Byung Yoon Choi
Seoul National University Bundang Hospital, South Korea
Scientific Tracks Abstracts: J Mol Genet Med
Cochlear glia-like supporting cells (GLSs) have been suggested to play an important role in the development and maintenance of an auditory system. However, genes that are primarily expressed in GLSs have never been clearly associated with progressive human deafness. Herein, we present a novel deafness locus and a new human auditory neuropathy spectrum disorder (ANSD) gene, AUDITORIN mainly expressed in GLSs. We specify p.R372X of AUDITORIN as a cause of the significant deterioration of speech perception in humans. AUDITORIN was shown to encode a novel, cationic channel, contributing to the enigmatic passive conductance current in GLSs. This current is abolished by gene-silencing or in p.R372X knock-in mouse in a dominant-negative fashion. Because the pathogenic effect of this variant was limited to GLSs, a cochlear implant that electrically stimulates spiral ganglion neurons was performed on the affected ANSD subjects and their speech perception ability was successfully restored. Our study elucidates an unprecedented pathological role of a cochlear GLSs by identifying a novel deafness gene and its causal relationship with ANSD, introducing a new disease entity called auditory gliopathy and paving the way for precision medicine in deafness.
Byung-Yoon Choi is both a geneticist and otologic surgeon. He has her expertise in genetic deafness and customized auditory rehabilitation based on genetic etiology. He pursues a discovery a new deafness gene and elucidation of a function of the genes. He is specially interested in application of the information obtained from the bench into clinics.
E-mail: choiby2010@gmail.com
Molecular and Genetic Medicine received 3919 citations as per Google Scholar report
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