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G-四链体作为超级增强子标记物BRD4的潜在捕获剂:体外配体敏感结合及共分离

G-quadruplexes as potential traps for superenhancer marker BRD4: ligand-sensitive binding and co-separation in vitro.

作者信息

Pavlova Iuliia I, Ivanova Olga M, Iudin Mikhail S, Surdina Anastasiya V, Barinov Nikolay A, Bogomiakova Margarita E, Oreshkov Sergey D, Shenkarev Zakhar O, Severov Vjacheslav V, Klinov Dmitriy V, Shender Victoria O, Bogomazova Alexandra N, Lagarkova Maria A, Varizhuk Anna M, Tsvetkov Vladimir B

机构信息

Lopukhin Federal Research and Clinical Center of Physical-Chemical Medicine, Malaya Pirogovskaya, 1a, 119435 Moscow, Russia.

Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Lopukhin Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency, Malaya Pirogovskaya, 1a, 119435 Moscow, Russia.

出版信息

Nucleic Acids Res. 2025 Jul 19;53(14). doi: 10.1093/nar/gkaf726.

DOI:10.1093/nar/gkaf726
PMID:40744496
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12311796/
Abstract

G-quadruplexes (G4s) are prevalent at promoters and superenhancers (SEs), exclude nucleosomes, and recruit transcription factors. This study sought to determine whether the nucleosome exclusion affects the recruitment of the SE marker BRD4, which typically binds to acetylated histones and facilitates SE-promoter contacts via the phase separation-dependent mechanism. Analyses of the available whole-genome data revealed that SEs with the highest G4 density were depleted of nucleosomes but not of BRD4. This led us to test the possibility of histone-independent BRD4 maintenance at G4-rich SEs. A typical SE G4 destabilized a nearby nucleosome in vitro and, unlike B-DNA, bound weakly to BRD4 bromodomains. Similar to an acetylated nucleosome, the G4 promoted phase separation in BRD4 solutions. This effect was not altered by the histone competitor JQ1. However, it was attenuated by two known G4 ligands, suggesting that they could disrupt SE-promoter communication in cells. Consistently, these ligands downregulated several genes regulated by G4-rich SE-contacting promoters more efficiently than they did SE-independent genes. Our findings underscore the significance of G4-rich SEs as transcriptional regulators and provide new insights into their organization.

摘要

G-四链体(G4s)在启动子和超级增强子(SEs)中普遍存在,排斥核小体并招募转录因子。本研究旨在确定核小体排斥是否会影响SE标记物BRD4的招募,BRD4通常与乙酰化组蛋白结合,并通过相分离依赖机制促进SE-启动子接触。对现有全基因组数据的分析表明,G4密度最高的SEs缺乏核小体,但不缺乏BRD4。这促使我们测试在富含G4的SEs处不依赖组蛋白维持BRD4的可能性。一个典型的SE G4在体外使附近的核小体不稳定,并且与B-DNA不同,它与BRD4溴结构域的结合较弱。与乙酰化核小体类似,G4在BRD4溶液中促进相分离。这种效应不受组蛋白竞争剂JQ1的影响。然而,它被两种已知的G4配体减弱,这表明它们可能破坏细胞中的SE-启动子通讯。一致地,这些配体比下调不依赖SE的基因更有效地下调了几个由富含G4的SE接触启动子调控的基因。我们的发现强调了富含G4的SEs作为转录调节因子的重要性,并为它们的组织提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2504/12311796/b7654266bed3/gkaf726fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2504/12311796/876f353ae84e/gkaf726figgra1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2504/12311796/75dee2e011a5/gkaf726fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2504/12311796/eae9437cb951/gkaf726fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2504/12311796/957b575f323d/gkaf726fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2504/12311796/29c38e2d9040/gkaf726fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2504/12311796/3be1ba46d9ce/gkaf726fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2504/12311796/b7654266bed3/gkaf726fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2504/12311796/876f353ae84e/gkaf726figgra1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2504/12311796/75dee2e011a5/gkaf726fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2504/12311796/eae9437cb951/gkaf726fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2504/12311796/957b575f323d/gkaf726fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2504/12311796/29c38e2d9040/gkaf726fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2504/12311796/3be1ba46d9ce/gkaf726fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2504/12311796/b7654266bed3/gkaf726fig6.jpg

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Int J Mol Sci. 2025 Jun 21;26(13):5979. doi: 10.3390/ijms26135979.
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Artificially inserted strong promoter containing multiple G-quadruplexes induces long-range chromatin modification.人工插入含有多个 G-四链体的强启动子诱导长距离染色质修饰。
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