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Long-Range Enhancer Interactions Are Prevalent in Mouse Embryonic Stem Cells and Are Reorganized upon Pluripotent State Transition
Transcriptional enhancers, including super-enhancers (SEs), form physical interactions with promoters to regulate cell-type-specific gene expression. SEs are characterized by high transcription factor occupancy and large domains of active chromatin, and they are commonly assigned to target promoters...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863031/ https://www.ncbi.nlm.nih.gov/pubmed/29514091 http://dx.doi.org/10.1016/j.celrep.2018.02.040 |
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author | Novo, Clara Lopes Javierre, Biola-Maria Cairns, Jonathan Segonds-Pichon, Anne Wingett, Steven W. Freire-Pritchett, Paula Furlan-Magaril, Mayra Schoenfelder, Stefan Fraser, Peter Rugg-Gunn, Peter J. |
author_facet | Novo, Clara Lopes Javierre, Biola-Maria Cairns, Jonathan Segonds-Pichon, Anne Wingett, Steven W. Freire-Pritchett, Paula Furlan-Magaril, Mayra Schoenfelder, Stefan Fraser, Peter Rugg-Gunn, Peter J. |
author_sort | Novo, Clara Lopes |
collection | PubMed |
description | Transcriptional enhancers, including super-enhancers (SEs), form physical interactions with promoters to regulate cell-type-specific gene expression. SEs are characterized by high transcription factor occupancy and large domains of active chromatin, and they are commonly assigned to target promoters using computational predictions. How promoter-SE interactions change upon cell state transitions, and whether transcription factors maintain SE interactions, have not been reported. Here, we used promoter-capture Hi-C to identify promoters that interact with SEs in mouse embryonic stem cells (ESCs). We found that SEs form complex, spatial networks in which individual SEs contact multiple promoters, and a rewiring of promoter-SE interactions occurs between pluripotent states. We also show that long-range promoter-SE interactions are more prevalent in ESCs than in epiblast stem cells (EpiSCs) or Nanog-deficient ESCs. We conclude that SEs form cell-type-specific interaction networks that are partly dependent on core transcription factors, thereby providing insights into the gene regulatory organization of pluripotent cells. |
format | Online Article Text |
id | pubmed-5863031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58630312018-03-23 Long-Range Enhancer Interactions Are Prevalent in Mouse Embryonic Stem Cells and Are Reorganized upon Pluripotent State Transition Novo, Clara Lopes Javierre, Biola-Maria Cairns, Jonathan Segonds-Pichon, Anne Wingett, Steven W. Freire-Pritchett, Paula Furlan-Magaril, Mayra Schoenfelder, Stefan Fraser, Peter Rugg-Gunn, Peter J. Cell Rep Article Transcriptional enhancers, including super-enhancers (SEs), form physical interactions with promoters to regulate cell-type-specific gene expression. SEs are characterized by high transcription factor occupancy and large domains of active chromatin, and they are commonly assigned to target promoters using computational predictions. How promoter-SE interactions change upon cell state transitions, and whether transcription factors maintain SE interactions, have not been reported. Here, we used promoter-capture Hi-C to identify promoters that interact with SEs in mouse embryonic stem cells (ESCs). We found that SEs form complex, spatial networks in which individual SEs contact multiple promoters, and a rewiring of promoter-SE interactions occurs between pluripotent states. We also show that long-range promoter-SE interactions are more prevalent in ESCs than in epiblast stem cells (EpiSCs) or Nanog-deficient ESCs. We conclude that SEs form cell-type-specific interaction networks that are partly dependent on core transcription factors, thereby providing insights into the gene regulatory organization of pluripotent cells. Cell Press 2018-03-06 /pmc/articles/PMC5863031/ /pubmed/29514091 http://dx.doi.org/10.1016/j.celrep.2018.02.040 Text en © 2018 The Author(s) http://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 Novo, Clara Lopes Javierre, Biola-Maria Cairns, Jonathan Segonds-Pichon, Anne Wingett, Steven W. Freire-Pritchett, Paula Furlan-Magaril, Mayra Schoenfelder, Stefan Fraser, Peter Rugg-Gunn, Peter J. Long-Range Enhancer Interactions Are Prevalent in Mouse Embryonic Stem Cells and Are Reorganized upon Pluripotent State Transition |
title | Long-Range Enhancer Interactions Are Prevalent in Mouse Embryonic Stem Cells and Are Reorganized upon Pluripotent State Transition |
title_full | Long-Range Enhancer Interactions Are Prevalent in Mouse Embryonic Stem Cells and Are Reorganized upon Pluripotent State Transition |
title_fullStr | Long-Range Enhancer Interactions Are Prevalent in Mouse Embryonic Stem Cells and Are Reorganized upon Pluripotent State Transition |
title_full_unstemmed | Long-Range Enhancer Interactions Are Prevalent in Mouse Embryonic Stem Cells and Are Reorganized upon Pluripotent State Transition |
title_short | Long-Range Enhancer Interactions Are Prevalent in Mouse Embryonic Stem Cells and Are Reorganized upon Pluripotent State Transition |
title_sort | long-range enhancer interactions are prevalent in mouse embryonic stem cells and are reorganized upon pluripotent state transition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863031/ https://www.ncbi.nlm.nih.gov/pubmed/29514091 http://dx.doi.org/10.1016/j.celrep.2018.02.040 |
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