Microtubule-sliding activity of a kinesin-8 promotes spindle assembly and spindle-length control

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Abstract

Molecular motors play critical roles in the formation of mitotic spindles, either through controlling the stability of individual microtubules, or by crosslinking and sliding microtubule arrays. Kinesin-8 motors are best known for their regulatory roles in controlling microtubule dynamics. They contain microtubule-destabilizing activities, and restrict spindle length in a wide variety of cell types and organisms. Here, we report an antiparallel microtubule-sliding activity of the budding yeast kinesin-8, Kip3. The in vivo importance of this sliding activity was established through the identification of complementary Kip3 mutants that separate the sliding activity and microtubule-destabilizing activity. In conjunction with Cin8, a kinesin-5 family member, the sliding activity of Kip3 promotes bipolar spindle assembly and the maintenance of genome stability. We propose a slide-disassemble model where the sliding and destabilizing activity of Kip3 balance during pre-anaphase. This facilitates normal spindle assembly. However, the destabilizing activity of Kip3 dominates in late anaphase, inhibiting spindle elongation and ultimately promoting spindle disassembly. © 2013 Macmillan Publishers Limited. All rights reserved.

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Su, X., Arellano-Santoyo, H., Portran, D., Gaillard, J., Vantard, M., Thery, M., & Pellman, D. (2013). Microtubule-sliding activity of a kinesin-8 promotes spindle assembly and spindle-length control. Nature Cell Biology, 15(8), 948–957. https://doi.org/10.1038/ncb2801

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