FAM20A is essential for amelogenesis, but is dispensable for dentinogenesis.

ABSTRACT: Mutations in the gene encoding family with sequence similarity 20, member A (FAM20A) caused amelogenesis imperfecta (AI), in humans. However, the roles of FAM20A in amelogenesis and dentinogenesis are poorly understood. In this study, we generated a Fam20a knockout (Sox2-Cre;Fam20a^fl/fl) mouse model by crossing Fam20a^fl/fl mice with Sox2-Cre transgenic mice, in which Fam20a was ablated in both dental epithelium and dental mesenchyme. We found that these mice developed an enamel phenotype that resembles human AI associated with FAM20A mutations, but did not have apparent dentin defects. The secretory stage ameloblasts in the mandibular incisors from the Sox2-Cre;Fam20a^fl/fl mice were shorter and detached from the enamel matrix, and subsequently lost their po

SUBMITTER: Li L 

PROVIDER: S-EPMC6861166 | biostudies-literature | 2019 Dec

REPOSITORIES: biostudies-literature