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

被引:136
作者
Hoskins, Bethan E.
Cramer, Carl H., II
Silvius, Derek
Zou, Dan
Raymond, Richard M., Jr.
Orten, Dana J.
Kimberling, William J.
Smith, Richard J. H.
Weil, Dominique
Petit, Christine
Otto, Edgar A.
Xu, Pin-Xian
Hildebrandt, Friedhelm
机构
[1] Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA
[3] McLaughlin Res Inst Biomed Sci, Great Falls, MT USA
[4] Boys Town Natl Res Hosp, Usher Syndrome Ctr, Omaha, NE 68131 USA
[5] Univ Iowa, Dept Otolaryngol, Iowa City, IA 52242 USA
[6] Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA
[7] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[8] Inst Pasteur, INSERM, UMRS587, Unite Genet Deficits Sensoriels, F-75015 Paris, France
[9] CUNY Mt Sinai Sch Med, Dept Human Genet, New York, NY 10029 USA
关键词
D O I
10.1086/513322
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:800 / 804
页数:5
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