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PMID: 10504567 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

K+ channels of Cf-9 transgenic tobacco guard cells as targets for Cladosporium fulvum Avr9 elicitor-dependent signal transduction.

The Plant journal : for cell and molecular biology ·Vol. 19 ·No. 4 ·1999-08-00 ·Pages 453-62

Blatt MR, Grabov A, Brearley J, Hammond-Kosack K, Jones JD

Abstract

The Cf-9 gene encodes an extracytosolic leucine-rich repeat (LRR) protein that is membrane anchored near its C-terminus. The protein confers resistance in tomato to races of the fungus Cladosporium fulvum expressing the corresponding avirulence gene Avr9. In Nicotiana tabacum the Cf-9 transgene confers sensitivity to the Avr9 elicitor, and leads on elicitation to a subset of defence responses qualitatively similar to those normally seen in the tomato host. One of the earliest responses, both in the native and transgenic hosts, results in K+ salt loss from the infected tissues. However, the mechanism(s) underlying this solute flux and its control is poorly understood. We have explored the actions of Avr9 on Cf-9 transgenic Nicotiana using guard cells as a model. Much detail of guard cell ion channels and their regulation is already known. Measurements were carried out on intact guard cells in epidermal peels, and the currents carried by inward- (IK,in) and outward-rectifying (IK,out) K+ channels were characterized under voltage clamp. Exposures to Avr9-containing extracts resulted in a 2.5- to 3-fold stimulation of IK,out and almost complete suppression of IK,in within 3-5 min. The K+ channel responses were irreversible. They were specific for the Avr9 elicitor, were not observed in guard cells of Nicotiana lacking the Cf-9 transgene and, from kinetic analyses, could be ascribed to changes in channel gating. Both K+ channel responses were found to be saturable functions of Avr9 concentration and were completely blocked in the presence of 0.5 microM staurosporine and 100 microM H7, both broad-range protein kinase antagonists. These results demonstrate the ability of the Cf-9 transgene to couple Avr9 elicitation specifically to a concerted action on two discrete K+ channels and they indicate a role for protein phosphorylation in Avr9/Cf-9 signal transduction leading to transport control.

MeSH Terms
1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine/pharmacology Animals Cladosporium/pathogenicity,physiology Electric Conductivity Fungal Proteins/antagonists & inhibitors,pharmacology Ion Channel Gating/drug effects Kinetics Membrane Glycoproteins/genetics,physiology Membrane Potentials/drug effects Patch-Clamp Techniques Phosphorylation/drug effects Plant Diseases/microbiology Plant Proteins/genetics,physiology Plants, Genetically Modified Plants, Toxic Potassium/metabolism Potassium Channels/metabolism Potassium Channels, Inwardly Rectifying Potassium Channels, Tandem Pore Domain Protein Serine-Threonine Kinases/antagonists & inhibitors,metabolism Signal Transduction/drug effects Staurosporine/pharmacology Tobacco/cytology,drug effects,metabolism,microbiology
Chemicals
Fungal Proteins Membrane Glycoproteins Plant Proteins Potassium Channels Potassium Channels, Inwardly Rectifying Potassium Channels, Tandem Pore Domain AVR9 protein, Cladosporium fulvum 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine Protein Serine-Threonine Kinases Staurosporine Potassium
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Blatt M R
Laboratory of Plant Physiology and Biophysics, Wye College, University of London, Wye, Kent, UK. mblatt@wye.ac.uk
Grabov A
Brearley J
Hammond-Kosack K
Jones J D
Article Info
Journal
The Plant journal : for cell and molecular biology
Abbr.
Plant J
ISSN
0960-7412
Published
1999-08-00
Pages
453-62
Language
English
Region
England
NLM ID
9207397
Subset
IM
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