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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.
Affiliation
  • Novo CL; Epigenetics Programme, Babraham Institute, Cambridge CB22 3AT, UK.
  • Javierre BM; Nuclear Dynamics Programme, Babraham Institute, Cambridge CB22 3AT, UK.
  • Cairns J; Nuclear Dynamics Programme, Babraham Institute, Cambridge CB22 3AT, UK.
  • Segonds-Pichon A; Bioinformatics Group, Babraham Institute, Cambridge CB22 3AT, UK.
  • Wingett SW; Bioinformatics Group, Babraham Institute, Cambridge CB22 3AT, UK.
  • Freire-Pritchett P; Nuclear Dynamics Programme, Babraham Institute, Cambridge CB22 3AT, UK.
  • Furlan-Magaril M; Nuclear Dynamics Programme, Babraham Institute, Cambridge CB22 3AT, UK.
  • Schoenfelder S; Nuclear Dynamics Programme, Babraham Institute, Cambridge CB22 3AT, UK.
  • Fraser P; Nuclear Dynamics Programme, Babraham Institute, Cambridge CB22 3AT, UK; Department of Biological Science, Florida State University, Tallahassee, FL 32306, USA.
  • Rugg-Gunn PJ; Epigenetics Programme, Babraham Institute, Cambridge CB22 3AT, UK; Wellcome Trust - Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge CB2 1QR, UK. Electronic address: peter.rugg-gunn@babraham.ac.uk.
Cell Rep ; 22(10): 2615-2627, 2018 03 06.
Article in En | MEDLINE | ID: mdl-29514091
ABSTRACT
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Differentiation / Enhancer Elements, Genetic / Pluripotent Stem Cells / Mouse Embryonic Stem Cells Type of study: Prognostic_studies Limits: Animals Language: En Journal: Cell Rep Year: 2018 Document type: Article Affiliation country: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Differentiation / Enhancer Elements, Genetic / Pluripotent Stem Cells / Mouse Embryonic Stem Cells Type of study: Prognostic_studies Limits: Animals Language: En Journal: Cell Rep Year: 2018 Document type: Article Affiliation country: Reino Unido
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