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Date and Time 2006-11-21 16:00:00 - 17:00:00
Venue Seminar Room A7F
Speaker Kazuhisa Kinoshita
Graduate School of Biostudies, Kyoto University
Title Molecular mechanism of microtubule dynamics in mitosis
Poster click here to download (PDF)
Host Fumio Matsuzaki
Summary Microtubules polymerize and depolymerize by the addition and loss of αβ-tubulin dimers from their ends. The discovery of dynamic instability revealed a tubulin-intrinsic mechanism for enhancing microtubule turnover. Microtubules exhibit dynamic instability when assembled from purified tubulin as well as in a physiological cytoplasmic environment. However, compared to purified tubulin, microtubules in vivo exhibit a faster polymerization rate and dramatically more frequent catastrophe, the transition from polymerization to depolymerization. The combination of rapid polymerization and high catastrophe rates is a hallmark of physiological microtubule dynamics and allows microtubules in cells to effectively search three-dimensional space and rapidly change spatial distributions.

How do microtubules in a physiological environment exhibit a high catastrophe rate while still maintaining a high polymerization rate? The studies using Xenopus egg extracts suggested that the microtubule-stabilizing protein XMAP215 and the microtubule-destabilizing kinesin MCAK have activities that may explain the ability of physiological microtubules. We have shown that a simple mixture of three purified components: tubulin, XMAP215 and MCAK can reconstitute essential features of physiological microtubule dynamics. Therefore, we propose that proper spatial and temporal regulation of the opposing activities of XMAP215 and MCAK is essential for modulation of microtubule dynamics during the cell cycle and spindle assembly. I also will talk about how XMAP215 is regulated to promote centrosome-specific microtubule assembly in mitosis.
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