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Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.
- Source :
-
Human molecular genetics [Hum Mol Genet] 2001 Feb 01; Vol. 10 (3), pp. 195-200. - Publication Year :
- 2001
-
Abstract
- We identified Eyes absent 4 (EYA4), a member of the vertebrate Eya family of transcriptional activators, as the causative gene of postlingual, progressive, autosomal dominant hearing loss at the DFNA10 locus. In two unrelated families from Belgium and the USA segregating for deafness at this locus, we found different mutations in EYA4, both of which create premature stop codons. Although EYA proteins interact with members of the SIX and DACH protein families in a conserved network that regulates early embryonic development, this finding shows that EYA4 is also important post-developmentally for continued function of the mature organ of Corti.
- Subjects :
- Age of Onset
Alternative Splicing
Animals
Base Sequence
Chromosome Mapping
Chromosomes, Human, Pair 6 genetics
Cochlea embryology
Cochlea metabolism
DNA chemistry
DNA genetics
DNA Mutational Analysis
Deafness pathology
Ear, Inner metabolism
Female
Hearing Loss, Sensorineural pathology
Humans
In Situ Hybridization
Male
Mice
Mice, Inbred CBA
Mutation
Pedigree
Polymorphism, Single Nucleotide
Polymorphism, Single-Stranded Conformational
RNA, Messenger genetics
RNA, Messenger metabolism
Rats
Rats, Sprague-Dawley
Deafness genetics
Hearing Loss, Sensorineural genetics
Trans-Activators genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0964-6906
- Volume :
- 10
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Human molecular genetics
- Publication Type :
- Academic Journal
- Accession number :
- 11159937
- Full Text :
- https://doi.org/10.1093/hmg/10.3.195