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. 2018 Aug 1;293(37):14342–14358. doi: 10.1074/jbc.RA118.005010

Figure 2.

Figure 2.

Polycomb proteins and associated histone modifications at the active and repressed CCND2 gene. A, schematic of the human CCND2 locus. Positions of PCR amplicons analyzed in B are shown below the coordinate scale. Note that amplicon 2 corresponds to the summit of MEL18 peak, and amplicon 5 corresponds to the CCND2 TSS (see Tables S4 and S5, for sequence information). B, ChIP profiles of MEL18, RING2, SUZ12, and H3K27me3 in NT2-D1 (left column) and TIG-3 (right column) cells. The immunoprecipitation of the ALX4 gene repressed by PcG in NT2-D1 and TIG-3 cells was used as positive control (for position of PCR amplicons see Fig. S11). The immunoprecipitation of a gene desert region (chromosome 12: 127711096–127713493; Hg19) was used as a negative control. Histograms for both are shown to the right of the each graph and are to the same y axis scale. All histograms and graphs show the average and the scatter (whiskers) between two independent experiments.