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. 2019 Jan 3;24(1):138–152.e8. doi: 10.1016/j.stem.2018.12.001

Figure 5.

Figure 5

Regulation of Meso-endoderm Differentiation by Dpf2 and Eed via Tbx3

(A) Clustering of Dpf2 binding events in ESCs and day 2 and 4 EBs. The genome was divided into 500-bp bins and a bin called bound (blue) or unbound (white) based on the presence of a DPF2 peak.

(B) GO analysis for enriched biological process for genes associated with DPF2 peaks from different clusters defined in (A), within ± 20 kb of the TSS.

(C) Transcript levels of the indicated endoderm markers in day 4 EBs from Dpf2fl/fl, Eed−/−, and Eed/Dpf2 double KO determined by qPCR.

(D) As in (C), except for pluripotency-associated genes in Dpf2fl/fl, Dpf2−/−, Eed−/−, and Dpf2 and Eed double KO ESCs.

(E) As in (C), except for Tbx3 in day 4 EBs from Dpf2fl/fl, Eed−/−, and Eed/Dpf2 double KO ESCs.

(F) As in (C), except for various endoderm markers in 4-day EBs induced from Eed−/− and Eed−/−/Tbx3 kd ESCs.

(G) As in (C), except for various mesoderm markers and Tbx3 in day 7 EBs from Dpf2fl/fl, Eed−/−, and Eed/Dpf2 double KO ESCs.

(H) As in (C), except for various neuroectoderm markers in day 6 EBs from Dpf2fl/fl, Dpf2−/−, and Eed/Dpf2 double KO ESCs.