Journal
CURRENT BIOLOGY
Volume 24, Issue 3, Pages 322-328Publisher
CELL PRESS
DOI: 10.1016/j.cub.2014.01.005
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Funding
- Netherlands Organization for Scientific Research (NWO) through an ALW-VICI
- Netherlands Organization for Scientific Research (NWO) through an ALW-VIDI
- Foundation for Fundamental Research on Matter (FOM), NWO
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Proper organization of microtubule networks depends on microtubule-associated proteins and motors that use different spatial cues to guide microtubule growth [1-3]. For example, it has been proposed that the uniform minus-end-out microtubule organization in dendrites of Drosophila neurons is maintained by steering of polymerizing microtubules along the stable ones by kinesin-2 motors bound to growing microtubule plus ends [4]. To explore the mechanics of kinesin-guided microtubule growth, we reconstituted this process in vitro. In the presence of microtubule plus-end tracking EB proteins, a constitutively active kinesin linked to the EB-interacting motif SxIP effectively guided polymerizing microtubules along other microtubules both in cells and in vitro. Experiments combined with modeling revealed that at angles larger than 90 degrees, guidance efficiency is determined by the force needed for microtubule bending. At angles smaller than 90 degrees, guidance requires microtubule growth, and guidance efficiency depends on the ability of kinesins to maintain contact between the two microtubules despite the geometrical constraints imposed by microtubule length and growth rate. Our findings provide a conceptual framework for understanding microtubule guidance during the generation of different types of microtubule arrays.
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