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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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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. |
format | Online Article Text |
id | pubmed-4717578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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