Literature DB >> 11278165

Identification of the protein product of the Coch gene (hereditary deafness gene) as the major component of bovine inner ear protein.

T Ikezono1, A Omori, S Ichinose, R Pawankar, A Watanabe, T Yagi.   

Abstract

In order to better understand the cause of hereditary hearing impairment, we have performed a proteomic analysis of the inner ear proteins using two-dimensional gel electrophoresis. In the process of analysis, we have found very unique properties of the bovine homologue of the human COCH gene product. The COCH gene is responsible for one of the hereditary hearing impairments, DFNA9, and was recently suggested to be a possible genetic factor contributing to Ménière's disease. The Coch protein constitutes 70% of bovine inner ear proteins and is composed of 16 different protein spots, with charge and size heterogeneity. Heterogeneity of this protein suggests that the Coch gene is processed in several ways, at the transcriptional and/or posttranslational level. Much knowledge has accumulated about the hereditary hearing impairment genes; however, little research has been done regarding the protein products of those genes. This is the first report to characterize the Coch protein. Study of the Coch protein might provide more information on the mechanism of hearing and vestibular disorders.

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Year:  2001        PMID: 11278165     DOI: 10.1016/s0925-4439(00)00101-0

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  28 in total

Review 1.  Immunosuppressive therapy for autoimmune inner ear disease.

Authors:  Maria C Buniel; Katie Geelan-Hansen; Peter C Weber; Vincent K Tuohy
Journal:  Immunotherapy       Date:  2009-05       Impact factor: 4.196

2.  Cochlin expression in vestibular endorgans obtained from patients with Meniere's disease.

Authors:  Audrey P Calzada; Ivan A Lopez; Luis Beltran Parrazal; Akira Ishiyama; Gail Ishiyama
Journal:  Cell Tissue Res       Date:  2012-09-20       Impact factor: 5.249

3.  Distinct vestibular phenotypes in DFNA9 families with COCH variants.

Authors:  Bong Jik Kim; Ah Reum Kim; Kyu-Hee Han; Yoon Chan Rah; Jaihwan Hyun; Brandon S Ra; Ja-Won Koo; Byung Yoon Choi
Journal:  Eur Arch Otorhinolaryngol       Date:  2016-01-13       Impact factor: 2.503

4.  Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

Authors:  Sanjoy K Bhattacharya; Edward J Rockwood; Scott D Smith; Vera L Bonilha; John S Crabb; Rachel W Kuchtey; Nahid G Robertson; Neal S Peachey; Cynthia C Morton; John W Crabb
Journal:  J Biol Chem       Date:  2004-12-03       Impact factor: 5.157

5.  Murine autoimmune hearing loss mediated by CD4+ T cells specific for inner ear peptides.

Authors:  C Arturo Solares; Andrea E Edling; Justin M Johnson; Moo-Jin Baek; Keiko Hirose; Gordon B Hughes; Vincent K Tuohy
Journal:  J Clin Invest       Date:  2004-04       Impact factor: 14.808

6.  Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorder.

Authors:  Tomoko Makishima; Clara I Rodriguez; Nahid G Robertson; Cynthia C Morton; Colin L Stewart; Andrew J Griffith
Journal:  Hum Genet       Date:  2005-10-28       Impact factor: 4.132

7.  Subcellular localisation, secretion, and post-translational processing of normal cochlin, and of mutants causing the sensorineural deafness and vestibular disorder, DFNA9.

Authors:  N G Robertson; S A Hamaker; V Patriub; J C Aster; C C Morton
Journal:  J Med Genet       Date:  2003-07       Impact factor: 6.318

Review 8.  Human hereditary hearing impairment: mouse models can help to solve the puzzle.

Authors:  Karen Vrijens; Lut Van Laer; Guy Van Camp
Journal:  Hum Genet       Date:  2008-09-11       Impact factor: 4.132

9.  A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction.

Authors:  Nahid G Robertson; Sherri M Jones; Theru A Sivakumaran; Anne B S Giersch; Sara A Jurado; Linda M Call; Constance E Miller; Stéphane F Maison; M Charles Liberman; Cynthia C Morton
Journal:  Hum Mol Genet       Date:  2008-08-12       Impact factor: 6.150

10.  Cochlin isoforms and their interaction with CTL2 (SLC44A2) in the inner ear.

Authors:  P K Kommareddi; T S Nair; Y Raphael; S A Telian; A H Kim; H A Arts; H K El-Kashlan; T E Carey
Journal:  J Assoc Res Otolaryngol       Date:  2007-10-10
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