Implications for tooth development on ENU-induced ectodermal dysplasia mice

BACKGROUND: In this study, the mutated phenotypes were produced by treatment of chemical mutagen, N‐ethyl‐N‐nitrosourea (ENU). We analyzed the mutated mice showing the specific phenotype of ectodermal dysplasia (ED) and examined the affected gene. METHODS: Phenotypes, including size, bone formation, and craniofacial morphology of ENU‐induced ED mice, were focused. Tooth development and expression of several molecules were analyzed by histologic observations and immunohistochemistry. We carried out genome‐wide screening and quantitative real‐time PCR to define the affected and related genes. RESULTS: As examined previously in human ectodermal dysplasia, ENU‐induced ED mice showed the specific morphologic deformities in tooth, hair, and craniofacial growth. Tooth development in the ENU‐induced ED mice ceased at early cap stage. In addition, skeletal staining showed retardation in craniofacial development. Finally, the affected gene, which would be involved in the mechanism of ED, was located between the marker D3Mit14 and D3Mit319 on chromosome 3. CONCLUSIONS: The affected gene in ENU‐induced ED mice showed several defects in ectodermal organogenesis and these results indicate that this gene plays an important role in mouse embryogenesis. Birth Defects Res (Part B) 2008. © 2008 Wiley‐Liss, Inc.