Kinesin-1 regulates microtubule dynamics via a c-Jun N-terminal kinase-dependent mechanism.

Abstract

In the kinesin family, all the molecular motors that have been implicated in the regulation of microtubule dynamics have been shown to stimulate microtubule depolymerization. Here, we report that kinesin-1 (also known as conventional kinesin or KIF5B) stimulates microtubule elongation and rescues. We show that microtubule-associated kinesin-1 carries the c-Jun N-terminal kinase (JNK) to allow its activation and that microtubule elongation requires JNK activity throughout the microtubule life cycle. We also show that kinesin-1 and JNK promoted microtubule rescues to similar extents. Stimulation of microtubule rescues by the kinesin-1/JNK pathway could not be accounted for by the rescue factor CLIP-170. Indeed only a dual inhibition of kinesin-1/JNK and CLIP-170 completely blocked rescues and led to extensive microtubule loss. We propose that the kinesin-1/JNK signaling pathway is a major regulator of microtubule dynamics in living cells and that it is required with the rescue factor CLIP-170 to allow cells to build their interphase microtubule network.

DOI: 10.1074/jbc.M109.007906

Cite this paper

@article{Daire2009Kinesin1RM, title={Kinesin-1 regulates microtubule dynamics via a c-Jun N-terminal kinase-dependent mechanism.}, author={Vanessa Daire and Julien Giustiniani and Ingrid Leroy-Gori and M{\'e}lanie Quesnoit and St{\'e}phanie Drevensek and Ariane Dimitrov and Franck Perez and Christian Po{\"{u}s}, journal={The Journal of biological chemistry}, year={2009}, volume={284 46}, pages={31992-2001} }