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Joint single-cell multiomic analysis in Wnt3a induced asymmetric stem cell division

Wnt signaling usually functions through a spatial gradient. Localized Wnt3a signaling can induce the asymmetric division of mouse embryonic stem cells, where proximal daughter cells maintain self-renewal and distal daughter cells acquire hallmarks of differentiation. Here, we develop an approach, sa...

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Autores principales: Sun, Zhongxing, Tang, Yin, Zhang, Yanjun, Fang, Yuan, Jia, Junqi, Zeng, Weiwu, Fang, Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8511096/
https://www.ncbi.nlm.nih.gov/pubmed/34642323
http://dx.doi.org/10.1038/s41467-021-26203-0
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author Sun, Zhongxing
Tang, Yin
Zhang, Yanjun
Fang, Yuan
Jia, Junqi
Zeng, Weiwu
Fang, Dong
author_facet Sun, Zhongxing
Tang, Yin
Zhang, Yanjun
Fang, Yuan
Jia, Junqi
Zeng, Weiwu
Fang, Dong
author_sort Sun, Zhongxing
collection PubMed
description Wnt signaling usually functions through a spatial gradient. Localized Wnt3a signaling can induce the asymmetric division of mouse embryonic stem cells, where proximal daughter cells maintain self-renewal and distal daughter cells acquire hallmarks of differentiation. Here, we develop an approach, same cell epigenome and transcriptome sequencing, to jointly profile the epigenome and transcriptome in the same single cell. Utilizing this method, we profiled H3K27me3 and H3K4me3 levels along with gene expression in mouse embryonic stem cells with localized Wnt3a signaling, revealing the cell type-specific maps of the epigenome and transcriptome in divided daughter cells. H3K27me3, but not H3K4me3, is correlated with gene expression changes during asymmetric cell division. Furthermore, cell clusters identified by H3K27me3 recapitulate the corresponding clusters defined by gene expression. Our study provides a convenient method to jointly profile the epigenome and transcriptome in the same cell and reveals mechanistic insights into the gene regulatory programs that maintain and reset stem cell fate during differentiation.
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spelling pubmed-85110962021-10-29 Joint single-cell multiomic analysis in Wnt3a induced asymmetric stem cell division Sun, Zhongxing Tang, Yin Zhang, Yanjun Fang, Yuan Jia, Junqi Zeng, Weiwu Fang, Dong Nat Commun Article Wnt signaling usually functions through a spatial gradient. Localized Wnt3a signaling can induce the asymmetric division of mouse embryonic stem cells, where proximal daughter cells maintain self-renewal and distal daughter cells acquire hallmarks of differentiation. Here, we develop an approach, same cell epigenome and transcriptome sequencing, to jointly profile the epigenome and transcriptome in the same single cell. Utilizing this method, we profiled H3K27me3 and H3K4me3 levels along with gene expression in mouse embryonic stem cells with localized Wnt3a signaling, revealing the cell type-specific maps of the epigenome and transcriptome in divided daughter cells. H3K27me3, but not H3K4me3, is correlated with gene expression changes during asymmetric cell division. Furthermore, cell clusters identified by H3K27me3 recapitulate the corresponding clusters defined by gene expression. Our study provides a convenient method to jointly profile the epigenome and transcriptome in the same cell and reveals mechanistic insights into the gene regulatory programs that maintain and reset stem cell fate during differentiation. Nature Publishing Group UK 2021-10-12 /pmc/articles/PMC8511096/ /pubmed/34642323 http://dx.doi.org/10.1038/s41467-021-26203-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sun, Zhongxing
Tang, Yin
Zhang, Yanjun
Fang, Yuan
Jia, Junqi
Zeng, Weiwu
Fang, Dong
Joint single-cell multiomic analysis in Wnt3a induced asymmetric stem cell division
title Joint single-cell multiomic analysis in Wnt3a induced asymmetric stem cell division
title_full Joint single-cell multiomic analysis in Wnt3a induced asymmetric stem cell division
title_fullStr Joint single-cell multiomic analysis in Wnt3a induced asymmetric stem cell division
title_full_unstemmed Joint single-cell multiomic analysis in Wnt3a induced asymmetric stem cell division
title_short Joint single-cell multiomic analysis in Wnt3a induced asymmetric stem cell division
title_sort joint single-cell multiomic analysis in wnt3a induced asymmetric stem cell division
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8511096/
https://www.ncbi.nlm.nih.gov/pubmed/34642323
http://dx.doi.org/10.1038/s41467-021-26203-0
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