Mechanosensitive genomic enhancers potentiate the cellular response to matrix stiffness

Epigenetic control of gene expression and cellular phenotype is influenced by changes in the local microenvironment, yet how mechanical cues precisely influence epigenetic state to regulate transcription remains largely unmapped. In this study, we combined genome-wide epigenome profiling, epigenome editing, and phenotypic and single-cell RNA sequencing CRISPR screening to identify a class of genomic enhancers that responds to the mechanical microenvironment. These "mechanoenhancers" can be preferentially activated on either soft or stiff extracellular matrix contexts and regulate transcription to influence critical cell functions including apoptosis, adhesion, proliferation, and migration. Epigenetic editing of mechanoenhancers reprograms the cellular response to the mechanical microenvironment and modulates the activation of disease-related genes in lung fibroblasts from healthy and fibrotic donors. Epigenetic editing of mechanoenhancers holds potential for precise targeting of mechanically driven diseases.

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Publication Details

Journal
Science
Published
2025-09-25
DOI
https://doi.org/10.1126/science.adl1988
Citations
7
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
5.64
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Mechanosensitive genomic enhancers potentiate the cellular response to matrix stiffness

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7 citations
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RNA Research and Splicing
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article

Mechanosensitive genomic enhancers potentiate the cellular response to matrix stiffness

Thomas J. Whitlow, Aleksandra Tata, Brenton D. Hoffman, Brian D. Cosgrove, Alexias Safi, Tongyu Sun, Yarui Diao, Lexi R. Bounds, Gregory E. Crawford, Alejandro Barrera, Nahid Iglesias, Charles A. Gersbach, Purushothama Rao Tata, Lingyun Song, Anthony Rizzo, Carson Key Taylor, Alan L Su
article en
7 citations

Abstract

Epigenetic control of gene expression and cellular phenotype is influenced by changes in the local microenvironment, yet how mechanical cues precisely influence epigenetic state to regulate transcription remains largely unmapped. In this study, we combined genome-wide epigenome profiling, epigenome editing, and phenotypic and single-cell RNA sequencing CRISPR screening to identify a class of genomic enhancers that responds to the mechanical microenvironment. These "mechanoenhancers" can be preferentially activated on either soft or stiff extracellular matrix contexts and regulate transcription to influence critical cell functions including apoptosis, adhesion, proliferation, and migration. Epigenetic editing of mechanoenhancers reprograms the cellular response to the mechanical microenvironment and modulates the activation of disease-related genes in lung fibroblasts from healthy and fibrotic donors. Epigenetic editing of mechanoenhancers holds potential for precise targeting of mechanically driven diseases.

ScienceVol. 390(6778)
Duke University (US), Duke Medical Center (US), Applied Genetic Technologies (United States) (US)
Openalex Percentile: Top 4%
RNA Research and Splicing
5.64
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