染色质
核小体
生物
染色体构象捕获
计算生物学
转录因子
真核转录
统一模型
抄写(语言学)
生物物理学
分辨率(逻辑)
DNA
生物系统
芯片排序
蛋白质结构
细胞生物学
物理
分子动力学
嘉雅宠物
基因表达调控
分子模型
组蛋白
模型系统
遗传学
转录前起始复合物
结构生物学
结合位点
基因表达
纳米尺度
血浆蛋白结合
模式生物
纳米技术
作者
Hangpeng Li,James Dalgleish,George Lister,Maria Julia Maristany,Jan Huertas,Ana M. Dopico-Fernandez,Joseph C. Hamley,Nicholas Denny,Gianna Bloye,Weijiao Zhang,Lance D. Hentges,Roman Doll,Ye Wei,Michela Maresca,Emilia Dimitrova,Lior Pytowski,Edward Tunnacliffe,Mira Kassouf,Douglas R. Higgs,Elzo de Wit
出处
期刊:Cell
[Cell Press]
日期:2025-11-05
卷期号:188 (25): 7175-7193.e19
被引量:8
标识
DOI:10.1016/j.cell.2025.10.013
摘要
Chromatin structure is a key determinant of gene expression in eukaryotes, but it has not been possible to define the structure of cis-regulatory elements at the scale of the proteins that bind them. Here, we generate multidimensional chromosome conformation capture (3C) maps at base-pair resolution using Micro Capture-C ultra (MCCu). This can resolve contacts between individual transcription factor motifs within cis-regulatory elements. Using degron systems, we show that removal of Mediator complex components alters fine-scale promoter structure and that nucleosome depletion plays a key role in transcription factor-driven enhancer-promoter contacts. We observe that chromatin is partitioned into nanoscale domains by nucleosome-depleted regions. This structural conformation is reproduced by chemically specific coarse-grained molecular dynamics simulations of the physicochemical properties of chromatin. Combining MCCu with molecular dynamics simulations and super-resolution microscopy allows us to propose a unified model in which the biophysical properties of chromatin orchestrate contacts between cis-regulatory elements.
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