Genomic Androgen Receptor-Occupied Regions with Different Functions, Defined by Histone Acetylation, Coregulators and Transcriptional Capacity
Figure 5
Occupancies of AR-coregulators on selected ARORs.
C4-2B cells were cultured in hormone-depleted medium for 3 days and then treated with 10 nM DHT or ethanol vehicle for 4 h. Conventional site-specific ChIP assays were performed with indicated antibodies. Nineteen ARORs and 2 negative control (NC) regions were examined by qPCR. The values are presented as percentage of input.