Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome

Bethan E. Hoskins, Carl H. Cramer, Derek Silvius, Dan Zou, Richard M. Raymond, Dana J. Orten, William J. Kimberling, Richard J.H. Smith, Dominique Weil, Christine Petit, Edgar A. Otto, Pin Xian Xu, Friedhelm Hildebrandt

Research output: Contribution to journalArticlepeer-review

164 Scopus citations

Abstract

Branchio-oto-renal syndrome (BOR) is an autosomal dominant developmental disorder characterized by the association of branchial arch defects, hearing loss, and renal anomalies. Mutations in EYA1 are known to cause BOR. More recently, mutations in SIX1, which interacts with EYA1, were identified as an additional cause of BOR. A second member of the SIX family of proteins, unc-39 (SIX5), has also been reported to directly interact with eya-1 in Caenorhabditis elegans. We hypothesized that this interaction would be conserved in humans and that interactors of EYA1 represent good candidate genes for BOR. We therefore screened a cohort of 95 patients with BOR for mutations in SIX5. Four different heterozygous missense mutations were identified in five individuals. Functional analyses of these mutations demonstrated that two mutations affect EYA1-SIX5 binding and the ability of SIX5 or the EYA1-SIX5 complex to activate gene transcription. We thereby identified heterozygous mutations in SIX5 as a novel cause of BOR.

Original languageEnglish
Pages (from-to)800-804
Number of pages5
JournalAmerican Journal of Human Genetics
Volume80
Issue number4
DOIs
StatePublished - Apr 2007

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