Tomato GLR3.3 and GLR3.5 mediate cold acclimation‐induced chilling tolerance by regulating apoplastic H2O2 production and redox homeostasis

Plant glutamate receptor‐like (GLR) genes play important roles in plant development and immune response. However, the functions of GLRs in abiotic stress response remain unclear. Here we show that cold acclimation at 12°C induced the transcripts of GLR3.3 and GLR3.5 with increased tolerance against...

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Published inPlant, cell and environment Vol. 42; no. 12; pp. 3326 - 3339
Main Authors Li, Huizi, Jiang, Xiaochun, Lv, Xiangzhang, Ahammed, Golam Jalal, Guo, Zhixin, Qi, Zhenyu, Yu, Jingquan, Zhou, Yanhong
Format Journal Article
LanguageEnglish
Published Oxford Wiley Subscription Services, Inc 01.12.2019
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Abstract Plant glutamate receptor‐like (GLR) genes play important roles in plant development and immune response. However, the functions of GLRs in abiotic stress response remain unclear. Here we show that cold acclimation at 12°C induced the transcripts of GLR3.3 and GLR3.5 with increased tolerance against a subsequent chilling at 4 °C. Silencing of GLR3.3 or/and GLR3.5 or application of the antagonist of ionotropic glutamate receptor 6,7‐dinitroquinoxaline‐2,3‐dione (DNQX), all compromised the acclimation‐induced increases in the transcripts of respiratory burst oxidase homolog1 (RBOH1), activity of NADPH oxidase, the accumulation of apoplastic H2O2 and the ratio of reduced glutathione (GSH) to oxidized glutathione (GSSG), resulting in an attenuated chilling tolerance; the effect, however, was rescued by foliar application of H2O2 or GSH. Both RBOH1‐silenced and glutathione biosynthesis genes, γ‐ glutamylcysteine synthetase (GSH1)‐ and glutathione synthetase (GSH2)‐cosilenced plants had decreased chilling tolerance with reduced GSH/GSSG ratio. Moreover, application of DNQX had little effects on the GSH/GSSG ratio and the tolerance in RBOH1‐silenced plants and GSH1‐ and GSH2‐cosilenced plants. These findings unmasked the functional hierarchy of GLR‐H2O2‐glutathione cascade and shed new light on cold response pathway in tomato plants. Silencing of the glutamate receptor‐like GLR3.3 or/and GLR3.5 in tomato compromises cold acclimation‐induced elevation in RBOH1‐dependent H2O2 and GSH content and ratio of GSH/GSSG, resulting in an attenuated cold tolerance.
AbstractList Plant glutamate receptor‐like (GLR) genes play important roles in plant development and immune response. However, the functions of GLRs in abiotic stress response remain unclear. Here we show that cold acclimation at 12°C induced the transcripts of GLR3.3 and GLR3.5 with increased tolerance against a subsequent chilling at 4 °C. Silencing of GLR3.3 or/and GLR3.5 or application of the antagonist of ionotropic glutamate receptor 6,7‐dinitroquinoxaline‐2,3‐dione (DNQX), all compromised the acclimation‐induced increases in the transcripts of respiratory burst oxidase homolog1 (RBOH1), activity of NADPH oxidase, the accumulation of apoplastic H2O2 and the ratio of reduced glutathione (GSH) to oxidized glutathione (GSSG), resulting in an attenuated chilling tolerance; the effect, however, was rescued by foliar application of H2O2 or GSH. Both RBOH1‐silenced and glutathione biosynthesis genes, γ‐ glutamylcysteine synthetase (GSH1)‐ and glutathione synthetase (GSH2)‐cosilenced plants had decreased chilling tolerance with reduced GSH/GSSG ratio. Moreover, application of DNQX had little effects on the GSH/GSSG ratio and the tolerance in RBOH1‐silenced plants and GSH1‐ and GSH2‐cosilenced plants. These findings unmasked the functional hierarchy of GLR‐H2O2‐glutathione cascade and shed new light on cold response pathway in tomato plants.
Plant glutamate receptor‐like (GLR) genes play important roles in plant development and immune response. However, the functions of GLRs in abiotic stress response remain unclear. Here we show that cold acclimation at 12°C induced the transcripts of GLR3.3 and GLR3.5 with increased tolerance against a subsequent chilling at 4 °C. Silencing of GLR3.3 or/and GLR3.5 or application of the antagonist of ionotropic glutamate receptor 6,7‐dinitroquinoxaline‐2,3‐dione (DNQX), all compromised the acclimation‐induced increases in the transcripts of respiratory burst oxidase homolog1 (RBOH1), activity of NADPH oxidase, the accumulation of apoplastic H2O2 and the ratio of reduced glutathione (GSH) to oxidized glutathione (GSSG), resulting in an attenuated chilling tolerance; the effect, however, was rescued by foliar application of H2O2 or GSH. Both RBOH1‐silenced and glutathione biosynthesis genes, γ‐ glutamylcysteine synthetase (GSH1)‐ and glutathione synthetase (GSH2)‐cosilenced plants had decreased chilling tolerance with reduced GSH/GSSG ratio. Moreover, application of DNQX had little effects on the GSH/GSSG ratio and the tolerance in RBOH1‐silenced plants and GSH1‐ and GSH2‐cosilenced plants. These findings unmasked the functional hierarchy of GLR‐H2O2‐glutathione cascade and shed new light on cold response pathway in tomato plants. Silencing of the glutamate receptor‐like GLR3.3 or/and GLR3.5 in tomato compromises cold acclimation‐induced elevation in RBOH1‐dependent H2O2 and GSH content and ratio of GSH/GSSG, resulting in an attenuated cold tolerance.
Author Zhou, Yanhong
Guo, Zhixin
Lv, Xiangzhang
Ahammed, Golam Jalal
Qi, Zhenyu
Yu, Jingquan
Jiang, Xiaochun
Li, Huizi
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Snippet Plant glutamate receptor‐like (GLR) genes play important roles in plant development and immune response. However, the functions of GLRs in abiotic stress...
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SubjectTerms Acclimation
Acclimatization
Biosynthesis
Chilling
Cold acclimation
Cold tolerance
Cooling
Foliar applications
Genes
Glutamic acid receptors
Glutathione
H2O2
Homeostasis
Homology
Hydrogen peroxide
Immune response
Immunological tolerance
NAD(P)H oxidase
Oxidase
redox signalling
Respiratory burst oxidase
respiratory burst oxidase homolog1
Tomatoes
γ-Glutamylcysteine
Title Tomato GLR3.3 and GLR3.5 mediate cold acclimation‐induced chilling tolerance by regulating apoplastic H2O2 production and redox homeostasis
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fpce.13623
https://www.proquest.com/docview/2327542378
Volume 42
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