A defined range of guard cell calcium oscillation parameters encodes stomatal movements
Gethyn J. Allen,
Sarah P. Chu,
Carrie L. Harrington,
Karin Schumacher,
Thomas Hoffmann,
Yat Y. Tang,
Erwin Grill and
Julian I. Schroeder ()
Additional contact information
Gethyn J. Allen: Cell and Developmental Biology Section, University of California, San Diego
Sarah P. Chu: Cell and Developmental Biology Section, University of California, San Diego
Carrie L. Harrington: Cell and Developmental Biology Section, University of California, San Diego
Karin Schumacher: ZMBP-Pflanzenphysiologie, Universität Tübingen
Thomas Hoffmann: Technische Universität, München Lehrstuhl fur Botanik
Yat Y. Tang: Cell and Developmental Biology Section, University of California, San Diego
Erwin Grill: Technische Universität, München Lehrstuhl fur Botanik
Julian I. Schroeder: Cell and Developmental Biology Section, University of California, San Diego
Nature, 2001, vol. 411, issue 6841, 1053-1057
Abstract:
Abstract Oscillations in cytosolic calcium concentration ([Ca2+]cyt) are central regulators of signal transduction cascades1, although the roles of individual [Ca2+]cyt oscillation parameters in regulating downstream physiological responses remain largely unknown. In plants, guard cells integrate environmental and endogenous signals to regulate the aperture of stomatal pores2 and [Ca2+]cyt oscillations are a fundamental component of stomatal closure3,4. Here we systematically vary [Ca2+]cyt oscillation parameters in Arabidopsis guard cells using a ‘calcium clamp’3,5,6,7 and show that [Ca2+]cyt controls stomatal closure by two mechanisms. Short-term ‘calcium-reactive’ closure occurred rapidly when [Ca2+]cyt was elevated, whereas the degree of long-term steady-state closure was ‘calcium programmed’ by [Ca2+]cyt oscillations within a defined range of frequency, transient number, duration and amplitude. Furthermore, in guard cells of the gca2 mutant8, [Ca2+]cyt oscillations induced by abscisic acid and extracellular calcium had increased frequencies and reduced transient duration, and steady-state stomatal closure was abolished. Experimentally imposing [Ca2+]cyt oscillations with parameters that elicited closure in the wild type restored long-term closure in gca2 stomata. These data show that a defined window of guard cell [Ca2+]cyt oscillation parameters programs changes in steady-state stomatal aperture.
Date: 2001
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DOI: 10.1038/35082575
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