| Literature DB >> 29348693 |
Anneke Kievit1, Federico Tessadori2,3, Hannie Douben4, Ingrid Jordens2, Madelon Maurice2, Jeannette Hoogeboom4, Raoul Hennekam5, Sheela Nampoothiri6, Hülya Kayserili7, Marco Castori8, Margo Whiteford9, Connie Motter10, Catherine Melver10, Michael Cunningham11, Anne Hing11, Nancy M Kokitsu-Nakata12, Siulan Vendramini-Pittoli12, Antonio Richieri-Costa12, Annette F Baas2, Corstiaan C Breugem13, Karen Duran2, Maarten Massink2, Patrick W B Derksen14, Wilfred F J van IJcken15, Leontine van Unen4, Fernando Santos-Simarro16, Pablo Lapunzina16, Vera L Gil-da Silva Lopes17, Elaine Lustosa-Mendes17, Max Krall18, Anne Slavotinek18, Victor Martinez-Glez16, Jeroen Bakkers3,19, Koen L I van Gassen2, Annelies de Klein4, Marie-José H van den Boogaard2, Gijs van Haaften20.
Abstract
Blepharocheilodontic syndrome (BCDS) consists of lagophthalmia, ectropion of the lower eyelids, distichiasis, euryblepharon, cleft lip/palate and dental anomalies and has autosomal dominant inheritance with variable expression. We identified heterozygous variants in two genes of the cadherin-catenin complex, CDH1, encoding E-cadherin, and CTNND1, encoding p120 catenin delta1 in 15 of 17 BCDS index patients, as was recently described in a different publication. CDH1 plays an essential role in epithelial cell adherence; CTNND1 binds to CDH1 and controls the stability of the complex. Functional experiments in zebrafish and human cells showed that the CDH1 variants impair the cell adhesion function of the cadherin-catenin complex in a dominant-negative manner. Variants in CDH1 have been linked to familial hereditary diffuse gastric cancer and invasive lobular breast cancer; however, no cases of gastric or breast cancer have been reported in our BCDS cases. Functional experiments reported here indicated the BCDS variants comprise a distinct class of CDH1 variants. Altogether, we identified the genetic cause of BCDS enabling DNA diagnostics and counseling, in addition we describe a novel class of dominant negative CDH1 variants.Entities:
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Year: 2018 PMID: 29348693 PMCID: PMC5838974 DOI: 10.1038/s41431-017-0010-5
Source DB: PubMed Journal: Eur J Hum Genet ISSN: 1018-4813 Impact factor: 4.246