2B). Figure 2 Activation of CgOPT1 transcription by IAA and during spore germination. A. Spores were germinated in pea extract and CgOPT1 expression was determined at various time points. Top – CgOPT1, bottom – rRNA. B. Expression of CgOPT1 in Tideglusib in vivo mycelia was determined after growing the fungus for 48 h in CD medium (0), CD supplemented with 500 μM tryptophol (Tol), or CD with 100 μM or 500 μM IAA. Top – CgOPT1, bottom – rRNA. C. The transgenic strain Pop-gfp6 was grown in CD media supplemented with various concentrations

of IAA. GFP levels were evaluated 48 h after culture inoculation. Control (0) contained an equal volume of ethanol. Low magnification image is presented as inset in each Temsirolimus manufacturer frame. The portion of the colony that is presented in higher magnification is designated by a small square within each inset. Bars = 20 μm. Further expression analyses were performed using a transgenic strain of C. gloeosporioides, Popt-gfp6, in which the GFP reporter gene is regulated by the CgOPT1 promoter. The GFP signal in spores was enhanced during germination with a peak at 12 h and then it decreased, similar to gene-expression results obtained by northern blot analysis (data not shown). To evaluate the response to auxin, the Popt-gfp6-transgenic isolate was grown in Czapek Dox (CD) medium supplemented with IAA and the GFP signal was monitored 48 h after culture inoculation. GFP fluorescence

was enhanced by IAA in a concentration-dependent manner, with saturation at 250 μM IAA (Fig. 2C). No change in GFP fluorescence was detected in https://www.selleckchem.com/products/JNJ-26481585.html media supplemented only with ethanol (the solvent used to dissolve IAA). Silencing of CgOPT1 transcription by RNA interference (RNAi) cgopt1-silenced mutants were generated and characterized. Because homologous integration does not work well in C. gloeosporioides f. sp. aeschynomene, mutants 4��8C were generated by RNA silencing. The wild-type strain was co-transformed with the RNAi cassette OptRi and the gGFP plasmid [19], which was used to confer resistance to hygromycin B. Some of the hygromycin-resistant colonies showed discoloration and reduced sporulation. Spores were collected from

culture plates of these isolates and germinated for 9 h in pea extract, conditions under which CgOPT1 gene expression is normally high (Fig. 2A). Variable levels of reduced CgOPT1 expression were noted in all isolates (Fig. 3). The phenotype of the cgopt1-silenced mutants was determined using isolates Ori51 and Ori83. Figure 3 Silencing of CgOPT1 gene expression. Spores of isolates obtained by transformation with the OptRi (RNAi) plasmid were germinated in pea extract. After 9 h, samples were collected and their RNA extracted. Reduced CgOPT1 gene expression is evident in all of the transgenic isolates. PathogeniCity Spore-inoculation experiments were performed using several spore dilutions: 104, 5 × 104, and 105 spores/ml.