Skip to main content
. Author manuscript; available in PMC: 2021 Oct 31.
Published in final edited form as: Science. 2021 Feb 5;371(6529):eabb4776. doi: 10.1126/science.abb4776

Fig. 4: Oct4 is dispensable for CNCC induction but essential for ectomesenchyme specification.

Fig. 4:

(A) Side and front views of E9.5 Oct4Flox/+; ActinCreER/+ and Oct4Flox/Flox; ActinCreER/+ embryos treated with tamoxifen at E6.5. Asterisks indicate reduced FNM in Oct4Flox/Flox; ActinCreER/+ embryos, black and yellow arrowheads point to BA1 and cephalic vesicle, respectively.

(B) Schematic representations of embryos shown in D. Asterisks indicate reduced FNM in Oct4Flox/Flox; ActinCreER/+ embryos, black and yellow arrowheads point to BA1 and cephalic vesicle, respectively.

(C) Side views of whole mount RNA FISH against Wnt1 performed on E8.5 Oct4Flox/+; ActinCreER/+ and Oct4Flox/Flox; ActinCreER/+ embryos treated with tamoxifen at E6.5. Images are maximum projections. Dashed line indicates the NF limit.

(D) Immunofluorescence against AP2α, pH3 and Sox10 within transverse cross-sections of E9.5 Oct4Flox/+; ActinCreER/+ and Oct4Flox/Flox; ActinCreER/+ embryos treated with tamoxifen at E6.5. Cranial ganglia (CG) are indicated by yellow dashed lines.

(E) Quantification of proportions of AP2α+ cells, Sox10+/AP2α+ cells and pH3+/Sox10+/AP2α+ cells in CG (top) and FNM (bottom). Error bars indicated mean ± SD. Mann-Whitney non-parametric statistical test; *** p < 0.001.