Fig. S4
furinA genetically interacts with edn1. Offspring of a furinAtg419/+ × edn1tf216b/+ cross were raised to adulthood. furinA/+;edn1/+ double heterozygote carriers were identified by PCR genotyping finclips. Double heterozygote carriers were mated and subsequent progeny were initially sorted into mutant and wild-type classes based on an open-mouth phenotype and ruffled fin phenotype. The heads of embryos were fixed and stained with Alcian green at 6 dpf and genomic DNA for genotyping was prepared from the tails. Loss of a single copy of edn1 in furinA mutants result in a high penetrance of severe reductions in the palatoquadrate (pq) and ceratohyal (ch) cartilages. edn1;furinA double mutants resemble edn1 single mutants. (A) wild-type, (B) furinAtg419, (C) furinAtg419;edn1tf216b/+, (D) edn1tf216b, (E) furinAtg419;edn1tf216b.
Reprinted from Developmental Biology, 295(1), Walker, M.B., Miller, C.T., Talbot, J.C., Stock, D.W., and Kimmel, C.B., Zebrafish furin mutants reveal intricacies in regulating Endothelin1 signaling in craniofacial patterning, 194-205, Copyright (2006) with permission from Elsevier. Full text @ Dev. Biol.