增强子
发起人
同源盒蛋白纳米
诱导多能干细胞
胚胎干细胞
生物
转录因子
染色质
外胚层
干细胞
遗传学
胚状体
细胞生物学
基因
基因表达
原肠化
作者
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. Rugg‐Gunn
出处
期刊:Cell Reports
[Elsevier]
日期:2018-03-01
卷期号:22 (10): 2615-2627
被引量:91
标识
DOI:10.1016/j.celrep.2018.02.040
摘要
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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