Skip to main content
letter
. 2009 Mar;19(3):372–380. doi: 10.1101/gr.084582.108

Figure 2.

Figure 2.

FOXA1 is required but not sufficient for high FAIRE enrichment at bound regulatory elements. (A) FOXA1 binding sites were divided into tertiles and the average FAIRE-chip signal (based on MAT scores, see Methods) for each subset of sites (low, medium, and high FAIRE) was calculated. Each subset was comprised of 645 sites. FAIRE-chip enrichments at FOXA1 LNCaP-specific sites were also analyzed. Data represent mean ± SEM of signals derived from MAT analysis of FAIRE-chip data. (B) FAIRE-qPCR experiments were performed in MCF7 cells to monitor FAIRE enrichment at the indicated categories of FOXA1 recruitment regions (at least 8 different sites were analyzed for each subset). Relative enrichment compared to negative control regions is shown. Data are mean ± SD from three independent experiments. (C) Signals from FOXA1 ChIP-chip in MCF7 cells within FOXA1 binding sites with low, medium or high FAIRE-chip enrichments. LNCaP-specific sites were also analyzed. Data represent means ± SEM of signals derived from MAT analysis of the FOXA1 ChIP-chip data from Lupien et al. (2008). (D) FAIRE-qPCR experiments performed as in B. Decrease in FAIRE enrichments triggered by FOXA1 silencing is shown. Data are mean ± SD from three independent experiments. *** and * Indicate a statistically significant difference between FOXA1 recruitment sites with high and low FAIRE enrichments (P < 0.001 and P < 0.05, respectively).