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Identification and characterisation of hypomethylated DNA loci controlling quantitative resistance in Arabidopsis
Variation in DNA methylation enables plants to inherit traits independently of changes to DNA sequence. Here, we have screened an Arabidopsis population of epigenetic recombinant inbred lines (epiRILs) for resistance against Hyaloperonospora arabidopsidis (Hpa). These lines share the same genetic ba...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6342528/ https://www.ncbi.nlm.nih.gov/pubmed/30608232 http://dx.doi.org/10.7554/eLife.40655 |
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author | Furci, Leonardo Jain, Ritushree Stassen, Joost Berkowitz, Oliver Whelan, James Roquis, David Baillet, Victoire Colot, Vincent Johannes, Frank Ton, Jurriaan |
author_facet | Furci, Leonardo Jain, Ritushree Stassen, Joost Berkowitz, Oliver Whelan, James Roquis, David Baillet, Victoire Colot, Vincent Johannes, Frank Ton, Jurriaan |
author_sort | Furci, Leonardo |
collection | PubMed |
description | Variation in DNA methylation enables plants to inherit traits independently of changes to DNA sequence. Here, we have screened an Arabidopsis population of epigenetic recombinant inbred lines (epiRILs) for resistance against Hyaloperonospora arabidopsidis (Hpa). These lines share the same genetic background, but show variation in heritable patterns of DNA methylation. We identified four epigenetic quantitative trait loci (epiQTLs) that provide quantitative resistance without reducing plant growth or resistance to other (a)biotic stresses. Phenotypic characterisation and RNA-sequencing analysis revealed that Hpa-resistant epiRILs are primed to activate defence responses at the relatively early stages of infection. Collectively, our results show that hypomethylation at selected pericentromeric regions is sufficient to provide quantitative disease resistance, which is associated with genome-wide priming of defence-related genes. Based on comparisons of global gene expression and DNA methylation between the wild-type and resistant epiRILs, we discuss mechanisms by which the pericentromeric epiQTLs could regulate the defence-related transcriptome. |
format | Online Article Text |
id | pubmed-6342528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63425282019-01-24 Identification and characterisation of hypomethylated DNA loci controlling quantitative resistance in Arabidopsis Furci, Leonardo Jain, Ritushree Stassen, Joost Berkowitz, Oliver Whelan, James Roquis, David Baillet, Victoire Colot, Vincent Johannes, Frank Ton, Jurriaan eLife Plant Biology Variation in DNA methylation enables plants to inherit traits independently of changes to DNA sequence. Here, we have screened an Arabidopsis population of epigenetic recombinant inbred lines (epiRILs) for resistance against Hyaloperonospora arabidopsidis (Hpa). These lines share the same genetic background, but show variation in heritable patterns of DNA methylation. We identified four epigenetic quantitative trait loci (epiQTLs) that provide quantitative resistance without reducing plant growth or resistance to other (a)biotic stresses. Phenotypic characterisation and RNA-sequencing analysis revealed that Hpa-resistant epiRILs are primed to activate defence responses at the relatively early stages of infection. Collectively, our results show that hypomethylation at selected pericentromeric regions is sufficient to provide quantitative disease resistance, which is associated with genome-wide priming of defence-related genes. Based on comparisons of global gene expression and DNA methylation between the wild-type and resistant epiRILs, we discuss mechanisms by which the pericentromeric epiQTLs could regulate the defence-related transcriptome. eLife Sciences Publications, Ltd 2019-01-04 /pmc/articles/PMC6342528/ /pubmed/30608232 http://dx.doi.org/10.7554/eLife.40655 Text en © 2019, Furci et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Plant Biology Furci, Leonardo Jain, Ritushree Stassen, Joost Berkowitz, Oliver Whelan, James Roquis, David Baillet, Victoire Colot, Vincent Johannes, Frank Ton, Jurriaan Identification and characterisation of hypomethylated DNA loci controlling quantitative resistance in Arabidopsis |
title | Identification and characterisation of hypomethylated DNA loci controlling quantitative resistance in Arabidopsis |
title_full | Identification and characterisation of hypomethylated DNA loci controlling quantitative resistance in Arabidopsis |
title_fullStr | Identification and characterisation of hypomethylated DNA loci controlling quantitative resistance in Arabidopsis |
title_full_unstemmed | Identification and characterisation of hypomethylated DNA loci controlling quantitative resistance in Arabidopsis |
title_short | Identification and characterisation of hypomethylated DNA loci controlling quantitative resistance in Arabidopsis |
title_sort | identification and characterisation of hypomethylated dna loci controlling quantitative resistance in arabidopsis |
topic | Plant Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6342528/ https://www.ncbi.nlm.nih.gov/pubmed/30608232 http://dx.doi.org/10.7554/eLife.40655 |
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