Nitrated cyclic GMP modulates guard cell signaling in Arabidopsis.
Journal: 2014/January - Plant Cell
ISSN: 1532-298X
Abstract:
Nitric oxide (NO) is a ubiquitous signaling molecule involved in diverse physiological processes, including plant senescence and stomatal closure. The NO and cyclic GMP (cGMP) cascade is the main NO signaling pathway in animals, but whether this pathway operates in plant cells, and the mechanisms of its action, remain unclear. Here, we assessed the possibility that the nitrated cGMP derivative 8-nitro-cGMP functions in guard cell signaling. Mass spectrometry and immunocytochemical analyses showed that abscisic acid and NO induced the synthesis of 8-nitro-cGMP in guard cells in the presence of reactive oxygen species. 8-Nitro-cGMP triggered stomatal closure, but 8-bromoguanosine 3',5'-cyclic monophosphate (8-bromo-cGMP), a membrane-permeating analog of cGMP, did not. However, in the dark, 8-bromo-cGMP induced stomatal opening but 8-nitro-cGMP did not. Thus, cGMP and its nitrated derivative play different roles in the signaling pathways that lead to stomatal opening and closure. Moreover, inhibitor and genetic studies showed that calcium, cyclic adenosine-5'-diphosphate-ribose, and SLOW ANION CHANNEL1 act downstream of 8-nitro-cGMP. This study therefore demonstrates that 8-nitro-cGMP acts as a guard cell signaling molecule and that a NO/8-nitro-cGMP signaling cascade operates in guard cells.
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Plant Cell 25(2): 558-571

Nitrated Cyclic GMP Modulates Guard Cell Signaling in <em>Arabidopsis</em><sup>[W]</sup>

Department of Horticultural Science, Faculty of Agriculture, Kagoshima University, Kagoshima 890-0065, Japan
Department of Microbiology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto 860-8556, Japan
Department of Bioscience and Biotechnology, Faculty of Agriculture, Kyushu University, Higashi-ku, Fukuoka 812-8581, Japan
Address correspondence to pj.ca.u-amihsogoak.irga@iawioms.
The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantcell.org) is: Takaaki Akaike (pj.ca.u-otomamuk.opg@kiakakat).
Online version contains Web-only data.
www.plantcell.org/cgi/doi/10.1105/tpc.112.105049
The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantcell.org) is: Takaaki Akaike (pj.ca.u-otomamuk.opg@kiakakat).www.plantcell.org/cgi/doi/10.1105/tpc.112.105049
Received 2012 Sep 11; Revised 2012 Dec 26; Accepted 2013 Jan 16.

Abstract

Nitric oxide (NO) is a ubiquitous signaling molecule involved in diverse physiological processes, including plant senescence and stomatal closure. The NO and cyclic GMP (cGMP) cascade is the main NO signaling pathway in animals, but whether this pathway operates in plant cells, and the mechanisms of its action, remain unclear. Here, we assessed the possibility that the nitrated cGMP derivative 8-nitro-cGMP functions in guard cell signaling. Mass spectrometry and immunocytochemical analyses showed that abscisic acid and NO induced the synthesis of 8-nitro-cGMP in guard cells in the presence of reactive oxygen species. 8-Nitro-cGMP triggered stomatal closure, but 8-bromoguanosine 3′,5′-cyclic monophosphate (8-bromo-cGMP), a membrane-permeating analog of cGMP, did not. However, in the dark, 8-bromo-cGMP induced stomatal opening but 8-nitro-cGMP did not. Thus, cGMP and its nitrated derivative play different roles in the signaling pathways that lead to stomatal opening and closure. Moreover, inhibitor and genetic studies showed that calcium, cyclic adenosine-5′-diphosphate-ribose, and SLOW ANION CHANNEL1 act downstream of 8-nitro-cGMP. This study therefore demonstrates that 8-nitro-cGMP acts as a guard cell signaling molecule and that a NO/8-nitro-cGMP signaling cascade operates in guard cells.

Abstract

Acknowledgments

We thank Koh Iba (Kyushu University, Japan) for kindly providing slac1-2. We thank members of the Vegetable Science Laboratory at Kagoshima University for help and suggestions. This work was supported by Grants-in-Aid for Scientific Research (B: 21390097) and Scientific Research on Innovative Areas (Research in a Proposed Research Area, 20117001 and 20117005) from the Ministry of Education, Sciences, Sports, and Technology, Japan.

Acknowledgments

AUTHOR CONTRIBUTIONS

S.I., T.A., and T.S. designed the research and analyzed data. T.J., Y.S., N.K., J.Y., N.Y., and S.I. performed research. S.I., T.A., T.S., and N.Y. wrote the article.

AUTHOR CONTRIBUTIONS

Notes

Glossary

ABAabscisic acid
NOnitric oxide
cGMPcyclic GMP
8-bromo-cGMP8-bromoguanosine 3′,5′-cyclic monophosphate
ROSreactive oxygen species
ODQ1-H-[1,2,4]oxadiazolo[4,3-a]quinoxaline-1-one
NOC51-hydroxy-2-oxo-3-(3-aminopropyl)-3-isopropyl-1-triazene
cPTIO2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide
MSmass spectrometry
m/zmass-to-charge ratio
SNAPS-nitroso-N-acetyl-dl-penicillamine
l-NAMEN-nitro-l-Arg methyl ester
LC-MS/MSliquid chromatography–tandem MS
MRMmultiple reaction monitoring
H2DCF-DA2,7-dichlorofluorescin diacetate
DAF-2 DAdiaminofluorescein–2 diacetate
H2O2hydrogen peroxide
cADPRcyclic adenosine-5′-diphosphate-ribose
RNSreactive nitrogen oxide species
Notes

Glossary

ABAabscisic acid
NOnitric oxide
cGMPcyclic GMP
8-bromo-cGMP8-bromoguanosine 3′,5′-cyclic monophosphate
ROSreactive oxygen species
ODQ1-H-[1,2,4]oxadiazolo[4,3-a]quinoxaline-1-one
NOC51-hydroxy-2-oxo-3-(3-aminopropyl)-3-isopropyl-1-triazene
cPTIO2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide
MSmass spectrometry
m/zmass-to-charge ratio
SNAPS-nitroso-N-acetyl-dl-penicillamine
l-NAMEN-nitro-l-Arg methyl ester
LC-MS/MSliquid chromatography–tandem MS
MRMmultiple reaction monitoring
H2DCF-DA2,7-dichlorofluorescin diacetate
DAF-2 DAdiaminofluorescein–2 diacetate
H2O2hydrogen peroxide
cADPRcyclic adenosine-5′-diphosphate-ribose
RNSreactive nitrogen oxide species
Glossary
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