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Cell Type–Specific Transcriptome Analysis Reveals a Major Role for Zeb1 and miR-200b in Mouse Inner Ear Morphogenesis

Cellular heterogeneity hinders the extraction of functionally significant results and inference of regulatory networks from wide-scale expression profiles of complex mammalian organs. The mammalian inner ear consists of the auditory and vestibular systems that are each composed of hair cells, suppor...

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Autores principales: Hertzano, Ronna, Elkon, Ran, Kurima, Kiyoto, Morrisson, Annie, Chan, Siaw-Lin, Sallin, Michelle, Biedlingmaier, Andrew, Darling, Douglas S., Griffith, Andrew J., Eisenman, David J., Strome, Scott E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3183091/
https://www.ncbi.nlm.nih.gov/pubmed/21980309
http://dx.doi.org/10.1371/journal.pgen.1002309
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author Hertzano, Ronna
Elkon, Ran
Kurima, Kiyoto
Morrisson, Annie
Chan, Siaw-Lin
Sallin, Michelle
Biedlingmaier, Andrew
Darling, Douglas S.
Griffith, Andrew J.
Eisenman, David J.
Strome, Scott E.
author_facet Hertzano, Ronna
Elkon, Ran
Kurima, Kiyoto
Morrisson, Annie
Chan, Siaw-Lin
Sallin, Michelle
Biedlingmaier, Andrew
Darling, Douglas S.
Griffith, Andrew J.
Eisenman, David J.
Strome, Scott E.
author_sort Hertzano, Ronna
collection PubMed
description Cellular heterogeneity hinders the extraction of functionally significant results and inference of regulatory networks from wide-scale expression profiles of complex mammalian organs. The mammalian inner ear consists of the auditory and vestibular systems that are each composed of hair cells, supporting cells, neurons, mesenchymal cells, other epithelial cells, and blood vessels. We developed a novel protocol to sort auditory and vestibular tissues of newborn mouse inner ears into their major cellular components. Transcriptome profiling of the sorted cells identified cell type–specific expression clusters. Computational analysis detected transcription factors and microRNAs that play key roles in determining cell identity in the inner ear. Specifically, our analysis revealed the role of the Zeb1/miR-200b pathway in establishing epithelial and mesenchymal identity in the inner ear. Furthermore, we detected a misregulation of the ZEB1 pathway in the inner ear of Twirler mice, which manifest, among other phenotypes, malformations of the auditory and vestibular labyrinth. The association of misregulation of the ZEB1/miR-200b pathway with auditory and vestibular defects in the Twirler mutant mice uncovers a novel mechanism underlying deafness and balance disorders. Our approach can be employed to decipher additional complex regulatory networks underlying other hearing and balance mouse mutants.
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spelling pubmed-31830912011-10-06 Cell Type–Specific Transcriptome Analysis Reveals a Major Role for Zeb1 and miR-200b in Mouse Inner Ear Morphogenesis Hertzano, Ronna Elkon, Ran Kurima, Kiyoto Morrisson, Annie Chan, Siaw-Lin Sallin, Michelle Biedlingmaier, Andrew Darling, Douglas S. Griffith, Andrew J. Eisenman, David J. Strome, Scott E. PLoS Genet Research Article Cellular heterogeneity hinders the extraction of functionally significant results and inference of regulatory networks from wide-scale expression profiles of complex mammalian organs. The mammalian inner ear consists of the auditory and vestibular systems that are each composed of hair cells, supporting cells, neurons, mesenchymal cells, other epithelial cells, and blood vessels. We developed a novel protocol to sort auditory and vestibular tissues of newborn mouse inner ears into their major cellular components. Transcriptome profiling of the sorted cells identified cell type–specific expression clusters. Computational analysis detected transcription factors and microRNAs that play key roles in determining cell identity in the inner ear. Specifically, our analysis revealed the role of the Zeb1/miR-200b pathway in establishing epithelial and mesenchymal identity in the inner ear. Furthermore, we detected a misregulation of the ZEB1 pathway in the inner ear of Twirler mice, which manifest, among other phenotypes, malformations of the auditory and vestibular labyrinth. The association of misregulation of the ZEB1/miR-200b pathway with auditory and vestibular defects in the Twirler mutant mice uncovers a novel mechanism underlying deafness and balance disorders. Our approach can be employed to decipher additional complex regulatory networks underlying other hearing and balance mouse mutants. Public Library of Science 2011-09-29 /pmc/articles/PMC3183091/ /pubmed/21980309 http://dx.doi.org/10.1371/journal.pgen.1002309 Text en Hertzano et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hertzano, Ronna
Elkon, Ran
Kurima, Kiyoto
Morrisson, Annie
Chan, Siaw-Lin
Sallin, Michelle
Biedlingmaier, Andrew
Darling, Douglas S.
Griffith, Andrew J.
Eisenman, David J.
Strome, Scott E.
Cell Type–Specific Transcriptome Analysis Reveals a Major Role for Zeb1 and miR-200b in Mouse Inner Ear Morphogenesis
title Cell Type–Specific Transcriptome Analysis Reveals a Major Role for Zeb1 and miR-200b in Mouse Inner Ear Morphogenesis
title_full Cell Type–Specific Transcriptome Analysis Reveals a Major Role for Zeb1 and miR-200b in Mouse Inner Ear Morphogenesis
title_fullStr Cell Type–Specific Transcriptome Analysis Reveals a Major Role for Zeb1 and miR-200b in Mouse Inner Ear Morphogenesis
title_full_unstemmed Cell Type–Specific Transcriptome Analysis Reveals a Major Role for Zeb1 and miR-200b in Mouse Inner Ear Morphogenesis
title_short Cell Type–Specific Transcriptome Analysis Reveals a Major Role for Zeb1 and miR-200b in Mouse Inner Ear Morphogenesis
title_sort cell type–specific transcriptome analysis reveals a major role for zeb1 and mir-200b in mouse inner ear morphogenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3183091/
https://www.ncbi.nlm.nih.gov/pubmed/21980309
http://dx.doi.org/10.1371/journal.pgen.1002309
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