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Zebrafish Otolith Biomineralization Requires Polyketide Synthase

Deflecting biomineralized crystals attached to vestibular hair cells are necessary for maintaining balance. Zebrafish (Danio rerio) are useful organisms to study these biomineralized crystals called otoliths, as many required genes are homologous to human otoconial development. We sought to identify...

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Autores principales: Thiessen, Kevin D., Grzegorski, Steven J., Chin, Yvonne, Higuchi, Lisa, Wilkinson, Christopher J., Shavit, Jordan A., Kramer, Kenneth L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531356/
https://www.ncbi.nlm.nih.gov/pubmed/30974150
http://dx.doi.org/10.1016/j.mod.2019.04.001
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author Thiessen, Kevin D.
Grzegorski, Steven J.
Chin, Yvonne
Higuchi, Lisa
Wilkinson, Christopher J.
Shavit, Jordan A.
Kramer, Kenneth L.
author_facet Thiessen, Kevin D.
Grzegorski, Steven J.
Chin, Yvonne
Higuchi, Lisa
Wilkinson, Christopher J.
Shavit, Jordan A.
Kramer, Kenneth L.
author_sort Thiessen, Kevin D.
collection PubMed
description Deflecting biomineralized crystals attached to vestibular hair cells are necessary for maintaining balance. Zebrafish (Danio rerio) are useful organisms to study these biomineralized crystals called otoliths, as many required genes are homologous to human otoconial development. We sought to identify and characterize the causative gene in a trio of homozygous recessive mutants, no content (nco) and corkscrew (csr), and vanished (vns), which fail to develop otoliths during early ear development. We show that nco, csr, and vns have potentially deleterious mutations in polyketide synthase (pks1), a multi-modular protein that has been previously implicated in biomineralization events in chordates and echinoderms. We found that Otoconin-90 (Oc90) expression within the otocyst is diffuse in nco and csr; therefore, it is not sufficient for otolith biomineralization in zebrafish. Similarly, normal localization of Otogelin, a protein required for otolith tethering in the otolithic membrane, is not sufficient for Oc90 attachment. Furthermore, eNOS signaling and Endothelin-1 signaling were the most up- and down-regulated pathways during otolith agenesis in nco, respectively. Our results demonstrate distinct processes for otolith nucleation and biomineralization in vertebrates and will be a starting point for models that are independent of Oc90-mediated seeding. This study will serve as a basis for investigating the role of eNOS signaling and Endothelin-1 signaling during otolith formation.
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spelling pubmed-65313562020-06-01 Zebrafish Otolith Biomineralization Requires Polyketide Synthase Thiessen, Kevin D. Grzegorski, Steven J. Chin, Yvonne Higuchi, Lisa Wilkinson, Christopher J. Shavit, Jordan A. Kramer, Kenneth L. Mech Dev Article Deflecting biomineralized crystals attached to vestibular hair cells are necessary for maintaining balance. Zebrafish (Danio rerio) are useful organisms to study these biomineralized crystals called otoliths, as many required genes are homologous to human otoconial development. We sought to identify and characterize the causative gene in a trio of homozygous recessive mutants, no content (nco) and corkscrew (csr), and vanished (vns), which fail to develop otoliths during early ear development. We show that nco, csr, and vns have potentially deleterious mutations in polyketide synthase (pks1), a multi-modular protein that has been previously implicated in biomineralization events in chordates and echinoderms. We found that Otoconin-90 (Oc90) expression within the otocyst is diffuse in nco and csr; therefore, it is not sufficient for otolith biomineralization in zebrafish. Similarly, normal localization of Otogelin, a protein required for otolith tethering in the otolithic membrane, is not sufficient for Oc90 attachment. Furthermore, eNOS signaling and Endothelin-1 signaling were the most up- and down-regulated pathways during otolith agenesis in nco, respectively. Our results demonstrate distinct processes for otolith nucleation and biomineralization in vertebrates and will be a starting point for models that are independent of Oc90-mediated seeding. This study will serve as a basis for investigating the role of eNOS signaling and Endothelin-1 signaling during otolith formation. 2019-04-08 2019-06 /pmc/articles/PMC6531356/ /pubmed/30974150 http://dx.doi.org/10.1016/j.mod.2019.04.001 Text en Submitted for possible open access publication under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Thiessen, Kevin D.
Grzegorski, Steven J.
Chin, Yvonne
Higuchi, Lisa
Wilkinson, Christopher J.
Shavit, Jordan A.
Kramer, Kenneth L.
Zebrafish Otolith Biomineralization Requires Polyketide Synthase
title Zebrafish Otolith Biomineralization Requires Polyketide Synthase
title_full Zebrafish Otolith Biomineralization Requires Polyketide Synthase
title_fullStr Zebrafish Otolith Biomineralization Requires Polyketide Synthase
title_full_unstemmed Zebrafish Otolith Biomineralization Requires Polyketide Synthase
title_short Zebrafish Otolith Biomineralization Requires Polyketide Synthase
title_sort zebrafish otolith biomineralization requires polyketide synthase
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531356/
https://www.ncbi.nlm.nih.gov/pubmed/30974150
http://dx.doi.org/10.1016/j.mod.2019.04.001
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