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The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice

Sucrose non-fermenting-1-related protein kinase-1 (SnRK1) belongs to a family of evolutionary conserved kinases with orthologs in all eukaryotes, ranging from yeasts (SnF1) to mammals (AMP-Activated kinase). These kinases sense energy deficits caused by nutrient limitation or stress and coordinate t...

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Autores principales: Filipe, Osvaldo, De Vleesschauwer, David, Haeck, Ashley, Demeestere, Kristof, Höfte, Monica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832823/
https://www.ncbi.nlm.nih.gov/pubmed/29497084
http://dx.doi.org/10.1038/s41598-018-22101-6
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author Filipe, Osvaldo
De Vleesschauwer, David
Haeck, Ashley
Demeestere, Kristof
Höfte, Monica
author_facet Filipe, Osvaldo
De Vleesschauwer, David
Haeck, Ashley
Demeestere, Kristof
Höfte, Monica
author_sort Filipe, Osvaldo
collection PubMed
description Sucrose non-fermenting-1-related protein kinase-1 (SnRK1) belongs to a family of evolutionary conserved kinases with orthologs in all eukaryotes, ranging from yeasts (SnF1) to mammals (AMP-Activated kinase). These kinases sense energy deficits caused by nutrient limitation or stress and coordinate the required adaptations to maintain energy homeostasis and survival. In plants, SnRK1 is a global regulator of plant metabolism and is also involved in abiotic stress responses. Its role in the response to biotic stress, however, is only starting to be uncovered. Here we studied the effect of altered SnRK1a expression on growth and plant defense in rice. OsSnRK1a overexpression interfered with normal growth and development and increased resistance against both (hemi)biotrophic and necrotrophic pathogens, while OsSnRK1a silencing in RNAi lines increased susceptibility. OsSnRK1a overexpression positively affected the salicylic acid pathway and boosted the jasmonate-mediated defense response after inoculation with the blast fungus Pyricularia oryzae. Together these findings strongly suggest OsSnRK1a to be involved in plant basal immunity and favor a model whereby OsSnRK1a acts as a master switch that regulates growth-immunity trade-offs.
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spelling pubmed-58328232018-03-05 The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice Filipe, Osvaldo De Vleesschauwer, David Haeck, Ashley Demeestere, Kristof Höfte, Monica Sci Rep Article Sucrose non-fermenting-1-related protein kinase-1 (SnRK1) belongs to a family of evolutionary conserved kinases with orthologs in all eukaryotes, ranging from yeasts (SnF1) to mammals (AMP-Activated kinase). These kinases sense energy deficits caused by nutrient limitation or stress and coordinate the required adaptations to maintain energy homeostasis and survival. In plants, SnRK1 is a global regulator of plant metabolism and is also involved in abiotic stress responses. Its role in the response to biotic stress, however, is only starting to be uncovered. Here we studied the effect of altered SnRK1a expression on growth and plant defense in rice. OsSnRK1a overexpression interfered with normal growth and development and increased resistance against both (hemi)biotrophic and necrotrophic pathogens, while OsSnRK1a silencing in RNAi lines increased susceptibility. OsSnRK1a overexpression positively affected the salicylic acid pathway and boosted the jasmonate-mediated defense response after inoculation with the blast fungus Pyricularia oryzae. Together these findings strongly suggest OsSnRK1a to be involved in plant basal immunity and favor a model whereby OsSnRK1a acts as a master switch that regulates growth-immunity trade-offs. Nature Publishing Group UK 2018-03-01 /pmc/articles/PMC5832823/ /pubmed/29497084 http://dx.doi.org/10.1038/s41598-018-22101-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Filipe, Osvaldo
De Vleesschauwer, David
Haeck, Ashley
Demeestere, Kristof
Höfte, Monica
The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice
title The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice
title_full The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice
title_fullStr The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice
title_full_unstemmed The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice
title_short The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice
title_sort energy sensor ossnrk1a confers broad-spectrum disease resistance in rice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832823/
https://www.ncbi.nlm.nih.gov/pubmed/29497084
http://dx.doi.org/10.1038/s41598-018-22101-6
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