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Landscape and evolutionary dynamics of terminal repeat retrotransposons in miniature in plant genomes

BACKGROUND: Terminal repeat retrotransposons in miniature (TRIMs) are a unique group of small long terminal repeat retrotransposons that are difficult to identify. Thus far, only a few TRIMs have been characterized in the euphyllophytes, and their evolutionary and biological significance as well as...

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Autores principales: Gao, Dongying, Li, Yupeng, Kim, Kyung Do, Abernathy, Brian, Jackson, Scott A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717578/
https://www.ncbi.nlm.nih.gov/pubmed/26781660
http://dx.doi.org/10.1186/s13059-015-0867-y
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author Gao, Dongying
Li, Yupeng
Kim, Kyung Do
Abernathy, Brian
Jackson, Scott A.
author_facet Gao, Dongying
Li, Yupeng
Kim, Kyung Do
Abernathy, Brian
Jackson, Scott A.
author_sort Gao, Dongying
collection PubMed
description BACKGROUND: Terminal repeat retrotransposons in miniature (TRIMs) are a unique group of small long terminal repeat retrotransposons that are difficult to identify. Thus far, only a few TRIMs have been characterized in the euphyllophytes, and their evolutionary and biological significance as well as their transposition mechanisms are poorly understood. RESULTS: Using a combination of de novo and homology-based methods, we annotate TRIMs in 48 plant genome sequences, spanning land plants to algae. The TRIMs are grouped into 156 families including 145 that were previously undefined. Notably, we identify the first TRIMs in a lycophyte and non-vascular plants. The majority of the TRIM families are highly conserved and shared within and between plant families. Unlike other long terminal repeat retrotransposons, TRIMs are enriched in or near genes; they are also targeted by sRNAs between 21 and 24 nucleotides in length, and are frequently found in CG body-methylated genes. Importantly, we also identify putative autonomous retrotransposons and very recent transpositions of a TRIM element in Oryza sativa. CONCLUSIONS: We perform the most comprehensive analysis of TRIM transposons thus far and report that TRIMs are ubiquitous across plant genomes. Our results show that TRIMs are more frequently associated with large and CG body-methylated genes that have undergone strong purifying selection. Our findings also indicate that TRIMs are likely derived from internal deletions of large long terminal repeat retrotransposons. Finally, our data and methodology are important resources for the characterization and evolutionary and genomic studies of long terminal repeat retrotransposons in other genomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0867-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-47175782016-01-20 Landscape and evolutionary dynamics of terminal repeat retrotransposons in miniature in plant genomes Gao, Dongying Li, Yupeng Kim, Kyung Do Abernathy, Brian Jackson, Scott A. Genome Biol Research BACKGROUND: Terminal repeat retrotransposons in miniature (TRIMs) are a unique group of small long terminal repeat retrotransposons that are difficult to identify. Thus far, only a few TRIMs have been characterized in the euphyllophytes, and their evolutionary and biological significance as well as their transposition mechanisms are poorly understood. RESULTS: Using a combination of de novo and homology-based methods, we annotate TRIMs in 48 plant genome sequences, spanning land plants to algae. The TRIMs are grouped into 156 families including 145 that were previously undefined. Notably, we identify the first TRIMs in a lycophyte and non-vascular plants. The majority of the TRIM families are highly conserved and shared within and between plant families. Unlike other long terminal repeat retrotransposons, TRIMs are enriched in or near genes; they are also targeted by sRNAs between 21 and 24 nucleotides in length, and are frequently found in CG body-methylated genes. Importantly, we also identify putative autonomous retrotransposons and very recent transpositions of a TRIM element in Oryza sativa. CONCLUSIONS: We perform the most comprehensive analysis of TRIM transposons thus far and report that TRIMs are ubiquitous across plant genomes. Our results show that TRIMs are more frequently associated with large and CG body-methylated genes that have undergone strong purifying selection. Our findings also indicate that TRIMs are likely derived from internal deletions of large long terminal repeat retrotransposons. Finally, our data and methodology are important resources for the characterization and evolutionary and genomic studies of long terminal repeat retrotransposons in other genomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0867-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-18 2016 /pmc/articles/PMC4717578/ /pubmed/26781660 http://dx.doi.org/10.1186/s13059-015-0867-y Text en © Gao et al. 2016 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
Gao, Dongying
Li, Yupeng
Kim, Kyung Do
Abernathy, Brian
Jackson, Scott A.
Landscape and evolutionary dynamics of terminal repeat retrotransposons in miniature in plant genomes
title Landscape and evolutionary dynamics of terminal repeat retrotransposons in miniature in plant genomes
title_full Landscape and evolutionary dynamics of terminal repeat retrotransposons in miniature in plant genomes
title_fullStr Landscape and evolutionary dynamics of terminal repeat retrotransposons in miniature in plant genomes
title_full_unstemmed Landscape and evolutionary dynamics of terminal repeat retrotransposons in miniature in plant genomes
title_short Landscape and evolutionary dynamics of terminal repeat retrotransposons in miniature in plant genomes
title_sort landscape and evolutionary dynamics of terminal repeat retrotransposons in miniature in plant genomes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717578/
https://www.ncbi.nlm.nih.gov/pubmed/26781660
http://dx.doi.org/10.1186/s13059-015-0867-y
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