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在巨噬细胞发育过程中,静态和动态DNA环形成AP-1结合的激活中心。

Static and Dynamic DNA Loops form AP-1-Bound Activation Hubs during Macrophage Development.

作者信息

Phanstiel Douglas H, Van Bortle Kevin, Spacek Damek, Hess Gaelen T, Shamim Muhammad Saad, Machol Ido, Love Michael I, Aiden Erez Lieberman, Bassik Michael C, Snyder Michael P

机构信息

Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, NC 27599, USA; Thurston Arthritis Research Center, University of North Carolina, Chapel Hill, NC 27599, USA; Department of Genetics, Stanford University, Stanford, CA 94305, USA.

Department of Genetics, Stanford University, Stanford, CA 94305, USA.

出版信息

Mol Cell. 2017 Sep 21;67(6):1037-1048.e6. doi: 10.1016/j.molcel.2017.08.006. Epub 2017 Sep 7.

Abstract

The three-dimensional arrangement of the human genome comprises a complex network of structural and regulatory chromatin loops important for coordinating changes in transcription during human development. To better understand the mechanisms underlying context-specific 3D chromatin structure and transcription during cellular differentiation, we generated comprehensive in situ Hi-C maps of DNA loops in human monocytes and differentiated macrophages. We demonstrate that dynamic looping events are regulatory rather than structural in nature and uncover widespread coordination of dynamic enhancer activity at preformed and acquired DNA loops. Enhancer-bound loop formation and enhancer activation of preformed loops together form multi-loop activation hubs at key macrophage genes. Activation hubs connect 3.4 enhancers per promoter and exhibit a strong enrichment for activator protein 1 (AP-1)-binding events, suggesting that multi-loop activation hubs involving cell-type-specific transcription factors represent an important class of regulatory chromatin structures for the spatiotemporal control of transcription.

摘要

人类基因组的三维排列包含一个复杂的结构和调控染色质环网络,这对于协调人类发育过程中转录的变化非常重要。为了更好地理解细胞分化过程中特定背景下三维染色质结构和转录的潜在机制,我们生成了人类单核细胞和分化巨噬细胞中DNA环的全面原位Hi-C图谱。我们证明,动态环化事件本质上是调控性的而非结构性的,并揭示了在预先形成和获得的DNA环处动态增强子活性的广泛协调。增强子结合的环形成和预先形成环的增强子激活共同在关键巨噬细胞基因处形成多环激活枢纽。激活枢纽每个启动子连接3.4个增强子,并在激活蛋白1(AP-1)结合事件中表现出强烈富集,这表明涉及细胞类型特异性转录因子的多环激活枢纽代表了一类重要的调控染色质结构,用于转录的时空控制。

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