Nature genetics · 2012
Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Riazuddin Saima, Belyantseva Inna A, Giese Arnaud P J, Lee Kwanghyuk, Indzhykulian Artur A, Nandamuri Sri Pratima, Yousaf Rizwan, Sinha Ghanshyam P, Lee Sue, Terrell David, Hegde Rashmi S, Ali Rana A, Anwar Saima, Andrade-Elizondo Paula B, Sirmaci Asli, Parise Leslie V, Basit Sulman, Wali Abdul, Ayub Muhammad, Ansar Muhammad, Ahmad Wasim, Khan Shaheen N, Akram Javed, Tekin Mustafa, Riazuddin Sheikh, Cook Tiffany, Buschbeck Elke K, Frolenkov Gregory I, Leal Suzanne M, Friedman Thomas B, Ahmed Zubair M
Аннотация
Sensorineural hearing loss is genetically heterogeneous. Here, we report that mutations in CIB2, which encodes a calcium- and integrin-binding protein, are associated with nonsyndromic deafness (DFNB48) and Usher syndrome type 1J (USH1J). One mutation in CIB2 is a prevalent cause of deafness DFNB48 in Pakistan; other CIB2 mutations contribute to deafness elsewhere in the world. In mice, CIB2 is localized to the mechanosensory stereocilia of inner ear hair cells and to retinal photoreceptor and pigmented epithelium cells. Consistent with molecular modeling predictions of calcium binding, CIB2 significantly decreased the ATP-induced calcium responses in heterologous cells, whereas mutations in deafness DFNB48 altered CIB2 effects on calcium responses. Furthermore, in zebrafish and Drosophila melanogaster, CIB2 is essential for the function and proper development of hair cells and retinal photoreceptor cells. We also show that CIB2 is a new member of the vertebrate Usher interactome.