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Otolith tethering in the zebrafish otic vesicle requires Otogelin and α-Tectorin

Otoliths are biomineralised structures important for balance and hearing in fish. Their counterparts in the mammalian inner ear, otoconia, have a primarily vestibular function. Otoliths and otoconia form over sensory maculae and are attached to the otolithic membrane, a gelatinous extracellular matr...

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Autores principales: Stooke-Vaughan, Georgina A., Obholzer, Nikolaus D., Baxendale, Sarah, Megason, Sean G., Whitfield, Tanya T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4360185/
https://www.ncbi.nlm.nih.gov/pubmed/25758224
http://dx.doi.org/10.1242/dev.116632
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author Stooke-Vaughan, Georgina A.
Obholzer, Nikolaus D.
Baxendale, Sarah
Megason, Sean G.
Whitfield, Tanya T.
author_facet Stooke-Vaughan, Georgina A.
Obholzer, Nikolaus D.
Baxendale, Sarah
Megason, Sean G.
Whitfield, Tanya T.
author_sort Stooke-Vaughan, Georgina A.
collection PubMed
description Otoliths are biomineralised structures important for balance and hearing in fish. Their counterparts in the mammalian inner ear, otoconia, have a primarily vestibular function. Otoliths and otoconia form over sensory maculae and are attached to the otolithic membrane, a gelatinous extracellular matrix that provides a physical coupling between the otolith and the underlying sensory epithelium. In this study, we have identified two proteins required for otolith tethering in the zebrafish ear, and propose that there are at least two stages to this process: seeding and maintenance. The initial seeding step, in which otolith precursor particles tether directly to the tips of hair cell kinocilia, fails to occur in the einstein (eis) mutant. The gene disrupted in eis is otogelin (otog); mutations in the human OTOG gene have recently been identified as causative for deafness and vestibular dysfunction (DFNB18B). At later larval stages, maintenance of otolith tethering to the saccular macula is dependent on tectorin alpha (tecta) function, which is disrupted in the rolling stones (rst) mutant. α-Tectorin (Tecta) is a major constituent of the tectorial membrane in the mammalian cochlea. Mutations in the human TECTA gene can cause either dominant (DFNA8/12) or recessive (DFNB21) forms of deafness. Our findings indicate that the composition of extracellular otic membranes is highly conserved between mammals and fish, reinforcing the view that the zebrafish is an excellent model system for the study of deafness and vestibular disease.
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spelling pubmed-43601852015-04-02 Otolith tethering in the zebrafish otic vesicle requires Otogelin and α-Tectorin Stooke-Vaughan, Georgina A. Obholzer, Nikolaus D. Baxendale, Sarah Megason, Sean G. Whitfield, Tanya T. Development Research Article Otoliths are biomineralised structures important for balance and hearing in fish. Their counterparts in the mammalian inner ear, otoconia, have a primarily vestibular function. Otoliths and otoconia form over sensory maculae and are attached to the otolithic membrane, a gelatinous extracellular matrix that provides a physical coupling between the otolith and the underlying sensory epithelium. In this study, we have identified two proteins required for otolith tethering in the zebrafish ear, and propose that there are at least two stages to this process: seeding and maintenance. The initial seeding step, in which otolith precursor particles tether directly to the tips of hair cell kinocilia, fails to occur in the einstein (eis) mutant. The gene disrupted in eis is otogelin (otog); mutations in the human OTOG gene have recently been identified as causative for deafness and vestibular dysfunction (DFNB18B). At later larval stages, maintenance of otolith tethering to the saccular macula is dependent on tectorin alpha (tecta) function, which is disrupted in the rolling stones (rst) mutant. α-Tectorin (Tecta) is a major constituent of the tectorial membrane in the mammalian cochlea. Mutations in the human TECTA gene can cause either dominant (DFNA8/12) or recessive (DFNB21) forms of deafness. Our findings indicate that the composition of extracellular otic membranes is highly conserved between mammals and fish, reinforcing the view that the zebrafish is an excellent model system for the study of deafness and vestibular disease. The Company of Biologists 2015-03-15 /pmc/articles/PMC4360185/ /pubmed/25758224 http://dx.doi.org/10.1242/dev.116632 Text en © 2015. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Stooke-Vaughan, Georgina A.
Obholzer, Nikolaus D.
Baxendale, Sarah
Megason, Sean G.
Whitfield, Tanya T.
Otolith tethering in the zebrafish otic vesicle requires Otogelin and α-Tectorin
title Otolith tethering in the zebrafish otic vesicle requires Otogelin and α-Tectorin
title_full Otolith tethering in the zebrafish otic vesicle requires Otogelin and α-Tectorin
title_fullStr Otolith tethering in the zebrafish otic vesicle requires Otogelin and α-Tectorin
title_full_unstemmed Otolith tethering in the zebrafish otic vesicle requires Otogelin and α-Tectorin
title_short Otolith tethering in the zebrafish otic vesicle requires Otogelin and α-Tectorin
title_sort otolith tethering in the zebrafish otic vesicle requires otogelin and α-tectorin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4360185/
https://www.ncbi.nlm.nih.gov/pubmed/25758224
http://dx.doi.org/10.1242/dev.116632
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