The Ca(2+) -dependent protein kinase CPK3 is required for MAPK-independent salt-stress acclimation in Arabidopsis

• Published in: The Plant journal : for cell and molecular biology 2010-08, Vol.63 (3), p.484-498
• Main Authors: Mehlmer, Norbert, Wurzinger, Bernhard, Stael, Simon, Hofmann-Rodrigues, Daniela, Csaszar, Edina, Pfister, Barbara, Bayer, Roman, Teige, Markus
• Format: Article
• Language: English
• Subjects: Arabidopsis - enzymology; Arabidopsis - physiology; Arabidopsis Proteins - metabolism; Calcium-Calmodulin-Dependent Protein Kinases - metabolism; Cell Membrane - enzymology; Cell Nucleus - enzymology; Mitogen-Activated Protein Kinases - metabolism; Protoplasts - enzymology; Sodium Chloride; Stress, Physiological
• ISSN: 1365-313X
• DOI: 10.1111/j.1365-313X.2010.04257.x

Plants use different signalling pathways to respond to external stimuli. Intracellular signalling via calcium-dependent protein kinases (CDPKs) or mitogen-activated protein kinases (MAPKs) present two major pathways that are widely used to react to a changing environment. Both CDPK and MAPK pathways are known to be involved in the signalling of abiotic and biotic stresses in animal, yeast and plant cells. Here, we show the essential function of the CDPK CPK3 (At4g23650) for salt stress acclimation in Arabidopsis thaliana, and test crosstalk between CPK3 and the major salt-stress activated MAPKs MPK4 and MPK6 in the salt stress response. CPK3 kinase activity was induced by salt and other stresses after transient overexpression in Arabidopsis protoplasts, but endogenous CPK3 appeared to be constitutively active in roots and leaves in a strictly Ca(2+) -dependent manner. cpk3 mutants show a salt-sensitive phenotype comparable with mutants in MAPK pathways. In contrast to animal cells, where crosstalk between Ca(2+) and MAPK signalling is well established, CPK3 seems to act independently of those pathways. Salt-induced transcriptional induction of known salt stress-regulated and MAPK-dependent marker genes was not altered, whereas post-translational protein phosphorylation patterns from roots of wild type and cpk3 plants revealed clear differences. A significant portion of CPK3 was found to be associated with the plasma membrane and the vacuole, both depending on its N-terminal myristoylation. An initial proteomic study led to the identification of 28 potential CPK3 targets, predominantly membrane-associated proteins.