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Identification of a novel EXT1 mutation in patients with hereditary multiple exostosis by exome sequencing

Hereditary multiple exostosis (HME) is an autosomal inherited skeletal disease whose etiology is not fully understood. To further understand the genetic spectrum of the disease, we analyzed a five-generation Chinese family with HME that have observable inheritance. Exome sequencing was performed on...

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Detalles Bibliográficos
Autores principales: LIU, HONGJIE, WU, SONG, DUAN, LI, ZHU, WEIMING, ZHANG, SHIQUAN, HU, XIAOXIAO, JIA, WENLONG, YANG, GUOSHENG, LIU, CHUNXIAO, LI, WEIPING, YANG, LEI, GUO, LIJUN, LIN, YOUCHENG, WANG, YONGQIANG, HE, MEIJIAN, YANG, ZHAO, HE, YINGYING, CAI, ZHIMING, WANG, DAPING
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306274/
https://www.ncbi.nlm.nih.gov/pubmed/25421355
http://dx.doi.org/10.3892/or.2014.3610
Descripción
Sumario:Hereditary multiple exostosis (HME) is an autosomal inherited skeletal disease whose etiology is not fully understood. To further understand the genetic spectrum of the disease, we analyzed a five-generation Chinese family with HME that have observable inheritance. Exome sequencing was performed on three HME individuals and three unaffected individuals from the family. A downstream study confirmed a new C deletion at codon 442 on exon 5 of the exostosin-1 (EXT1) gene as the only pathogenic site which generated a stop codon and caused the truncation of the protein. We rediscovered the deletion in other affected individuals but not in the unaffected individuals from the family. Upon immunohistochemistry assay, we found that the EXT1 protein level of the patients with the novel mutation in our study was less than the level in the patients without the EXT1 mutation from another unrelated family. For a deeper understanding, we analyzed the mutation spectrum of the EXT1 gene. The present study should facilitate a further understanding of HME.