1. Copper stress-induced changes in leaf soluble proteome of Cu-sensitive and tolerantAgrostis capillarisL. populations
- Author
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Jean-William Dupuy, Elena Hego, Michel Mench, Aurélien Barré, Christophe Plomion, Céline Lalanne, Sébastien Vilain, Stéphane Claverol, Marc Bonneu, Biodiversité, Gènes & Communautés (BioGeCo), Institut National de la Recherche Agronomique (INRA)-Université de Bordeaux (UB), Bordeaux INP, Université de Bordeaux (UB), Centre Génomique Fonctionnelle, Plateforme Protéome, and Université Sciences et Technologies - Bordeaux 1
- Subjects
Chlorophyll ,0301 basic medicine ,Copper Sulfate ,Proteome ,Ribulose-Bisphosphate Carboxylase ,[SDV]Life Sciences [q-bio] ,Pentose phosphate pathway ,Photosynthesis ,Agrostis ,Biochemistry ,03 medical and health sciences ,chemistry.chemical_compound ,Gene Expression Regulation, Plant ,Stress, Physiological ,oxidative stress ,LC-MS/MS ,Molecular Biology ,mass spectrometry ,Agrostis capillaris ,2. Zero hunger ,chemistry.chemical_classification ,photosynthesis ,biology ,Chlorophyll A ,Gene Expression Profiling ,RuBisCO ,plant proteomics ,Molecular Sequence Annotation ,heat-shock protein ,biology.organism_classification ,Adaptation, Physiological ,Plant Leaves ,Cytochrome b6f Complex ,Gene Ontology ,030104 developmental biology ,Enzyme ,Isocitrate dehydrogenase ,Solubility ,chemistry ,biology.protein ,Chlorophyll Binding Proteins ,Energy Metabolism - 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).
- Published
- 2016
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