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      The Arabidopsis Golgi-localized GDP-L-fucose transporter is required for plant development

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          Abstract

          Nucleotide sugar transport across Golgi membranes is essential for the luminal biosynthesis of glycan structures. Here we identify GDP-fucose transporter 1 (GFT1), an Arabidopsis nucleotide sugar transporter that translocates GDP- L-fucose into the Golgi lumen. Using proteo-liposome-based transport assays, we show that GFT preferentially transports GDP- L-fucose over other nucleotide sugars in vitro, while GFT1-silenced plants are almost devoid of L-fucose in cell wall-derived xyloglucan and rhamnogalacturonan II. Furthermore, these lines display reduced L-fucose content in N-glycan structures accompanied by severe developmental growth defects. We conclude that GFT1 is the major nucleotide sugar transporter for import of GDP- L-fucose into the Golgi and is required for proper plant growth and development.

          Abstract

          Nucleotide sugars are transported from the cytoplasm to the Golgi lumen where they are incorporated into cell wall polysaccharides and used for glycosylation of proteins and lipids. Here the authors identify GFT1, an Arabidopsis Golgi-localized GDP-fucose transporter that is required for plant growth and development

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          Most cited references40

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          NIH Image to ImageJ: 25 years of image analysis.

          For the past 25 years NIH Image and ImageJ software have been pioneers as open tools for the analysis of scientific images. We discuss the origins, challenges and solutions of these two programs, and how their history can serve to advise and inform other software projects.
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            Genome-wide insertional mutagenesis of Arabidopsis thaliana.

            J Alonso (2003)
            Over 225,000 independent Agrobacterium transferred DNA (T-DNA) insertion events in the genome of the reference plant Arabidopsis thaliana have been created that represent near saturation of the gene space. The precise locations were determined for more than 88,000 T-DNA insertions, which resulted in the identification of mutations in more than 21,700 of the approximately 29,454 predicted Arabidopsis genes. Genome-wide analysis of the distribution of integration events revealed the existence of a large integration site bias at both the chromosome and gene levels. Insertion mutations were identified in genes that are regulated in response to the plant hormone ethylene.
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              A multicolored set of in vivo organelle markers for co-localization studies in Arabidopsis and other plants.

              Genome sequencing has resulted in the identification of a large number of uncharacterized genes with unknown functions. It is widely recognized that determination of the intracellular localization of the encoded proteins may aid in identifying their functions. To facilitate these localization experiments, we have generated a series of fluorescent organelle markers based on well-established targeting sequences that can be used for co-localization studies. In particular, this organelle marker set contains indicators for the endoplasmic reticulum, the Golgi apparatus, the tonoplast, peroxisomes, mitochondria, plastids and the plasma membrane. All markers were generated with four different fluorescent proteins (FP) (green, cyan, yellow or red FPs) in two different binary plasmids for kanamycin or glufosinate selection, respectively, to allow for flexible combinations. The labeled organelles displayed characteristic morphologies consistent with previous descriptions that could be used for their positive identification. Determination of the intracellular distribution of three previously uncharacterized proteins demonstrated the usefulness of the markers in testing predicted subcellular localizations. This organelle marker set should be a valuable resource for the plant community for such co-localization studies. In addition, the Arabidopsis organelle marker lines can also be employed in plant cell biology teaching labs to demonstrate the distribution and dynamics of these organelles.
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                Author and article information

                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group
                2041-1723
                06 July 2016
                2016
                : 7
                : 12119
                Affiliations
                [1 ]Joint BioEnergy Institute, Physical Biosciences Division, Lawrence Berkeley National Laboratory , Berkeley, California 94702, USA
                [2 ]ARC Centre of Excellence in Plant Cell Walls, School of BioSciences, The University of Melbourne , Melbourne, VIC 3010, Australia
                [3 ]Department of Plant and Environmental Sciences, Faculty of Science, University of Copenhagen , Copenhagen DK-1871, Denmark
                [4 ]Department of Plant and Microbial Biology, University of California , Berkeley, California 94720, USA
                [5 ]Centro de Biotecnología Vegetal, Facultad de Ciencias Biológicas, Universidad Andrés Bello , Santiago RM 8370146, Chile
                [6 ]Fondo de Areas Prioritarias Center for Genome Regulation , Santiago RM 8370146, Chile
                Author notes
                [*]

                These authors contributed equally to this study.

                Article
                ncomms12119
                10.1038/ncomms12119
                4935801
                27381418
                ab15b33c-355d-4087-9e79-9ae9feda77d3
                Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 05 May 2015
                : 01 June 2016
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