Publication | Open Access
Identification of Pathogenesis-Associated Genes by T-DNA–Mediated Insertional Mutagenesis in <i>Botrytis cinerea</i>: A Type 2A Phosphoprotein Phosphatase and an SPT3 Transcription Factor Have Significant Impact on Virulence
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Citations
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References
2011
Year
EngineeringMicrobial PathogensGeneticsMolecular BiologyPlant PathologyMolecular GeneticsPathogen EffectorType 2ATranscriptional RegulationBiosynthesisPlant Pathogen EffectorPathogenesis-associated GenesHost-pathogen InteractionsPhosphoprotein PhosphataseVirulence FactorSpt3 SubunitPathogen CharacterizationGene ReplacementAgrobacterium Tumefaciens-mediated TransformationFungal PathogenPathogenesisGenetic EngineeringMicrobiologyHost ResistanceMedicineMutagenesis
Agrobacterium tumefaciens-mediated transformation (ATMT) was used to generate an insertional mutant library of the gray mold fungus Botrytis cinerea. From a total of 2,367 transformants, 68 mutants showing significant reduction in virulence on tomato and bean plants were analyzed in detail. As reported for other fungal ATMT libraries, integrations were mostly single copy, occurred preferentially in noncoding (regulatory) regions, and were frequently accompanied by small deletions of the target sequences and loss of parts of the border sequence. Two T-DNA integration events that were found to be linked to virulence were characterized in more detail: a catalytic subunit of a PP2A serine/threonine protein phosphatase (BcPP2Ac) and the SPT3 subunit of a Spt-Ada-Gcn5-acetyltransferase (SAGA-like) transcriptional regulator complex. Gene replacement and silencing approaches revealed that both Bcpp2Ac and SPT3 are crucial for virulence, growth, and differentiation as well as for resistance to H(2)O(2) in B. cinerea.
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