Transcriptional Activation and Production of Tryptophan-Derived Secondary Metabolites in Arabidopsis Roots Contributes to the Defense against the Fungal Vascular Pathogen Verticillium longisporum

2012 | journal article. A publication with affiliation to the University of Göttingen.

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​Transcriptional Activation and Production of Tryptophan-Derived Secondary Metabolites in Arabidopsis Roots Contributes to the Defense against the Fungal Vascular Pathogen Verticillium longisporum​
Iven, T.; Koenig, S.; Singh, S.; Braus-Stromeyer, S. A.; Bischoff, M.; Tietze, L. F. & Braus, G. H. et al.​ (2012) 
Molecular Plant5(6) pp. 1389​-1402​.​ DOI: https://doi.org/10.1093/mp/sss044 

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Authors
Iven, Tim; Koenig, Stefanie; Singh, Seema; Braus-Stromeyer, Susanna A.; Bischoff, Matthias; Tietze, Lutz Friedjan; Braus, Gerhard H.; Lipka, Volker; Feussner, Ivo; Droege-Laser, Wolfgang
Abstract
The soil-borne fungal pathogen Verticillium longisporum causes vascular disease on Brassicaceae host plants such as oilseed rape. The fungus colonizes the root xylem and moves upwards to the foliage where disease symptoms become visible. Using Arabidopsis as a model for early gene induction, we performed root transcriptome analyses in response to hyphal growth immediately after spore germination and during penetration of the root cortex, respectively. Infected roots showed a rapid reprogramming of gene expression such as activation of transcription factors, stress-, and defense-related genes. Here, we focused on the highly coordinated gene induction resulting in the production of tryptophan-derived secondary metabolites. Previous studies in leaves showed that enzymes encoded by CYP81F2 and PEN2 (PENETRATION2)execute the formation of antifungal indole glucosinolate (IGS) metabolites. In Verticillium-infected roots, we found transcriptional activation of CYP81F2 and the PEN2 homolog PEL1 (PEN2-LIKE1), but no increase in antifungal IGS breakdown products. In contrast, indole-3-carboxylic acid (I3CA) and the phytoalexin camalexin accumulated in infected roots but only camalexin inhibited Verticillium growth in vitro. Whereas genetic disruption of the individual metabolic pathways leading to either camalexin or CYP81F2-dependent IGS metabolites did not alter Verticillium-induced disease symptoms, a cyp79b2 cyp79b3 mutant impaired in both branches resulted in significantly enhanced susceptibility. Hence, our data provide an insight into root-specific early defenses and suggest tryptophan-derived metabolites as active antifungal compounds against a vascular pathogen.
Issue Date
2012
Status
published
Publisher
Oxford Univ Press
Journal
Molecular Plant 
ISSN
1752-9867; 1674-2052
Sponsor
DFG Research Unit [FOR546]

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