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Mapping the evolving landscape of super-enhancers during cell differentiation
BACKGROUND: Super-enhancers are clusters of enhancer elements that play critical roles in the maintenance of cell identity. Current investigations on super-enhancers are centered on the established ones in static cell types. How super-enhancers are established during cell differentiation remains obs...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8442463/ https://www.ncbi.nlm.nih.gov/pubmed/34526084 http://dx.doi.org/10.1186/s13059-021-02485-x |
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author | Kai, Yan Li, Bin E. Zhu, Ming Li, Grace Y. Chen, Fei Han, Yingli Cha, Hye Ji Orkin, Stuart H. Cai, Wenqing Huang, Jialiang Yuan, Guo-Cheng |
author_facet | Kai, Yan Li, Bin E. Zhu, Ming Li, Grace Y. Chen, Fei Han, Yingli Cha, Hye Ji Orkin, Stuart H. Cai, Wenqing Huang, Jialiang Yuan, Guo-Cheng |
author_sort | Kai, Yan |
collection | PubMed |
description | BACKGROUND: Super-enhancers are clusters of enhancer elements that play critical roles in the maintenance of cell identity. Current investigations on super-enhancers are centered on the established ones in static cell types. How super-enhancers are established during cell differentiation remains obscure. RESULTS: Here, by developing an unbiased approach to systematically analyze the evolving landscape of super-enhancers during cell differentiation in multiple lineages, we discover a general trend where super-enhancers emerge through three distinct temporal patterns: conserved, temporally hierarchical, and de novo. The three types of super-enhancers differ further in association patterns in target gene expression, functional enrichment, and 3D chromatin organization, suggesting they may represent distinct structural and functional subtypes. Furthermore, we dissect the enhancer repertoire within temporally hierarchical super-enhancers, and find enhancers that emerge at early and late stages are enriched with distinct transcription factors, suggesting that the temporal order of establishment of elements within super-enhancers may be directed by underlying DNA sequence. CRISPR-mediated deletion of individual enhancers in differentiated cells shows that both the early- and late-emerged enhancers are indispensable for target gene expression, while in undifferentiated cells early enhancers are involved in the regulation of target genes. CONCLUSIONS: In summary, our analysis highlights the heterogeneity of the super-enhancer population and provides new insights to enhancer functions within super-enhancers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02485-x. |
format | Online Article Text |
id | pubmed-8442463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84424632021-09-15 Mapping the evolving landscape of super-enhancers during cell differentiation Kai, Yan Li, Bin E. Zhu, Ming Li, Grace Y. Chen, Fei Han, Yingli Cha, Hye Ji Orkin, Stuart H. Cai, Wenqing Huang, Jialiang Yuan, Guo-Cheng Genome Biol Research BACKGROUND: Super-enhancers are clusters of enhancer elements that play critical roles in the maintenance of cell identity. Current investigations on super-enhancers are centered on the established ones in static cell types. How super-enhancers are established during cell differentiation remains obscure. RESULTS: Here, by developing an unbiased approach to systematically analyze the evolving landscape of super-enhancers during cell differentiation in multiple lineages, we discover a general trend where super-enhancers emerge through three distinct temporal patterns: conserved, temporally hierarchical, and de novo. The three types of super-enhancers differ further in association patterns in target gene expression, functional enrichment, and 3D chromatin organization, suggesting they may represent distinct structural and functional subtypes. Furthermore, we dissect the enhancer repertoire within temporally hierarchical super-enhancers, and find enhancers that emerge at early and late stages are enriched with distinct transcription factors, suggesting that the temporal order of establishment of elements within super-enhancers may be directed by underlying DNA sequence. CRISPR-mediated deletion of individual enhancers in differentiated cells shows that both the early- and late-emerged enhancers are indispensable for target gene expression, while in undifferentiated cells early enhancers are involved in the regulation of target genes. CONCLUSIONS: In summary, our analysis highlights the heterogeneity of the super-enhancer population and provides new insights to enhancer functions within super-enhancers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02485-x. BioMed Central 2021-09-15 /pmc/articles/PMC8442463/ /pubmed/34526084 http://dx.doi.org/10.1186/s13059-021-02485-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Kai, Yan Li, Bin E. Zhu, Ming Li, Grace Y. Chen, Fei Han, Yingli Cha, Hye Ji Orkin, Stuart H. Cai, Wenqing Huang, Jialiang Yuan, Guo-Cheng Mapping the evolving landscape of super-enhancers during cell differentiation |
title | Mapping the evolving landscape of super-enhancers during cell differentiation |
title_full | Mapping the evolving landscape of super-enhancers during cell differentiation |
title_fullStr | Mapping the evolving landscape of super-enhancers during cell differentiation |
title_full_unstemmed | Mapping the evolving landscape of super-enhancers during cell differentiation |
title_short | Mapping the evolving landscape of super-enhancers during cell differentiation |
title_sort | mapping the evolving landscape of super-enhancers during cell differentiation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8442463/ https://www.ncbi.nlm.nih.gov/pubmed/34526084 http://dx.doi.org/10.1186/s13059-021-02485-x |
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