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Resolution: standard / high Figure 6.
AR binding displays three distinct modes of androgen receptor-DNA interaction that
are specific to ligand-activated androgen receptor. (a) K-means clustering of LNCaP-induced DNase-seq signal into three consistent clusters
within AR binding sites. (b) K-means clustering (k = 3) was repeated 100 times on both LNCaP and LNCaP-induced
DNase-seq data around all DHS sites with a full-site canonical AR motif. Shown is
the distribution of correlations between cluster centers for each run. The asterisk
denotes the statistically significant difference between the correlation distributions
(Mann-Whitney P < 2.2e-16). (c) Motif analysis of the entire 25 bp span up- and downstream from AR motif matches for
each cluster. MEME motifs identified within this interval (E < 0.1, E-value shown
below logo) are shown in logo format. Motifs that significantly match a known motif
(E < 0.05, by TomTom) are marked with an asterisk. The name of the most significant
match according to TomTom is indicated next to the logo, as is the percentage of regions
that contain the enriched motif. For matches resembling FOX family factors, we note
that these motifs are very similar to each other. DNase-seq signal is shown as the
aggregate signal from all cluster members with the dotted lines marking the location
of the AR motif within the plot. AR: androgen receptor; bp: base pairs; DHS: DNase
I hypersensitive; DNase-seq: DNase I hypersensitivity analysis coupled with high-throughput
sequencing; FOX: Forkhead box; NF1C: nuclear factor 1 C-type.
Tewari et al. Genome Biology 2012 13:R88 doi:10.1186/gb-2012-13-10-r88 |