The H2O2-induced transcript levels of most of the genes tested de

The H2O2-induced transcript levels of most of the genes tested depended strongly on ChAP1, and several required Skn7 for full induction. The gene for glutathione reductase (GLR1) was only twofold induced in Δchap1 compared with 52-fold in WT and 16-fold and Δskn7. In the double mutant, the transcript level was similar to the basal level in the untreated control, indicating that either transcription factor is sufficient only for partial expression, while both transcription factors are required for full expression (Fig. 2). TRX2 showed the same

pattern as GLR1, but the additive effect was not statistically significant. The TRR1 gene is under the regulation of ChAP1 alone. While superoxide dismutase (SOD1) expression is not strongly decreased by loss of either ChAP1 or Skn7 alone, the GS-1101 concentration double mutant failed Protease Inhibitor Library research buy to upregulate the expression of SOD1. The catalase genes CAT1 and CAT3 seem ChAP1 dependent and Skn7 independent; however, this regulation is not significant at P < 0.01 by the multiple-comparison t-test used here. CAT2 is expressed in all three mutants. The expression of γ-glutamylcysteine

synthetase (GSH1) was also tested, and only minor upregulation was observed in WT and Δskn7. To test whether both ChAP1 and Skn7 contribute to virulence on the host, infection assays on maize were carried out. To inoculate undetached maize leaves, maize plants were grown in hydroponics (as described in the Materials and Methods section) for 12 days, the plants were removed from the medium and transferred into a tray where the roots were kept moist. Spores from Δchap1, Δskn7, Δchap1-Δskn7 (ΔΔ) and WT were prepared in ddW with 0.02% Tween 20; at least four plants were used for each mutant, and the second leaf was inoculated with three 7-μL droplets containing about 500 spores. Lesion areas were measured using imagej software from images taken 2 days after inoculation (Fig. 3a). Δchap1 and Δskn7 mutants were not significantly different in virulence from WT, whereas ΔΔ showed significantly smaller lesions (about 30% smaller, Fig. 3b). This demonstrates an additive contribution of the

two transcription factors that are lacking in the double mutant. These contributions may promote the ability GNA12 to counteract the plant’s oxidative burst as well as other stresses the pathogen encounters during infection. Thus, the double mutant may be sensitive to the HR or other plant defenses, preventing spreading of the mutant and resulting in smaller lesions than those formed by the WT. In vitro experiments showed that in response to some stressors, there is no additive contribution, whereas for others there is (Fig. 1). Loss of either of these transcription factors results in hypersensitivity to oxidants in plate assays, and the contribution of each is reflected in the expression of genes whose products allow the cell to cope with oxidative stress. ChAP1 is critical for increased expression of GLR1, TRR1, and TRX2 in response to hydrogen peroxide (Fig.

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