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      Endogenous levels of cytokinins, indole-3-acetic acid and abscisic acid in in vitro grown potato: A contribution to potato hormonomics

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          Abstract

          A number of scientific reports published to date contain data on endogenous levels of various phytohormones in potato ( Solanum tuberosum L.) but a complete cytokinin profile of potato tissues, that would include data on all particular molecular forms of cytokinin, has still been missing. In this work, endogenous levels of all analytically detectable isoprenoid cytokinins, as well as the auxin indole-3-acetic acid (IAA), and abscisic acid (ABA) have been determined in shoots and roots of 30 day old in vitro grown potato (cv. Désirée). The results presented here are generally similar to other data reported for in vitro grown potato plants, whereas greenhouse-grown plants typically contain lower levels of ABA, possibly indicating that in vitro grown potato is exposed to chronic stress. Cytokinin N-glucosides, particularly N7-glucosides, are the dominant cytokinin forms in both shoots and roots of potato, whereas nucleobases, as the bioactive forms of cytokinins, comprise a low proportion of cytokinin levels in tissues of potato. Differences in phytohormone composition between shoots and roots of potato suggest specific patterns of transport and/or differences in tissue-specific metabolism of plant hormones. These results represent a contribution to understanding the hormonomics of potato, a crop species of extraordinary economic importance.

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          Cytokinins: activity, biosynthesis, and translocation.

          Cytokinins (CKs) play a crucial role in various phases of plant growth and development, but the basic molecular mechanisms of their biosynthesis and signal transduction only recently became clear. The progress was achieved by identifying a series of key genes encoding enzymes and proteins controlling critical steps in biosynthesis, translocation, and signaling. Basic schemes for CK homeostasis and root/shoot communication at the whole-plant level can now be devised. This review summarizes recent findings on the relationship between CK structural variation and activity, distinct features in CK biosynthesis between higher plants and Agrobacterium infected plants, CK translocation at whole-plant and cellular levels, and CKs as signaling molecules for nutrient status via root-shoot communication.
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            The Arabidopsis cytochrome P450 CYP707A encodes ABA 8'-hydroxylases: key enzymes in ABA catabolism.

            The hormonal action of abscisic acid (ABA) in plants is controlled by the precise balance between its biosynthesis and catabolism. In plants, ABA 8'-hydroxylation is thought to play a predominant role in ABA catabolism. ABA 8'-hydroxylase was shown to be a cytochrome P450 (P450); however, its corresponding gene had not been identified. Through phylogenetic and DNA microarray analyses during seed imbibition, the candidate genes for this enzyme were narrowed down from 272 Arabidopsis P450 genes. These candidate genes were functionally expressed in yeast to reveal that members of the CYP707A family, CYP707A1-CYP707A4, encode ABA 8'-hydroxylases. Expression analyses revealed that CYP707A2 is responsible for the rapid decrease in ABA level during seed imbibition. During drought stress conditions, all CYP707A genes were upregulated, and upon rehydration a significant increase in mRNA level was observed. Consistent with the expression analyses, cyp707a2 mutants exhibited hyperdormancy in seeds and accumulated six-fold greater ABA content than wild type. These results demonstrate that CYP707A family genes play a major regulatory role in controlling the level of ABA in plants.
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              Abscisic Acid and abiotic stress signaling.

              Abiotic stress is severe environmental stress, which impairs crop production on irrigated land worldwide. Overall, the susceptibility or tolerance to the stress in plants is a coordinated action of multiple stress responsive genes, which also cross-talk with other components of stress signal transduction pathways. Plant responses to abiotic stress can be determined by the severity of the stress and by the metabolic status of the plant. Abscisic acid (ABA) is a phytohormone critical for plant growth and development and plays an important role in integrating various stress signals and controlling downstream stress responses. Plants have to adjust ABA levels constantly in responce to changing physiological and environmental conditions. To date, the mechanisms for fine-tuning of ABA levels remain elusive. The mechanisms by which plants respond to stress include both ABA-dependent and ABA-independent processes. Various transcription factors such as DREB2A/2B, AREB1, RD22BP1 and MYC/MYB are known to regulate the ABA-responsive gene expression through interacting with their corrosponding cis-acting elements such as DRE/CRT, ABRE and MYCRS/MYBRS, respectively. Understanding these mechanisms is important to improve stress tolerance in crops plants. This article first describes the general pathway for plant stress response followed by roles of ABA and transcription factors in stress tolerance including the regulation of ABA biosynthesis.
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                Author and article information

                Contributors
                martin@ibiss.bg.ac.rs
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                26 February 2020
                26 February 2020
                2020
                : 10
                : 3437
                Affiliations
                [1 ]ISNI 0000 0001 2166 9385, GRID grid.7149.b, Department of Plant Physiology, Institute for Biological Research “Siniša Stanković” – National Institute of Republic of Serbia, , University of Belgrade, ; Bulevar Despota Stefana 142, 11060 Belgrade, Serbia
                [2 ]ISNI 0000 0004 0613 3592, GRID grid.419008.4, Laboratory of Hormonal Regulations in Plants, , Institute of Experimental Botany of the Czech Academy of Sciences, ; Rozvojová 263, CZ-165 02 Prague 6, Czech Republic
                [3 ]ISNI 0000 0004 0613 3592, GRID grid.419008.4, Laboratory of Mass Spectrometry, , Institute of Experimental Botany of the Czech Academy of Sciences, ; Rozvojová 263, CZ-165 02 Prague 6, Czech Republic
                [4 ]Mining and Metallurgy Institute, Zeleni Bulevar 35, 19219 Bor, Serbia
                [5 ]ISNI 0000 0001 2166 9385, GRID grid.7149.b, Department of Plant Physiology, Faculty of Biology, , University of Belgrade, ; Studentski trg 16, 11000 Belgrade, Serbia
                Author information
                http://orcid.org/0000-0002-7014-9818
                http://orcid.org/0000-0001-7878-7788
                http://orcid.org/0000-0002-9394-3854
                http://orcid.org/0000-0001-7412-6982
                http://orcid.org/0000-0001-6796-2608
                http://orcid.org/0000-0002-2715-0944
                http://orcid.org/0000-0002-8869-0020
                http://orcid.org/0000-0002-8385-7549
                http://orcid.org/0000-0003-0301-1250
                http://orcid.org/0000-0002-7034-9780
                Article
                60412
                10.1038/s41598-020-60412-9
                7044434
                32103086
                31ac09a8-1eac-4c3f-93aa-ed35bbfda9ff
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 29 October 2019
                : 7 February 2020
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100004564, Ministarstvo Prosvete, Nauke i Tehnološkog Razvoja (Ministry of Education, Science and Technological Development of the Republic of Serbia);
                Award ID: OI173015
                Award ID: OI173015
                Award Recipient :
                Categories
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                © The Author(s) 2020

                Uncategorized
                auxin,cytokinin
                Uncategorized
                auxin, cytokinin

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