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- W2144519600 abstract "The development of the vertebrate face relies on the regionalization of neural crest-derived skeletal precursors along the dorsoventral (DV) axis. Here we show that Jagged-Notch signaling ensures dorsal identity within the hyoid and mandibular components of the facial skeleton by repressing ventral fates. In a genetic screen in zebrafish, we identified a loss-of-function mutation in jagged 1b (jag1b) that results in dorsal expansion of ventral gene expression and partial transformation of the dorsal hyoid skeleton to a ventral morphology. Conversely, misexpression of human jagged 1 (JAG1) represses ventral gene expression and dorsalizes the ventral hyoid and mandibular skeletons. We further show that jag1b is expressed specifically in dorsal skeletal precursors, where it acts through the Notch2 receptor to activate hey1 expression. Whereas Jagged-Notch positive feedback propagates jag1b expression throughout the dorsal domain, Endothelin 1 (Edn1) inhibits jag1b and hey1 expression in the ventral domain. Strikingly, reduction of Jag1b or Notch2 function partially rescues the ventral defects of edn1 mutants, indicating that Edn1 promotes facial skeleton development in part by inhibiting Jagged-Notch signaling in ventral skeletal precursors. Together, these results indicate a novel function of Jagged-Notch signaling in ensuring dorsal identity within broad fields of facial skeletal precursors." @default.
- W2144519600 created "2016-06-24" @default.
- W2144519600 creator A5010005812 @default.
- W2144519600 creator A5082104814 @default.
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- W2144519600 date "2010-06-01" @default.
- W2144519600 modified "2023-10-16" @default.
- W2144519600 title "Jagged-Notch signaling ensures dorsal skeletal identity in the vertebrate face" @default.
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- W2144519600 doi "https://doi.org/10.1242/dev.049056" @default.
- W2144519600 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2867320" @default.
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