Regulation of chromatin modifications through coordination of nucleus size and epithelial cell morphology heterogeneity

Cell morphology heterogeneity is pervasive in epithelial collectives, yet the underlying mechanisms driving such heterogeneity and its consequential biological ramifications remain elusive. Here, we observed a consistent correlation between the epithelial cell morphology and nucleus morphology during crowding, revealing a persistent log-normal probability distribution characterizing both cell and nucleus areas across diverse epithelial model systems. We showed that this morphological diversity arises from asymmetric partitioning during cell division. Next, we provide insights into the impact of nucleus morphology on chromatin modifications. We demonstrated that constraining nucleus leads to downregulation of the euchromatic mark H3K9ac and upregulation of the heterochromatic mark H3K27me3. Furthermore, we showed that nucleus size regulates H3K27me3 levels through histone demethylase UTX. These findings highlight the significance of cell morphology heterogeneity as a driver of chromatin state diversity, shaping functional variability within epithelial tissues.

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Publication Details

Journal
Communications Biology
Published
2025-02-20
DOI
https://doi.org/10.1038/s42003-025-07677-w
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
0.00

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article

Regulation of chromatin modifications through coordination of nucleus size and epithelial cell morphology heterogeneity

Jimmy Kuang‐Hsien Hu, Dapeng Bi, Alexandra G. Bermudez, Neil Y. C. Lin et al.
Communications Biology
Genomics and Chromatin Dynamics
article

Regulation of chromatin modifications through coordination of nucleus size and epithelial cell morphology heterogeneity

Jimmy Kuang‐Hsien Hu, Dapeng Bi, Alexandra G. Bermudez, Neil Y. C. Lin, Zoe D. Latham, J. Alex
article en

Abstract

Cell morphology heterogeneity is pervasive in epithelial collectives, yet the underlying mechanisms driving such heterogeneity and its consequential biological ramifications remain elusive. Here, we observed a consistent correlation between the epithelial cell morphology and nucleus morphology during crowding, revealing a persistent log-normal probability distribution characterizing both cell and nucleus areas across diverse epithelial model systems. We showed that this morphological diversity arises from asymmetric partitioning during cell division. Next, we provide insights into the impact of nucleus morphology on chromatin modifications. We demonstrated that constraining nucleus leads to downregulation of the euchromatic mark H3K9ac and upregulation of the heterochromatic mark H3K27me3. Furthermore, we showed that nucleus size regulates H3K27me3 levels through histone demethylase UTX. These findings highlight the significance of cell morphology heterogeneity as a driver of chromatin state diversity, shaping functional variability within epithelial tissues.

Communications BiologyVol. 8(1)
QB3 (US), Northeastern University (US), University of California, Los Angeles (US), Quantitative BioSciences (US)
National Science Foundation, Alfred P. Sloan Foundation, National Institutes of Health, Division of Physics, National Institute of General Medical Sciences, National Institute of Dental and Craniofacial Research, Division of Materials Research, Division of Chemical, Bioengineering, Environmental, and Transport Systems, Division of Civil, Mechanical and Manufacturing Innovation, Division of Biological Infrastructure
Life in Land
Openalex Percentile: Top 97%
Genomics and Chromatin Dynamics
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