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TINC- 一种在单基因座分辨率下解析调控复合物的方法-揭示了 Nanog 启动子处广泛存在的蛋白质复合物。

TINC- A Method to Dissect Regulatory Complexes at Single-Locus Resolution- Reveals an Extensive Protein Complex at the Nanog Promoter.

机构信息

Department of Anatomy and Developmental Biology, Monash University, Clayton, VIC 3800, Australia; Development and Stem Cells Program, Monash Biomedicine Discovery Institute, Clayton, VIC 3800, Australia; Australian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800, Australia.

Australian Research Council Centre of Excellence in Plant Energy Biology, The University of Western Australia, Perth, WA 6009, Australia; Harry Perkins Institute of Medical Research, Nedlands, WA 6009, Australia.

出版信息

Stem Cell Reports. 2020 Dec 8;15(6):1246-1259. doi: 10.1016/j.stemcr.2020.11.005.

Abstract

Cellular identity is ultimately dictated by the interaction of transcription factors with regulatory elements (REs) to control gene expression. Advances in epigenome profiling techniques have significantly increased our understanding of cell-specific utilization of REs. However, it remains difficult to dissect the majority of factors that interact with these REs due to the lack of appropriate techniques. Therefore, we developed TINC: TALE-mediated isolation of nuclear chromatin. Using this new method, we interrogated the protein complex formed at the Nanog promoter in embryonic stem cells (ESCs) and identified many known and previously unknown interactors, including RCOR2. Further interrogation of the role of RCOR2 in ESCs revealed its involvement in the repression of lineage genes and the fine-tuning of pluripotency genes. Consequently, using the Nanog promoter as a paradigm, we demonstrated the power of TINC to provide insight into the molecular makeup of specific transcriptional complexes at individual REs as well as into cellular identity control in general.

摘要

细胞身份最终由转录因子与调控元件(REs)的相互作用决定,以控制基因表达。 表观基因组分析技术的进步极大地提高了我们对细胞特异性利用 REs 的理解。 然而,由于缺乏适当的技术,仍然难以剖析与这些 RE 相互作用的大多数因素。 因此,我们开发了 TINC:TALE 介导的核染色质分离。 使用这种新方法,我们在胚胎干细胞(ESCs)中检测了 Nanog 启动子处形成的蛋白质复合物,并鉴定了许多已知和以前未知的相互作用因子,包括 RCOR2。 进一步研究 RCOR2 在 ESCs 中的作用表明其参与谱系基因的抑制和多能性基因的微调。 因此,我们使用 Nanog 启动子作为范例,证明了 TINC 的力量,可以深入了解单个 RE 上特定转录复合物的分子组成,以及细胞身份控制的一般情况。

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