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Cut-and-Paste Transposons in Fungi with Diverse Lifestyles
Transposable elements (TEs) shape genomes via recombination and transposition, lead to chromosomal rearrangements, create new gene neighborhoods, and alter gene expression. They play key roles in adaptation either to symbiosis in Amanita genus or to pathogenicity in Pyrenophora tritici-repentis. Des...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5751038/ https://www.ncbi.nlm.nih.gov/pubmed/29228286 http://dx.doi.org/10.1093/gbe/evx261 |
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author | Muszewska, Anna Steczkiewicz, Kamil Stepniewska-Dziubinska, Marta Ginalski, Krzysztof |
author_facet | Muszewska, Anna Steczkiewicz, Kamil Stepniewska-Dziubinska, Marta Ginalski, Krzysztof |
author_sort | Muszewska, Anna |
collection | PubMed |
description | Transposable elements (TEs) shape genomes via recombination and transposition, lead to chromosomal rearrangements, create new gene neighborhoods, and alter gene expression. They play key roles in adaptation either to symbiosis in Amanita genus or to pathogenicity in Pyrenophora tritici-repentis. Despite growing evidence of their importance, the abundance and distribution of mobile elements replicating in a “cut-and-paste” fashion is barely described so far. In order to improve our knowledge on this old and ubiquitous class of transposable elements, 1,730 fungal genomes were scanned using both de novo and homology-based approaches. DNA TEs have been identified across the whole data set and display uneven distribution from both DNA TE classification and fungal taxonomy perspectives. DNA TE content correlates with genome size, which confirms that many transposon families proliferate simultaneously. In contrast, it is independent from intron density, average gene distance and GC content. TE count is associated with species’ lifestyle and tends to be elevated in plant symbionts and decreased in animal parasites. Lastly, we found that fungi with both RIP and RNAi systems have more total DNA TE sequences but less elements retaining a functional transposase, what reflects stringent control over transposition. |
format | Online Article Text |
id | pubmed-5751038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57510382018-01-05 Cut-and-Paste Transposons in Fungi with Diverse Lifestyles Muszewska, Anna Steczkiewicz, Kamil Stepniewska-Dziubinska, Marta Ginalski, Krzysztof Genome Biol Evol Research Article Transposable elements (TEs) shape genomes via recombination and transposition, lead to chromosomal rearrangements, create new gene neighborhoods, and alter gene expression. They play key roles in adaptation either to symbiosis in Amanita genus or to pathogenicity in Pyrenophora tritici-repentis. Despite growing evidence of their importance, the abundance and distribution of mobile elements replicating in a “cut-and-paste” fashion is barely described so far. In order to improve our knowledge on this old and ubiquitous class of transposable elements, 1,730 fungal genomes were scanned using both de novo and homology-based approaches. DNA TEs have been identified across the whole data set and display uneven distribution from both DNA TE classification and fungal taxonomy perspectives. DNA TE content correlates with genome size, which confirms that many transposon families proliferate simultaneously. In contrast, it is independent from intron density, average gene distance and GC content. TE count is associated with species’ lifestyle and tends to be elevated in plant symbionts and decreased in animal parasites. Lastly, we found that fungi with both RIP and RNAi systems have more total DNA TE sequences but less elements retaining a functional transposase, what reflects stringent control over transposition. Oxford University Press 2017-12-08 /pmc/articles/PMC5751038/ /pubmed/29228286 http://dx.doi.org/10.1093/gbe/evx261 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Muszewska, Anna Steczkiewicz, Kamil Stepniewska-Dziubinska, Marta Ginalski, Krzysztof Cut-and-Paste Transposons in Fungi with Diverse Lifestyles |
title | Cut-and-Paste Transposons in Fungi with Diverse Lifestyles |
title_full | Cut-and-Paste Transposons in Fungi with Diverse Lifestyles |
title_fullStr | Cut-and-Paste Transposons in Fungi with Diverse Lifestyles |
title_full_unstemmed | Cut-and-Paste Transposons in Fungi with Diverse Lifestyles |
title_short | Cut-and-Paste Transposons in Fungi with Diverse Lifestyles |
title_sort | cut-and-paste transposons in fungi with diverse lifestyles |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5751038/ https://www.ncbi.nlm.nih.gov/pubmed/29228286 http://dx.doi.org/10.1093/gbe/evx261 |
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