Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86.

TitleMutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86.
Publication TypeJournal Article
Year of Publication2014
AuthorsRehman, AU, Santos-Cortez, RLyn P, Morell, RJ, Drummond, MC, Ito, T, Lee, K, Khan, AA, Basra, MAsim R, Wasif, N, Ayub, M, Ali, RA, Raza, SI, Nickerson, DA, Shendure, J, Bamshad, M, Riazuddin, S, Billington, N, Khan, SN, Friedman, PL, Griffith, AJ, Ahmad, W, Riazuddin, S, Leal, SM, Friedman, TB
Corporate AuthorsUniversity of Washington Center for Mendelian Genomics
JournalAm J Hum Genet
Volume94
Issue1
Pagination144-52
Date Published2014 Jan 02
ISSN1537-6605
KeywordsAlleles, Amino Acid Sequence, Carrier Proteins, Chromosomes, Human, Pair 16, Consanguinity, Deafness, Epilepsy, Exome, Exons, Female, Genes, Recessive, Genetic Loci, Genome-Wide Association Study, Heterozygote, Homozygote, Humans, Male, Molecular Sequence Data, Mutation, Pakistan, Pedigree, Phenotype, Polymorphism, Single Nucleotide, RNA, Messenger, Sequence Analysis, DNA
Abstract

Inherited deafness is clinically and genetically heterogeneous. We recently mapped DFNB86, a locus associated with nonsyndromic deafness, to chromosome 16p. In this study, whole-exome sequencing was performed with genomic DNA from affected individuals from three large consanguineous families in which markers linked to DFNB86 segregate with profound deafness. Analyses of these data revealed homozygous mutation c.208G>T (p.Asp70Tyr) or c.878G>C (p.Arg293Pro) in TBC1D24 as the underlying cause of deafness in the three families. Sanger sequence analysis of TBC1D24 in an additional large family in which deafness segregates with DFNB86 identified the c.208G>T (p.Asp70Tyr) substitution. These mutations affect TBC1D24 amino acid residues that are conserved in orthologs ranging from fruit fly to human. Neither variant was observed in databases of single-nucleotide variants or in 634 chromosomes from ethnically matched control subjects. TBC1D24 in the mouse inner ear was immunolocalized predominantly to spiral ganglion neurons, indicating that DFNB86 deafness might be an auditory neuropathy spectrum disorder. Previously, six recessive mutations in TBC1D24 were reported to cause seizures (hearing loss was not reported) ranging in severity from epilepsy with otherwise normal development to epileptic encephalopathy resulting in childhood death. Two of our four families in which deafness segregates with mutant alleles of TBC1D24 were available for neurological examination. Cosegregation of epilepsy and deafness was not observed in these two families. Although the causal relationship between genotype and phenotype is not presently understood, our findings, combined with published data, indicate that recessive alleles of TBC1D24 can cause either epilepsy or nonsyndromic deafness.

DOI10.1016/j.ajhg.2013.12.004
Alternate JournalAm. J. Hum. Genet.
PubMed ID24387994
PubMed Central IDPMC3882911
Grant ListU54 HG006493 / HG / NHGRI NIH HHS / United States
Z01 DC000060 / DC / NIDCD NIH HHS / United States
R01 DC011651 / DC / NIDCD NIH HHS / United States
N01 HG065403 / HG / NHGRI NIH HHS / United States
R01 DC011748 / DC / NIDCD NIH HHS / United States
Z01 DC000039 / DC / NIDCD NIH HHS / United States
DC000039-16 / DC / NIDCD NIH HHS / United States
R01 DC003594 / DC / NIDCD NIH HHS / United States
DC000060-12 / DC / NIDCD NIH HHS / United States
Z01 HL004232 / HL / NHLBI NIH HHS / United States
T32 DC000039 / DC / NIDCD NIH HHS / United States
K08 HL004232 / HL / NHLBI NIH HHS / United States
UM1 HG006493 / HG / NHGRI NIH HHS / United States
R01 DC011803 / DC / NIDCD NIH HHS / United States