Hedgehog signaling is required for cranial neural crest morphogenesis and chondrogenesis at the midline in the zebrafish skull
Development Wada et al.
132: 3977
DEV01943 Supplementary Material
Files in this Data Supplement:
Supplemental Figure 1
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Fig. S1. Labeling
of individual premigratory NC cells with iontophoresis at 13 hpf, and their
descendants in the ANC. (A,B) NC dorsal to the eye form medial ethmoid. (C,D)
NC posterior to the eye form trabecular cartilage.
Supplemental Figure 2
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Fig. S2. A
comparison of iontophoretic and PKH26 labeling of postmigratory NC cells at 22
hpf. (A,B,E,F,I,J) Iontophoresis; (C,D,G,H,K,L) PKH26. (A-D) NC at the anterior
end of the head forms medial ethmoid. (E-H) NC beneath the eye forms lateral
ethmoid and trabecular cartilage. (I-L) NC posterior to the eye forms
trabeculae.
Supplemental Figure 3
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Fig. S3. NC
transplants from smu mutant donors migrate but do not form
cartilage in wild-type hosts. (A) Schematic representation of transplantation.
(B-E) Lateral (B) and dorsal (C-E) views of Alcian-Blue-stained mosaic larvae,
whole mounted at 5 dpf. Transplanted mutant cells (brown) never form cartilage,
unlike wild-type controls.
Movie 1
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Movie 1. A 6-hour,
confocal time-lapsed movie of a sox10:egfp transgenic showing
cranial NC migration. Lateral view. Confocal stacks were collected every 10
minutes from 14-20 hpf, and projected at each time point. (A-C) Initially,
labeled NC cells remain posterior to the forming optic vesicle, and then begin
to migrate dorsal or medial to the optic vesicle. (D) Examples of migration
paths of individual cells followed through stacks in this movie.