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      The reduction in maize leaf growth under mild drought affects the transition between cell division and cell expansion and cannot be restored by elevated gibberellic acid levels

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          Summary

          Growth is characterized by the interplay between cell division and cell expansion, two processes that occur separated along the growth zone at the maize leaf. To gain further insight into the transition between cell division and cell expansion, conditions were investigated in which the position of this transition zone was positively or negatively affected. High levels of gibberellic acid ( GA) in plants overexpressing the GA biosynthesis gene GA20‐ OXIDASE ( GA20 OX‐1 OE ) shifted the transition zone more distally, whereas mild drought, which is associated with lowered GA biosynthesis, resulted in a more basal positioning. However, the increased levels of GA in the GA20 OX‐1 OE line were insufficient to convey tolerance to the mild drought treatment, indicating that another mechanism in addition to lowered GA levels is restricting growth during drought. Transcriptome analysis with high spatial resolution indicated that mild drought specifically induces a reprogramming of transcriptional regulation in the division zone. ‘Leaf Growth Viewer’ was developed as an online searchable tool containing the high‐resolution data.

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          Most cited references68

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          Photosynthesis and drought: can we make metabolic connections from available data?

          Photosynthesis is one of the key processes to be affected by water deficits, via decreased CO2 diffusion to the chloroplast and metabolic constraints. The relative impact of those limitations varies with the intensity of the stress, the occurrence (or not) of superimposed stresses, and the species we are dealing with. Total plant carbon uptake is further reduced due to the concomitant or even earlier inhibition of growth. Leaf carbohydrate status, altered directly by water deficits or indirectly (via decreased growth), acts as a metabolic signal although its role is not totally clear. Other relevant signals acting under water deficits comprise: abscisic acid (ABA), with an impact on stomatal aperture and the regulation at the transcription level of a large number of genes related to plant stress response; other hormones that act either concurrently (brassinosteroids, jasmonates, and salycilic acid) or antagonistically (auxin, cytokinin, or ethylene) with ABA; and redox control of the energy balance of photosynthetic cells deprived of CO2 by stomatal closure. In an attempt to systematize current knowledge on the complex network of interactions and regulation of photosynthesis in plants subjected to water deficits, a meta-analysis has been performed covering >450 papers published in the last 15 years. This analysis shows the interplay of sugars, reactive oxygen species (ROS), and hormones with photosynthetic responses to drought, involving many metabolic events. However, more significantly it highlights (i) how fragmented and often non-comparable the results are and (ii) how hard it is to relate molecular events to plant physiological status, namely photosynthetic activity, and to stress intensity. Indeed, the same data set usually does not integrate these different levels of analysis. Considering these limitations, it was hard to find a general trend, particularly concerning molecular responses to drought, with the exception of the genes ABI1 and ABI3. These genes, irrespective of the stress type (acute versus chronic) and intensity, show a similar response to water shortage in the two plant systems analysed (Arabidopsis and barley). Both are associated with ABA-mediated metabolic responses to stress and the regulation of stomatal aperture. Under drought, ABI1 transcription is up-regulated while ABI3 is usually down-regulated. Recently ABI3 has been hypothesized to be essential for successful drought recovery.
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            Regulation of water, salinity, and cold stress responses by salicylic acid

            Salicylic acid (SA) is a naturally occurring phenolic compound. SA plays an important role in the regulation of plant growth, development, ripening, and defense responses. The role of SA in the plant–pathogen relationship has been extensively investigated. In addition to defense responses, SA plays an important role in the response to abiotic stresses, including drought, low temperature, and salinity stresses. It has been suggested that SA has great agronomic potential to improve the stress tolerance of agriculturally important crops. However, the utility of SA is dependent on the concentration of the applied SA, the mode of application, and the state of the plants (e.g., developmental stage and acclimation). Generally, low concentrations of applied SA alleviate the sensitivity to abiotic stresses, and high concentrations of applied induce high levels of oxidative stress, leading to a decreased tolerance to abiotic stresses. In this article, the effects of SA on the water stress responses and regulation of stomatal closure are reviewed.
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              Aquaporins: highly regulated channels controlling plant water relations.

              Plant growth and development are dependent on tight regulation of water movement. Water diffusion across cell membranes is facilitated by aquaporins that provide plants with the means to rapidly and reversibly modify water permeability. This is done by changing aquaporin density and activity in the membrane, including posttranslational modifications and protein interaction that act on their trafficking and gating. At the whole organ level aquaporins modify water conductance and gradients at key "gatekeeper" cell layers that impact on whole plant water flow and plant water potential. In this way they may act in concert with stomatal regulation to determine the degree of isohydry/anisohydry. Molecular, physiological, and biophysical approaches have demonstrated that variations in root and leaf hydraulic conductivity can be accounted for by aquaporins but this must be integrated with anatomical considerations. This Update integrates these data and emphasizes the central role played by aquaporins in regulating plant water relations.
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                Author and article information

                Contributors
                dirk.inze@ugent.vib.be
                Journal
                Plant Biotechnol J
                Plant Biotechnol. J
                10.1111/(ISSN)1467-7652
                PBI
                Plant Biotechnology Journal
                John Wiley and Sons Inc. (Hoboken )
                1467-7644
                1467-7652
                04 September 2017
                February 2018
                : 16
                : 2 ( doiID: 10.1111/pbi.2018.16.issue-2 )
                : 615-627
                Affiliations
                [ 1 ] Department of Plant Biotechnology and Bioinformatics Ghent University Gent Belgium
                [ 2 ] Center for Plant Systems Biology VIB Gent Belgium
                [ 3 ] Growth Regulation Research Group Plant Science Center RIKEN Yokohama Japan
                [ 4 ] Plant Productivity Systems Research Group Plant Science Center RIKEN Yokohama Japan
                [ 5 ] Department of Biology University of Antwerp Antwerp Belgium
                Author notes
                [*] [* ] Correspondence (Tel +32 9 331 38 00; fax +32 9 331 38 09; email dirk.inze@ 123456ugent.vib.be )
                [†]

                These authors contributed equally.

                Article
                PBI12801
                10.1111/pbi.12801
                5787831
                28730636
                f8193c63-30d9-4592-893b-bd38f7e793f7
                © 2017 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 01 June 2017
                : 07 July 2017
                : 12 July 2017
                Page count
                Figures: 7, Tables: 2, Pages: 13, Words: 10605
                Funding
                Funded by: European Research Council under the European Community's Seventh Framework Programme
                Award ID: FP7/2007‐2013
                Award ID: 339341‐AMAIZE]11
                Funded by: Ghent University (‘Bijzonder Onderzoeksfonds Methusalem Project’
                Funded by: BOF08/01M00408
                Funded by: Multidisciplinary Research Partnership ‘Biotechnology for a Sustainable Economy’
                Award ID: 01MR0510W
                Funded by: Interuniversity Attraction Poles Programme
                Award ID: IUAP P7/29
                Funded by: Chinese Scholarship Council
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                pbi12801
                February 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.3.1.2 mode:remove_FC converted:29.01.2018

                Biotechnology
                maize,mild drought,gibberellic acid,cell division
                Biotechnology
                maize, mild drought, gibberellic acid, cell division

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