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CTCF缺失使增强子介导的基因激活与染色质枢纽形成解偶联。

CTCF depletion decouples enhancer-mediated gene activation from chromatin hub formation.

作者信息

Karpinska Magdalena A, Zhu Yi, Fakhraei Ghazvini Zahra, Ramasamy Shyam, Barbieri Mariano, Cao T B Ngoc, Varahram Natalie, Aljahani Abrar, Lidschreiber Michael, Papantonis Argyris, Oudelaar A Marieke

机构信息

Genome Organization and Regulation, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.

Georg August University of Göttingen, Göttingen, Germany.

出版信息

Nat Struct Mol Biol. 2025 May 13. doi: 10.1038/s41594-025-01555-z.

Abstract

Enhancers and promoters interact in three-dimensional (3D) chromatin structures to regulate gene expression. Here we characterize the mechanisms that drive the formation and function of these structures in a lymphoid-to-myeloid transdifferentiation system. Based on analyses at base pair resolution, we demonstrate a close correlation between binding of regulatory proteins, formation of chromatin interactions and gene expression. Multi-way interaction analyses and computational modeling show that tissue-specific gene loci are organized into chromatin hubs, characterized by cooperative interactions between multiple enhancers, promoters and CTCF-binding sites. While depletion of CTCF strongly impairs the formation of these chromatin hubs, the effects of CTCF depletion on gene expression are modest and can be explained by rewired enhancer-promoter interactions. These findings demonstrate a role for enhancer-promoter interactions in gene regulation that is independent of cooperative interactions in chromatin hubs. Together, these results contribute to our understanding of the structure-function relationship of the genome during cellular differentiation.

摘要

增强子和启动子在三维(3D)染色质结构中相互作用以调控基因表达。在此,我们阐述了在淋巴细胞向髓细胞转分化系统中驱动这些结构形成和功能的机制。基于碱基对分辨率的分析,我们证明了调控蛋白的结合、染色质相互作用的形成与基因表达之间存在密切关联。多路相互作用分析和计算模型表明,组织特异性基因位点被组织成染色质枢纽,其特征是多个增强子、启动子和CTCF结合位点之间的协同相互作用。虽然CTCF的缺失强烈损害了这些染色质枢纽的形成,但CTCF缺失对基因表达的影响较小,并且可以通过增强子 - 启动子相互作用的重新连接来解释。这些发现证明了增强子 - 启动子相互作用在基因调控中的作用,该作用独立于染色质枢纽中的协同相互作用。总之,这些结果有助于我们理解细胞分化过程中基因组的结构 - 功能关系。

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