| Literature DB >> 18351662 |
Mary Anne Potok1, Kelly B Cha, Andrea Hunt, Michelle L Brinkmeier, Michael Leitges, Andreas Kispert, Sally A Camper.
Abstract
We examined the role of WNT signaling in pituitary development by characterizing the pituitary phenotype of three WNT knockout mice and assessing the expression of WNT pathway components. Wnt5a mutants have expanded domains of Fgf10 and bone morphogenetic protein expression in the ventral diencephalon and a reduced domain of LHX3 expression in Rathke's pouch. Wnt4 mutants have mildly reduced cell differentiation, reduced POU1F1 expression, and mild anterior lobe hypoplasia. Wnt4, Wnt5a double mutants exhibit an additive pituitary phenotype of dysmorphology and mild hypoplasia. Wnt6 mutants have no obvious pituitary phenotype. We surveyed WNT expression and identified transcripts for numerous Wnts, Frizzleds, and downstream pathway members in the pituitary and ventral diencephalon. These findings support the emerging model that WNT signaling affects the pituitary gland via effects on ventral diencephalon signaling, and suggest additional Wnt genes that are worthy of functional studies. (c) 2008 Wiley-Liss, Inc.Entities:
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Year: 2008 PMID: 18351662 PMCID: PMC2799114 DOI: 10.1002/dvdy.21511
Source DB: PubMed Journal: Dev Dyn ISSN: 1058-8388 Impact factor: 3.780