Multiparametric real-time sensing of cytosolic physiology links hypoxia responses to mitochondrial electron transport.
Multiparametric real-time sensing of cytosolic physiology links hypoxia responses to mitochondrial electron transport.
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DOI:
10.1111/nph.16093
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发表时间:
2019-09
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通讯作者:
Stephan Wagner;Janina Steinbeck;Philippe Fuchs;Sophie Lichtenauer;Marlene Elsässer;Jos H. M. Schippers;Thomas Nietzel;Cristina Ruberti;Olivier Van Aken;A. Meyer;Joost T. van Dongen;Romy R. Schmidt;M. Schwarzländer
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作者:
Stephan Wagner;Janina Steinbeck;Philippe Fuchs;Sophie Lichtenauer;Marlene Elsässer;Jos H. M. Schippers;Thomas Nietzel;Cristina Ruberti;Olivier Van Aken;A. Meyer;Joost T. van Dongen;Romy R. Schmidt;M. Schwarzländer
•Hypoxia regularly occurs during plant development and can be induced by the environment, for example through flooding. •To understand how plant tissue physiology responds to progressing oxygen restriction, we aimed at monitoring subcellular physiology in real-time and in vivo. We establish a fluorescent protein sensor-based system for multiparametric monitoring of dynamic changes in subcellular physiology of living Arabidopsis thaliana leaves, and exemplify its applicability for hypoxia stress. •By monitoring cytosolic dynamics of MgATP2-, free Ca2+ concentration, pH, NAD redox status and glutathione redox status in parallel, linked to transcriptional and metabolic responses, we generate an integrated picture of the physiological response to progressing hypoxia. We show that the physiological changes are surprisingly robust, even when plant carbon status is modified as achieved by sucrose feeding or extended night. Inhibition of the mitochondrial respiratory chain causes dynamics of cytosolic physiology that are remarkably similar to those under oxygen depletion, highlighting mitochondrial electron transport as key determinant of the cellular consequences of hypoxia beyond the organelle. •A broadly applicable system for parallel in vivo sensing of plant stress physiology is established to map out the physiological context under which both mitochondrial retrograde signaling and low oxygen signaling occur, indicating shared upstream stimuli. This article is protected by copyright. All rights reserved.