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Copper stress‐induced changes in leaf soluble proteome of Cu‐sensitive and tolerant Agrostis capillaris L. populations
Authors:Elena Hego  Sébastien Vilain  Aurélien Barré  Stéphane Claverol  Jean‐William Dupuy  Céline Lalanne  Marc Bonneu  Christophe Plomion  Michel Mench
Institution:1. UMR1202 BIOGECO, University of Bordeaux, Pessac Cedex, France;2. UMR1202 BIOGECO, INRA, Cestas cedex, France;3. Bordeaux INP, Univ. Bordeaux, Bordeaux, France;4. Centre de Génomique Fonctionnelle, Centre de Bioinformatique de Bordeaux, Univ. Bordeaux, Bordeaux, France;5. Centre de Génomique Fonctionnelle, Plateforme Protéome, Univ. Bordeaux, Bordeaux, France;6. Bordeaux INP, Centre de Génomique Fonctionnelle, Plateforme Protéome, Univ. Bordeaux, France
Abstract:Changes in leaf soluble proteome were explored in 3‐month‐old plants of metallicolous (M) and nonmetallicolous (NM) Agrostis capillaris L. populations exposed to increasing Cu concentrations (1–50 μM) to investigate molecular mechanisms underlying plant responses to Cu excess and tolerance of M plants. Plants were cultivated on perlite (CuSO4 spiked‐nutrient solution). Soluble proteins, extracted by the trichloroacetic acid/acetone procedure, were separated with 2‐DE (linear 4–7 pH gradient). Analysis of CCB‐stained gels (PDQuest) reproducibly detected 214 spots, and 64 proteins differentially expressed were identified using LC‐MS/MS. In both populations, Cu excess impacted both light‐dependent (OEE, cytochrome b6‐f complex, and chlorophyll a‐b binding protein), and ‐independent (RuBisCO) photosynthesis reactions, more intensively in NM leaves (ferredoxin‐NADP reductase and metalloprotease FTSH2). In both populations, upregulation of isocitrate dehydrogenase and cysteine/methionine synthases respectively suggested increased isocitrate oxidation and enhanced need for S‐containing amino‐acids, likely for chelation and detoxification. In NM leaves, an increasing need for energetic compounds was indicated by the stimulation of ATPases, glycolysis, pentose phosphate pathway, and Calvin cycle enzymes; impacts on protein metabolism and oxidative stress increase were respectively suggested by the rise of chaperones and redox enzymes. Overexpression of a HSP70 may be pivotal for M Cu tolerance by protecting protein metabolism. All MS data have been deposited in the ProteomeXchange with the dataset identifier PXD001930 ( http//proteomecentral.proteomexchange.org/dataset/PXD001930 ).
Keywords:Heat‐shock protein  MS‐LC‐MS/MS  Oxidative stress  Photosynthesis  Plant proteomics
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