Literature DB >> 16301217

Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells.

Avital Adato1, Gaëlle Lefèvre, Benjamin Delprat, Vincent Michel, Nicolas Michalski, Sébastien Chardenoux, Dominique Weil, Aziz El-Amraoui, Christine Petit.   

Abstract

Usher syndrome type IIa (USH2A) combines moderate to severe congenital hearing impairment and retinitis pigmentosa. It is the most common genetic form of USH. USH2A encodes usherin, which was previously defined as a basement membrane protein. A much larger USH2A transcript predicted to encode a transmembrane (TM) isoform was recently reported. Here, we address the role of TM usherin in the inner ear. Analysis of the usherin alternative transcripts in the murine inner ear revealed the existence of several predicted TM usherin isoforms with modular ectodomains of different lengths. In addition, we identified in the usherin cytoplasmic region a predicted 24 amino acid peptide, derived from a newly defined exon that is predominantly expressed in the inner ear but not in the retina. In mouse and rat inner ears, we show that TM usherin is present at the base of the differentiating stereocilia, which make up the mechanosensitive hair bundles receptive to sound. The usherin immunolabeling is transient in the hair bundles of cochlear hair cells (HCs), but persists in mature hair bundles of vestibular HCs. Several lines of evidence support the involvement of TM usherin in the composition of the ankle links, a subset of filamentous lateral links connecting stereocilia at the base. By co-immunoprecipitation and in vitro binding assays, we establish that the usherin cytodomain can bind to whirlin and harmonin, two PDZ domain-containing proteins that are defective in genetic forms of isolated deafness and USH type I, respectively. These PDZ proteins are suitable to provide the anchoring of interstereocilia lateral links to the F-actin core of stereocilia. Our results strongly suggest that congenital deafness in USH type I and type II shares similar pathogenic mechanisms, i.e. the disruption of hair bundle links-mediated adhesion forces that are essential for the proper organization of growing hair bundles.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16301217     DOI: 10.1093/hmg/ddi416

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  101 in total

1.  Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79.

Authors:  Atteeq Ur Rehman; Robert J Morell; Inna A Belyantseva; Shahid Y Khan; Erich T Boger; Mohsin Shahzad; Zubair M Ahmed; Saima Riazuddin; Shaheen N Khan; Sheikh Riazuddin; Thomas B Friedman
Journal:  Am J Hum Genet       Date:  2010-02-18       Impact factor: 11.025

2.  Mutational screening of the USH2A gene in Spanish USH patients reveals 23 novel pathogenic mutations.

Authors:  Gema Garcia-Garcia; Maria J Aparisi; Teresa Jaijo; Regina Rodrigo; Ana M Leon; Almudena Avila-Fernandez; Fiona Blanco-Kelly; Sara Bernal; Rafael Navarro; Manuel Diaz-Llopis; Montserrat Baiget; Carmen Ayuso; Jose M Millan; Elena Aller
Journal:  Orphanet J Rare Dis       Date:  2011-10-17       Impact factor: 4.123

3.  Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II.

Authors:  E Aller; T Jaijo; M Beneyto; C Nájera; S Oltra; C Ayuso; M Baiget; M Carballo; G Antiñolo; D Valverde; F Moreno; C Vilela; D Collado; H Pérez-Garrigues; A Navea; J M Millán
Journal:  J Med Genet       Date:  2006-11       Impact factor: 6.318

4.  Regulated vesicular trafficking of specific PCDH15 and VLGR1 variants in auditory hair cells.

Authors:  Marisa Zallocchi; Duane Delimont; Daniel T Meehan; Dominic Cosgrove
Journal:  J Neurosci       Date:  2012-10-03       Impact factor: 6.167

5.  Photoreceptors in whirler mice show defective transducin translocation and are susceptible to short-term light/dark changes-induced degeneration.

Authors:  Mei Tian; Weimin Wang; Duane Delimont; Linda Cheung; Marisa Zallocchi; Dominic Cosgrove; You-Wei Peng
Journal:  Exp Eye Res       Date:  2013-11-07       Impact factor: 3.467

Review 6.  Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.

Authors:  Pranav Mathur; Jun Yang
Journal:  Biochim Biophys Acta       Date:  2014-12-04

7.  Assembling stable hair cell tip link complex via multidentate interactions between harmonin and cadherin 23.

Authors:  Lifeng Pan; Jing Yan; Lin Wu; Mingjie Zhang
Journal:  Proc Natl Acad Sci U S A       Date:  2009-03-18       Impact factor: 11.205

8.  An USH2A founder mutation is the major cause of Usher syndrome type 2 in Canadians of French origin and confirms common roots of Quebecois and Acadians.

Authors:  Inga Ebermann; Robert K Koenekoop; Irma Lopez; Lara Bou-Khzam; Renée Pigeon; Hanno J Bolz
Journal:  Eur J Hum Genet       Date:  2008-07-30       Impact factor: 4.246

9.  Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.

Authors:  Mounira Hmani-Aifa; Zeineb Benzina; Fareeha Zulfiqar; Houria Dhouib; Amber Shahzadi; Abdelmonem Ghorbel; Ahmed Rebaï; Peter Söderkvist; Sheikh Riazuddin; William J Kimberling; Hammadi Ayadi
Journal:  Eur J Hum Genet       Date:  2008-10-15       Impact factor: 4.246

10.  Biochemical characterization of native Usher protein complexes from a vesicular subfraction of tracheal epithelial cells.

Authors:  Marisa Zallocchi; Joseph H Sisson; Dominic Cosgrove
Journal:  Biochemistry       Date:  2010-02-16       Impact factor: 3.162

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.