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Gibberellin signaling mediates lateral root inhibition in response to K(+)-deprivation

The potassium ion (K(+)) is vital for plant growth and development, and K(+)-deprivation leads to reduced crop yields. Here we describe phenotypic, transcriptomic, and mutant analyses to investigate the signaling mechanisms mediating root architectural changes in Arabidopsis (Arabidopsis thaliana) C...

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Autores principales: Hetherington, Flora M, Kakkar, Medhavi, Topping, Jennifer F, Lindsey, Keith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8133588/
https://www.ncbi.nlm.nih.gov/pubmed/33793923
http://dx.doi.org/10.1093/plphys/kiaa093
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author Hetherington, Flora M
Kakkar, Medhavi
Topping, Jennifer F
Lindsey, Keith
author_facet Hetherington, Flora M
Kakkar, Medhavi
Topping, Jennifer F
Lindsey, Keith
author_sort Hetherington, Flora M
collection PubMed
description The potassium ion (K(+)) is vital for plant growth and development, and K(+)-deprivation leads to reduced crop yields. Here we describe phenotypic, transcriptomic, and mutant analyses to investigate the signaling mechanisms mediating root architectural changes in Arabidopsis (Arabidopsis thaliana) Columbia. We showed effects on root architecture are mediated through a reduction in cell division in the lateral root (LR) meristems, the rate of LR initiation is reduced but LR density is unaffected, and primary root growth is reduced only slightly. This was primarily regulated through gibberellic acid (GA) signaling, which leads to the accumulation of growth-inhibitory DELLA proteins. The short LR phenotype was rescued by exogenous application of GA but not of auxin or by the inhibition of ethylene signaling. RNA-seq analysis showed upregulation by K(+)-deprivation of the transcription factors JUNGBRUNNEN1 (JUB1) and the C-repeat-binding factor (CBF)/dehydration-responsive element-binding factor 1 regulon, which are known to regulate GA signaling and levels that regulate DELLAs. Transgenic overexpression of JUB1 and CBF1 enhanced responses to K(+) stress. Attenuation of the reduced LR growth response occurred in mutants of the CBF1 target gene SFR6, implicating a role for JUB1, CBF1, and SFR6 in the regulation of LR growth in response to K(+)-deprivation via DELLAs. We propose this represents a mechanism to limit horizontal root growth in conditions where K(+) is available deeper in the soil.
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spelling pubmed-81335882021-05-25 Gibberellin signaling mediates lateral root inhibition in response to K(+)-deprivation Hetherington, Flora M Kakkar, Medhavi Topping, Jennifer F Lindsey, Keith Plant Physiol Regular Issue The potassium ion (K(+)) is vital for plant growth and development, and K(+)-deprivation leads to reduced crop yields. Here we describe phenotypic, transcriptomic, and mutant analyses to investigate the signaling mechanisms mediating root architectural changes in Arabidopsis (Arabidopsis thaliana) Columbia. We showed effects on root architecture are mediated through a reduction in cell division in the lateral root (LR) meristems, the rate of LR initiation is reduced but LR density is unaffected, and primary root growth is reduced only slightly. This was primarily regulated through gibberellic acid (GA) signaling, which leads to the accumulation of growth-inhibitory DELLA proteins. The short LR phenotype was rescued by exogenous application of GA but not of auxin or by the inhibition of ethylene signaling. RNA-seq analysis showed upregulation by K(+)-deprivation of the transcription factors JUNGBRUNNEN1 (JUB1) and the C-repeat-binding factor (CBF)/dehydration-responsive element-binding factor 1 regulon, which are known to regulate GA signaling and levels that regulate DELLAs. Transgenic overexpression of JUB1 and CBF1 enhanced responses to K(+) stress. Attenuation of the reduced LR growth response occurred in mutants of the CBF1 target gene SFR6, implicating a role for JUB1, CBF1, and SFR6 in the regulation of LR growth in response to K(+)-deprivation via DELLAs. We propose this represents a mechanism to limit horizontal root growth in conditions where K(+) is available deeper in the soil. Oxford University Press 2021-01-06 /pmc/articles/PMC8133588/ /pubmed/33793923 http://dx.doi.org/10.1093/plphys/kiaa093 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Issue
Hetherington, Flora M
Kakkar, Medhavi
Topping, Jennifer F
Lindsey, Keith
Gibberellin signaling mediates lateral root inhibition in response to K(+)-deprivation
title Gibberellin signaling mediates lateral root inhibition in response to K(+)-deprivation
title_full Gibberellin signaling mediates lateral root inhibition in response to K(+)-deprivation
title_fullStr Gibberellin signaling mediates lateral root inhibition in response to K(+)-deprivation
title_full_unstemmed Gibberellin signaling mediates lateral root inhibition in response to K(+)-deprivation
title_short Gibberellin signaling mediates lateral root inhibition in response to K(+)-deprivation
title_sort gibberellin signaling mediates lateral root inhibition in response to k(+)-deprivation
topic Regular Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8133588/
https://www.ncbi.nlm.nih.gov/pubmed/33793923
http://dx.doi.org/10.1093/plphys/kiaa093
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