Genome-Wide Association Study Identifies Nox3 as a Critical Gene for Susceptibility to Noise-Induced Hearing Loss e1005094

• Published in: PLoS genetics Vol. 11; no. 4
• Main Authors: Lavinsky, Joel, Crow, Amanda L, Pan, Calvin, Wang, Juemei, Aaron, Ksenia A, Ho, Maria K, Li, Qingzhong, Salehide, Pehzman, Myint, Anthony, Monges-Hernadez, Maya, Eskin, Eleazar, Allayee, Hooman, Lusis, Aldons J, Friedman, Rick A
• Format: Journal Article
• Language: English
• Published: San Francisco Public Library of Science 01-04-2015
• Subjects: Enzymes; Genes; Genomes; Hearing loss; Hearing protection; Noise; Population; Rodents; Studies; Twins; United States > US
• ISSN: 1553-7390; 1553-7404
• DOI: 10.1371/journal.pgen.1005094

In the United States, roughly 10% of the population is exposed daily to hazardous levels of noise in the workplace. Twin studies estimate heritability for noise-induced hearing loss (NIHL) of approximately 36%, and strain specific variation in sensitivity has been demonstrated in mice. Based upon the difficulties inherent to the study of NIHL in humans, we have turned to the study of this complex trait in mice. We exposed 5 week-old mice from the Hybrid Mouse Diversity Panel (HMDP) to a 10 kHz octave band noise at 108 dB for 2 hours and assessed the permanent threshold shift 2 weeks post exposure using frequency specific stimuli. These data were then used in a genome-wide association study (GWAS) using the Efficient Mixed Model Analysis (EMMA) to control for population structure. In this manuscript we describe our GWAS, with an emphasis on a significant peak for susceptibility to NIHL on chromosome 17 within a haplotype block containing NADPH oxidase-3 (Nox3). Our peak was detected after an 8 kHz tone burst stimulus. Nox3 mutants and heterozygotes were then tested to validate our GWAS. The mutants and heterozygotes demonstrated a greater susceptibility to NIHL specifically at 8 kHz both on measures of distortion product otoacoustic emissions (DPOAE) and on auditory brainstem response (ABR). We demonstrate that this sensitivity resides within the synaptic ribbons of the cochlea in the mutant animals specifically at 8 kHz. Our work is the first GWAS for NIHL in mice and elucidates the power of our approach to identify tonotopic genetic susceptibility to NIHL.