Bridging-Induced Phase Separation and Loop Extrusion Drive Noise in Chromatin Transcription

Cell-to-cell heterogeneity in transcription, or transcriptional noise, is important in cellular development and in disease. The molecular mechanisms driving it are, however, elusive and ill-understood. Here, we use computer simulations to explore the role of 3D chromatin structure in driving transcriptional noise. We study a simple polymer model where proteins-modeling complexes of transcription factors and polymerases-bind multivalently to transcription units-modeling regulatory elements such as promoters and enhancers. We also include cohesinlike factors that extrude chromatin loops that are important for the physiological folding of chromosomes. We find that transcription factor binding creates spatiotemporal patterning and a highly variable correlation time in transcriptional dynamics, which is linked to the cell-to-cell variation in gene expression. Loop extrusion also contributes to noise, as the stochastic nature of this process leads to different networks of cohesin loops in different cells in our model. Our results could be tested with single-cell experiments and provide a pathway to understanding the principles underlying transcriptional plasticity in vivo.

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Publication Details

Journal
Physical Review Letters
Published
2025-10-08
DOI
https://doi.org/10.1103/bjq4-xnsy
Citations
4
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
3.22

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article

Bridging-Induced Phase Separation and Loop Extrusion Drive Noise in Chromatin Transcription

Davide Marenduzzo, Cleis Battaglia, Giada Forte, Michael Chiang et al.
4 citations
Physical Review Letters
Genomics and Chromatin Dynamics
3.22
article

Bridging-Induced Phase Separation and Loop Extrusion Drive Noise in Chromatin Transcription

Davide Marenduzzo, Cleis Battaglia, Giada Forte, Michael Chiang, Chris A. Brackley
article en
4 citations

Abstract

Cell-to-cell heterogeneity in transcription, or transcriptional noise, is important in cellular development and in disease. The molecular mechanisms driving it are, however, elusive and ill-understood. Here, we use computer simulations to explore the role of 3D chromatin structure in driving transcriptional noise. We study a simple polymer model where proteins-modeling complexes of transcription factors and polymerases-bind multivalently to transcription units-modeling regulatory elements such as promoters and enhancers. We also include cohesinlike factors that extrude chromatin loops that are important for the physiological folding of chromosomes. We find that transcription factor binding creates spatiotemporal patterning and a highly variable correlation time in transcriptional dynamics, which is linked to the cell-to-cell variation in gene expression. Loop extrusion also contributes to noise, as the stochastic nature of this process leads to different networks of cohesin loops in different cells in our model. Our results could be tested with single-cell experiments and provide a pathway to understanding the principles underlying transcriptional plasticity in vivo.

Physical Review LettersVol. 135(15)
Edinburgh Cancer Research (GB), Institute of Genetics and Cancer (GB), University of Edinburgh (GB)
Wellcome Trust, Leverhulme Trust, Medical Research Council
Openalex Percentile: Top 7%
Genomics and Chromatin Dynamics
3.22
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