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. 2014 Mar 31;111(15):E1491–E1500. doi: 10.1073/pnas.1400568111

Fig. 4.

Fig. 4.

Hh, but not Wnt, signaling is disrupted in Sas4−/− mutants. (AD) Hh-dependent ventral cell types in the neural tube of E9.5 wild-type and Sas4−/− p53−/− embryos. In Sas4−/− p53−/− embryos floor plate cells (FOXA2, red) and V3 interneurons (NKX2.2, green) are absent (compare A and B), and PAX6+ interneurons (green) occupy the ventral neural tube (compare C and D). (E and F) The activity of the canonical Wnt reporter TOPGAL (blue) is normal in E8.5 Sas4−/− mutants. (GL) The PCP noncanonical Wnt signaling protein VANGL2 (green) localizes to the anterior/posterior (horizontal) faces of the cells in the embryonic node of both wild-type (GI) and Sas4−/− p53−/− embryos (JL) at E7.75. Rhodamine-conjugated phalloidin (red) marks F-actin at cell borders. (Scale bars: 300 µm in AF, 3 µm in GL.)