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Calcineurin-Responsive Zinc Finger Transcription Factor CRZ1 of Botrytis cinerea Is Required for Growth, Development, and Full Virulence on Bean Plants

Calcineurin-Responsive Zinc Finger Transcription Factor CRZ1 of Botrytis cinerea Is Required for... Calcineurin-Responsive Zinc Finger Transcription Factor CRZ1 of Botrytis cinerea Is Required for Growth, Development, and Full Virulence on Bean Plants ▿ Julia Schumacher 1 , Inigo F. de Larrinoa 2 and Bettina Tudzynski 1 , * 1 Institut für Botanik, Westfälische Wilhelms-Universität Münster, Schlossgarten 3, 48149 Münster, Germany 2 Departamento de Química Aplicada, Facultad de Ciencias Químicas, Universidad del País Vasco (UPV/EHU), Po. de Manuel de Lardizabal 3, 20018 San Sebastián, Spain ABSTRACT Recently, we showed that the α subunit BCG1 of a heterotrimeric G protein is an upstream activator of the Ca 2+ /calmodulin-dependent phosphatase calcineurin in the gray mold fungus Botrytis cinerea . To identify the transcription factor acting downstream of BCG1 and calcineurin, we cloned the gene encoding the B. cinerea homologue of CRZ1 (“CRaZy,” c alcineurin- r esponsive z inc finger transcription factor), the mediator of calcineurin function in yeast. BcCRZ1 is able to partially complement the corresponding Saccharomyces cerevisiae mutant, and the subcellular localization of the green fluorescent protein-BcCRZ1 fusion product in yeast cells depends on the calcium level and calcineurin activity. Bc crz1 deletion mutants are not able to grow on minimal media and grow slowly on media containing plant extracts. Hyphal morphology, conidiation, and sclerotium formation are impaired. The cell wall and membrane integrity, stress response (extreme pH, H 2 O 2 , Ca 2+ , Li + ), and ability of the hyphae to penetrate the intact plant surface are affected in the mutants. However, BcCRZ1 is almost dispensable for the conidium-derived infection of bean plants. The addition of Mg 2+ restores the growth rate, conidiation, and penetration and improves the cell wall integrity but has no impact on sclerotium formation or hypersensitivity to Ca 2+ and H 2 O 2 . The expression of a set of recently identified BCG1- and calcineurin-dependent genes is also affected in ΔBc crz1 mutants, confirming that this transcription factor acts downstream of calcineurin in B. cinerea . Since the Bc crz1 mutants still respond to calcineurin inhibitors, we conclude that BcCRZ1 is not the only target of calcineurin. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Eukaryotic Cell American Society For Microbiology

Calcineurin-Responsive Zinc Finger Transcription Factor CRZ1 of Botrytis cinerea Is Required for Growth, Development, and Full Virulence on Bean Plants

Calcineurin-Responsive Zinc Finger Transcription Factor CRZ1 of Botrytis cinerea Is Required for Growth, Development, and Full Virulence on Bean Plants

