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A Highlights from MBoC Selection: MAP65/Ase1 promote microtubule flexibility
Authors:D. Portran  M. Zoccoler  J. Gaillard  V. Stoppin-Mellet  E. Neumann  I. Arnal  J. L. Martiel  M. Vantard
Affiliation:University of California, Davis;aLaboratoire de Physiologie Cellulaire et Végétale, Institut de Recherches en Technologies et Sciences pour le Vivant, UMR CNRS, CEA, INRA, Université Joseph Fourier, 38054 Grenoble, France;bInstitut de Biologie Structurale Jean-Pierre Ebel, CNRS, CEA, Université Joseph Fourier, Grenoble 38027, France;cInstitut de Neurosciences, INSERM, Université Joseph Fourier, La Tronche 38706, France
Abstract:
Microtubules (MTs) are dynamic cytoskeletal elements involved in numerous cellular processes. Although they are highly rigid polymers with a persistence length of 1–8 mm, they may exhibit a curved shape at a scale of few micrometers within cells, depending on their biological functions. However, how MT flexural rigidity in cells is regulated remains poorly understood. Here we ask whether MT-associated proteins (MAPs) could locally control the mechanical properties of MTs. We show that two major cross-linkers of the conserved MAP65/PRC1/Ase1 family drastically decrease MT rigidity. Their MT-binding domain mediates this effect. Remarkably, the softening effect of MAP65 observed on single MTs is maintained when MTs are cross-linked. By reconstituting physical collisions between growing MTs/MT bundles, we further show that the decrease in MT stiffness induced by MAP65 proteins is responsible for the sharp bending deformations observed in cells when they coalign at a steep angle to create bundles. Taken together, these data provide new insights into how MAP65, by modifying MT mechanical properties, may regulate the formation of complex MT arrays.
Keywords:
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