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Transcriptional activity and epigenetic regulation of transposable elements in the symbiotic fungus Rhizophagus irregularis
Arbuscular mycorrhizal (AM) fungi form mutualistic relationships with most land plant species. AM fungi have long been considered as ancient asexuals. Long-term clonal evolution would be remarkable for a eukaryotic lineage and suggests the importance of alternative mechanisms to promote genetic vari...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647823/ https://www.ncbi.nlm.nih.gov/pubmed/34772700 http://dx.doi.org/10.1101/gr.275752.121 |
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author | Dallaire, Alexandra Manley, Bethan F. Wilkens, Maya Bista, Iliana Quan, Clement Evangelisti, Edouard Bradshaw, Charles R. Ramakrishna, Navin B. Schornack, Sebastian Butter, Falk Paszkowski, Uta Miska, Eric A. |
author_facet | Dallaire, Alexandra Manley, Bethan F. Wilkens, Maya Bista, Iliana Quan, Clement Evangelisti, Edouard Bradshaw, Charles R. Ramakrishna, Navin B. Schornack, Sebastian Butter, Falk Paszkowski, Uta Miska, Eric A. |
author_sort | Dallaire, Alexandra |
collection | PubMed |
description | Arbuscular mycorrhizal (AM) fungi form mutualistic relationships with most land plant species. AM fungi have long been considered as ancient asexuals. Long-term clonal evolution would be remarkable for a eukaryotic lineage and suggests the importance of alternative mechanisms to promote genetic variability facilitating adaptation. Here, we assessed the potential of transposable elements for generating such genomic diversity. The dynamic expression of TEs during Rhizophagus irregularis spore development suggests ongoing TE activity. We find Mutator-like elements located near genes belonging to highly expanded gene families. Whole-genome epigenomic profiling of R. irregularis provides direct evidence of DNA methylation and small RNA production occurring at TE loci. Our results support a model in which TE activity shapes the genome, while DNA methylation and small RNA–mediated silencing keep their overproliferation in check. We propose that a well-controlled TE activity directly contributes to genome evolution in AM fungi. |
format | Online Article Text |
id | pubmed-8647823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-86478232021-12-15 Transcriptional activity and epigenetic regulation of transposable elements in the symbiotic fungus Rhizophagus irregularis Dallaire, Alexandra Manley, Bethan F. Wilkens, Maya Bista, Iliana Quan, Clement Evangelisti, Edouard Bradshaw, Charles R. Ramakrishna, Navin B. Schornack, Sebastian Butter, Falk Paszkowski, Uta Miska, Eric A. Genome Res Research Arbuscular mycorrhizal (AM) fungi form mutualistic relationships with most land plant species. AM fungi have long been considered as ancient asexuals. Long-term clonal evolution would be remarkable for a eukaryotic lineage and suggests the importance of alternative mechanisms to promote genetic variability facilitating adaptation. Here, we assessed the potential of transposable elements for generating such genomic diversity. The dynamic expression of TEs during Rhizophagus irregularis spore development suggests ongoing TE activity. We find Mutator-like elements located near genes belonging to highly expanded gene families. Whole-genome epigenomic profiling of R. irregularis provides direct evidence of DNA methylation and small RNA production occurring at TE loci. Our results support a model in which TE activity shapes the genome, while DNA methylation and small RNA–mediated silencing keep their overproliferation in check. We propose that a well-controlled TE activity directly contributes to genome evolution in AM fungi. Cold Spring Harbor Laboratory Press 2021-12 /pmc/articles/PMC8647823/ /pubmed/34772700 http://dx.doi.org/10.1101/gr.275752.121 Text en © 2021 Dallaire et al.; Published by Cold Spring Harbor Laboratory Press https://creativecommons.org/licenses/by/4.0/This article, published in Genome Research, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Dallaire, Alexandra Manley, Bethan F. Wilkens, Maya Bista, Iliana Quan, Clement Evangelisti, Edouard Bradshaw, Charles R. Ramakrishna, Navin B. Schornack, Sebastian Butter, Falk Paszkowski, Uta Miska, Eric A. Transcriptional activity and epigenetic regulation of transposable elements in the symbiotic fungus Rhizophagus irregularis |
title | Transcriptional activity and epigenetic regulation of transposable elements in the symbiotic fungus Rhizophagus irregularis |
title_full | Transcriptional activity and epigenetic regulation of transposable elements in the symbiotic fungus Rhizophagus irregularis |
title_fullStr | Transcriptional activity and epigenetic regulation of transposable elements in the symbiotic fungus Rhizophagus irregularis |
title_full_unstemmed | Transcriptional activity and epigenetic regulation of transposable elements in the symbiotic fungus Rhizophagus irregularis |
title_short | Transcriptional activity and epigenetic regulation of transposable elements in the symbiotic fungus Rhizophagus irregularis |
title_sort | transcriptional activity and epigenetic regulation of transposable elements in the symbiotic fungus rhizophagus irregularis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647823/ https://www.ncbi.nlm.nih.gov/pubmed/34772700 http://dx.doi.org/10.1101/gr.275752.121 |
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