Epigenetics Programme, Babraham Institute, Cambridge CB22 3AT, UK.
Nuclear Dynamics Programme, Babraham Institute, Cambridge CB22 3AT, UK.
Cell Rep. 2018 Mar 6;22(10):2615-2627. doi: 10.1016/j.celrep.2018.02.040.
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.
转录增强子,包括超级增强子(SEs),与启动子形成物理相互作用,以调节细胞类型特异性基因表达。SE 的特征是转录因子占据率高,活性染色质的大区域,并且通常使用计算预测将它们分配给靶启动子。在细胞状态转变过程中,启动子-SE 相互作用如何变化,以及转录因子是否保持 SE 相互作用,尚未有报道。在这里,我们使用启动子捕获 Hi-C 来鉴定在小鼠胚胎干细胞(ESCs)中与 SE 相互作用的启动子。我们发现 SE 形成复杂的空间网络,其中单个 SE 与多个启动子接触,并且在多能状态之间发生启动子-SE 相互作用的重新布线。我们还表明,长距离启动子-SE 相互作用在 ESCs 中比在胚胎外干细胞(EpiSCs)或 Nanog 缺陷型 ESCs 中更为普遍。我们得出结论,SE 形成细胞类型特异性相互作用网络,部分依赖于核心转录因子,从而为多能细胞的基因调控组织提供了见解。