ZFIN ID: ZDB-PUB-111027-51
Examination of a palatogenic gene program in zebrafish
Swartz, M.E., Sheehan-Rooney, K., Dixon, M.J., and Eberhart, J.K.
Date: 2011
Source: Developmental dynamics : an official publication of the American Association of Anatomists 240(9): 2204-2220 (Journal)
Registered Authors: Eberhart, Johann, Sheehan-Rooney, Kelly, Swartz, Mary
Keywords: cranial neural crest cells, palatal skeleton, zebrafish, anterior neurocranium, gene regulatory network, fate mapping
MeSH Terms: Animals; Fibroblast Growth Factor 10/genetics; Fibroblast Growth Factor 10/metabolism; Gene Expression Regulation, Developmental; In Situ Hybridization (all 19) expand
PubMed: 22016187 Full text @ Dev. Dyn.
FIGURES   (current status)

Human palatal clefting is debilitating and difficult to rectify surgically. Animal models enhance our understanding of palatogenesis and are essential in strategies designed to ameliorate palatal malformations in humans. Recent studies have shown that the zebrafish palate, or anterior neurocranium, is under similar genetic control to the amniote palatal skeleton. We extensively analyzed palatogenesis in zebrafish to determine the similarity of gene expression and function across vertebrates. By 36 hours postfertilization (hpf) palatogenic cranial neural crest cells reside in homologous regions of the developing face compared with amniote species. Transcription factors and signaling molecules regulating mouse palatogenesis are expressed in similar domains during palatogenesis in zebrafish. Functional investigation of a subset of these genes, fgf10a, tgfb2, pax9, and smad5 revealed their necessity in zebrafish palatogenesis. Collectively, these results suggest that the gene regulatory networks regulating palatogenesis may be conserved across vertebrate species, demonstrating the utility of zebrafish as a model for palatogenesis.