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PAX9 基因突变与牙齿缺失:综述

PAX9 gene mutations and tooth agenesis: A review.

机构信息

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.

出版信息

Clin Genet. 2017 Nov;92(5):467-476. doi: 10.1111/cge.12986. Epub 2017 Mar 30.

Abstract

Paired box 9 (PAX9) is one of the best-known transcription factors involved in the development of human dentition. Mutations in PAX9 gene could, therefore, seriously influence the number, position and morphology of the teeth in an affected individual. To date, over 50 mutations in the gene have been reported as associated with various types of dental agenesis (congenitally missing teeth) and other inherited dental defects or variations. The most common consequence of PAX9 gene mutation is the autosomal-dominant isolated (non-syndromic) oligodontia or hypodontia. In the present review, we are summarizing all known PAX9 mutations as well as their nature and precise loci in the DNA sequence of the gene. Where necessary, we have revised the loci of the mutations in line with the reference sequence of the PAX9 gene as it appears in the current DNA databases.

摘要

配对盒基因 9(PAX9)是参与人类牙齿发育的最知名的转录因子之一。因此,PAX9 基因突变会严重影响受影响个体牙齿的数量、位置和形态。迄今为止,已有 50 多种基因突变被报道与各种类型的牙齿缺失(先天性缺牙)和其他遗传性牙齿缺陷或变异有关。PAX9 基因突变的最常见后果是常染色体显性遗传孤立(非综合征性)少牙症或无牙症。在本综述中,我们总结了所有已知的 PAX9 突变及其在基因 DNA 序列中的性质和精确位置。在必要时,我们根据当前 DNA 数据库中 PAX9 基因的参考序列对突变位置进行了修正。

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