Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2021
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
_version_ 1784610675496058880
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
work_keys_str_mv AT dallairealexandra transcriptionalactivityandepigeneticregulationoftransposableelementsinthesymbioticfungusrhizophagusirregularis
AT manleybethanf transcriptionalactivityandepigeneticregulationoftransposableelementsinthesymbioticfungusrhizophagusirregularis
AT wilkensmaya transcriptionalactivityandepigeneticregulationoftransposableelementsinthesymbioticfungusrhizophagusirregularis
AT bistailiana transcriptionalactivityandepigeneticregulationoftransposableelementsinthesymbioticfungusrhizophagusirregularis
AT quanclement transcriptionalactivityandepigeneticregulationoftransposableelementsinthesymbioticfungusrhizophagusirregularis
AT evangelistiedouard transcriptionalactivityandepigeneticregulationoftransposableelementsinthesymbioticfungusrhizophagusirregularis
AT bradshawcharlesr transcriptionalactivityandepigeneticregulationoftransposableelementsinthesymbioticfungusrhizophagusirregularis
AT ramakrishnanavinb transcriptionalactivityandepigeneticregulationoftransposableelementsinthesymbioticfungusrhizophagusirregularis
AT schornacksebastian transcriptionalactivityandepigeneticregulationoftransposableelementsinthesymbioticfungusrhizophagusirregularis
AT butterfalk transcriptionalactivityandepigeneticregulationoftransposableelementsinthesymbioticfungusrhizophagusirregularis
AT paszkowskiuta transcriptionalactivityandepigeneticregulationoftransposableelementsinthesymbioticfungusrhizophagusirregularis
AT miskaerica transcriptionalactivityandepigeneticregulationoftransposableelementsinthesymbioticfungusrhizophagusirregularis