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Files in this Data Supplement:
Fig. S1. Neural crest cells migrate superior to the stomodeum in smo- embryos. (A,C) Kaede protein was photoconverted at 12 hpf in wild-type (A) or smoh- (C) embryos. (B,D) At 18 hpf, neural crest cells had migrated dorsal to the stomodeum (arrow) in both wild-type (B) and smo- (D) embryos.
Fig. S2. Expression of shh is maintained in presumptive endoderm but not presumptive stomodeum of smoh- embryos. (A,B) Cross-sections taken at the posterior edge of the eye (arrowhead) show shh is expressed in presumptive stomodeum of wild-type (A, arrow), but not smoh- (B) embryos. (C,D) More posterior sections, still through the first arch, show shh is expressed by presumptive medial endoderm in both wild-type (C, arrow) and smoh- (D, arrow) embryos.
Fig. S3. Epithelial integrity of the stomodeum is intact in smo- embryos. Epithelial markers p63 (A,B) and pan-cadherin (C,D) are expressed in the stomodeum of both wild-type (A,C) and smo- embryos (B,D).
Fig. S4. Rescue of anterior craniofacial outgrowth by wild-type stomodeum in smo- embryos. (A,B) Confocal images show outgrowth of the developing anterior craniofacial domain (arrow) in 48 hpf wild-type (A) and smo- embryos receiving wild-type stomodeum transplants (B). (C) No outgrowth is evident in smo- embryos not receiving transplants.
Movie 1. Wild-type first arch crest cell migration and condensation.
Movie 2. Failure of crest cells to condense on the stomodeal roof in smo mutants.
Movie 3. Anterior craniofacial crest cells migrate posterior to the eye in smo- embryos.
Movie 4. Wild-type crest cells fail to condense on the stomodeal roof and migrate posterior to the eye in smo- hosts.
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