Premium
Novel mutations identified in patients with tooth agenesis by whole‐exome sequencing
Author(s) -
Zhao Kai,
Lian Meifei,
Zou Duohong,
Huang Wei,
Zhou Wenjie,
Shen Yihan,
Wang Feng,
Wu Yiqun
Publication year - 2019
Publication title -
oral diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.953
H-Index - 87
eISSN - 1601-0825
pISSN - 1354-523X
DOI - 10.1111/odi.13002
Subject(s) - exome sequencing , genetics , mutation , phenotype , biology , in silico , hypodontia , gene , medicine , dentistry
Objectives To identify potentially pathogenic mutations for tooth agenesis by whole‐exome sequencing. Subjects and Methods Ten Chinese families including five families with ectodermal dysplasia (syndromic tooth agenesis) and five families with selective tooth agenesis were included. Whole‐exome sequencing was performed using genomic DNA. Potentially pathogenic mutations were identified after data filtering and screening. The pathogenicity of novel variants was investigated by segregation analysis, in silico analysis, and functional studies. Results One novel mutation (c.441_442insACTCT) and three reported mutations (c.252delT, c.463C>T, and c.1013C>T) in EDA were identified in families with ectodermal dysplasia. The novel EDA mutation was co‐segregated with phenotype. A functional study revealed that NF‐κB activation was compromised by the identified mutations. The secretion of active EDA was also compromised detection by western blotting. Novel Wnt10A mutations (c.521T>C and c.653T>G) and EVC2 mutation (c.1472C>T) were identified in families with selective tooth agenesis. The Wnt10A c.521T>C mutation and the EVC2 c.1472C>T mutation were considered as pathogenic for affecting highly conserved amino acids, co‐segregated with phenotype and predicted to be disease‐causing by SIFT and PolyPhen2. Moreover, several reported mutations in PAX9, Wnt10A, and FGFR3 were also detected. Conclusions Our study expanded our knowledge on tooth agenesis spectrum by identifying novel variants.