(A) Graph depicting interaction between the five regulatory motifs measured by synergy and cooccurrence. (A) Graph depicting interaction between the five.

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(A) Graph depicting interaction between the five regulatory motifs measured by synergy and cooccurrence. (A) Graph depicting interaction between the five regulatory motifs measured by synergy and cooccurrence. A pair of motifs connected by a thick red line has a synergistic effect on expression and pairs connected by a thin blue line are significantly more highly cooccurring in individual promoters. These interactions were computed using all genes on the array. In addition, we calculated cooccurrence interaction given only the genes in the cluster (i.e. considering the total number of genes in the cluster and the number of cluster's genes containing each motif as a background), and found even there several significant interactions (blue dotted lines). Since for some of the motifs, the motif database contains multiple variants, we unified all variants of the same motif into one node, and an edge in the graph connects two motifs if at least one of the variants of the two motifs is either synergistic or highly cooccurring. (B, C) Combinogram analyses (Pilpel et al, 2001) using the five regulatory motifs during the transformation process (B) and HeLa cell cycle (C). All the varying genes in the respective arrays were used in the analysis. The upper and middle parts of the Combinogram are depicted as before (Pilpel et al, 2001), while the lower part is modified. Briefly, the middle section of the Combinogram depicts the motif composition of each gene set defined by motif combination (GMC; see Materials and methods). Each vertical column represents a single GMC. A black square indicates that the particular motif is present in the promoters of all the genes in that GMC. A white square indicates that none of the genes in the GMC contain the particular motif. The top section of the graph shows the dendrogram analysis that assesses the similarity in expression profiles of each GMC using normalized Euclidean distances between the average expression profiles of the genes in the GMC as a measure of distance. The lower part of this modified Combinogram displays the mean expression profiles of the genes in each GMC; color‐coded as in Figure 1. The numbers of genes in each GMC appear below the dendrogram. The three main branch points in the dendrogram in (B) are represented as 1–3 (in circles). In the present analysis, only genes that contain the motifs in their preferred distance relative to TSS (as depicted in Figure 2) were considered, as genes that contain the motifs, yet away from the preferred location, display no clear expression patterns (not shown). Since CHR motif has a strong strand bias in addition, and since genes that contain this motif yet on the nonpreferred strand have a non‐coherent expression profile (Supplementary Figure S6), for this motif we considered only genes that contain it in the preferred strand and distance from the TSS. Yuval Tabach et al. Mol Syst Biol 2005;1:2005.0022 © as stated in the article, figure or figure legend