| First Author | Lana-Elola E | Year | 2011 |
| Journal | Hum Mol Genet | Volume | 20 |
| Issue | 20 | Pages | 4005-15 |
| PubMed ID | 21821669 | Mgi Jnum | J:175841 |
| Mgi Id | MGI:5287524 | Doi | 10.1093/hmg/ddr329 |
| Citation | Lana-Elola E, et al. (2011) Noggin null allele mice exhibit a microform of holoprosencephaly. Hum Mol Genet 20(20):4005-15 |
| abstractText | Holoprosencephaly (HPE) is a heterogeneous craniofacial and neural developmental anomaly characterized in its most severe form by the failure of the forebrain to divide. In humans, HPE is associated with disruption of Sonic hedgehog and Nodal signaling pathways, but the role of other signaling pathways has not yet been determined. In this study, we analyzed mice which, due to the lack of the Bmp antagonist Noggin, exhibit elevated Bmp signaling. Noggin(-/-) mice exhibited a solitary median maxillary incisor that developed from a single dental placode, early midfacial narrowing as well as abnormalities in the developing hyoid bone, pituitary gland and vomeronasal organ. In Noggin(-/-) mice, the expression domains of Shh, as well as the Shh target genes Ptch1 and Gli1, were reduced in the frontonasal region at key stages of early facial development. Using E10.5 facial cultures, we show that excessive BMP4 results in reduced Fgf8 and Ptch1 expression. These data suggest that increased Bmp signaling in Noggin(-/-) mice results in downregulation of the hedgehog pathway at a critical stage when the midline craniofacial structures are developing, which leads to a phenotype consistent with a microform of HPE. |
