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H(2)O(2) and Ca(2+) Signaling Crosstalk Counteracts ABA to Induce Seed Germination

Seed germination is a critical stage and the first step in the plant’s life cycle. H(2)O(2) and Ca(2+) act as important signal molecules in regulating plant growth and development and in providing defense against numerous stresses; however, their crosstalk in modulating seed germination remains larg...

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Autores principales: Cheng, Mengjie, Guo, Yanliang, Liu, Qing, Nan, Sanwa, Xue, Yuxing, Wei, Chunhua, Zhang, Yong, Luan, Feishi, Zhang, Xian, Li, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9404710/
https://www.ncbi.nlm.nih.gov/pubmed/36009313
http://dx.doi.org/10.3390/antiox11081594
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author Cheng, Mengjie
Guo, Yanliang
Liu, Qing
Nan, Sanwa
Xue, Yuxing
Wei, Chunhua
Zhang, Yong
Luan, Feishi
Zhang, Xian
Li, Hao
author_facet Cheng, Mengjie
Guo, Yanliang
Liu, Qing
Nan, Sanwa
Xue, Yuxing
Wei, Chunhua
Zhang, Yong
Luan, Feishi
Zhang, Xian
Li, Hao
author_sort Cheng, Mengjie
collection PubMed
description Seed germination is a critical stage and the first step in the plant’s life cycle. H(2)O(2) and Ca(2+) act as important signal molecules in regulating plant growth and development and in providing defense against numerous stresses; however, their crosstalk in modulating seed germination remains largely unaddressed. In the current study, we report that H(2)O(2) and Ca(2+) counteracted abscisic acid (ABA) to induce seed germination in melon and Arabidopsis by modulating ABA and gibberellic acid (GA(3)) balance. H(2)O(2) treatment induced a Ca(2+) influx in melon seeds accompanied by the upregulation of cyclic nucleotide-gated ion channel (CNGC) 20, which encodes a plasma membrane Ca(2+)-permeable channel. However, the inhibition of cytoplasmic free Ca(2+) elevation in the melon seeds and Arabidopsis mutant atcngc20 compromised H(2)O(2)-induced germination under ABA stress. CaCl(2) induced H(2)O(2) accumulation accompanied by the upregulation of respiratory burst oxidase homologue (RBOH) D and RBOHF in melon seeds with ABA pretreatment. However, inhibition of H(2)O(2) accumulation in the melon seeds and Arabidopsis mutant atrbohd and atrbohf abolished CaCl(2)-induced germination under ABA stress. The current study reveals a novel mechanism in which H(2)O(2) and Ca(2+) signaling crosstalk offsets ABA to induce seed germination. H(2)O(2) induces Ca(2+) influx, which in turn increases H(2)O(2) accumulation, thus forming a reciprocal positive-regulatory loop to maintain a balance between ABA and GA(3) and promote seed germination under ABA stress.
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spelling pubmed-94047102022-08-26 H(2)O(2) and Ca(2+) Signaling Crosstalk Counteracts ABA to Induce Seed Germination Cheng, Mengjie Guo, Yanliang Liu, Qing Nan, Sanwa Xue, Yuxing Wei, Chunhua Zhang, Yong Luan, Feishi Zhang, Xian Li, Hao Antioxidants (Basel) Article Seed germination is a critical stage and the first step in the plant’s life cycle. H(2)O(2) and Ca(2+) act as important signal molecules in regulating plant growth and development and in providing defense against numerous stresses; however, their crosstalk in modulating seed germination remains largely unaddressed. In the current study, we report that H(2)O(2) and Ca(2+) counteracted abscisic acid (ABA) to induce seed germination in melon and Arabidopsis by modulating ABA and gibberellic acid (GA(3)) balance. H(2)O(2) treatment induced a Ca(2+) influx in melon seeds accompanied by the upregulation of cyclic nucleotide-gated ion channel (CNGC) 20, which encodes a plasma membrane Ca(2+)-permeable channel. However, the inhibition of cytoplasmic free Ca(2+) elevation in the melon seeds and Arabidopsis mutant atcngc20 compromised H(2)O(2)-induced germination under ABA stress. CaCl(2) induced H(2)O(2) accumulation accompanied by the upregulation of respiratory burst oxidase homologue (RBOH) D and RBOHF in melon seeds with ABA pretreatment. However, inhibition of H(2)O(2) accumulation in the melon seeds and Arabidopsis mutant atrbohd and atrbohf abolished CaCl(2)-induced germination under ABA stress. The current study reveals a novel mechanism in which H(2)O(2) and Ca(2+) signaling crosstalk offsets ABA to induce seed germination. H(2)O(2) induces Ca(2+) influx, which in turn increases H(2)O(2) accumulation, thus forming a reciprocal positive-regulatory loop to maintain a balance between ABA and GA(3) and promote seed germination under ABA stress. MDPI 2022-08-17 /pmc/articles/PMC9404710/ /pubmed/36009313 http://dx.doi.org/10.3390/antiox11081594 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cheng, Mengjie
Guo, Yanliang
Liu, Qing
Nan, Sanwa
Xue, Yuxing
Wei, Chunhua
Zhang, Yong
Luan, Feishi
Zhang, Xian
Li, Hao
H(2)O(2) and Ca(2+) Signaling Crosstalk Counteracts ABA to Induce Seed Germination
title H(2)O(2) and Ca(2+) Signaling Crosstalk Counteracts ABA to Induce Seed Germination
title_full H(2)O(2) and Ca(2+) Signaling Crosstalk Counteracts ABA to Induce Seed Germination
title_fullStr H(2)O(2) and Ca(2+) Signaling Crosstalk Counteracts ABA to Induce Seed Germination
title_full_unstemmed H(2)O(2) and Ca(2+) Signaling Crosstalk Counteracts ABA to Induce Seed Germination
title_short H(2)O(2) and Ca(2+) Signaling Crosstalk Counteracts ABA to Induce Seed Germination
title_sort h(2)o(2) and ca(2+) signaling crosstalk counteracts aba to induce seed germination
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9404710/
https://www.ncbi.nlm.nih.gov/pubmed/36009313
http://dx.doi.org/10.3390/antiox11081594
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