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. 2017 Aug 9;6:e28440. doi: 10.7554/eLife.28440

Figure 3. Dynamic patterns of developmental enhancer occupancy across distantly related species.

(a) Hierarchical clustering of ChIP signal of CRMs with high, intermediate and low binding conservation, as classified using Jaccard distance (Figure 2). Each row corresponds to an orthologous CRM, and each column to a condition, with 14 D. melanogaster conditions followed by their equivalent 14 D. virilis conditions. The vertical dashed line delimits data from both species, while the horizontal colored bars indicate the TF. All three heatmaps are visualized using the quantitative ChIP-signal shown in the scale in lower right. (b) Differential motif analysis on early vs late Twi bound enhancers indicates that the regulation of these elements is largely conserved. Heatmap shows fold enrichment (early vs late bound enhancers, log2) of all motifs with >2 fold significant enrichment in one of the two species. *p<0.05; **p<0.01; ***p<0.001 indicates significance in that species. Color indicates motif enrichment, which is generally in the same direction in both species, even when significant in only one species.

DOI: http://dx.doi.org/10.7554/eLife.28440.006

Figure 3.

Figure 3—figure supplement 1. ChIP-chip and ChIP-seq signals are highly correlated.

Figure 3—figure supplement 1.

ChIP-chip and ChIP-seq signal for Mef2 over all D. melanogaster CRMs are plotted here. ChIP-chip signals correspond to mean ChIP-chip intensity signals calculated over 200 bp sliding window with 35 bp steps along the CRM length. ChIP-seq signals correspond to Log2(IP/input). Mef2 ChIP-seq signals over D. melanogaster 8,008 CRMs were generated previously (Bonn et al., 2012). Pearson correlation coefficient between both sets is shown.