| Literature DB >> 26444186 |
Ahmad N Abou Tayoun1,2,3, Heather Mason-Suares2,4, Ashley L Frisella2, Mark Bowser2, Elizabeth Duffy2, Lisa Mahanta2, Birgit Funke2,4, Heidi L Rehm2,4, Sami S Amr2,4.
Abstract
Pathogenic variants at the DFNB1 locus encompassing the GJB2 and GJB6 genes account for 50% of autosomal-recessive, congenital nonsyndromic hearing loss in the United States. Most cases are caused by sequence variants within the GJB2 gene, but a significant number of DFNB1 patients carry a large deletion (GJB6-D13S1830) in trans with a GJB2 variant. This deletion lies upstream of GJB2 and was shown to reduce GJB2 expression by disrupting unidentified regulatory elements. First-tier genetic testing for hearing loss includes GJB2 sequence and GJB6-D13S1830 deletion analysis; however, several other deletions in this locus, each with distinct breakpoints, have been reported in DFNB1 patients and are missed by current panels. Here, we report the development of a targeted droplet digital polymerase chain reaction-based assay for comprehensive copy-number analysis at the DFNB1 locus that detects all deletions reported to date. This assay increased detection rates in a multiethnic cohort of 87 hearing loss patients with only one identified pathogenic GJB2 variant. We identify two deletions, one of which is novel, in two patients (2/87 or 2.3%), suggesting that other pathogenic deletions at the DFNB1 locus may be missed. Mapping the assayed DFNB1 deletions also revealed a ∼ 95 kb critical region, which may harbor the GJB2 regulatory element(s).Entities:
Keywords: DFNB1; GJB2; autosomal-recessive sensorineural hearing loss; copy-number variants; droplet digital PCR
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Year: 2015 PMID: 26444186 DOI: 10.1002/humu.22912
Source DB: PubMed Journal: Hum Mutat ISSN: 1059-7794 Impact factor: 4.878