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Insight into the regulatory mechanism of dynamic chromatin 3D interactions during cardiomyocyte differentiation in human

Cardiogenesis is an extremely complicated process involved with DNA regulatory elements, and trans factors regulate gene expression pattern spatiotemporally. Enhancers, as the well-known DNA elements, activate target gene expression by transcription factors (TFs) occupied to organize dynamic three-d...

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Autores principales: Liu, Hui, Ma, Yingying, Yu, Jiaxin, Chen, Xiang, Wang, Shuyuan, Jia, Yijie, Ding, Na, Jin, Xiaoyan, Zhang, Yunpeng, Xu, Juan, Li, Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10462852/
https://www.ncbi.nlm.nih.gov/pubmed/37650118
http://dx.doi.org/10.1016/j.omtn.2023.07.033
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author Liu, Hui
Ma, Yingying
Yu, Jiaxin
Chen, Xiang
Wang, Shuyuan
Jia, Yijie
Ding, Na
Jin, Xiaoyan
Zhang, Yunpeng
Xu, Juan
Li, Xia
author_facet Liu, Hui
Ma, Yingying
Yu, Jiaxin
Chen, Xiang
Wang, Shuyuan
Jia, Yijie
Ding, Na
Jin, Xiaoyan
Zhang, Yunpeng
Xu, Juan
Li, Xia
author_sort Liu, Hui
collection PubMed
description Cardiogenesis is an extremely complicated process involved with DNA regulatory elements, and trans factors regulate gene expression pattern spatiotemporally. Enhancers, as the well-known DNA elements, activate target gene expression by transcription factors (TFs) occupied to organize dynamic three-dimensional (3D) interactions, which when affected or interrupted might cause heart defects or diseases. In this study, we integrated transcriptome, 3D genome, and regulatome to reorganize the global 3D genome in cardiomyogenesis, showing a gradually decreased trend of both chromatin interactions and topological associating domains (TADs) during cardiomyocyte differentiation. And almost all of the chromatin interactions occurred within the same or between adjacent TADs involved with enhancers, indicating that dynamical rewiring of enhancer-related chromatin interactions in the continuous expansive TADs is closely correlated to cardiogenesis. Moreover, we found stage-specific interactions activate stage-specific expression to be involved within corresponding biological functions, and the stage-specific combined regulations of enhancers and binding TFs form connected networks to control stage-specific expression and biological processes, which promote cardiomyocyte differentiation. Finally, we identified markers based on regulatory networks, which might drive cardiac development. This study demonstrates the power of enhancer interactome combined with active TFs to reveal insights into transcriptional regulatory networks during cardiomyogenesis.
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spelling pubmed-104628522023-08-30 Insight into the regulatory mechanism of dynamic chromatin 3D interactions during cardiomyocyte differentiation in human Liu, Hui Ma, Yingying Yu, Jiaxin Chen, Xiang Wang, Shuyuan Jia, Yijie Ding, Na Jin, Xiaoyan Zhang, Yunpeng Xu, Juan Li, Xia Mol Ther Nucleic Acids Original Article Cardiogenesis is an extremely complicated process involved with DNA regulatory elements, and trans factors regulate gene expression pattern spatiotemporally. Enhancers, as the well-known DNA elements, activate target gene expression by transcription factors (TFs) occupied to organize dynamic three-dimensional (3D) interactions, which when affected or interrupted might cause heart defects or diseases. In this study, we integrated transcriptome, 3D genome, and regulatome to reorganize the global 3D genome in cardiomyogenesis, showing a gradually decreased trend of both chromatin interactions and topological associating domains (TADs) during cardiomyocyte differentiation. And almost all of the chromatin interactions occurred within the same or between adjacent TADs involved with enhancers, indicating that dynamical rewiring of enhancer-related chromatin interactions in the continuous expansive TADs is closely correlated to cardiogenesis. Moreover, we found stage-specific interactions activate stage-specific expression to be involved within corresponding biological functions, and the stage-specific combined regulations of enhancers and binding TFs form connected networks to control stage-specific expression and biological processes, which promote cardiomyocyte differentiation. Finally, we identified markers based on regulatory networks, which might drive cardiac development. This study demonstrates the power of enhancer interactome combined with active TFs to reveal insights into transcriptional regulatory networks during cardiomyogenesis. American Society of Gene & Cell Therapy 2023-08-01 /pmc/articles/PMC10462852/ /pubmed/37650118 http://dx.doi.org/10.1016/j.omtn.2023.07.033 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Liu, Hui
Ma, Yingying
Yu, Jiaxin
Chen, Xiang
Wang, Shuyuan
Jia, Yijie
Ding, Na
Jin, Xiaoyan
Zhang, Yunpeng
Xu, Juan
Li, Xia
Insight into the regulatory mechanism of dynamic chromatin 3D interactions during cardiomyocyte differentiation in human
title Insight into the regulatory mechanism of dynamic chromatin 3D interactions during cardiomyocyte differentiation in human
title_full Insight into the regulatory mechanism of dynamic chromatin 3D interactions during cardiomyocyte differentiation in human
title_fullStr Insight into the regulatory mechanism of dynamic chromatin 3D interactions during cardiomyocyte differentiation in human
title_full_unstemmed Insight into the regulatory mechanism of dynamic chromatin 3D interactions during cardiomyocyte differentiation in human
title_short Insight into the regulatory mechanism of dynamic chromatin 3D interactions during cardiomyocyte differentiation in human
title_sort insight into the regulatory mechanism of dynamic chromatin 3d interactions during cardiomyocyte differentiation in human
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10462852/
https://www.ncbi.nlm.nih.gov/pubmed/37650118
http://dx.doi.org/10.1016/j.omtn.2023.07.033
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