Abstract
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.
Funder
NSF | BIO | Division of Biological Infrastructure
NSF | ENG/OAD | Division of Chemical, Bioengineering, Environmental, and Transport Systems
NSF | ENG/OAD | Division of Civil, Mechanical and Manufacturing Innovation
U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences
NSF | Directorate for Mathematical & Physical Sciences | Division of Materials Research
NSF | Directorate for Mathematical & Physical Sciences | Division of Physics
U.S. Department of Health & Human Services | NIH | National Institute of Dental and Craniofacial Research
Publisher
Springer Science and Business Media LLC