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BZR1 Regulates Brassinosteroid-Mediated Activation of AMT1;2 in Rice

Although it is known that brassinosteroids (BRs) play pleiotropic roles in plant growth and development, their roles in plant nutrient uptake remain unknown. Here, we hypothesized that BRs directly regulate ammonium uptake by activating the expression of rice AMT1-type genes. Exogenous BR treatment...

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Autores principales: Yang, Shuo, Yuan, Depeng, Zhang, Yang, Sun, Qian, Xuan, Yuan Hu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247761/
https://www.ncbi.nlm.nih.gov/pubmed/34220889
http://dx.doi.org/10.3389/fpls.2021.665883
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author Yang, Shuo
Yuan, Depeng
Zhang, Yang
Sun, Qian
Xuan, Yuan Hu
author_facet Yang, Shuo
Yuan, Depeng
Zhang, Yang
Sun, Qian
Xuan, Yuan Hu
author_sort Yang, Shuo
collection PubMed
description Although it is known that brassinosteroids (BRs) play pleiotropic roles in plant growth and development, their roles in plant nutrient uptake remain unknown. Here, we hypothesized that BRs directly regulate ammonium uptake by activating the expression of rice AMT1-type genes. Exogenous BR treatment upregulated both AMT1;1 and AMT1;2 expression, while this induction was impaired in the BR-receptor gene BRI1 mutant d61-1. We then focused on brassinazole-resistant 1 (BZR1), a central hub of the BR signaling pathway, demonstrating the important role of this signaling pathway in regulating AMT1 expression and rice roots NH(4)(+) uptake. The results showed that BR-induced expression of AMT1;2 was suppressed in BZR1 RNAi plants but was increased in bzr1-D, a gain-of-function BZR1 mutant. Further EMSA and ChIP analyses showed that BZR1 bound directly to the BRRE motif located in the promoter region of AMT1;2. Moreover, cellular ammonium contents, (15)NH(4)(+) uptake, and the regulatory effect of methyl-ammonium on root growth are strongly dependent on the levels of BZR1. Overexpression lines of BRI1 and BZR1 and Genetic combination of them mutants showed that BZR1 activates AMT1;2 expression downstream of BRI1. In conclusion, the findings suggest that BRs regulation of NH4(+) uptake in rice involves transcription regulation of ammonium transporters.
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spelling pubmed-82477612021-07-02 BZR1 Regulates Brassinosteroid-Mediated Activation of AMT1;2 in Rice Yang, Shuo Yuan, Depeng Zhang, Yang Sun, Qian Xuan, Yuan Hu Front Plant Sci Plant Science Although it is known that brassinosteroids (BRs) play pleiotropic roles in plant growth and development, their roles in plant nutrient uptake remain unknown. Here, we hypothesized that BRs directly regulate ammonium uptake by activating the expression of rice AMT1-type genes. Exogenous BR treatment upregulated both AMT1;1 and AMT1;2 expression, while this induction was impaired in the BR-receptor gene BRI1 mutant d61-1. We then focused on brassinazole-resistant 1 (BZR1), a central hub of the BR signaling pathway, demonstrating the important role of this signaling pathway in regulating AMT1 expression and rice roots NH(4)(+) uptake. The results showed that BR-induced expression of AMT1;2 was suppressed in BZR1 RNAi plants but was increased in bzr1-D, a gain-of-function BZR1 mutant. Further EMSA and ChIP analyses showed that BZR1 bound directly to the BRRE motif located in the promoter region of AMT1;2. Moreover, cellular ammonium contents, (15)NH(4)(+) uptake, and the regulatory effect of methyl-ammonium on root growth are strongly dependent on the levels of BZR1. Overexpression lines of BRI1 and BZR1 and Genetic combination of them mutants showed that BZR1 activates AMT1;2 expression downstream of BRI1. In conclusion, the findings suggest that BRs regulation of NH4(+) uptake in rice involves transcription regulation of ammonium transporters. Frontiers Media S.A. 2021-06-17 /pmc/articles/PMC8247761/ /pubmed/34220889 http://dx.doi.org/10.3389/fpls.2021.665883 Text en Copyright © 2021 Yang, Yuan, Zhang, Sun and Xuan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Yang, Shuo
Yuan, Depeng
Zhang, Yang
Sun, Qian
Xuan, Yuan Hu
BZR1 Regulates Brassinosteroid-Mediated Activation of AMT1;2 in Rice
title BZR1 Regulates Brassinosteroid-Mediated Activation of AMT1;2 in Rice
title_full BZR1 Regulates Brassinosteroid-Mediated Activation of AMT1;2 in Rice
title_fullStr BZR1 Regulates Brassinosteroid-Mediated Activation of AMT1;2 in Rice
title_full_unstemmed BZR1 Regulates Brassinosteroid-Mediated Activation of AMT1;2 in Rice
title_short BZR1 Regulates Brassinosteroid-Mediated Activation of AMT1;2 in Rice
title_sort bzr1 regulates brassinosteroid-mediated activation of amt1;2 in rice
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247761/
https://www.ncbi.nlm.nih.gov/pubmed/34220889
http://dx.doi.org/10.3389/fpls.2021.665883
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