A cis-acting sequence homologous to the yeast filamentation and invasion response element regulates expression of a pectinase gene from the bean pathogen Colletotrichum lindemuthianum

Phytopathogenic fungi secrete hydrolytic enzymes that degrade plant cell walls, notably pectinases. The signaling pathway(s) that control pectinase gene expression are currently unknown in filamentous fungi. Recently, the green fluorescent protein coding sequence was used as a reporter gene to study...

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Veröffentlicht in:The Journal of biological chemistry 2002-08, Vol.277 (32), p.29125-29131
Hauptverfasser: Herbert, Corentin, Jacquet, Christophe, Borel, Charlotte, Esquerre-Tugaye, Marie-Therese, Dumas, Bernard
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container_end_page 29131
container_issue 32
container_start_page 29125
container_title The Journal of biological chemistry
container_volume 277
creator Herbert, Corentin
Jacquet, Christophe
Borel, Charlotte
Esquerre-Tugaye, Marie-Therese
Dumas, Bernard
description Phytopathogenic fungi secrete hydrolytic enzymes that degrade plant cell walls, notably pectinases. The signaling pathway(s) that control pectinase gene expression are currently unknown in filamentous fungi. Recently, the green fluorescent protein coding sequence was used as a reporter gene to study the expression of CLPG2, a gene encoding an endopolygalacturonase of the bean pathogen Colletotrichum lindemuthianum. CLPG2 is transcriptionally induced by pectin in the axenic culture of the fungus and during formation of the appressorium, an infection structure specialized in plant tissue penetration. In the present study, promoter deletion and mutagenesis, as well as gel shift mobility assays, allowed for the first time identification of cis-acting elements that bind protein factors and are essential for the regulation of a pectinase gene. We found that two different adjacent DNA motifs are combined to form an active element that shows a strong sequence homology with the yeast filamentation and invasion response element. The same element is required for the transcriptional activation of CLPG2 by pectin and during appressorium development. This study strongly suggests that the control of virulence genes of fungal plant pathogens, such as pectinases, involves the formation of a complex of transcriptional activators similar to those regulating the invasive growth in yeast.
doi_str_mv 10.1074/jbc.M201489200
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source MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Base Sequence
Chromosome Mapping
DNA - metabolism
Fabaceae - microbiology
Fungal Proteins - biosynthesis
Fungal Proteins - genetics
Fungi - pathogenicity
Gene Deletion
Gene Expression Regulation, Enzymologic
Genetic Vectors
Glucose - metabolism
Green Fluorescent Proteins
Luminescent Proteins - metabolism
Microscopy, Fluorescence
Models, Biological
Molecular Sequence Data
Mutagenesis, Site-Directed
Plant Diseases - microbiology
Polygalacturonase - biosynthesis
Polygalacturonase - genetics
Promoter Regions, Genetic
Protein Binding
Protoplasts - metabolism
Recombinant Fusion Proteins - metabolism
Signal Transduction
Transcription, Genetic
title A cis-acting sequence homologous to the yeast filamentation and invasion response element regulates expression of a pectinase gene from the bean pathogen Colletotrichum lindemuthianum
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