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Agroinfiltration is a versatile tool that facilitates comparative analyses of Avr9/Cf-9-induced and Avr4/Cf-4-induced necrosis.

Identifieur interne : 000888 ( Main/Exploration ); précédent : 000887; suivant : 000889

Agroinfiltration is a versatile tool that facilitates comparative analyses of Avr9/Cf-9-induced and Avr4/Cf-4-induced necrosis.

Auteurs : R A Van Der Hoorn [Pays-Bas] ; F. Laurent ; R. Roth ; P J De Wit

Source :

RBID : pubmed:10755307

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English descriptors

Abstract

The avirulence genes Avr9 and Avr4 from the fungal tomato pathogen Cladosporium fulvum encode extracellular proteins that elicit a hypersensitive response when injected into leaves of tomato plants carrying the matching resistance genes, Cf-9 and Cf-4, respectively. We successfully expressed both Avr9 and Avr4 genes in tobacco with the Agrobacterium tumefaciens transient transformation assay (agroinfiltration). In addition, we expressed the matching resistance genes, Cf-9 and Cf-4, through agroinfiltration. By combining transient Cf gene expression with either transgenic plants expressing one of the gene partners, Potato virus X (PVX)-mediated Avr gene expression, or elicitor injections, we demonstrated that agroinfiltration is a reliable and versatile tool to study Avr/Cf-mediated recognition. Significantly, agroinfiltration can be used to quantify and compare Avr/Cf-induced responses. Comparison of different Avr/Cf-interactions within one tobacco leaf showed that Avr9/Cf-9-induced necrosis developed slower than necrosis induced by Avr4/Cf-4. Quantitative analysis demonstrated that this temporal difference was due to a difference in Avr gene activities. Transient expression of matching Avr/Cf gene pairs in a number of plant families indicated that the signal transduction pathway required for Avr/Cf-induced responses is conserved within solanaceous species. Most non-solanaceous species did not develop specific Avr/Cf-induced responses. However, co-expression of the Avr4/Cf-4 gene pair in lettuce resulted in necrosis, providing the first proof that a resistance (R) gene can function in a different plant family.

DOI: 10.1094/MPMI.2000.13.4.439
PubMed: 10755307


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Le document en format XML

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<nlm:affiliation>Laboratory of Phytopathology, Wageningen University, The Netherlands.</nlm:affiliation>
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<term>Cladosporium (genetics)</term>
<term>Cladosporium (metabolism)</term>
<term>Fungal Proteins (genetics)</term>
<term>Fungal Proteins (metabolism)</term>
<term>Lycopersicon esculentum (genetics)</term>
<term>Lycopersicon esculentum (metabolism)</term>
<term>Membrane Glycoproteins (genetics)</term>
<term>Membrane Glycoproteins (metabolism)</term>
<term>Necrosis (MeSH)</term>
<term>Plant Proteins (genetics)</term>
<term>Plant Proteins (metabolism)</term>
<term>Signal Transduction (genetics)</term>
<term>Signal Transduction (physiology)</term>
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<term>Agrobacterium tumefaciens (génétique)</term>
<term>Cladosporium (génétique)</term>
<term>Cladosporium (métabolisme)</term>
<term>Glycoprotéines membranaires (génétique)</term>
<term>Glycoprotéines membranaires (métabolisme)</term>
<term>Lycopersicon esculentum (génétique)</term>
<term>Lycopersicon esculentum (métabolisme)</term>
<term>Nécrose (MeSH)</term>
<term>Protéines fongiques (génétique)</term>
<term>Protéines fongiques (métabolisme)</term>
<term>Protéines végétales (génétique)</term>
<term>Protéines végétales (métabolisme)</term>
<term>Transduction du signal (génétique)</term>
<term>Transduction du signal (physiologie)</term>
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<term>Agrobacterium tumefaciens</term>
<term>Cladosporium</term>
<term>Lycopersicon esculentum</term>
<term>Signal Transduction</term>
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<term>Agrobacterium tumefaciens</term>
<term>Cladosporium</term>
<term>Glycoprotéines membranaires</term>
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<term>Protéines végétales</term>
<term>Transduction du signal</term>
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<term>Fungal Proteins</term>
<term>Lycopersicon esculentum</term>
<term>Membrane Glycoproteins</term>
<term>Plant Proteins</term>
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<term>Lycopersicon esculentum</term>
<term>Protéines fongiques</term>
<term>Protéines végétales</term>
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<term>Transduction du signal</term>
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<keywords scheme="MESH" qualifier="physiology" xml:lang="en">
<term>Signal Transduction</term>
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<keywords scheme="MESH" xml:lang="en">
<term>Necrosis</term>
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<div type="abstract" xml:lang="en">The avirulence genes Avr9 and Avr4 from the fungal tomato pathogen Cladosporium fulvum encode extracellular proteins that elicit a hypersensitive response when injected into leaves of tomato plants carrying the matching resistance genes, Cf-9 and Cf-4, respectively. We successfully expressed both Avr9 and Avr4 genes in tobacco with the Agrobacterium tumefaciens transient transformation assay (agroinfiltration). In addition, we expressed the matching resistance genes, Cf-9 and Cf-4, through agroinfiltration. By combining transient Cf gene expression with either transgenic plants expressing one of the gene partners, Potato virus X (PVX)-mediated Avr gene expression, or elicitor injections, we demonstrated that agroinfiltration is a reliable and versatile tool to study Avr/Cf-mediated recognition. Significantly, agroinfiltration can be used to quantify and compare Avr/Cf-induced responses. Comparison of different Avr/Cf-interactions within one tobacco leaf showed that Avr9/Cf-9-induced necrosis developed slower than necrosis induced by Avr4/Cf-4. Quantitative analysis demonstrated that this temporal difference was due to a difference in Avr gene activities. Transient expression of matching Avr/Cf gene pairs in a number of plant families indicated that the signal transduction pathway required for Avr/Cf-induced responses is conserved within solanaceous species. Most non-solanaceous species did not develop specific Avr/Cf-induced responses. However, co-expression of the Avr4/Cf-4 gene pair in lettuce resulted in necrosis, providing the first proof that a resistance (R) gene can function in a different plant family.</div>
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