Šerý Omar, Bonczek Ondřej, Hloušková Alena, Černochová Pavlína, Vaněk Jiří, Míšek Ivan, Krejčí Přemysl, Izakovičová Hollá Lydie
Laboratory of DNA Diagnostics, Department of Biochemistry, Faculty of Science, Masaryk University, Brno, Czech Republic; Laboratory of Animal Embryology, Institute of Animal Physiology and Genetics, The Academy of Sciences of the Czech Republic, Brno, Czech Republic.
Eur J Oral Sci. 2015 Apr;123(2):65-71. doi: 10.1111/eos.12170. Epub 2015 Feb 14.
Tooth agenesis is one of the most common developmental anomalies in humans. To date, many mutations involving paired box 9 (PAX9), msh homeobox 1 (MSX1), and axin 2 (AXIN2) genes have been identified. The aim of the present study was to perform screening for mutations and/or polymorphisms using the capillary sequencing method in the critical regions of PAX9 and MSX1 genes in a group of 270 individuals with tooth agenesis and in 30 healthy subjects of Czech origin. This screening revealed a previously unknown heterozygous g.9527G>T mutation in the PAX9 gene in monozygotic twins with oligodontia and three additional affected family members. The same variant was not found in healthy relatives. This mutation is located in intron 2, in the region recognized as the splice site between exon 2 and intron 2. We hypothesize that the error in pre-mRNA splicing may lead to lower expression of PAX9 protein and could have contributed to the development of tooth agenesis in the affected subjects.
牙齿发育不全是人类最常见的发育异常之一。迄今为止,已经鉴定出许多涉及配对盒9(PAX9)、肌节同源盒1(MSX1)和轴抑制蛋白2(AXIN2)基因的突变。本研究的目的是采用毛细管测序法,对270名牙齿发育不全个体和30名捷克裔健康受试者的PAX9和MSX1基因关键区域进行突变和/或多态性筛查。该筛查在患有少牙症的同卵双胞胎及另外三名受影响家庭成员中发现了PAX9基因中一个先前未知的杂合g.9527G>T突变。在健康亲属中未发现相同变异。该突变位于内含子2中,处于外显子2和内含子2之间被认为是剪接位点的区域。我们推测,前体mRNA剪接错误可能导致PAX9蛋白表达降低,并可能促成了受影响受试者牙齿发育不全的发生。