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. 2019 Apr 18;9:6278. doi: 10.1038/s41598-019-42179-w

Figure 3.

Figure 3

Maternal DCAF13 affects zygotic genome activation by the two-cell stage. (a) Detection of newly synthesized RNA by 5-ethynyl uridine (EU) (in green) incorporation and the activity of polymerase II (POLII) (PSII in red) in two-cell embryos of Dcaf13+/+ or Dcaf13−/+ is shown (top), and the measurement of the intensity was indicated (bottom). Scale bar, 20 µm. *** to p < 0.001. Dcaf13+/+ (n = 10), Dcaf13−/+ (n = 10). (b) Heat map and cluster tree represented the relative mRNA levels of total transcripts in Dcaf13fl/fl and Dcaf13fl/fl;Zp3-Cre MII oocytes as well as Dcaf13+/+ or Dcaf13−/+ two-cell embryos. (c) Gene scatter plots showed that transcript levels increasing more than three folds in Dcaf13fl/fl;Zp3-Cre MII oocytes (Dcaf13fl/fl;Zp3-Cre/Dcaf13fl/fl > 3) were upregulated (red); Transcript levels decreasing more than three folds (Dcaf13fl/fl/Dcaf13fl/fl;Zp3-Cre > 3) were downregulated (blue) (top). Transcript levels increasing more than three folds in Dcaf13−/+ two-cell embryos were upregulated (red); transcript levels decreasing more than three folds in Dcaf13−/+ two-cell embryos were downregulated (blue) (bottom). (d) Gene ontology (GO) analysis plot and heat map indicated the function of transcripts whose levels increased (red) or decreased (blue) in Dcaf13−/+ two-cell embryos compared to control. (e) Heat map described the level change of transcripts encoding ribosomal proteins grouped by ribosome large and small subunit in Dcaf13−/+ two-cell embryos. The fold changes (Dcaf13−/+/Dcaf13+/+) were listed at the top of the boxes from white to blue (from large to small).