Department of Orthodontics and Dentofacial Orthopedics, Institute of Health Biosciences, The University of Tokushima Graduate School, Tokushima, Japan.
J Dent Res. 2014 Mar;93(3):245-9. doi: 10.1177/0022034513519801. Epub 2014 Jan 16.
PAX9 is a transcription factor expressed in the tooth mesenchyme during tooth morphogenesis. In Pax9-null mice, tooth development is arrested at the bud stage. In humans, heterozygous mutations in PAX9 have been associated with non-syndromic tooth agenesis, predominantly in the molars. Here, we report 2 novel mutations in the paired domain of PAX9, a three-nucleotide deletion (73-75 delATC) and a missense mutation (C146T), in two unrelated Japanese patients with non-syndromic tooth agenesis. The individual with the 73-75del ATC mutation was missing all maxillary molars and mandibular second and third molars. The individual with the C146T mutation was missing the mandibular central incisors, maxillary second premolars, and first molars, along with all second and third molars. Both mutations affected amino acids that are highly conserved among different species and are critical for DNA binding. When both mutants were transfected to COS7 cells, nuclear localization of PAX9 proteins was not affected. However, reduced expression of the mutant proteins and almost no transcriptional activity of the target BMP4 gene were observed, suggesting haploinsufficiency of PAX9 as the cause of non-syndromic tooth agenesis.
PAX9 是一种在牙齿发生过程中表达于牙间质的转录因子。在 Pax9 基因敲除的小鼠中,牙齿发育在萌芽期停滞。在人类中,PAX9 的杂合突变与非综合征性牙齿缺失有关,主要影响磨牙。在这里,我们报道了 2 例非综合征性牙齿缺失的日本患者 PAX9 配对结构域中的 2 个新突变,一个是三核苷酸缺失(73-75delATC),另一个是错义突变(C146T)。73-75delATC 突变的个体缺失所有上颌磨牙和下颌第二和第三磨牙。C146T 突变的个体缺失下颌中切牙、上颌第二前磨牙和第一磨牙,以及所有第二和第三磨牙。这两个突变都影响了不同物种高度保守的氨基酸,这些氨基酸对 DNA 结合至关重要。当这两种突变体转染 COS7 细胞时,PAX9 蛋白的核定位没有受到影响。然而,观察到突变体蛋白的表达减少,以及靶基因 BMP4 的几乎没有转录活性,提示 PAX9 的单倍不足是导致非综合征性牙齿缺失的原因。