| Literature DB >> 28686854 |
Yavuz Bayram1, Janson J White1, Nursel Elcioglu2, Megan T Cho3, Neda Zadeh4, Asuman Gedikbasi5, Sukru Palanduz5, Sukru Ozturk5, Kivanc Cefle5, Ozgur Kasapcopur6, Zeynep Coban Akdemir1, Davut Pehlivan7, Amber Begtrup3, Claudia M B Carvalho1, Ingrid Sophie Paine1, Ali Mentes8, Kivanc Bektas-Kayhan9, Ender Karaca1, Shalini N Jhangiani10, Donna M Muzny10, Richard A Gibbs11, James R Lupski12.
Abstract
Hereditary gingival fibromatosis (HGF) is the most common genetic form of gingival fibromatosis that develops as a slowly progressive, benign, localized or generalized enlargement of keratinized gingiva. HGF is a genetically heterogeneous disorder and can be transmitted either as an autosomal-dominant or autosomal-recessive trait or appear sporadically. To date, four loci (2p22.1, 2p23.3-p22.3, 5q13-q22, and 11p15) have been mapped to autosomes and one gene (SOS1) has been associated with the HGF trait observed to segregate in a dominant inheritance pattern. Here we report 11 individuals with HGF from three unrelated families. Whole-exome sequencing (WES) revealed three different truncating mutations including two frameshifts and one nonsense variant in RE1-silencing transcription factor (REST) in the probands from all families and further genetic and genomic analyses confirmed the WES-identified findings. REST is a transcriptional repressor that is expressed throughout the body; it has different roles in different cellular contexts, such as oncogenic and tumor-suppressor functions and hematopoietic and cardiac differentiation. Here we show the consequences of germline final-exon-truncating mutations in REST for organismal development and the association with the HGF phenotype.Entities:
Keywords: RE1-silencing transcription factor; REST; gingival fibromatosis; mosaic mutation; nonsense-mediated decay; whole-exome sequencing
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Year: 2017 PMID: 28686854 PMCID: PMC5501868 DOI: 10.1016/j.ajhg.2017.06.006
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025