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Long-Range Enhancer Interactions Are Prevalent in Mouse Embryonic Stem Cells and Are Reorganized upon Pluripotent State Transition
Author(s) -
Clara Lopes Novo,
Biola M. Javierre,
Jonathan Cairns,
Anne Segonds-Pichon,
Steven W. Wingett,
Paula Freire-Pritchett,
Mayra Furlan-Magaril,
Stefan Schoenfelder,
Peter Fraser,
Peter J. RuggGunn
Publication year - 2018
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2018.02.040
Subject(s) - promoter , enhancer , homeobox protein nanog , embryonic stem cell , induced pluripotent stem cell , biology , transcription factor , chromatin , epiblast , microbiology and biotechnology , genetics , stem cell , embryoid body , gene , gene expression , gastrulation
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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