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  Pep1, a Secreted Effector Protein of Ustilago maydis, Is Required for Successful Invasion of Plant Cells

Doehlemann, G., van der Linde, K., Aßmann, D., Schwammbach, D., Hof, A., Mohanty, A., et al. (2009). Pep1, a Secreted Effector Protein of Ustilago maydis, Is Required for Successful Invasion of Plant Cells. PLoS Pathogens, 5(2): e1000290, pp. 1-16. doi:10.1371/journal.ppat.1000290.

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Doehlemann, Gunther1, Autor           
van der Linde, Karina1, Autor           
Aßmann, Daniela1, Autor           
Schwammbach, Daniela1, Autor           
Hof, Alexander1, Autor           
Mohanty, Amitabh, Autor
Jackson, David, Autor
Kahmann, Regine2, Autor           
Affiliations:
1Department of Organismic Interactions, Alumni, Max Planck Institute for Terrestrial Microbiology, Max Planck Society, ou_3266313              
2Emeriti Molecular Phytopathology, Max Planck Institute for Terrestrial Microbiology, Max Planck Society, ou_3266291              

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 Zusammenfassung: The basidiomycete Ustilago maydis causes smut disease in maize. Colonization of the host plant is initiated by direct penetration of cuticle and cell wall of maize epidermis cells. The invading hyphae are surrounded by the plant plasma membrane and proliferate within the plant tissue. We identified a novel secreted protein, termed Pep1, that is essential for penetration. Disruption mutants of pep1 are not affected in saprophytic growth and develop normal infection structures. However, Deltapep1 mutants arrest during penetration of the epidermal cell and elicit a strong plant defense response. Using Affymetrix maize arrays, we identified 116 plant genes which are differentially regulated in Deltapep1 compared to wild type infections. Most of these genes are related to plant defense. By in vivo immunolocalization, live-cell imaging and plasmolysis approaches, we detected Pep1 in the apoplastic space as well as its accumulation at sites of cell-to-cell passages. Site-directed mutagenesis identified two of the four cysteine residues in Pep1 as essential for function, suggesting that the formation of disulfide bridges is crucial for proper protein folding. The barley covered smut fungus Ustilago hordei contains an ortholog of pep1 which is needed for penetration of barley and which is able to complement the U. maydis Deltapep1 mutant. Based on these results, we conclude that Pep1 has a conserved function essential for establishing compatibility that is not restricted to the U. maydis / maize interaction.

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Sprache(n): eng - English
 Datum: 2009-02
 Publikationsstatus: Erschienen
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 Ort, Verlag, Ausgabe: -
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 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: eDoc: 441567
DOI: 10.1371/journal.ppat.1000290
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Titel: PLoS Pathogens
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 5 (2) Artikelnummer: e1000290 Start- / Endseite: 1 - 16 Identifikator: -