Fig. 5
From: Phospho-code of a conserved transcriptional factor underpins fungal virulence

Binding of CgCrzA to the promoter regions of CgCHS5 and CgCHS6. A, B Quantitative RT-PCR analysis of CgCHS5/6 expression in the ΔCgcrzA mutant and wild-type in response to CFW. HY and CO indicates hypha and conidia, respectively. Error bars represent standard deviation. Asterisks indicate a significant difference at P < 0.01. C and D Electrophoretic Mobility Shift Assay (EMSA) demonstrating the binding of CgCrzAS280D protein to the putative promoter sequences of CgCHS5 (C) and CgCHS6 (D). The band shift of the promoter with increasing concentration of CgCrzAS280D protein. GST indicates glutathione S-transferase tag protein. E and F Incubation of the Alex660-labelled full-length promoter DNA in the absence (leftmost lane) or presence (second to the sixth lane) of purified CgCrzAS280D and GST proteins (rightmost lane). Unlabelled DNA was added as a binding competitor, with increasing amounts in the third to sixth lanes