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Novel compound heterozygous TMC1 mutations associated with autosomal recessive hearing loss in a Chinese family.

ABSTRACT: Hereditary nonsyndromic hearing loss is highly heterogeneous and most patients with a presumed genetic etiology lack a specific diagnosis. It has been estimated that several hundred genes may be associated with this sensory deficit in humans. Here, we identified compound heterozygous mutations in the TMC1 gene as the cause of recessively inherited sensorineural hearing loss by using whole-exome sequencing in a family with two deaf siblings. Sanger sequencing confirmed that both siblings inherited a missense mutation, c.589G>A p.G197R (maternal allele), and a nonsense mutation, c.1171C>T p.Q391X (paternal allele), in TMC1. We also used DNA from 50 Chinese familial patients with ARNSHL and 208 ethnicity-matched negative samples to perform extended variants analysis. Both variants co-segregated in family 1953, which had the hearing loss phenotype, but were absent in 50 patients and 208 ethnicity-matched controls. Therefore, we concluded that the hearing loss in this family was caused by novel compound heterozygous mutations in TMC1.

SUBMITTER: Gao X 

PROVIDER: S-EPMC3653921 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

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Novel compound heterozygous TMC1 mutations associated with autosomal recessive hearing loss in a Chinese family.

Gao Xue X   Su Yu Y   Guan Li-Ping LP   Yuan Yong-Yi YY   Huang Sha-Sha SS   Lu Yu Y   Wang Guo-Jian GJ   Han Ming-Yu MY   Yu Fei F   Song Yue-Shuai YS   Zhu Qing-Yan QY   Wu Jing J   Dai Pu P  

PloS one 20130514 5

Hereditary nonsyndromic hearing loss is highly heterogeneous and most patients with a presumed genetic etiology lack a specific diagnosis. It has been estimated that several hundred genes may be associated with this sensory deficit in humans. Here, we identified compound heterozygous mutations in the TMC1 gene as the cause of recessively inherited sensorineural hearing loss by using whole-exome sequencing in a family with two deaf siblings. Sanger sequencing confirmed that both siblings inherite  ...[more]

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