中介复合物调节增强子-启动子相互作用。

The Mediator complex regulates enhancer-promoter interactions.

机构信息

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

Department of Molecular Biology, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.

出版信息

Nat Struct Mol Biol. 2023 Jul;30(7):991-1000. doi: 10.1038/s41594-023-01027-2. Epub 2023 Jul 10.

Abstract

Enhancer-mediated gene activation generally requires physical proximity between enhancers and their target gene promoters. However, the molecular mechanisms by which interactions between enhancers and promoters are formed are not well understood. Here, we investigate the function of the Mediator complex in the regulation of enhancer-promoter interactions, by combining rapid protein depletion and high-resolution MNase-based chromosome conformation capture approaches. We show that depletion of Mediator leads to reduced enhancer-promoter interaction frequencies, which are associated with a strong decrease in gene expression. In addition, we find increased interactions between CTCF-binding sites upon Mediator depletion. These changes in chromatin architecture are associated with a redistribution of the Cohesin complex on chromatin and a reduction in Cohesin occupancy at enhancers. Together, our results indicate that the Mediator and Cohesin complexes contribute to enhancer-promoter interactions and provide insights into the molecular mechanisms by which communication between enhancers and promoters is regulated.

摘要

增强子介导的基因激活通常需要增强子与其靶基因启动子之间的物理接近。然而,增强子与启动子之间相互作用形成的分子机制尚不清楚。在这里,我们通过结合快速蛋白消耗和高分辨率 MNase 基于染色质构象捕获方法来研究中介体复合物在调节增强子-启动子相互作用中的功能。我们表明,中介体的消耗导致增强子-启动子相互作用频率降低,这与基因表达的强烈下降有关。此外,我们发现中介体消耗后 CTCF 结合位点之间的相互作用增加。染色质结构的这些变化与染色质上黏合蛋白复合物的重新分布以及增强子上黏合蛋白占据的减少有关。总之,我们的结果表明,中介体和黏合蛋白复合物有助于增强子-启动子相互作用,并提供了对增强子和启动子之间通讯调控的分子机制的深入了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a099/10352134/6f9ff8d48bf6/41594_2023_1027_Fig1_HTML.jpg

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