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First published online October 19, 2007; 10.1104/pp.107.104752 Plant Physiology 145:1658-1669 (2007) © 2007 American Society of Plant Biologists OPEN ACCESS ARTICLE
Oxo-Phytodienoic Acid-Containing Galactolipids in Arabidopsis: Jasmonate Signaling Dependence1,[W],[OA]Department of Plant and Environmental Sciences, Göteborg University, SE–405 30 Gothenburg, Sweden (O.K., M.E.); Plant and Soil Science Laboratory, Department of Agricultural Sciences, Faculty of Life Sciences, University of Copenhagen, 1871 Frederiksberg C, Denmark (M.X.A.); Division of Chemistry II, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, SE–17177 Stockholm, Sweden (M.H.); Biolipox AB, SE–171 65 Solna, Sweden (Å.B.); Department of Plant Biochemistry, Albrecht-von-Haller-Institute for Plant Sciences, Georg-August-University Göttingen, D–37077 Goettingen, Germany (C.G., I.F.); College of Pharmacy, Oregon State University, Corvallis, Oregon 97331 (K.L.M.); and Center for Marine Biotechnology and Biomedicine, Scripps Institution of Oceanography, University of California, San Diego, California 92093–0212 (W.H.G.)
The jasmonate family of phytohormones, as represented by 12-oxo-phytodienoic acid (OPDA), dinor-phytodienoic acid (dn-OPDA), and jasmonic acid in Arabidopsis (Arabidopsis thaliana), has been implicated in a vast array of different developmental processes and stress responses. Recent reports indicate that OPDA and dn-OPDA occur not only as free acids in Arabidopsis, but also as esters with complex lipids, so-called arabidopsides. Recently, we showed that recognition of the two bacterial effector proteins AvrRpm1 and AvrRpt2 induced high levels of a molecule consisting of two OPDAs and one dn-OPDA esterified to a monogalactosyl diacylglycerol moiety, named arabidopside E. In this study, we demonstrate that the synthesis of arabidopsides is mainly independent of the prokaryotic lipid biosynthesis pathway in the chloroplast, and, in addition to what previously has been reported, arabidopside E as well as an all-OPDA analog, arabidopside G, described here accumulated during the hypersensitive response and in response to wounding. We also show that different signaling pathways lead to the formation of arabidopsides during the hypersensitive response and the wounding response, respectively. However, the formation of arabidopsides during both responses is dependent on an intact jasmonate signaling pathway. Additionally, we report inhibition of growth of the fungal necrotrophic pathogen Botrytis cinerea and in planta release of free jasmonates in a time frame that overlaps with the observed reduction of arabidopside levels. Thus, arabidopsides may have a dual function: as antipathogenic substances and as storage compounds that allow the slow release of free jasmonates.
1 This work was supported by the Lennanders Foundation (to M.X.A.), by the P. E. Lindahls Foundation (to M.X.A.), by the Carl Tryggers Foundation (to M.X.A.), by the Swedish Council for Environment, Agricultural Sciences and Spatial Planning (project no. 229–2004–833 to M.H.), by the Magnus Bergvalls Foundation (to M.E.), by Innovationsbron Väst (to M.E.), and by the Carl Tryggers Foundation (to M.E.). 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 (www.plantphysiol.org) is: Mats Ellerström (mats.ellerstrom{at}dpes.gu.se). [W] The online version of this article contains Web-only data. [OA] Open Access articles can be viewed online without a subscription. www.plantphysiol.org/cgi/doi/10.1104/pp.107.104752 * Corresponding author; e-mail mats.ellerstrom{at}dpes.gu.se. Received June 29, 2007; accepted October 9, 2007; published October 19, 2007. Related articles in Plant Physiol.:
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