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Whole genome comparative analysis of transposable elements provides new insight into mechanisms of their inactivation in fungal genomes

BACKGROUND: Transposable Elements (TEs) are key components that shape the organization and evolution of genomes. Fungi have developed defense mechanisms against TE invasion such as RIP (Repeat-Induced Point mutation), MIP (Methylation Induced Premeiotically) and Quelling (RNA interference). RIP inac...

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Autores principales: Amselem, Joëlle, Lebrun, Marc-Henri, Quesneville, Hadi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352252/
https://www.ncbi.nlm.nih.gov/pubmed/25766680
http://dx.doi.org/10.1186/s12864-015-1347-1
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author Amselem, Joëlle
Lebrun, Marc-Henri
Quesneville, Hadi
author_facet Amselem, Joëlle
Lebrun, Marc-Henri
Quesneville, Hadi
author_sort Amselem, Joëlle
collection PubMed
description BACKGROUND: Transposable Elements (TEs) are key components that shape the organization and evolution of genomes. Fungi have developed defense mechanisms against TE invasion such as RIP (Repeat-Induced Point mutation), MIP (Methylation Induced Premeiotically) and Quelling (RNA interference). RIP inactivates repeated sequences by promoting Cytosine to Thymine mutations, whereas MIP only methylates TEs at C residues. Both mechanisms require specific cytosine DNA Methyltransferases (RID1/Masc1) of the Dnmt1 superfamily. RESULTS: We annotated TE sequences from 10 fungal genomes with different TE content (1-70%). We then used these TE sequences to carry out a genome-wide analysis of C to T mutations biases. Genomes from either Ascomycota or Basidiomycota that were massively invaded by TEs (Blumeria, Melampsora, Puccinia) were characterized by a low frequency of C to T mutation bias (10-20%), whereas other genomes displayed intermediate to high frequencies (25-75%). We identified several dinucleotide signatures at these C to T mutation sites (CpA, CpT, and CpG). Phylogenomic analysis of fungal Dnmt1 MTases revealed a previously unreported association between these dinucleotide signatures and the presence/absence of sub-classes of Dnmt1. CONCLUSIONS: We identified fungal genomes containing large numbers of TEs with many C to T mutations associated with species-specific dinucleotide signatures. This bias suggests that a basic defense mechanism against TE invasion similar to RIP is widespread in fungi, although the efficiency and specificity of this mechanism differs between species. Our analysis revealed that dinucleotide signatures are associated with the presence/absence of specific Dnmt1 subfamilies. In particular, an RID1-dependent RIP mechanism was found only in Ascomycota. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1347-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-43522522015-03-08 Whole genome comparative analysis of transposable elements provides new insight into mechanisms of their inactivation in fungal genomes Amselem, Joëlle Lebrun, Marc-Henri Quesneville, Hadi BMC Genomics Research Article BACKGROUND: Transposable Elements (TEs) are key components that shape the organization and evolution of genomes. Fungi have developed defense mechanisms against TE invasion such as RIP (Repeat-Induced Point mutation), MIP (Methylation Induced Premeiotically) and Quelling (RNA interference). RIP inactivates repeated sequences by promoting Cytosine to Thymine mutations, whereas MIP only methylates TEs at C residues. Both mechanisms require specific cytosine DNA Methyltransferases (RID1/Masc1) of the Dnmt1 superfamily. RESULTS: We annotated TE sequences from 10 fungal genomes with different TE content (1-70%). We then used these TE sequences to carry out a genome-wide analysis of C to T mutations biases. Genomes from either Ascomycota or Basidiomycota that were massively invaded by TEs (Blumeria, Melampsora, Puccinia) were characterized by a low frequency of C to T mutation bias (10-20%), whereas other genomes displayed intermediate to high frequencies (25-75%). We identified several dinucleotide signatures at these C to T mutation sites (CpA, CpT, and CpG). Phylogenomic analysis of fungal Dnmt1 MTases revealed a previously unreported association between these dinucleotide signatures and the presence/absence of sub-classes of Dnmt1. CONCLUSIONS: We identified fungal genomes containing large numbers of TEs with many C to T mutations associated with species-specific dinucleotide signatures. This bias suggests that a basic defense mechanism against TE invasion similar to RIP is widespread in fungi, although the efficiency and specificity of this mechanism differs between species. Our analysis revealed that dinucleotide signatures are associated with the presence/absence of specific Dnmt1 subfamilies. In particular, an RID1-dependent RIP mechanism was found only in Ascomycota. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1347-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-02-28 /pmc/articles/PMC4352252/ /pubmed/25766680 http://dx.doi.org/10.1186/s12864-015-1347-1 Text en © Amselem et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Article
Amselem, Joëlle
Lebrun, Marc-Henri
Quesneville, Hadi
Whole genome comparative analysis of transposable elements provides new insight into mechanisms of their inactivation in fungal genomes
title Whole genome comparative analysis of transposable elements provides new insight into mechanisms of their inactivation in fungal genomes
title_full Whole genome comparative analysis of transposable elements provides new insight into mechanisms of their inactivation in fungal genomes
title_fullStr Whole genome comparative analysis of transposable elements provides new insight into mechanisms of their inactivation in fungal genomes
title_full_unstemmed Whole genome comparative analysis of transposable elements provides new insight into mechanisms of their inactivation in fungal genomes
title_short Whole genome comparative analysis of transposable elements provides new insight into mechanisms of their inactivation in fungal genomes
title_sort whole genome comparative analysis of transposable elements provides new insight into mechanisms of their inactivation in fungal genomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352252/
https://www.ncbi.nlm.nih.gov/pubmed/25766680
http://dx.doi.org/10.1186/s12864-015-1347-1
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