Rapid Avr9- and Cf-9–Dependent Activation of MAP Kinases in Tobacco Cell Cultures and Leaves: Convergence of Resistance Gene, Elicitor, Wound, and Salicylate Responses
- 1 February 1999
- journal article
- Published by Oxford University Press (OUP) in Plant Cell
- Vol. 11 (2) , 273-287
- https://doi.org/10.1105/tpc.11.2.273
Abstract
The Cf-9 resistance (R) gene from tomato confers resistance to the fungal pathogen Cladosporium fulvum expressing the corresponding, pathogen-derived avirulence gene product Avr9. To understand how an initial R/Avr recognition event is transmitted and triggers the induction of plant defenses, we investigated early Avr9/Cf-9–dependent activation of protein kinases in transgenic tobacco expressing the Cf-9 gene. We identified two protein kinases of 46 and 48 kD, using myelin basic protein as substrate, that became rapidly activated in a strictly gene-for-gene manner within 2 to 5 min after Avr9 elicitation in both Cf9 tobacco plants and derived cell cultures. Studies with pharmacological inhibitors and effectors revealed that Ca2+ influx and a phosphorylation event(s) are required for kinase activation, but neither enzyme is involved in the Avr9-dependent synthesis of active oxygen species. The activation of both kinases is achieved via post-translational mechanisms, and the activation but not inactivation step includes tyrosine phosphorylation. Using specific antibodies, we found that the 46- and 48-kD kinases were similiar to WIPK (for wound-induced protein kinase) and SIPK (for salicylic acid–induced protein kinase), two previously characterized mitogen-activated protein (MAP) kinases from tobacco. In addition, Cf9 tobacco plants and cell cultures showed an Avr9-dependent accumulation of the WIPK transcript. Cf9 tobacco suspension cultures are thus a unique system in which to analyze the earliest events in R gene function. These data indicate that (1) the R/Avr–mediated induction of plant defense is accomplished via several parallel signaling mechanisms, and (2) R/Avr–dependent signal transduction pathways are interlinked at MAP kinases with responses of plants not only to non-race-specific elicitors but also to abiotic stimuli, such as wounding and mechanical stress.Keywords
This publication has 61 references indexed in Scilit:
- The search for physiological substrates of MAP and SAP kinases in mammalian cellsTrends in Cell Biology, 1997
- Receptor-Mediated Activation of a MAP Kinase in Pathogen Defense of PlantsScience, 1997
- THE OXIDATIVE BURST IN PLANT DISEASE RESISTANCEAnnual Review of Plant Biology, 1997
- Initiation of Plant Disease Resistance by Physical Interaction of AvrPto and Pto KinaseScience, 1996
- Mechanosensors in plantsNature, 1996
- Two genes that encode ribosomal‐protein S6 kinase homologs are induced by cold or salinity stress in Arabidopsis thalianaFEBS Letters, 1995
- The MAP kinase cascade is essential for diverse signal transduction pathwaysTrends in Biochemical Sciences, 1993
- The plant homologue of MAP kinase is expressed in a cell cycle‐dependent and organ‐specific mannerThe Plant Journal, 1993
- cPLA2 is phosphorylated and activated by MAP kinaseCell, 1993
- Microtubule‐associated‐protein (MAP) kinase activated by nerve growth factor and epidermal growth factor in PC12 cellsEuropean Journal of Biochemistry, 1990