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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-9404710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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