Guard cell abscisic acid signalling and engineering drought hardiness in plants

By J. Schroeder, J. Kwak, G. J. Allen. Nature, 2001

814 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/a830ecf1b8d2f35a6aa280823c31fddb0a4e64bf

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Citations in the corpus

The role of ABA and MAPK signaling pathways in plant abiotic stress responses. (2014, background): “The membrane depolarization caused by anion efflux via ion channels activates outward-rectifying K + (K + out ) channels and results in K + efflux from guard cells (Schroeder et al., 2001a).”
Physiology and molecular biology of stress tolerance in plants (2006, background): “Calcium ions act as a second messenger in intracellular signal transduction during ABA signaling (Schroeder et al., 2001).”
ABA signal transduction at the crossroad of biotic and abiotic stress responses. (2012, background): “Typically the S-type anion channels and outward K-channels are activated by ABA, whereas inward K+ channels are inactivated, leading to net ionic efflux and decrease in guard cell turgor (Schroeder et al. 2001b; Nilson & Assmann 2007;Ward et al. 2008; Wasilewska et al. 2008; Kim et al. 2010).”
Early abscisic acid signal transduction mechanisms: newly discovered components and newly emerging questions. (2010, background): “Stomatal aperture is regulated by the coordinated actions of ion channels at the plasma membrane and tonoplast (for review, see Schroeder et al. 2001).”
Hydrogen peroxide is involved in abscisic acid-induced stomatal closure in Vicia faba. (2001, background): “ABA, which is widely accepted as a stress signal, induces a reduction in stomatal aperture in a concentration-dependent manner (Schroeder et al., 2001).”
Over-expression of the stress-induced OsWRKY45 enhances disease resistance and drought tolerance in Arabidopsis (2009, background): “In response to drought-induced stress, ABA is synthesized and triggers a calciumactivated signalling cascade in guard cells, resulting in stomatal closure (Schroeder et al., 2001).”
Effect of Deficit Irrigation and Reduced N Fertilization on Plant Growth, Root Morphology and Water Use Efficiency of Tomato Grown in Soilless Culture (2021, background): “The increase in IWUE may be possible due to the decrease in stomatal conductance caused by the increased signal transduction network of guard cells [31].”
Identification of Two Protein Kinases Required for Abscisic Acid Regulation of Seed Germination, Root Growth, and Gene Expression in Arabidopsis[W] (2007, background): “…including seed dormancy and germination and seedling growth, as well as in controlling many abiotic stress responses (LeonKloosterziel et al., 1996; Schroeder et al., 2001; Bray, 2002; Finkelstein and Gibson, 2002; Zhu, 2002; Assmann, 2003; Chow and McCourt, 2004;Yamaguchi-Shinozaki and Shinozaki,…”
Differences in some morphological, physiological, and biochemical responses to drought stress in two contrasting populations of Populus przewalskii (2006, methodology): “2006 Copyright Physiologia Plantarum 2006, ISSN 0031-9317 tissue, as suggested by many previous studies (Kozlowski and Pallardy 2002, Luan 2002, Schroeder et al. 2001).”
Improving water use efficiency in grapevines: potential physiological targets for biotechnological improvement. (2010, background): “Among genes involved in ABA signalling and ABA-mediated stomatal closure, protein kinases (like OST1) act as positive regulators while type 2C protein phosphatases (PP2C) and farnesyltransferases (like ERA1) act as negative regulators (Schroeder et al. 2001).”
Signal transduction during cold, salt, and drought stresses in plants (2011, background): “Although the receptors for ROS are unknown at present, it has been suggested that plant cells sense ROS via at least three different mechanisms: (1) unidentified receptor proteins; (2) redox-sensitive transcription factors, such as NPR1 or HSFs; and (3) direct inhibition of phosphatases by ROS [101–”