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Updated: Jun 30, 2025

Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers
Published on: September 20, 2018
Transcription-induced active forces suppress chromatin motion
Sucheol Shin1, Guang Shi1,2, Hyun Woo Cho3
1Department of Chemistry, The University of Texas at Austin, Austin, TX 78712.
Active mechanical forces from RNA polymerase II (RNAPII) surprisingly suppress human interphase chromosome mobility during transcription. This study models how these forces impact chromatin dynamics, revealing a transient ordering mechanism.
Area of Science:
- Biophysics
- Molecular Biology
- Genomics
Background:
- Interphase chromosome organization is increasingly understood through experimental techniques.
- Chromatin dynamics, particularly during functional states like transcription, remain less understood.
- Experiments show decreased locus motility during human transcription, counterintuitive to expected chromatin opening.
Purpose of the Study:
- To investigate how active mechanical forces (F) influence chromatin dynamical properties.
- To explain the counterintuitive observation of decreased locus mobility during transcription.
Main Methods:
- Development of a minimal active copolymer model for interphase chromosomes.
- Simulation of locus movements under varying active forces (F).
Main Results:
- Locus movements in gene-rich regions are suppressed at intermediate forces (F) and enhanced at low forces.
- Intermediate forces cause increased bond lengths and a transient disorder-to-order transition, reducing mobility.
- This force-dependent dynamics preserves chromosome organization and may nucleate dynamic networks.
Conclusions:
- The model explains the experimentally observed suppression of chromatin mobility during transcription.
- A transient ordering mechanism in gene-rich regions, driven by mechanical forces, is proposed.
- This mechanism could be crucial for forming dynamic networks involving transcription machinery and chromatin.
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