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Epigenetic landscape reveals MECOM as an endothelial lineage regulator
A comprehensive understanding of endothelial cell lineage specification will advance cardiovascular regenerative medicine. Recent studies found that unique epigenetic signatures preferentially regulate cell identity genes. We thus systematically investigate the epigenetic landscape of endothelial ce...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130150/ https://www.ncbi.nlm.nih.gov/pubmed/37185814 http://dx.doi.org/10.1038/s41467-023-38002-w |
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author | Lv, Jie Meng, Shu Gu, Qilin Zheng, Rongbin Gao, Xinlei Kim, Jun-dae Chen, Min Xia, Bo Zuo, Yihan Zhu, Sen Zhao, Dongyu Li, Yanqiang Wang, Guangyu Wang, Xin Meng, Qingshu Cao, Qi Cooke, John P. Fang, Longhou Chen, Kaifu Zhang, Lili |
author_facet | Lv, Jie Meng, Shu Gu, Qilin Zheng, Rongbin Gao, Xinlei Kim, Jun-dae Chen, Min Xia, Bo Zuo, Yihan Zhu, Sen Zhao, Dongyu Li, Yanqiang Wang, Guangyu Wang, Xin Meng, Qingshu Cao, Qi Cooke, John P. Fang, Longhou Chen, Kaifu Zhang, Lili |
author_sort | Lv, Jie |
collection | PubMed |
description | A comprehensive understanding of endothelial cell lineage specification will advance cardiovascular regenerative medicine. Recent studies found that unique epigenetic signatures preferentially regulate cell identity genes. We thus systematically investigate the epigenetic landscape of endothelial cell lineage and identify MECOM to be the leading candidate as an endothelial cell lineage regulator. Single-cell RNA-Seq analysis verifies that MECOM-positive cells are exclusively enriched in the cell cluster of bona fide endothelial cells derived from induced pluripotent stem cells. Our experiments demonstrate that MECOM depletion impairs human endothelial cell differentiation, functions, and Zebrafish angiogenesis. Through integrative analysis of Hi-C, DNase-Seq, ChIP-Seq, and RNA-Seq data, we find MECOM binds enhancers that form chromatin loops to regulate endothelial cell identity genes. Further, we identify and verify the VEGF signaling pathway to be a key target of MECOM. Our work provides important insights into epigenetic regulation of cell identity and uncovered MECOM as an endothelial cell lineage regulator. |
format | Online Article Text |
id | pubmed-10130150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101301502023-04-27 Epigenetic landscape reveals MECOM as an endothelial lineage regulator Lv, Jie Meng, Shu Gu, Qilin Zheng, Rongbin Gao, Xinlei Kim, Jun-dae Chen, Min Xia, Bo Zuo, Yihan Zhu, Sen Zhao, Dongyu Li, Yanqiang Wang, Guangyu Wang, Xin Meng, Qingshu Cao, Qi Cooke, John P. Fang, Longhou Chen, Kaifu Zhang, Lili Nat Commun Article A comprehensive understanding of endothelial cell lineage specification will advance cardiovascular regenerative medicine. Recent studies found that unique epigenetic signatures preferentially regulate cell identity genes. We thus systematically investigate the epigenetic landscape of endothelial cell lineage and identify MECOM to be the leading candidate as an endothelial cell lineage regulator. Single-cell RNA-Seq analysis verifies that MECOM-positive cells are exclusively enriched in the cell cluster of bona fide endothelial cells derived from induced pluripotent stem cells. Our experiments demonstrate that MECOM depletion impairs human endothelial cell differentiation, functions, and Zebrafish angiogenesis. Through integrative analysis of Hi-C, DNase-Seq, ChIP-Seq, and RNA-Seq data, we find MECOM binds enhancers that form chromatin loops to regulate endothelial cell identity genes. Further, we identify and verify the VEGF signaling pathway to be a key target of MECOM. Our work provides important insights into epigenetic regulation of cell identity and uncovered MECOM as an endothelial cell lineage regulator. Nature Publishing Group UK 2023-04-25 /pmc/articles/PMC10130150/ /pubmed/37185814 http://dx.doi.org/10.1038/s41467-023-38002-w Text en © The Author(s) 2023, corrected publication 2023 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 Lv, Jie Meng, Shu Gu, Qilin Zheng, Rongbin Gao, Xinlei Kim, Jun-dae Chen, Min Xia, Bo Zuo, Yihan Zhu, Sen Zhao, Dongyu Li, Yanqiang Wang, Guangyu Wang, Xin Meng, Qingshu Cao, Qi Cooke, John P. Fang, Longhou Chen, Kaifu Zhang, Lili Epigenetic landscape reveals MECOM as an endothelial lineage regulator |
title | Epigenetic landscape reveals MECOM as an endothelial lineage regulator |
title_full | Epigenetic landscape reveals MECOM as an endothelial lineage regulator |
title_fullStr | Epigenetic landscape reveals MECOM as an endothelial lineage regulator |
title_full_unstemmed | Epigenetic landscape reveals MECOM as an endothelial lineage regulator |
title_short | Epigenetic landscape reveals MECOM as an endothelial lineage regulator |
title_sort | epigenetic landscape reveals mecom as an endothelial lineage regulator |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130150/ https://www.ncbi.nlm.nih.gov/pubmed/37185814 http://dx.doi.org/10.1038/s41467-023-38002-w |
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