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. 2020 Mar 26;14(4):551–560. doi: 10.1016/j.stemcr.2020.02.011

Figure 4.

Figure 4

Dnmt3a and Tet2 Loss of Function Alter Hematopoietic Progenitor Function through Distinct Molecular Mechanisms

(A) Principal-component analysis plot of gene expression in ControlVav HSCs (n = 3) and MPP3 (n = 4), Dnmt3a-KOVav HSCs (n = 3), and Tet2-KOVav HSCs (n = 4) and MPP3 (n = 4).

(B) Venn diagrams displaying DEG overlap in Dnmt3a-KOVav and Tet2-KOVav HSCs compared with ControlVav HSCs.

(C) Heatmaps displaying DEGs (p < 0.05, fold-change >1 or <−1) between ControlVav and Tet2-KOVav HSCs and MPP3.

(D) Gene set enrichment analysis showing differentially regulated pathways between ControlVav and Tet2-KOVav MPP3.

(E) Gene score enrichment plot of “Hallmark TNFα Signaling via NFkB” gene set in Tet2-KOVav MPP3.

(F) ATAC-seq heatmaps from ControlVav, Dnmt3a-KOVav, and Tet2-KOVav mice. Signals displayed are peaks 1 kb up- and downstream of transcription start sites of protein coding genes.

(G) Multi-dimensional scaling plot with distances approximating the largest log2 fold-changes in the top 500 peaks between ATAC-seq samples.