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致癌转录因子在单个三阴性乳腺癌细胞中指示启动子增强子枢纽。

Oncogenic transcription factors instruct promoter-enhancer hubs in individual triple negative breast cancer cells.

机构信息

Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.

Penn Epigenetics Institute, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.

出版信息

Sci Adv. 2024 Aug 9;10(32):eadl4043. doi: 10.1126/sciadv.adl4043. Epub 2024 Aug 7.

Abstract

Sequencing-based mapping of ensemble pairwise interactions among regulatory elements support the existence of topological assemblies known as promoter-enhancer hubs or cliques in cancer. Yet, prevalence, regulators, and functions of promoter-enhancer hubs in individual cancer cells remain unclear. Here, we systematically integrated functional genomics, transcription factor screening, and optical mapping of promoter-enhancer interactions to identify key promoter-enhancer hubs, examine heterogeneity of their assembly, determine their regulators, and elucidate their role in gene expression control in individual triple negative breast cancer (TNBC) cells. Optical mapping of individual and alleles revealed the existence of frequent multiway interactions among promoters and enhancers within spatial hubs. Our single-allele studies further demonstrated that lineage-determining SOX9 and signaling-dependent NOTCH1 transcription factors compact and hubs. Together, our findings suggest that promoter-enhancer hubs are dynamic and heterogeneous topological assemblies, which are controlled by oncogenic transcription factors and facilitate subtype-restricted gene expression in cancer.

摘要

基于测序的调控元件相互作用图谱支持拓扑组装的存在,这些组装被称为癌症中的启动子-增强子枢纽或类团。然而,在单个癌细胞中,启动子-增强子枢纽的普遍性、调节因子和功能仍不清楚。在这里,我们系统地整合了功能基因组学、转录因子筛选和启动子-增强子相互作用的光学作图,以鉴定关键的启动子-增强子枢纽,研究其组装的异质性,确定其调节因子,并阐明它们在单个三阴性乳腺癌 (TNBC) 细胞中的基因表达调控中的作用。单个 和 等位基因的光学作图揭示了在空间枢纽内,启动子和增强子之间存在频繁的多向相互作用。我们的单等位基因研究进一步表明,谱系决定因子 SOX9 和信号依赖性 NOTCH1 转录因子使 和 枢纽紧缩。总之,我们的研究结果表明,启动子-增强子枢纽是动态的、异质的拓扑组装,由致癌转录因子控制,并促进癌症中亚型特异性的基因表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb94/11305386/e3b3f39127bd/sciadv.adl4043-f1.jpg

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