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      WUSCHEL-related homeobox1 (WOX1) regulates vein patterning and leaf size in Cucumis sativus

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          Abstract

          In plants, WUSCHEL-related homeobox1 ( WOX1) homologs promote lamina mediolateral outgrowth. However, the downstream components linking WOX1 and lamina development remain unclear. In this study, we revealed the roles of WOX1 in palmate leaf expansion in cucumber ( Cucumis sativus). A cucumber mango fruit ( mf) mutant, resulting from truncation of a WOX1-type protein (CsWOX1), displayed abnormal lamina growth and defects in the development of secondary and smaller veins. CsWOX1 was expressed in the middle mesophyll and leaf margins and rescued defects of the Arabidopsis wox1 prs double mutant. Transcriptomic analysis revealed that genes involved in auxin polar transport and auxin response were highly associated with leaf development. Analysis of the cucumber mf rl ( round leaf) double mutant revealed that CsWOX1 functioned in vein development via PINOID (CsPID1)-controlled auxin transport. Overexpression of CsWOX1 in cucumber ( CsWOX1-OE) affected vein patterning and produced ‘butterfly-shaped’ leaves. CsWOX1 physically interacted with CsTCP4a, which may account for the abnormal lamina development in the mf mutant line and the smaller leaves in the CsWOX1-OE plants. Our findings demonstrated that CsWOX1 regulates cucumber leaf vein development by modulating auxin polar transport; moreover, CsWOX1 regulates leaf size by controlling CIN-TCP genes.

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          Floral dip: a simplified method forAgrobacterium-mediated transformation ofArabidopsis thaliana

          The Agrobacterium vacuum infiltration method has made it possible to transform Arabidopsis thaliana without plant tissue culture or regeneration. In the present study, this method was evaluated and a substantially modified transformation method was developed. The labor-intensive vacuum infiltration process was eliminated in favor of simple dipping of developing floral tissues into a solution containing Agrobacterium tumefaciens, 5% sucrose and 500 microliters per litre of surfactant Silwet L-77. Sucrose and surfactant were critical to the success of the floral dip method. Plants inoculated when numerous immature floral buds and few siliques were present produced transformed progeny at the highest rate. Plant tissue culture media, the hormone benzylamino purine and pH adjustment were unnecessary, and Agrobacterium could be applied to plants at a range of cell densities. Repeated application of Agrobacterium improved transformation rates and overall yield of transformants approximately twofold. Covering plants for 1 day to retain humidity after inoculation also raised transformation rates twofold. Multiple ecotypes were transformable by this method. The modified method should facilitate high-throughput transformation of Arabidopsis for efforts such as T-DNA gene tagging, positional cloning, or attempts at targeted gene replacement.
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            Plant ABC proteins--a unified nomenclature and updated inventory.

            The ABC superfamily comprises both membrane-bound transporters and soluble proteins involved in a broad range of processes, many of which are of considerable agricultural, biotechnological and medical potential. Completion of the Arabidopsis and rice genome sequences has revealed a particularly large and diverse complement of plant ABC proteins in comparison with other organisms. Forward and reverse genetics, together with heterologous expression, have uncovered many novel roles for plant ABC proteins, but this progress has been accompanied by a confusing proliferation of names for plant ABC genes and their products. A consolidated nomenclature will provide much-needed clarity and a framework for future research.
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              Regulation of polar auxin transport by AtPIN1 in Arabidopsis vascular tissue.

              Polar auxin transport controls multiple developmental processes in plants, including the formation of vascular tissue. Mutations affecting the PIN-FORMED (PIN1) gene diminish polar auxin transport in Arabidopsis thaliana inflorescence axes. The AtPIN1gene was found to encode a 67-kilodalton protein with similarity to bacterial and eukaryotic carrier proteins, and the AtPIN1 protein was detected at the basal end of auxin transport-competent cells in vascular tissue. AtPIN1 may act as a transmembrane component of the auxin efflux carrier.
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                Author and article information

                Contributors
                lizheng82@nwsuaf.edu.cn
                Journal
                Hortic Res
                Hortic Res
                Horticulture Research
                Nature Publishing Group UK (London )
                2662-6810
                2052-7276
                1 November 2020
                1 November 2020
                2020
                : 7
                : 182
                Affiliations
                [1 ]GRID grid.144022.1, ISNI 0000 0004 1760 4150, State Key Laboratory of Crop Stress Biology in Arid Areas, College of Horticulture, , Northwest A&F University, ; Yangling, Shaanxi 712100 China
                [2 ]GRID grid.22935.3f, ISNI 0000 0004 0530 8290, Department of Vegetable Sciences, Beijing Key Laboratory of Growth and Developmental Regulation for Protected Vegetable Crops, , China Agricultural University, ; Beijing, 100193 China
                [3 ]GRID grid.28803.31, ISNI 0000 0001 0701 8607, USDA-ARS, Vegetable Crops Research Unit, Horticulture Department, , University of Wisconsin, ; Madison, WI 53706 USA
                [4 ]GRID grid.257160.7, ISNI 0000 0004 1761 0331, College of Horticulture and Landscape Architecture, , Hunan Agricultural University, ; Changsha, Hunan 410128 China
                Author information
                http://orcid.org/0000-0001-9457-2234
                Article
                404
                10.1038/s41438-020-00404-y
                7603520
                33328463
                1c02f99e-2d70-4bfe-a61a-8df88380cd47
                © 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
                : 16 July 2020
                : 28 August 2020
                : 3 September 2020
                Funding
                Funded by: National Key Research and Development Program of China (SQ2019YFD100067) National Natural Science Foundation of China (No. 31672150, and 31872111)
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                © The Author(s) 2020

                non-model organisms,transgenic organisms
                non-model organisms, transgenic organisms

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