Literature DB >> 26609154

Progressive Hearing Loss in Mice Carrying a Mutation in Usp53.

Marcin Kazmierczak1, Suzan L Harris1, Piotr Kazmierczak2, Prahar Shah1, Valentin Starovoytov1, Kevin K Ohlemiller3, Martin Schwander4.   

Abstract

Disordered protein ubiquitination has been linked to neurodegenerative disease, yet its role in inner ear homeostasis and hearing loss is essentially unknown. Here we show that progressive hearing loss in the ethylnitrosourea-generated mambo mouse line is caused by a mutation in Usp53, a member of the deubiquitinating enzyme family. USP53 contains a catalytically inactive ubiquitin-specific protease domain and is expressed in cochlear hair cells and a subset of supporting cells. Although hair cell differentiation is unaffected in mambo mice, outer hair cells degenerate rapidly after the first postnatal week. USP53 colocalizes and interacts with the tight junction scaffolding proteins TJP1 and TJP2 in polarized epithelial cells, suggesting that USP53 is part of the tight junction complex. The barrier properties of tight junctions of the stria vascularis appeared intact in a biotin tracer assay, but the endocochlear potential is reduced in adult mambo mice. Hair cell degeneration in mambo mice precedes endocochlear potential decline and is rescued in cochlear organotypic cultures in low potassium milieu, indicating that hair cell loss is triggered by extracellular factors. Remarkably, heterozygous mambo mice show increased susceptibility to noise injury at high frequencies. We conclude that USP53 is a novel tight junction-associated protein that is essential for the survival of auditory hair cells and normal hearing in mice, possibly by modulating the barrier properties and mechanical stability of tight junctions. SIGNIFICANCE STATEMENT: Hereditary hearing loss is extremely prevalent in the human population, but many genes linked to hearing loss remain to be discovered. Forward genetics screens in mice have facilitated the identification of genes involved in sensory perception and provided valuable animal models for hearing loss in humans. This involves introducing random mutations in mice, screening the mice for hearing defects, and mapping the causative mutation. Here, we have identified a mutation in the Usp53 gene that causes progressive hearing loss in the mambo mouse line. We demonstrate that USP53 is a catalytically inactive deubiquitinating enzyme and a novel component of tight junctions that is necessary for sensory hair cell survival and inner ear homeostasis.
Copyright © 2015 the authors 0270-6474/15/3515582-17$15.00/0.

Entities:  

Keywords:  Usp53; hearing loss; inner ear; mambo mice; tight junction; ubiquitin

Mesh:

Substances:

Year:  2015        PMID: 26609154      PMCID: PMC4659823          DOI: 10.1523/JNEUROSCI.1965-15.2015

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  71 in total

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Authors:  Emily Steed; Maria S Balda; Karl Matter
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Review 10.  Tight junctions: molecular architecture and function.

Authors:  Saima Aijaz; Maria S Balda; Karl Matter
Journal:  Int Rev Cytol       Date:  2006
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1.  Conditional deletion of pejvakin in adult outer hair cells causes progressive hearing loss in mice.

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Journal:  Neuroscience       Date:  2017-01-09       Impact factor: 3.590

2.  In vivo base editing restores sensory transduction and transiently improves auditory function in a mouse model of recessive deafness.

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7.  Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran.

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Review 8.  The role of ubiquitination and deubiquitination in the regulation of cell junctions.

Authors:  Junting Cai; Miranda K Culley; Yutong Zhao; Jing Zhao
Journal:  Protein Cell       Date:  2017-10-27       Impact factor: 14.870

9.  Expanding etiology of progressive familial intrahepatic cholestasis.

Authors:  Sarah Af Henkel; Judy H Squires; Mary Ayers; Armando Ganoza; Patrick Mckiernan; James E Squires
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10.  Knockdown of Ubiquitin-Specific Protease 53 Enhances the Radiosensitivity of Human Cervical Squamous Cell Carcinoma by Regulating DNA Damage-Binding Protein 2.

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