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Natural variation of BSK3 tunes brassinosteroid signaling to regulate root foraging under low nitrogen

Developmental plasticity of root system architecture is crucial for plant performance in nutrient-poor soils. Roots of plants grown under mild nitrogen (N) deficiency show a foraging response characterized by increased root length but mechanisms underlying this developmental plasticity are still elu...

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Autores principales: Jia, Zhongtao, Giehl, Ricardo F. H., Meyer, Rhonda C., Altmann, Thomas, von Wirén, Nicolaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542857/
https://www.ncbi.nlm.nih.gov/pubmed/31147541
http://dx.doi.org/10.1038/s41467-019-10331-9
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author Jia, Zhongtao
Giehl, Ricardo F. H.
Meyer, Rhonda C.
Altmann, Thomas
von Wirén, Nicolaus
author_facet Jia, Zhongtao
Giehl, Ricardo F. H.
Meyer, Rhonda C.
Altmann, Thomas
von Wirén, Nicolaus
author_sort Jia, Zhongtao
collection PubMed
description Developmental plasticity of root system architecture is crucial for plant performance in nutrient-poor soils. Roots of plants grown under mild nitrogen (N) deficiency show a foraging response characterized by increased root length but mechanisms underlying this developmental plasticity are still elusive. By employing natural variation in Arabidopsis accessions, we show that the brassinosteroid (BR) signaling kinase BSK3 modulates root elongation under mild N deficiency. In particular, a proline to leucine substitution in the predicted kinase domain of BSK3 enhances BR sensitivity and signaling to increase the extent of root elongation. We further show that low N specifically upregulates transcript levels of the BR co-receptor BAK1 to activate BR signaling and stimulate root elongation. Altogether, our results uncover a role of BR signaling in root elongation under low N. The BSK3 alleles identified here provide targets for improving root growth of crops growing under limited N conditions.
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spelling pubmed-65428572019-06-03 Natural variation of BSK3 tunes brassinosteroid signaling to regulate root foraging under low nitrogen Jia, Zhongtao Giehl, Ricardo F. H. Meyer, Rhonda C. Altmann, Thomas von Wirén, Nicolaus Nat Commun Article Developmental plasticity of root system architecture is crucial for plant performance in nutrient-poor soils. Roots of plants grown under mild nitrogen (N) deficiency show a foraging response characterized by increased root length but mechanisms underlying this developmental plasticity are still elusive. By employing natural variation in Arabidopsis accessions, we show that the brassinosteroid (BR) signaling kinase BSK3 modulates root elongation under mild N deficiency. In particular, a proline to leucine substitution in the predicted kinase domain of BSK3 enhances BR sensitivity and signaling to increase the extent of root elongation. We further show that low N specifically upregulates transcript levels of the BR co-receptor BAK1 to activate BR signaling and stimulate root elongation. Altogether, our results uncover a role of BR signaling in root elongation under low N. The BSK3 alleles identified here provide targets for improving root growth of crops growing under limited N conditions. Nature Publishing Group UK 2019-05-30 /pmc/articles/PMC6542857/ /pubmed/31147541 http://dx.doi.org/10.1038/s41467-019-10331-9 Text en © The Author(s) 2019 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
Jia, Zhongtao
Giehl, Ricardo F. H.
Meyer, Rhonda C.
Altmann, Thomas
von Wirén, Nicolaus
Natural variation of BSK3 tunes brassinosteroid signaling to regulate root foraging under low nitrogen
title Natural variation of BSK3 tunes brassinosteroid signaling to regulate root foraging under low nitrogen
title_full Natural variation of BSK3 tunes brassinosteroid signaling to regulate root foraging under low nitrogen
title_fullStr Natural variation of BSK3 tunes brassinosteroid signaling to regulate root foraging under low nitrogen
title_full_unstemmed Natural variation of BSK3 tunes brassinosteroid signaling to regulate root foraging under low nitrogen
title_short Natural variation of BSK3 tunes brassinosteroid signaling to regulate root foraging under low nitrogen
title_sort natural variation of bsk3 tunes brassinosteroid signaling to regulate root foraging under low nitrogen
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542857/
https://www.ncbi.nlm.nih.gov/pubmed/31147541
http://dx.doi.org/10.1038/s41467-019-10331-9
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