DNA probes used for EMSAs were prepared by labeling at the 3′ end with digoxigenin (DIG)-11-ddUTP. The DNA-protein binding reactions were carried out at 20 °C in a final volume of 10 μL mixture containing 3 fmol of DIG-labeled probe, 0.5 µg of salmon sperm DNA, 0.1 µg of poly-(l-lysine), and 50 ng of purified ht-IphR (0.8 pmol dimer) in a binding buffer [20 mM HEPES, 1 mM EDTA, 10 mM (NH4)2SO4, 1 mM dithiothreitol, 0.2% (w/v) Tween 20, and 30 mM KCl, pH 7.6] for 20 min following the same procedure described earlier (Kamimura et al., 2010). When required,

effectors Wnt inhibitor including IPA or unlabeled fragments shown in Fig. S1 were added to a final concentration of 1 mM or 3 μM, respectively. Gel electrophoresis and the detection of signals were carried out as described previously (Kamimura et al., 2010). In a previous study, E6 cells harboring a lacZ reporter plasmid, pZSH2 containing a 1794 bp region upstream from the iphA start codon, showed 88-fold higher β-galactosidase activity in the presence of IPA (Fukuhara et al., 2010). To determine the iphA www.selleckchem.com/products/DAPT-GSI-IX.html promoter region, a set of deletion plasmids of pZSH2 was constructed and used for the promoter assay (Fig. 1a). The inducible expressions of the iphA promoter variants were observed in

IPA-grown E6 cells harboring pZSM1, pZSP08, pZSN06, pZSNE530, and pZSNE347. On the other hand, no promoter activity was shown in E6 cells harboring pZSNE198. These results suggested that the region sufficient for the IPA-dependent induction of the iphA promoter was located within a 160 bp region upstream from the iphA start codon. The transcription start site of iphA was determined by primer extension analyses using total RNA isolated from E6 and the iphR mutant (DEIR) cells. A 159-nucleotides (nt) DNA fragment was observed when using total RNA from E6 cells grown in the presence of IPA (Fig. 1b); however, no significant extension product was seen in the absence of IPA

(data not shown). From these results, the transcription start site of the iph operon was determined to be a cytosine located 49 bp upstream of the iphA start codon (Fig. 1c). Putative −35 and −10 sequences separated by 16 nt were found upstream of the transcription start site. We also found two inverted repeat sequences IR1 Lumacaftor chemical structure and IR2. In the case of DEIR, a 159-nt DNA fragment appeared regardless of the presence of IPA in the cultures (data not shown). These results supported that the iph operon is negatively autoregulated by IphR. To further identify the iphA promoter region, pZ347, pZ284, pZ274, and pZ255 were constructed and used for the promoter assays (Fig. 1c). The inducible expression of the iphA promoter was observed in E6 cells harboring pZ347, pZ284, and pZ274 (Table 1). However, cells harboring pZ255, which lacks the putative −35 sequence, showed no promoter activity.