دورية أكاديمية
Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome.
| العنوان: | Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. |
|---|---|
| المؤلفون: | Alharatani, R, Ververi, A, Beleza-Meireles, A, Ji, W, Mis, E, Patterson, QT, Griffin, JN, Bhujel, N, Chang, CA, Dixit, A, Konstantino, M, Healy, C, Hannan, S, Neo, N, Cash, A, Li, D, Bhoj, E, Zackai, EH, Cleaver, R, Baralle, D, McEntagart, M, Newbury-Ecob, R, Scott, R, Hurst, JA, Au, PYB, Hosey, MT, Khokha, M, Marciano, DK, Lakhani, SA, Liu, KJ |
| بيانات النشر: | Oxford University Press |
| سنة النشر: | 2020 |
| المجموعة: | St George's University of London: Repository |
| الوصف: | CTNND1 encodes the p120-catenin (p120) protein, which has a wide range of functions, including the maintenance of cell-cell junctions, regulation of the epithelial-mesenchymal transition and transcriptional signalling. Due to advances in next-generation sequencing, CTNND1 has been implicated in human diseases including cleft palate and blepharocheilodontic (BCD) syndrome albeit only recently. In this study, we identify eight novel protein-truncating variants, six de novo, in 13 participants from nine families presenting with craniofacial dysmorphisms including cleft palate and hypodontia, as well as congenital cardiac anomalies, limb dysmorphologies and neurodevelopmental disorders. Using conditional deletions in mice as well as CRISPR/Cas9 approaches to target CTNND1 in Xenopus, we identified a subset of phenotypes that can be linked to p120-catenin in epithelial integrity and turnover, and additional phenotypes that suggest mesenchymal roles of CTNND1. We propose that CTNND1 variants have a wider developmental role than previously described and that variations in this gene underlie not only cleft palate and BCD but may be expanded to a broader velocardiofacial-like syndrome. |
| نوع الوثيقة: | article in journal/newspaper |
| وصف الملف: | application/pdf |
| اللغة: | English |
| العلاقة: | https://openaccess.sgul.ac.uk/id/eprint/112552/1/ddaa050.pdfTest; Alharatani, R; Ververi, A; Beleza-Meireles, A; Ji, W; Mis, E; Patterson, QT; Griffin, JN; Bhujel, N; Chang, CA; Dixit, A; et al. Alharatani, R; Ververi, A; Beleza-Meireles, A; Ji, W; Mis, E; Patterson, QT; Griffin, JN; Bhujel, N; Chang, CA; Dixit, A; Konstantino, M; Healy, C; Hannan, S; Neo, N; Cash, A; Li, D; Bhoj, E; Zackai, EH; Cleaver, R; Baralle, D; McEntagart, M; Newbury-Ecob, R; Scott, R; Hurst, JA; Au, PYB; Hosey, MT; Khokha, M; Marciano, DK; Lakhani, SA; Liu, KJ (2020) Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. Hum Mol Genet, 29 (11). pp. 1900-1921. ISSN 1460-2083 https://doi.org/10.1093/hmg/ddaa050Test SGUL Authors: McEntagart, Meriel |
| الإتاحة: | https://doi.org/10.1093/hmg/ddaa050Test https://openaccess.sgul.ac.uk/id/eprint/112552Test/ https://openaccess.sgul.ac.uk/id/eprint/112552/1/ddaa050.pdfTest |
| حقوق: | cc_by_4 |
| رقم الانضمام: | edsbas.E29FB66A |
| قاعدة البيانات: | BASE |
| الوصف غير متاح. |