fusicoccin and systemin

Leaf wounding and the wound signaling peptide systemin induce expression of wound response genes while the fungal toxin fusicoccin (FC) induces expression of pathogenesis-related genes. Consistent with their functional differences, FC and systemin regulate the extracellular pH in opposite ways, with systemin inducing an alkalinization and FC an acidification response. Here we show that systemin, wounding and FC activate the same mitogen-activated protein kinases (MAPKs; MPKs) MPK1 and 2 in tomato (Lycopersicon esculentum) leaves and L. peruvianum suspension-cultured cells. Wounding and FC activated an additional MAPK, MPK3. Pronounced differences were observed with regard to MAPK activation kinetics. FC induced prolonged, and systemin transient activity of the MAPKs. This shows that functionally different elicitors engage the same signaling components, yet induce signal-specific activation dynamics. A comparative analysis of pH effects and MAPK activity in response to specific treatments revealed that the kinetics of pH changes and MAPK activation did not correlate. Simultaneous application of FC and systemin did not lead to immediate pH changes but resulted in rapid increases in MAPK activity. Furthermore, changes in extracellular pH could be induced without concomitant MAPK activation by exchanging conditioned medium with fresh medium. This shows that changes in the extracellular pH are neither required nor sufficient for MAPK activation, suggesting that signaling pathways involving MAPKs and extracellular pH changes operate in parallel and are not part of the same linear pathway.

Topics: Enzyme Activation; Extracellular Fluid; Glycosides; Hydrogen-Ion Concentration; Mitogen-Activated Protein Kinases; Mycotoxins; Peptides; Plant Leaves; Plant Proteins; Solanum lycopersicum

Among the early responses of Lycopersicon peruvianum suspension-cultured cells to the polypeptide wound signal systemin are the alkalinization of the culture medium and the activation of a 48-kDa mitogen-activated protein kinase (MAPK). Here, we report that both responses are induced in the cells by exposure to ultraviolet-B (UV-B) radiation. Suramin, an inhibitor of systemin receptor function, strongly inhibited the UV-B-induced medium alkalinization and MAPK activity. The UV-B response was also reduced when cells were initially treated with systemin or the systemin antagonist Ala-17-systemin, which competitively inhibits binding of systemin to the systemin receptor. Cells that were initially treated with either UV-B or systemin exhibited a strongly reduced response to a subsequent elicitation with systemin. The desensitization was transient, reaching a maximum at 30-60 min after the initial treatment. Several hours later, depending on the initial UV-B dose or systemin concentration, the cells regained their initial responsiveness. When cells were irradiated with low doses of UV-B and subsequently treated with systemin, the UV-B response reached levels higher than the response without UV-B treatment. The data provide evidence for an involvement of the systemin receptor and/or systemin-responsive signaling elements in the UV-B response.

Topics: Adenosine Triphosphatases; Alanine; Cell Membrane; Cells, Cultured; Glycosides; Peptides; Signal Transduction; Solanum lycopersicum; Suramin; Time Factors; Ultraviolet Rays