A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

被引:414
作者
Yasunaga, S
Grati, M
Cohen-Salmon, M
El-Amraoui, A
Mustapha, M
Salem, N
El-Zir, E
Loiselet, J
Petit, C
机构
[1] Inst Pasteur, CNRS, URA 1968, Unite Genet Deficits Sensoriels, F-75724 Paris 15, France
[2] St Josephs Univ, Fac Med, Biochim Lab, Beyrouth, Lebanon
[3] Hop Sacre Coeur, Clin Audiol, Baabda, Brazilia, Lebanon
关键词
D O I
10.1038/7693
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Using a candidate gene approach, we identified a novel human gene, OTOF, underlying an autosomal recessive, nonsyndromic prelingual deafness, DFNB9. The same nonsense mutation was detected in four unrelated affected families of Lebanese origin. OTOF is the second member of a mammalian gene family related to Caenorhabditis elegans fer-1. It encodes a predicted cytosolic protein (of 1,230 aa) with three C2 domains and a single carboxy-terminal transmembrane domain. The sequence homologies and predicted structure of otoferlin, the protein encoded by OTOF, suggest its involvement in vesicle membrane fusion. In the inner ear, the expression of the orthologous mouse gene, mainly in the sensory hair cells, indicates that such a role could apply to synaptic vesicles.
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收藏
页码:363 / 369
页数:7
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