RESUMEN

Nonsyndromic orofacial cleft (NSOFC) is a complex disease of still unclear genetic etiology. To investigate the contribution of rare epithelial cadherin (CDH1) gene variants to NSOFC, we target sequenced 221 probands. Candidate variants were evaluated via in vitro, in silico, or segregation analyses. Three probably pathogenic variants (c.760G>A [p.Asp254Asn], c.1023T>G [p.Tyr341*], and c.2351G>A [p.Arg784His]) segregated according to autosomal dominant inheritance in four nonsyndromic cleft lip with or without cleft palate (NSCL/P) families (Lod score: 5.8 at θ = 0; 47% penetrance). A fourth possibly pathogenic variant (c.387+5G>A) was also found, but further functional analyses are needed (overall prevalence of CDH1 candidate variants: 2%; 15.4% among familial cases). CDH1 mutational burden was higher among probands from familial cases when compared to that of controls (P = 0.002). We concluded that CDH1 contributes to NSCL/P with mainly rare, moderately penetrant variants, and CDH1 haploinsufficiency is the likely etiological mechanism.

Asunto(s)

Encéfalo/anomalías , Cadherinas/genética , Labio Leporino/genética , Fisura del Paladar/genética , Variación Genética , Alelos , Sustitución de Aminoácidos , Animales , Antígenos CD , Cadherinas/química , Línea Celular , Labio Leporino/diagnóstico , Fisura del Paladar/diagnóstico , Análisis Mutacional de ADN , Genotipo , Mutación de Línea Germinal , Humanos , Mutación , Sistemas de Lectura Abierta , Penetrancia