Cell confinement initiates a delayed but heritable loss of chromosomes

Heritable genetic changes continually arise in cancer, especially in solid tumors where cells sometimes appear compressed. Rare heritable losses of chromosomes in live cells are quantified here with chromosome reporters (ChReporters) that reveal similar levels of loss after imposing a threshold level of confinement. Compression to ~60% of interphase height ruptures few nuclei compared to deeper compression but perturbs mitotic spindles and prolongs pro/metaphase. Chromosome mis-segregation into micronuclei is discovered only <i>after</i> release from modest confinement, but arrest and death predominate. All such effects are phenocopied by Nocodazole washout that generates a 'memory' of prolonged mitosis, and effects differ from the rapid induction of micronuclei by a spindle assembly checkpoint inhibitor and by a clinical CDK4/6-inhibitor of cell cycle entry. Single-cell-RNA-sequencing confirms chromosome loss days after confinement and reveals persistence of chromosome segregation pathways. Chromosome losses as mitotic memories of confinement ultimately address knowledge gaps in mechanobiology and cancer evolution.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-02-03
DOI
https://doi.org/10.64898/2026.02.03.703566
Primary Topic
Microtubule and mitosis dynamics
Type
article
Field-Weighted Citation Impact
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article

Cell confinement initiates a delayed but heritable loss of chromosomes

Mai Wang, Steven H. Phan, Kayla R. Snare, G. Nader et al.
bioRxiv (Cold Spring Harbor Laboratory)
Microtubule and mitosis dynamics
article

Cell confinement initiates a delayed but heritable loss of chromosomes

Mai Wang, Steven H. Phan, Kayla R. Snare, G. Nader, Dennis E. Discher, P. Rompolas, Jeneille Deans, Jonah Kandell
article en

Abstract

Heritable genetic changes continually arise in cancer, especially in solid tumors where cells sometimes appear compressed. Rare heritable losses of chromosomes in live cells are quantified here with chromosome reporters (ChReporters) that reveal similar levels of loss after imposing a threshold level of confinement. Compression to ~60% of interphase height ruptures few nuclei compared to deeper compression but perturbs mitotic spindles and prolongs pro/metaphase. Chromosome mis-segregation into micronuclei is discovered only <i>after</i> release from modest confinement, but arrest and death predominate. All such effects are phenocopied by Nocodazole washout that generates a 'memory' of prolonged mitosis, and effects differ from the rapid induction of micronuclei by a spindle assembly checkpoint inhibitor and by a clinical CDK4/6-inhibitor of cell cycle entry. Single-cell-RNA-sequencing confirms chromosome loss days after confinement and reveals persistence of chromosome segregation pathways. Chromosome losses as mitotic memories of confinement ultimately address knowledge gaps in mechanobiology and cancer evolution.

bioRxiv (Cold Spring Harbor Laboratory)
Children's Hospital of Philadelphia (US), University of Pennsylvania (US)
Good health and well-being
Openalex Percentile: Top 70%
Microtubule and mitosis dynamics
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