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. 2009 Oct;19(10):1732–1741. doi: 10.1101/gr.092353.109

Figure 4.

Figure 4.

Some histone mark signals are higher in internal exons than in introns in a transcription-dependent manner. (A) For highly expressed genes, the average histone mark signal in exon-expression groups (low and high) (see Fig. 1) was compared to the respective medium-expressed exons to determine whether the signal was above (yellow), below (green) or at the same level (gray). The classes were determined by calculating the fold change (log2) of the average signals in the high-expression and low-expression categories to the average signal in the medium-expression one and then further discretized to above (>0.25), below (<–0.25) or at medium (between –0.25 and 0.25) level. (B) For the alternative hypothesis, that the signal in exons (in each exon-expression group) is higher than in corresponding succeeding introns, paired Wilcoxon signed rank test P-values (-log10) are depicted below each histone mark. Asterisks indicate significant (<0.001, horizontal black line) P-values. Highly relevant histone marks showing (1) any of the major identified trends in A; (2) significantly higher signal in exons than introns (B); and (3) lack of preferential accumulation at TSS-proximal regions (manual inspection) are highlighted (A). (C) Footprints of H3K36me3 (red) and H3K27me3 (blue) signals (±1-kb window) in human T-cells centered on intron/exon junctions of internal exons in highly expressed genes in the three exon-expression groups: high, medium, and low. (D) Median values and interquartile ranges of the exon average signals in the exon-expression groups high, medium, and low in Class 1 (H3K36me3, H3K79me1, and H2BK5me1), Class 2 (H3K27me2 and H3K27me3), and Class 3 (H3K27me1). Significant differences in distributions were tested for the high/medium- and low/medium-expression groups. An asterisk below or above the interquartile ranges indicates significantly (Wilcoxon rank sum test P-value < 10−5) lower or greater signal distribution compared to medium-expressed exons.