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FACT safeguards promoter topology by maintaining nucleosomes and restricting chromatin factor spreading

Abstract:

Facilitates chromatin transcription (FACT) is a histone chaperone that displaces and re-assembles histones during transcription. Recent studies have reported a minor role for FACT in chromatin architecture. We have recently shown that active gene promoters form nanoscale domains and proposed they are created by the biophysical properties of nucleosome-free regions. Here we use base-pair resolution Micro Capture-C ultra to show that, following FACT degradation, nanoscale domains are lost and subnucleosomal chromatin interactions are rearranged at active promoters. Nucleosome-free regions at these promoters expand and chromatin-binding factors invade the newly accessible chromatin, indicating FACT maintains the integrity of active promoters by opposing DNA-binding factor spreading into gene bodies. Finally, we show increased interactions between promoters across topologically associating domains, suggesting large-scale structural changes upon FACT loss. Thus, we demonstrate FACT plays a major role in chromatin organisation and provide in vivo evidence that nucleosomes drive both local and long-range chromatin architecture.

Publication status:
Published
Peer review status:
Peer reviewed

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Preprint server copy:
10.64898/2026.02.18.706382

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Radcliffe Department of Medicine
Sub department:
RDM-Weatherall Inst of Molecular Medicine
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Radcliffe Department of Medicine
Sub department:
RDM-Weatherall Inst of Molecular Medicine
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Radcliffe Department of Medicine
Sub department:
RDM-Weatherall Inst of Molecular Medicine
Role:
Author
ORCID:
0000-0002-8326-5260
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Radcliffe Department of Medicine
Sub department:
RDM-Weatherall Inst of Molecular Medicine
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Radcliffe Department of Medicine
Sub department:
RDM-Weatherall Inst of Molecular Medicine
Role:
Author


More from this funder
Funder identifier:
https://ror.org/029chgv08
Grant:
225220/Z/22/Z
224135/Z/21/Z


Preprint server:
bioRxiv
Publication date:
2026-02-19
DOI:
Server owner:
Cold Spring Harbor Laboratory


Language:
English
Pubs id:
2384946
Local pid:
pubs:2384946
Deposit date:
2026-06-18
ARK identifier:

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