Drosophila genus
title_sort genomic landscape and evolutionary dynamics of mariner transposable elements within the drosophila genus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4161770/
https://www.ncbi.nlm.nih.gov/pubmed/25163909
http://dx.doi.org/10.1186/1471-2164-15-727
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