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A Critical E-box in Barhl1 3′ Enhancer Is Essential for Auditory Hair Cell Differentiation
Barhl1, a mouse homologous gene of Drosophila BarH class homeobox genes, is highly expressed within the inner ear and crucial for the long-term maintenance of auditory hair cells that mediate hearing and balance, yet little is known about the molecular events underlying Barhl1 regulation and functio...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562609/ https://www.ncbi.nlm.nih.gov/pubmed/31096644 http://dx.doi.org/10.3390/cells8050458 |
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author | Hou, Kun Jiang, Hui Karim, Md. Rezaul Zhong, Chao Xu, Zhouwen Liu, Lin Guan, Minxin Shao, Jianzhong Huang, Xiao |
author_facet | Hou, Kun Jiang, Hui Karim, Md. Rezaul Zhong, Chao Xu, Zhouwen Liu, Lin Guan, Minxin Shao, Jianzhong Huang, Xiao |
author_sort | Hou, Kun |
collection | PubMed |
description | Barhl1, a mouse homologous gene of Drosophila BarH class homeobox genes, is highly expressed within the inner ear and crucial for the long-term maintenance of auditory hair cells that mediate hearing and balance, yet little is known about the molecular events underlying Barhl1 regulation and function in hair cells. In this study, through data mining and in vitro report assay, we firstly identified Barhl1 as a direct target gene of Atoh1 and one E-box (E3) in Barhl1 3’ enhancer is crucial for Atoh1-mediated Barhl1 activation. Then we generated a mouse embryonic stem cell (mESC) line carrying disruptions on this E3 site E-box (CAGCTG) using CRISPR/Cas9 technology and this E3 mutated mESC line is further subjected to an efficient stepwise hair cell differentiation strategy in vitro. Disruptions on this E3 site caused dramatic loss of Barhl1 expression and significantly reduced the number of induced hair cell-like cells, while no affections on the differentiation toward early primitive ectoderm-like cells and otic progenitors. Finally, through RNA-seq profiling and gene ontology (GO) enrichment analysis, we found that this E3 box was indispensable for Barhl1 expression to maintain hair cell development and normal functions. We also compared the transcriptional profiles of induced cells from CDS mutated and E3 mutated mESCs, respectively, and got very consistent results except the Barhl1 transcript itself. These observations indicated that Atoh1-mediated Barhl1 expression could have important roles during auditory hair cell development. In brief, our findings delineate the detail molecular mechanism of Barhl1 expression regulation in auditory hair cell differentiation. |
format | Online Article Text |
id | pubmed-6562609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-65626092019-06-17 A Critical E-box in Barhl1 3′ Enhancer Is Essential for Auditory Hair Cell Differentiation Hou, Kun Jiang, Hui Karim, Md. Rezaul Zhong, Chao Xu, Zhouwen Liu, Lin Guan, Minxin Shao, Jianzhong Huang, Xiao Cells Article Barhl1, a mouse homologous gene of Drosophila BarH class homeobox genes, is highly expressed within the inner ear and crucial for the long-term maintenance of auditory hair cells that mediate hearing and balance, yet little is known about the molecular events underlying Barhl1 regulation and function in hair cells. In this study, through data mining and in vitro report assay, we firstly identified Barhl1 as a direct target gene of Atoh1 and one E-box (E3) in Barhl1 3’ enhancer is crucial for Atoh1-mediated Barhl1 activation. Then we generated a mouse embryonic stem cell (mESC) line carrying disruptions on this E3 site E-box (CAGCTG) using CRISPR/Cas9 technology and this E3 mutated mESC line is further subjected to an efficient stepwise hair cell differentiation strategy in vitro. Disruptions on this E3 site caused dramatic loss of Barhl1 expression and significantly reduced the number of induced hair cell-like cells, while no affections on the differentiation toward early primitive ectoderm-like cells and otic progenitors. Finally, through RNA-seq profiling and gene ontology (GO) enrichment analysis, we found that this E3 box was indispensable for Barhl1 expression to maintain hair cell development and normal functions. We also compared the transcriptional profiles of induced cells from CDS mutated and E3 mutated mESCs, respectively, and got very consistent results except the Barhl1 transcript itself. These observations indicated that Atoh1-mediated Barhl1 expression could have important roles during auditory hair cell development. In brief, our findings delineate the detail molecular mechanism of Barhl1 expression regulation in auditory hair cell differentiation. MDPI 2019-05-15 /pmc/articles/PMC6562609/ /pubmed/31096644 http://dx.doi.org/10.3390/cells8050458 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hou, Kun Jiang, Hui Karim, Md. Rezaul Zhong, Chao Xu, Zhouwen Liu, Lin Guan, Minxin Shao, Jianzhong Huang, Xiao A Critical E-box in Barhl1 3′ Enhancer Is Essential for Auditory Hair Cell Differentiation |
title | A Critical E-box in Barhl1 3′ Enhancer Is Essential for Auditory Hair Cell Differentiation |
title_full | A Critical E-box in Barhl1 3′ Enhancer Is Essential for Auditory Hair Cell Differentiation |
title_fullStr | A Critical E-box in Barhl1 3′ Enhancer Is Essential for Auditory Hair Cell Differentiation |
title_full_unstemmed | A Critical E-box in Barhl1 3′ Enhancer Is Essential for Auditory Hair Cell Differentiation |
title_short | A Critical E-box in Barhl1 3′ Enhancer Is Essential for Auditory Hair Cell Differentiation |
title_sort | critical e-box in barhl1 3′ enhancer is essential for auditory hair cell differentiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562609/ https://www.ncbi.nlm.nih.gov/pubmed/31096644 http://dx.doi.org/10.3390/cells8050458 |
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