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      Oryza sativa H +-ATPase (OSA) is Involved in the Regulation of Dumbbell-Shaped Guard Cells of Rice

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          Abstract

          The stomatal apparatus consists of a pair of guard cells and regulates gas exchange between the leaf and atmosphere. In guard cells, blue light (BL) activates H +-ATPase in the plasma membrane through the phosphorylation of its penultimate threonine, mediating stomatal opening. Although this regulation is thought to be widely adopted among kidney-shaped guard cells in dicots, the molecular basis underlying that of dumbbell-shaped guard cells in monocots remains unclear. Here, we show that H +-ATPases are involved in the regulation of dumbbell-shaped guard cells. Stomatal opening of rice was promoted by the H +-ATPase activator fusicoccin and by BL, and the latter was suppressed by the H +-ATPase inhibitor vanadate. Using H +-ATPase antibodies, we showed the presence of phosphoregulation of the penultimate threonine in Oryza sativa H +-ATPases (OSAs) and localization of OSAs in the plasma membrane of guard cells. Interestingly, we identified one H +-ATPase isoform, OSA7, that is preferentially expressed among the OSA genes in guard cells, and found that loss of function of OSA7 resulted in partial insensitivity to BL. We conclude that H +-ATPase is involved in BL-induced stomatal opening of dumbbell-shaped guard cells in monocotyledon species.

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          Most cited references47

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          Light regulation of stomatal movement.

          Stomatal pores, each surrounded by a pair of guard cells, regulate CO2 uptake and water loss from leaves. Stomatal opening is driven by the accumulation of K+ salts and sugars in guard cells, which is mediated by electrogenic proton pumps in the plasma membrane and/or metabolic activity. Opening responses are achieved by coordination of light signaling, light-energy conversion, membrane ion transport, and metabolic activity in guard cells. In this review, we focus on recent progress in blue- and red-light-dependent stomatal opening. Because the blue-light response of stomata appears to be strongly affected by red light, we discuss underlying mechanisms in the interaction between blue-light signaling and guard cell chloroplasts.
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            GUARD CELL SIGNAL TRANSDUCTION.

            Guard cells surround stomatal pores in the epidermis of plant leaves and stems. Stomatal pore opening is essential for CO2 influx into leaves for photosynthetic carbon fixation. In exchange, plants lose over 95% of their water via transpiration to the atmosphere. Signal transduction mechanisms in guard cells integrate hormonal stimuli, light signals, water status, CO2, temperature, and other environmental conditions to modulate stomatal apertures for regulation of gas exchange and plant survival under diverse conditions. Stomatal guard cells have become a highly developed model system for characterizing early signal transduction mechanisms in plants and for elucidating how individual signaling mechanisms can interact within a network in a single cell. In this review we focus on recent advances in understanding signal transduction mechanisms in guard cells.
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              SAUR Inhibition of PP2C-D Phosphatases Activates Plasma Membrane H+-ATPases to Promote Cell Expansion in Arabidopsis.

              The plant hormone auxin promotes cell expansion. Forty years ago, the acid growth theory was proposed, whereby auxin promotes proton efflux to acidify the apoplast and facilitate the uptake of solutes and water to drive plant cell expansion. However, the underlying molecular and genetic bases of this process remain unclear. We have previously shown that the SAUR19-24 subfamily of auxin-induced SMALL AUXIN UP-RNA (SAUR) genes promotes cell expansion. Here, we demonstrate that SAUR proteins provide a mechanistic link between auxin and plasma membrane H(+)-ATPases (PM H(+)-ATPases) in Arabidopsis thaliana. Plants overexpressing stabilized SAUR19 fusion proteins exhibit increased PM H(+)-ATPase activity, and the increased growth phenotypes conferred by SAUR19 overexpression are dependent upon normal PM H(+)-ATPase function. We find that SAUR19 stimulates PM H(+)-ATPase activity by promoting phosphorylation of the C-terminal autoinhibitory domain. Additionally, we identify a regulatory mechanism by which SAUR19 modulates PM H(+)-ATPase phosphorylation status. SAUR19 as well as additional SAUR proteins interact with the PP2C-D subfamily of type 2C protein phosphatases. We demonstrate that these phosphatases are inhibited upon SAUR binding, act antagonistically to SAURs in vivo, can physically interact with PM H(+)-ATPases, and negatively regulate PM H(+)-ATPase activity. Our findings provide a molecular framework for elucidating auxin-mediated control of plant cell expansion. © 2014 American Society of Plant Biologists. All rights reserved.
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                Author and article information

                Journal
                Plant Cell Physiol
                Plant Cell Physiol
                pcp
                pcellphys
                Plant and Cell Physiology
                Oxford University Press
                0032-0781
                1471-9053
                June 2016
                05 April 2016
                05 April 2016
                : 57
                : 6
                : 1220-1230
                Affiliations
                1Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya, 464-8602 Japan
                2Institute for Advanced Research, Nagoya University, Chikusa, Nagoya, 464-8602 Japan
                3Genetically Modified Organism Research Center, National Institute of Agrobiological Sciences, Tsukuba, 305-8602 Japan
                4Center of Gene Research, Nagoya University, Chikusa, Nagoya, 464-8602 Japan
                5Institute of Plant Science and Resources, Okayama University, Chuo 2-20-1, Kurashiki, 710-0046 Japan
                6Bioscience Center, Nagoya University, Chikusa, Nagoya, 464-8601 Japan
                7Institute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Chikusa, Nagoya, 464-8602 Japan
                Author notes
                [* ]Corresponding author: E-mail, kinoshita@ 123456bio.nagoya-u.ac.jp ; Fax, +81-52-789-4778.
                Article
                pcw070
                10.1093/pcp/pcw070
                4904443
                27048369
                16a746a1-a877-41ee-9941-34d2e5fd9681
                © The Author 2016. Published by Oxford University Press on behalf of Japanese Society of Plant Physiologists.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 20 February 2016
                : 30 March 2016
                Page count
                Pages: 11
                Categories
                Regular Papers

                Plant science & Botany
                dumbbell-type stomata,h+-atpase,light-induced stomatal opening,rice
                Plant science & Botany
                dumbbell-type stomata, h+-atpase, light-induced stomatal opening, rice

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