Mechanically-induced Septin Networks Protect Nuclear Integrity

The cytoskeleton is a key mediator of mechanical interactions in cells, but specific contributions of septins remains unclear. Septins preferentially localize with a subset of actin stress fibers positioned under the nucleus, where they are situated between the membrane and stress fibers. Removing the nucleus from the cell results in the loss of these subnuclear septin-decorated stress fibers. Surprisingly, however, their formation can be rescued using a large glass bead in place of the nucleus. Similarly, applying a compressive force to the cell via confinement, whether externally or through internally generated actomyosin forces, results in increased septin accumulation in regions where the nucleus engages the cell cortex. Finally, loss of septin filaments via knockdown of SEPT7 increases the likelihood of nuclear membrane rupture during confinement. Together these data suggest that septins act as a dynamic mechanosensitive protective mechanism to buffer mechanical forces on the nucleus.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-01-21
DOI
https://doi.org/10.64898/2026.01.20.700414
Citations
1
Primary Topic
Fungal and yeast genetics research
Type
article
Field-Weighted Citation Impact
22.24
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article

Mechanically-induced Septin Networks Protect Nuclear Integrity

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Fungal and yeast genetics research
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article

Mechanically-induced Septin Networks Protect Nuclear Integrity

Patrick W. Oakes, Jesse Aaron, Owen Puls, Harikrushnan Balasubramanian, Alexia Caillier, Joseph J. Tidei, T. Chew, Shreya Chandrasekar, Jordan R. Beach, Satya Khuon, Rachel Lee, Margaret E Utgaard
article en
1 citations

Abstract

The cytoskeleton is a key mediator of mechanical interactions in cells, but specific contributions of septins remains unclear. Septins preferentially localize with a subset of actin stress fibers positioned under the nucleus, where they are situated between the membrane and stress fibers. Removing the nucleus from the cell results in the loss of these subnuclear septin-decorated stress fibers. Surprisingly, however, their formation can be rescued using a large glass bead in place of the nucleus. Similarly, applying a compressive force to the cell via confinement, whether externally or through internally generated actomyosin forces, results in increased septin accumulation in regions where the nucleus engages the cell cortex. Finally, loss of septin filaments via knockdown of SEPT7 increases the likelihood of nuclear membrane rupture during confinement. Together these data suggest that septins act as a dynamic mechanosensitive protective mechanism to buffer mechanical forces on the nucleus.

bioRxiv (Cold Spring Harbor Laboratory)
Loyola University Chicago (US), Janelia Research Campus (US)
Openalex Percentile: Top 2%
Fungal and yeast genetics research
22.24
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