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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...

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Autores principales: Jimenez, Erin, Slevin, Claire C., Song, Wei, Chen, Zelin, Frederickson, Stephen C., Gildea, Derek, Wu, Weiwei, Elkahloun, Abdel G., Ovcharenko, Ivan, Burgess, Shawn M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
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.
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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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