Novel mutation of the initiation codon of PAX9 causes oligodontia.

Abstract

Tooth development is under strict genetic control. Oligodontia is defined as the congenital absence of 6 or more permanent teeth, excluding the third molar. The occurrence of non-syndromic oligodontia is poorly understood, but in recent years several cases have been described where a single gene mutation is associated with oligodontia. Several studies have shown that MSX1 and PAX9 play a role in early tooth development. We screened one family with non-syndromic oligodontia for mutations in MSX1 and PAX9. The pedigree showed an autosomal-dominant pattern of inheritance. Direct sequencing and restriction enzyme analysis revealed a novel heterozygous A to G transition mutation in the AUG initiation codon of PAX9 in exon 1 in the affected members of the family. This is the first mutation found in the initiation codon of PAX9, and we suggest that it causes haploinsufficiency.

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@article{Klein2005NovelMO, title={Novel mutation of the initiation codon of PAX9 causes oligodontia.}, author={Mary L. Klein and Pia Nieminen and Laura Lammi and Erik Niebuhr and Sven Kreiborg}, journal={Journal of dental research}, year={2005}, volume={84 1}, pages={43-7} }