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. Author manuscript; available in PMC: 2016 Sep 1.
Published in final edited form as: Dev Biol. 2015 Jun 6;405(1):21–32. doi: 10.1016/j.ydbio.2015.05.024

Figure 6. Transcriptional control of stomach mesenchyme.

Figure 6

(A-B) Principal component analysis (A) and unsupervised hierarchical clustering (B) of gene expression profiles indicates reproducible data from replicate samples and similarities between cultured wild-type stomach and Barx1Int mesenchyme. (C) Heatmaps of mRNAs altered >2-fold in wild-type (WT) stomachs (left) and Barx1Int intestines (right), both compared to WT intestines. Red, elevated expression; blue, reduced expression. (D) Venn diagrams representing transcripts expressed at higher (red) and lower (blue) levels in control stomachs and Barx1Int intestines compared to WT intestines. (E) qRT-PCR evidence for expression of Flag-tagged Barx1 in immortalized embryonic stomach mesenchymal cells. (F) Significant enrichment of the BARX1 consensus motif at occupied sites. (G) Graph showing evolutionary conservation of BARX1 binding sites in 8 mammalian species. (H) Integrated Genome Viewer traces of input (blue) and BARX1 ChIP (crimson) fragment reads (tag counts are represented on the y-axis) at 3 significant binding sites (top 3 examples), including the Barx1 gene, and in the Isl1 locus (bottom example).