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DNA demethylases target promoter transposable elements to positively regulate stress responsive genes in Arabidopsis
BACKGROUND: DNA demethylases regulate DNA methylation levels in eukaryotes. Arabidopsis encodes four DNA demethylases, DEMETER (DME), REPRESSOR OF SILENCING 1 (ROS1), DEMETER-LIKE 2 (DML2), and DML3. While DME is involved in maternal specific gene expression during seed development, the biological f...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189188/ https://www.ncbi.nlm.nih.gov/pubmed/25228471 http://dx.doi.org/10.1186/s13059-014-0458-3 |
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author | Le, Tuan-Ngoc Schumann, Ulrike Smith, Neil A Tiwari, Sameer Au, Phil Chi Khang Zhu, Qian-Hao Taylor, Jennifer M Kazan, Kemal Llewellyn, Danny J Zhang, Ren Dennis, Elizabeth S Wang, Ming-Bo |
author_facet | Le, Tuan-Ngoc Schumann, Ulrike Smith, Neil A Tiwari, Sameer Au, Phil Chi Khang Zhu, Qian-Hao Taylor, Jennifer M Kazan, Kemal Llewellyn, Danny J Zhang, Ren Dennis, Elizabeth S Wang, Ming-Bo |
author_sort | Le, Tuan-Ngoc |
collection | PubMed |
description | BACKGROUND: DNA demethylases regulate DNA methylation levels in eukaryotes. Arabidopsis encodes four DNA demethylases, DEMETER (DME), REPRESSOR OF SILENCING 1 (ROS1), DEMETER-LIKE 2 (DML2), and DML3. While DME is involved in maternal specific gene expression during seed development, the biological function of the remaining DNA demethylases remains unclear. RESULTS: We show that ROS1, DML2, and DML3 play a role in fungal disease resistance in Arabidopsis. A triple DNA demethylase mutant, rdd (ros1 dml2 dml3), shows increased susceptibility to the fungal pathogen Fusarium oxysporum. We identify 348 genes differentially expressed in rdd relative to wild type, and a significant proportion of these genes are downregulated in rdd and have functions in stress response, suggesting that DNA demethylases maintain or positively regulate the expression of stress response genes required for F. oxysporum resistance. The rdd-downregulated stress response genes are enriched for short transposable element sequences in their promoters. Many of these transposable elements and their surrounding sequences show localized DNA methylation changes in rdd, and a general reduction in CHH methylation, suggesting that RNA-directed DNA methylation (RdDM), responsible for CHH methylation, may participate in DNA demethylase-mediated regulation of stress response genes. Many of the rdd-downregulated stress response genes are downregulated in the RdDM mutants nrpd1 and nrpe1, and the RdDM mutants nrpe1 and ago4 show enhanced susceptibility to F. oxysporum infection. CONCLUSIONS: Our results suggest that a primary function of DNA demethylases in plants is to regulate the expression of stress response genes by targeting promoter transposable element sequences. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-014-0458-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4189188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41891882014-10-10 DNA demethylases target promoter transposable elements to positively regulate stress responsive genes in Arabidopsis Le, Tuan-Ngoc Schumann, Ulrike Smith, Neil A Tiwari, Sameer Au, Phil Chi Khang Zhu, Qian-Hao Taylor, Jennifer M Kazan, Kemal Llewellyn, Danny J Zhang, Ren Dennis, Elizabeth S Wang, Ming-Bo Genome Biol Research BACKGROUND: DNA demethylases regulate DNA methylation levels in eukaryotes. Arabidopsis encodes four DNA demethylases, DEMETER (DME), REPRESSOR OF SILENCING 1 (ROS1), DEMETER-LIKE 2 (DML2), and DML3. While DME is involved in maternal specific gene expression during seed development, the biological function of the remaining DNA demethylases remains unclear. RESULTS: We show that ROS1, DML2, and DML3 play a role in fungal disease resistance in Arabidopsis. A triple DNA demethylase mutant, rdd (ros1 dml2 dml3), shows increased susceptibility to the fungal pathogen Fusarium oxysporum. We identify 348 genes differentially expressed in rdd relative to wild type, and a significant proportion of these genes are downregulated in rdd and have functions in stress response, suggesting that DNA demethylases maintain or positively regulate the expression of stress response genes required for F. oxysporum resistance. The rdd-downregulated stress response genes are enriched for short transposable element sequences in their promoters. Many of these transposable elements and their surrounding sequences show localized DNA methylation changes in rdd, and a general reduction in CHH methylation, suggesting that RNA-directed DNA methylation (RdDM), responsible for CHH methylation, may participate in DNA demethylase-mediated regulation of stress response genes. Many of the rdd-downregulated stress response genes are downregulated in the RdDM mutants nrpd1 and nrpe1, and the RdDM mutants nrpe1 and ago4 show enhanced susceptibility to F. oxysporum infection. CONCLUSIONS: Our results suggest that a primary function of DNA demethylases in plants is to regulate the expression of stress response genes by targeting promoter transposable element sequences. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-014-0458-3) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-17 2014 /pmc/articles/PMC4189188/ /pubmed/25228471 http://dx.doi.org/10.1186/s13059-014-0458-3 Text en © Le et al.; licensee BioMed Central Ltd. 2014 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 Le, Tuan-Ngoc Schumann, Ulrike Smith, Neil A Tiwari, Sameer Au, Phil Chi Khang Zhu, Qian-Hao Taylor, Jennifer M Kazan, Kemal Llewellyn, Danny J Zhang, Ren Dennis, Elizabeth S Wang, Ming-Bo DNA demethylases target promoter transposable elements to positively regulate stress responsive genes in Arabidopsis |
title | DNA demethylases target promoter transposable elements to positively regulate stress responsive genes in Arabidopsis |
title_full | DNA demethylases target promoter transposable elements to positively regulate stress responsive genes in Arabidopsis |
title_fullStr | DNA demethylases target promoter transposable elements to positively regulate stress responsive genes in Arabidopsis |
title_full_unstemmed | DNA demethylases target promoter transposable elements to positively regulate stress responsive genes in Arabidopsis |
title_short | DNA demethylases target promoter transposable elements to positively regulate stress responsive genes in Arabidopsis |
title_sort | dna demethylases target promoter transposable elements to positively regulate stress responsive genes in arabidopsis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189188/ https://www.ncbi.nlm.nih.gov/pubmed/25228471 http://dx.doi.org/10.1186/s13059-014-0458-3 |
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