32
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Identification of the Abundant Hydroxyproline-Rich Glycoproteins in the Root Walls of Wild-Type Arabidopsis, an ext3 Mutant Line, and Its Phenotypic Revertant

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Extensins are members of the cell wall hydroxyproline-rich glycoprotein (HRGP) superfamily that form covalently cross-linked networks in primary cell walls. A knockout mutation in EXT3 ( AT1G21310), the gene coding EXTENSIN 3 (EXT3) in Arabidopsis Landsberg erecta resulted in a lethal phenotype, although about 20% of the knockout plants have an apparently normal phenotype (ANP). In this study the root cell wall HRGP components of wild-type, ANP and the ext3 mutant seedlings were characterized by peptide fractionation of trypsin digested anhydrous hydrogen fluoride deglycosylated wall residues and by sequencing using LC-MS/MS. Several HRGPs, including EXT3, were identified in the wild-type root walls but not in walls of the ANP and lethal mutant. Indeed the ANP walls and walls of mutants displaying the lethal phenotype possessed HRGPs, but the profiles suggest that changes in the amount and perhaps type may account for the corresponding phenotypes.

          Related collections

          Most cited references71

          • Record: found
          • Abstract: found
          • Article: not found

          Cellular organisation of the Arabidopsis thaliana root.

          The anatomy of the developing root of Arabidopsis is described using conventional histological techniques, scanning and transmission electron microscopy. The root meristem is derived from cells of the hypophysis and adjacent cells of the embryo proper. The postembryonic organization of the root is apparent in the mature embryo and is maintained in the growing primary root after germination. Cell number and location is relatively invariant in the primary root, with 8 cortical and endodermal cell files but more variable numbers of pericycle and epidermal cells. The organisation of cells in lateral roots is similar to that of the primary root but with more variability in the numbers of cell files in each layer. [3H]thymidine labeling of actively growing roots indicates that a quiescent centre of four central cells (derived from the hypophysis) is located between the root cap columella and the stele. This plate of four cells is surrounded by three groups of cells in, proximal, distal and lateral positions. The labeling patterns of these cells suggest that they are the initials for the files of cells that comprise the root. They give rise to four sets of cell files: the stele, the cortex and endodermis, the epidermis and lateral root-cap and the columella. A model of meristem activity is proposed based on these data. This description of Arabidopsis root structure underpins future work on the developmental genetics of root morphogenesis.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            An Arabidopsis cell wall proteoglycan consists of pectin and arabinoxylan covalently linked to an arabinogalactan protein.

            Plant cell walls are comprised largely of the polysaccharides cellulose, hemicellulose, and pectin, along with ∼10% protein and up to 40% lignin. These wall polymers interact covalently and noncovalently to form the functional cell wall. Characterized cross-links in the wall include covalent linkages between wall glycoprotein extensins between rhamnogalacturonan II monomer domains and between polysaccharides and lignin phenolic residues. Here, we show that two isoforms of a purified Arabidopsis thaliana arabinogalactan protein (AGP) encoded by hydroxyproline-rich glycoprotein family protein gene At3g45230 are covalently attached to wall matrix hemicellulosic and pectic polysaccharides, with rhamnogalacturonan I (RG I)/homogalacturonan linked to the rhamnosyl residue in the arabinogalactan (AG) of the AGP and with arabinoxylan attached to either a rhamnosyl residue in the RG I domain or directly to an arabinosyl residue in the AG glycan domain. The existence of this wall structure, named ARABINOXYLAN PECTIN ARABINOGALACTAN PROTEIN1 (APAP1), is contrary to prevailing cell wall models that depict separate protein, pectin, and hemicellulose polysaccharide networks. The modified sugar composition and increased extractability of pectin and xylan immunoreactive epitopes in apap1 mutant aerial biomass support a role for the APAP1 proteoglycan in plant wall architecture and function.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Elicitor- and wound-induced oxidative cross-linking of a proline-rich plant cell wall protein: a novel, rapid defense response.

              Treatment of bean or soybean cells with fungal elicitor or glutathione causes a rapid insolubilization of preexisting (hydroxy)proline-rich structural proteins in the cell wall. This insolubilization, which involves H2O2-mediated oxidative cross-linking, is initiated within 2 min and is complete within 10 min under optimal conditions, and hence, precedes the expression of transcription-dependent defenses. Cross-linking is also under developmental control during hypocotyl growth and in tissues subject to mechanical stress such as the stem-petiole junction. Stimulus-dependent oxidative cross-linking of wall structural proteins is a novel site of cellular regulation with potentially important functions in cell maturation and toughening of cell walls in the initial stages of plant defense.
                Bookmark

                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Plants (Basel)
                Plants (Basel)
                plants
                Plants
                MDPI
                2223-7747
                21 January 2015
                March 2015
                : 4
                : 1
                : 85-111
                Affiliations
                [1 ]Department of Chemistry and Biochemistry, Ohio University, Athens, OH 45701, USA; E-Mails: Boxofjacky@ 123456gmail.com (D.Y.); held@ 123456ohio.edu (M.A.H.); af844006@ 123456gmail.com (A.N.F.); kielisze@ 123456helios.phy.ohiou.edu (M.J.K.)
                [2 ]Department of Biochemistry and Molecular Biology, University of Massachusetts, Amherst, MA 01003, USA; E-Mails: mcannon@ 123456biochem.umass.edu (M.C.C.); tuiray76@ 123456gmail.com (T.R.); sahap76@ 123456gmail.com (P.S.)
                [3 ]Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, OK 74078, USA; E-Mail: Andrew.mort@ 123456okstate.edu
                Author notes
                [†]

                These authors contributed equally to this work.

                [* ]Author to whom correspondence should be addressed; E-Mail: yuc27@ 123456psu.edu ; Tel.: +1-814-441-0263.
                Article
                plants-04-00085
                10.3390/plants4010085
                4844335
                27135319
                ca5ad8b4-c8fe-428e-83e6-dc28d5a4f299
                © 2015 by the authors; licensee MDPI, Basel, Switzerland.

                This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 09 November 2014
                : 15 January 2015
                Categories
                Article

                arabidopsis root,cell wall,hydroxyproline-rich glycoprotein,extensin 3,lrx,prp4,proteomics

                Comments

                Comment on this article