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First published online March 9, 2007; 10.1104/pp.106.094227 Plant Physiology 144:419-431 (2007) © 2007 American Society of Plant Biologists OPEN ACCESS ARTICLE
A Genomic Approach to Suberin Biosynthesis and Cork Differentiation1,[C],[W],[OA]Laboratori del suro, Department of Biology, Facultat de Ciències, Universitat de Girona, Campus Montilivi sn. 17071 Girona, Spain (M.S., O.S., M.M., G.H., M.F.); and Platform for Integrated Clone Management, Austrian Research Center, A2444 Seibersdorf, Austria (S.F.)
Cork (phellem) is a multilayered dead tissue protecting plant mature stems and roots and plant healing tissues from water loss and injuries. Cork cells are made impervious by the deposition of suberin onto cell walls. Although suberin deposition and cork formation are essential for survival of land plants, molecular studies have rarely been conducted on this tissue. Here, we address this question by combining suppression subtractive hybridization together with cDNA microarrays, using as a model the external bark of the cork tree (Quercus suber), from which bottle cork is obtained. A suppression subtractive hybridization library from cork tree bark was prepared containing 236 independent sequences; 69% showed significant homology to database sequences and they corresponded to 135 unique genes. Out of these genes, 43.5% were classified as the main pathways needed for cork biosynthesis. Furthermore, 19% could be related to regulatory functions. To identify genes more specifically required for suberin biosynthesis, cork expressed sequence tags were printed on a microarray and subsequently used to compare cork (phellem) to a non-suberin-producing tissue such as wood (xylem). Based on the results, a list of candidate genes relevant for cork was obtained. This list includes genes for the synthesis, transport, and polymerization of suberin monomers such as components of the fatty acid elongase complexes, ATP-binding cassette transporters, and acyltransferases, among others. Moreover, a number of regulatory genes induced in cork have been identified, including MYB, No-Apical-Meristem, and WRKY transcription factors with putative functions in meristem identity and cork differentiation.
1 This work was supported by the Spanish Ministerio de Ciencia y Tecnología (grant no. AGL200300416), by Ministerio de Educación y Ciencia (FPI grant to O.S.), by the European Social Funds and the Departament d'Universitats, Investigació i Societat de la Informació of Catalonia (FI and BE grants to M.S.), and by the European Forest Genomic Network (STSM to M.S. and O.S.). 2 These authors contributed equally to the article. The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (http://www.plantphysiol.org) is: Mercè Figueras (merce.figueras{at}udg.es). [C] Some figures in this article are displayed in color online but in black and white in the print edition. [W] Online version contains Web-only data. [OA] Open Access articles can be viewed online without a subscription. www.plantphysiol.org/cgi/doi/10.1104/pp.106.094227 * Corresponding author; e-mail merce.figueras{at}udg.es; fax 34972418150. Received October 19, 2006; accepted March 2, 2007; published March 9, 2007. Related articles in Plant Physiol.:
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