Signal-specific recruitment of EZH2 onto the miR-101-2 promoter in JR1 cells after EZH2 down-regulation. (A) ChIP assays on JR1 cells 72Â h after EZH2 or CTR siRNA transfection showing the recruitment of EZH2 and the levels of histone H3 trimethylation on Lys27 (H3K27me3) on miR-101-2, MCK, and SMAD6 (as negative control) regulatory regions. Normal rabbit IgG were used as negative control. Graphs represent the percent of immunoprecipitated material relative to input DNA. (B) mRNA levels (RT-qPCR) of pri-miR-101-2 in JR1 cells 48Â h after EZH2 siRNA treatment were normalized to GAPDH levels and expressed as fold increase over CTR siRNA.