Eukaryotic Cell , Volume 7 (4): 584 – Apr 1, 2008

Abstract

Calcineurin-Responsive Zinc Finger Transcription Factor CRZ1 of Botrytis cinerea Is Required for Growth, Development, and Full Virulence on Bean Plants ▿ Julia Schumacher 1 , Inigo F. de Larrinoa 2 and Bettina Tudzynski 1 , * 1 Institut für Botanik, Westfälische Wilhelms-Universität Münster, Schlossgarten 3, 48149 Münster, Germany 2 Departamento de Química Aplicada, Facultad de Ciencias Químicas, Universidad del País Vasco (UPV/EHU), Po. de Manuel de Lardizabal 3, 20018 San Sebastián, Spain ABSTRACT Recently, we showed that the α subunit BCG1 of a heterotrimeric G protein is an upstream activator of the Ca 2+ /calmodulin-dependent phosphatase calcineurin in the gray mold fungus Botrytis cinerea . To identify the transcription factor acting downstream of BCG1 and calcineurin, we cloned the gene encoding the B. cinerea homologue of CRZ1 (“CRaZy,” c alcineurin- r esponsive z inc finger transcription factor), the mediator of calcineurin function in yeast. BcCRZ1 is able to partially complement the corresponding Saccharomyces cerevisiae mutant, and the subcellular localization of the green fluorescent protein-BcCRZ1 fusion product in yeast cells depends on the calcium level and calcineurin activity. Bc crz1 deletion mutants are not able to grow on minimal media and grow slowly on media containing plant extracts. Hyphal morphology, conidiation, and sclerotium formation are impaired. The cell wall and membrane integrity, stress response (extreme pH, H 2 O 2 , Ca 2+ , Li + ), and ability of the hyphae to penetrate the intact plant surface are affected in the mutants. However, BcCRZ1 is almost dispensable for the conidium-derived infection of bean plants. The addition of Mg 2+ restores the growth rate, conidiation, and penetration and improves the cell wall integrity but has no impact on sclerotium formation or hypersensitivity to Ca 2+ and H 2 O 2 . The expression of a set of recently identified BCG1- and calcineurin-dependent genes is also affected in ΔBc crz1 mutants, confirming that this transcription factor acts downstream of calcineurin in B. cinerea . Since the Bc crz1 mutants still respond to calcineurin inhibitors, we conclude that BcCRZ1 is not the only target of calcineurin.

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Publisher
American Society For Microbiology
Copyright
Copyright © 2008 by the American society for Microbiology.
ISSN
1535-9778
eISSN
1535-9786
DOI
10.1128/EC.00426-07
pmid
18263765
Publisher site
See Article on Publisher Site

Abstract

Calcineurin-Responsive Zinc Finger Transcription Factor CRZ1 of Botrytis cinerea Is Required for Growth, Development, and Full Virulence on Bean Plants ▿ Julia Schumacher 1 , Inigo F. de Larrinoa 2 and Bettina Tudzynski 1 , * 1 Institut für Botanik, Westfälische Wilhelms-Universität Münster, Schlossgarten 3, 48149 Münster, Germany 2 Departamento de Química Aplicada, Facultad de Ciencias Químicas, Universidad del País Vasco (UPV/EHU), Po. de Manuel de Lardizabal 3, 20018 San Sebastián, Spain ABSTRACT Recently, we showed that the α subunit BCG1 of a heterotrimeric G protein is an upstream activator of the Ca 2+ /calmodulin-dependent phosphatase calcineurin in the gray mold fungus Botrytis cinerea . To identify the transcription factor acting downstream of BCG1 and calcineurin, we cloned the gene encoding the B. cinerea homologue of CRZ1 (“CRaZy,” c alcineurin- r esponsive z inc finger transcription factor), the mediator of calcineurin function in yeast. BcCRZ1 is able to partially complement the corresponding Saccharomyces cerevisiae mutant, and the subcellular localization of the green fluorescent protein-BcCRZ1 fusion product in yeast cells depends on the calcium level and calcineurin activity. Bc crz1 deletion mutants are not able to grow on minimal media and grow slowly on media containing plant extracts. Hyphal morphology, conidiation, and sclerotium formation are impaired. The cell wall and membrane integrity, stress response (extreme pH, H 2 O 2 , Ca 2+ , Li + ), and ability of the hyphae to penetrate the intact plant surface are affected in the mutants. However, BcCRZ1 is almost dispensable for the conidium-derived infection of bean plants. The addition of Mg 2+ restores the growth rate, conidiation, and penetration and improves the cell wall integrity but has no impact on sclerotium formation or hypersensitivity to Ca 2+ and H 2 O 2 . The expression of a set of recently identified BCG1- and calcineurin-dependent genes is also affected in ΔBc crz1 mutants, confirming that this transcription factor acts downstream of calcineurin in B. cinerea . Since the Bc crz1 mutants still respond to calcineurin inhibitors, we conclude that BcCRZ1 is not the only target of calcineurin.

Journal

Eukaryotic CellAmerican Society For Microbiology

Published: Apr 1, 2008

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