Taxane-induced conformational changes in the microtubule lattice activate GEF-H1-dependent RhoA signalling

Abstract Taxanes are widely used chemotherapeutic agents that perturb cell division. They also exert effects during interphase, but the underlying mechanisms are poorly understood. Here we show that taxanes activate RhoA signalling and induce actin remodelling by releasing the RhoA activator GEF-H1 from microtubules. This taxane-induced release of GEF-H1 occurs rapidly, is independent of tubulin post-translational modifications, and can be recapitulated using purified proteins. In vitro reconstitution assays combined with analyses of microtubule structure revealed that microtubule binding by GEF-H1 is inhibited by microtubule-stabilizing ligands that expand the microtubule lattice, such as taxanes and GMPCPP, but not by others, including GTPγS and discodermolide, which stabilize a compacted microtubule lattice. Our findings demonstrate that alterations in microtubule lattice conformation can activate key signalling pathways, offering insights into the mode of action of taxanes and the possible origins of their side effects.

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Publication Details

Journal
Nature Cell Biology
Published
2026-09-24
DOI
https://doi.org/10.1038/s41556-026-02079-4
Primary Topic
Microtubule and mitosis dynamics
Type
article
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article

Taxane-induced conformational changes in the microtubule lattice activate GEF-H1-dependent RhoA signalling

Michel Olivier Steinmetz, Joyce C. M. Meiring, Zdeněk Lánský, Stuart C. Howes et al.
Nature Cell Biology
Microtubule and mitosis dynamics
article

Taxane-induced conformational changes in the microtubule lattice activate GEF-H1-dependent RhoA signalling

Michel Olivier Steinmetz, Joyce C. M. Meiring, Zdeněk Lánský, Stuart C. Howes, Samantha J. Stehbens, Saishree S. Iyer, Anna S. Akhmanova, Lukas C. Kapitein, Varsha Mahapatra, Kelly E. Stecker, Harriet A. J. Saunders, José Fernando Díaz, Matteo Giono, Sung Ryul Choi, Ilya Grigoriev, Andressa Pelster Jose, Daan Morren, Ioanna Metallidou, Ruijie Liu, Alex Moore, Adela Karhanova, Marèl F. M. Spoelstra, Molly S. C. Gravett
article en

Abstract

Abstract Taxanes are widely used chemotherapeutic agents that perturb cell division. They also exert effects during interphase, but the underlying mechanisms are poorly understood. Here we show that taxanes activate RhoA signalling and induce actin remodelling by releasing the RhoA activator GEF-H1 from microtubules. This taxane-induced release of GEF-H1 occurs rapidly, is independent of tubulin post-translational modifications, and can be recapitulated using purified proteins. In vitro reconstitution assays combined with analyses of microtubule structure revealed that microtubule binding by GEF-H1 is inhibited by microtubule-stabilizing ligands that expand the microtubule lattice, such as taxanes and GMPCPP, but not by others, including GTPγS and discodermolide, which stabilize a compacted microtubule lattice. Our findings demonstrate that alterations in microtubule lattice conformation can activate key signalling pathways, offering insights into the mode of action of taxanes and the possible origins of their side effects.

Nature Cell Biology
The University of Queensland (AU), University of Applied Sciences Utrecht (NL), University of Basel (CH), Utrecht University (NL), Charles University (CZ), Paul Scherrer Institute (CH), Czech Academy of Sciences, Institute of Biotechnology (CZ), Netherlands Metabolomics Centre (NL), Centro de Investigaciones Biológicas Margarita Salas (ES), Institute for Molecular Bioscience (AU)
Openalex Percentile: Top 15%
Microtubule and mitosis dynamics
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