4F). The results suggest

that ZNF191 may act as a mediator of serum induction of β-catenin mRNA expression in HCC cells. It is clear that ZNF191 can positively regulate mRNA and protein levels of β-catenin. Next we sought to determine the mechanism of this regulation. To this end we assessed whether overexpression of ZNF191 has any effect on transcription activity of the CTNNB1 promoter. Promoter luciferase assay indicated that ZNF191 can increase the transcription activity of the full-length CTNNB1 promoter (PGL3-HBCP, gift of Prof. R.H. Dashwood, Oregon State University) by about 3.5-fold compared with transfecting control vector (Fig. 5A). Furthermore, this activation was in a dose-dependent manner (Fig. 5B). Compared with the full-length isoform of ZNF191 (ZNF191-FU), the short isoform of ZNF191 (ZNF191-NF, without C2H2 zinc finger domain) had no activation effect on CTNNB1 www.selleckchem.com/products/jq1.html promoter (Fig. 5B). This result suggests that ZNF191 exerts this activation function role by way of C2H2

zinc finger domain. Because cyclin D1 is the downstream gene of β-catenin, we assessed the effect of ZNF191 on CCND1 promoter. Figure 5C shows that ZNF191 increased CCND1 promoter by 6.4-fold. Mutation in the LEF/TCF site (the binding site of β-catenin) of the CCND1 promoter resulted in a much lower increase (3.2-fold) in transcription activity. In vivo ChIP assays showed that ZNF191 cannot directly bind to the CCND1 promoter (-962CD1), including the LEF/TCF site of the CCND1 promoter (Supporting Fig. 4). The results suggest that activation of CCND1 promoter by ZNF191 is through β-catenin, but not through direct binding of endogenous ZNF191 to the promoter. Dabrafenib research buy Next, in order to identify ZNF191 response regions in the CTNNB1 promoter, various lengths of CTNNB1 5′-flanking region (Fig. 5D) were transfected into HEK-293T cells with pCMV-Myc-ZNF191 to determine the promoter transcriptional activities.

The luciferase reporter assay indicated that the construct P(-1407/+93) exhibited the maximum luciferase activity, which was much higher than that of P(-2692/+93) and P(-1907/+93). P(-907/+93) and P(-409/+93) constructs displayed modest promoter activity (Fig. 4E). These results suggest that nucleotide (nt)-1407/-907 of the CTNNB1 promoter region is Chlormezanone indispensable to elicit transcriptional response for ZNF191. The finding that potential binding sites for ZNF191 are located at nt-1407/-907 of CTNNB1 promoter region prompted us to determine whether ZNF191 is directly binding to the CTNNB1 promoter. With delicate analysis of the nucleotide sequences of the 5′-flanking region (-1467/-907) of the β-catenin gene (Fig. 6A, top), we found that sequences ATTAATT at nt-1244 of the CTNNB1 promoter are similar to ATTCATT (within three repetitions of [TCAT] motif, TCATTCATTCAT, defined previously as ZNF191 interacting motif21). We hypothesized that ZNF191 may directly bind to the CTNNB1 promoter at this candidate site (Fig. 6A).