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A regulatory network of Sox and Six transcription factors initiate a cell fate transformation during hearing regeneration in adult zebrafish
Using adult zebrafish inner ears as a model for sensorineural regeneration, we ablated the mechanosensory receptors and characterized the single-cell epigenome and transcriptome at consecutive time points during hair cell regeneration. We utilized deep learning on the regeneration-induced open chrom...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540346/ https://www.ncbi.nlm.nih.gov/pubmed/36212030 http://dx.doi.org/10.1016/j.xgen.2022.100170 |
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author | Jimenez, Erin Slevin, Claire C. Song, Wei Chen, Zelin Frederickson, Stephen C. Gildea, Derek Wu, Weiwei Elkahloun, Abdel G. Ovcharenko, Ivan Burgess, Shawn M. |
author_facet | Jimenez, Erin Slevin, Claire C. Song, Wei Chen, Zelin Frederickson, Stephen C. Gildea, Derek Wu, Weiwei Elkahloun, Abdel G. Ovcharenko, Ivan Burgess, Shawn M. |
author_sort | Jimenez, Erin |
collection | PubMed |
description | Using adult zebrafish inner ears as a model for sensorineural regeneration, we ablated the mechanosensory receptors and characterized the single-cell epigenome and transcriptome at consecutive time points during hair cell regeneration. We utilized deep learning on the regeneration-induced open chromatin sequences and identified cell-specific transcription factor (TF) motif patterns. Enhancer activity correlated with gene expression and identified potential gene regulatory networks. A pattern of overlapping Sox- and Six-family TF gene expression and binding motifs was detected, suggesting a combinatorial program of TFs driving regeneration and cell identity. Pseudotime analysis of single-cell transcriptomic data suggested that support cells within the sensory epithelium changed cell identity to a “progenitor” cell population that could differentiate into hair cells. We identified a 2.6 kb DNA enhancer upstream of the sox2 promoter that, when deleted, showed a dominant phenotype that resulted in a hair-cell-regeneration-specific deficit in both the lateral line and adult inner ear. |
format | Online Article Text |
id | pubmed-9540346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-95403462022-10-07 A regulatory network of Sox and Six transcription factors initiate a cell fate transformation during hearing regeneration in adult zebrafish Jimenez, Erin Slevin, Claire C. Song, Wei Chen, Zelin Frederickson, Stephen C. Gildea, Derek Wu, Weiwei Elkahloun, Abdel G. Ovcharenko, Ivan Burgess, Shawn M. Cell Genom Article Using adult zebrafish inner ears as a model for sensorineural regeneration, we ablated the mechanosensory receptors and characterized the single-cell epigenome and transcriptome at consecutive time points during hair cell regeneration. We utilized deep learning on the regeneration-induced open chromatin sequences and identified cell-specific transcription factor (TF) motif patterns. Enhancer activity correlated with gene expression and identified potential gene regulatory networks. A pattern of overlapping Sox- and Six-family TF gene expression and binding motifs was detected, suggesting a combinatorial program of TFs driving regeneration and cell identity. Pseudotime analysis of single-cell transcriptomic data suggested that support cells within the sensory epithelium changed cell identity to a “progenitor” cell population that could differentiate into hair cells. We identified a 2.6 kb DNA enhancer upstream of the sox2 promoter that, when deleted, showed a dominant phenotype that resulted in a hair-cell-regeneration-specific deficit in both the lateral line and adult inner ear. Elsevier 2022-08-22 /pmc/articles/PMC9540346/ /pubmed/36212030 http://dx.doi.org/10.1016/j.xgen.2022.100170 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jimenez, Erin Slevin, Claire C. Song, Wei Chen, Zelin Frederickson, Stephen C. Gildea, Derek Wu, Weiwei Elkahloun, Abdel G. Ovcharenko, Ivan Burgess, Shawn M. A regulatory network of Sox and Six transcription factors initiate a cell fate transformation during hearing regeneration in adult zebrafish |
title | A regulatory network of Sox and Six transcription factors initiate a cell fate transformation during hearing regeneration in adult zebrafish |
title_full | A regulatory network of Sox and Six transcription factors initiate a cell fate transformation during hearing regeneration in adult zebrafish |
title_fullStr | A regulatory network of Sox and Six transcription factors initiate a cell fate transformation during hearing regeneration in adult zebrafish |
title_full_unstemmed | A regulatory network of Sox and Six transcription factors initiate a cell fate transformation during hearing regeneration in adult zebrafish |
title_short | A regulatory network of Sox and Six transcription factors initiate a cell fate transformation during hearing regeneration in adult zebrafish |
title_sort | regulatory network of sox and six transcription factors initiate a cell fate transformation during hearing regeneration in adult zebrafish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540346/ https://www.ncbi.nlm.nih.gov/pubmed/36212030 http://dx.doi.org/10.1016/j.xgen.2022.100170 |
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