Enhancers and super-enhancers have an equivalent regulatory role in embryonic stem cells through regulation of single or multiple genes

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Figure 3.
Figure 3.

Transcriptional control of Dppa5a and Ooep by multiple enhancers. (A) Schematic representation of the Dppa5a/Ooep locus. Transcription factor-bound regions (red bars), MED1 and H3K27ac ChIP-seq and RNA-seq data obtained from the CODEX database are shown. Predicted enhancers (prEnh) and called super-enhancers (SEs) are shown in black. The deleted enhancer clusters, ΔEC(DppUp) and ΔEC(DppDn), are shown with a line that links the 5′ and 3′ gRNA targets. All data are displayed on the mm10 assembly of the UCSC Genome Browser. (B) Deletion of EC(DppDn) in clones carrying a homozygous deletion of EC(DppUp) greatly affects expression of the linked Dppa5a and Ooep alleles. Allele-specific primers detect 129 or Cast RNA in RT-qPCR from F1 ES, Δ129/+, Δ+/Cast, and Δ129/Cast clones. Expression is shown relative to the F1 ES 129 value. Error bars represent SEM. Significant differences from the F1 ES values are indicated: (*) P < 0.05, (**) P < 0.01, (***) P < 0.001. Significant differences from the parent ΔEC-Up129/Cast clone are indicated: (ΟΟ) P < 0.01, (ΟΟΟ) P < 0.001.

This Article

  1. Genome Res. 27: 246-258

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