REVIEW article

Front. Cell Dev. Biol.

Sec. Morphogenesis and Patterning

Volume 13 - 2025 | doi: 10.3389/fcell.2025.1634252

This article is part of the Research TopicReconstitution Methods in Cell BiologyView all articles

How the chromatin landscape influences nuclear morphology

Provisionally accepted
  • 1The University of Texas Southwestern Medical Center, Dallas, United States
  • 2Molecular Biology, University of Wyoming, Laramie, WY, United States

The final, formatted version of the article will be published soon.

Nuclear morphology is a defining cellular feature, differing based on cell type, tissue type, and species. In healthy cells, nuclear morphology is generally tightly regulated and maintained; however, dynamic changes in nuclear morphology are observed under certain conditions, for instance in early embryos and in some immune cells. Deviations in normal nuclear morphology are linked to numerous diseases, including most cancers and premature aging syndromes. Many regulators of nuclear morphology have been identified, encompassing both intranuclear, cytoplasmic, and extracellular factors. Of note, recent studies have converged on chromatin and chromatin-associated proteins as key determinants of nuclear morphology and dynamics. In this review we discuss how the chromatin landscape regulates nuclear morphology in both normal and diseased cellular states. Additionally, we highlight emerging technologies that promise to bridge critical gaps in our understanding of nuclear morphology, including new approaches to probe nuclear structure and the use of synthetic cells.

Keywords: nuclear size, Nuclear shape, Chromatin structure, chromatin modifications, Cancer, epigenetics, Xenopus egg extract, Microscopy

Received: 23 May 2025; Accepted: 24 Jun 2025.

Copyright: © 2025 Sengupta, Prabha and Levy. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Sourabh Sengupta, The University of Texas Southwestern Medical Center, Dallas, United States
Daniel L. Levy, Molecular Biology, University of Wyoming, Laramie, 82071, WY, United States

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