2025/11/05 by Hangpeng Li, James Dalgleish, George Lister +22 · 1 voice · 18 citations
Biochemistry, Genetics and Molecular Biology · #Chromatin #Chromosome conformation capture #DNA #DNA and Nucleic Acid Chemistry #Developmental Biology and Gene Regulation #Eukaryotic transcription #Genomics and Chromatin Dynamics #Nucleosome #Resolution (logic) #Transcription (linguistics) #Transcription factor #Unified Model
paper · doi:10.1016/j.cell.2025.10.013
published in Cell 188(25), 7175-7193.e19 (Cell Press)
openalex created_date 2025/11/05 · openalex publication_date 2025/11/05 · openalex updated_date 2026/08/03
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.