CAMSAP2 organizes a γ-tubulin-independent microtubule nucleation centre
Imasaki, T.; Kikkawa, S.; Niwa, S.; Saijo-Hamano, Y.; Shigematsu, H.; Aoyama, K.; Mitsuoka, K.; Aoki, M.; Sakamot, A.; Tomabechi, Y.; Sakai, N.; Shirouz, M.; Taguchi, S.; Yamagish, Y.; Setsu, T.; Sakihama, Y.; Shimizu, T.; Nitta, E.; Takeichi, M.; Nitta, R.
Show abstract
Microtubules are dynamic polymers consisting of {beta}-tubulin heterodimers. The initial polymerization process, called microtubule nucleation, occurs spontaneously via {beta}-tubulin. Since a large energy barrier prevents microtubule nucleation in cells, the {gamma}-tubulin ring complex is recruited to the centrosome to overcome the nucleation barrier. However, detachment of a considerable number of microtubules from the centrosome is known to contribute to fundamental processes in cells. Here, we present evidence that minus-end-binding calmodulin-regulated spectrin-associated protein 2 (CAMSAP2) serves as a strong nucleator for microtubule formation from soluble {beta}-tubulin independent of {gamma}-tubulin. CAMSAP2 significantly reduces the nucleation barrier close to the critical concentration for microtubule polymerization by stabilizing the longitudinal contacts among {beta}-tubulins. CAMSAP2 clusters together with {beta}-tubulin to generate nucleation intermediates, from which numerous microtubules radiate, forming aster-like structures. Our findings suggest that CAMSAP2 supports microtubule growth by organizing a nucleation centre as well as by stabilizing microtubule nucleation intermediates.
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