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A Force-Induced Directional Switch of a Molecular Motor Enables Parallel Microtubule Bundle Formation
Author(s) -
Maxim I. Molodtsov,
Christine Mieck,
Jeroen Dobbelaere,
Alexander Dammermann,
Stefan Westermann,
Alipasha Vaziri
Publication year - 2016
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2016.09.029
Subject(s) - microtubule , kinesin , biology , microtubule organizing center , microtubule nucleation , molecular motor , bundle , mechanism (biology) , microbiology and biotechnology , dynein , physics , centrosome , cell , genetics , materials science , cell cycle , quantum mechanics , composite material
Microtubule-organizing centers (MTOCs) nucleate microtubules that can grow autonomously in any direction. To generate bundles of parallel microtubules originating from a single MTOC, the growth of multiple microtubules needs to coordinated, but the underlying mechanism is unknown. Here, we show that a conserved two-component system consisting of the plus-end tracker EB1 and the minus-end-directed molecular motor Kinesin-14 is sufficient to promote parallel microtubule growth. The underlying mechanism relies on the ability of Kinesin-14 to guide growing plus ends along existing microtubules. The generality of this finding is supported by yeast, Drosophila, and human EB1/Kinesin-14 pairs. We demonstrate that plus-end guiding involves a directional switch of the motor due to a force applied via a growing microtubule end. The described mechanism can account for the generation of parallel microtubule networks required for a broad range of cellular functions such as spindle assembly or cell polarization.

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