Differences in Intrinsic Tubulin Dynamic Properties Contribute to Spindle Length Control in Xenopus Species
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Hirst, William
Biswas, Abin
Mahalingan, Kishore K
Reber, Simone
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Cell Press
Abstract
The function of cellular organelles relates not only to their molecular composition but also to their size. However, how the size of dynamic mesoscale structures is established and maintained remains poorly understood [1–3]. Mitotic spindle length, for example, varies several-fold among cell types and among different organisms [4]. Although most studies on spindle size control focus on changes in proteins that regulate
microtubule dynamics [5–8], the contribution of the spindle’s main building block, the ab-tubulin heterodimer, has yet to be studied. Apart from microtubule-associated proteins and motors, two factors have
been shown to contribute to the heterogeneity of microtubule dynamics: tubulin isoform composition [9,
10] and post-translational modifications [11]. In the past, studying the contribution of tubulin and microtubules to spindle assembly has been limited by the fact that physiologically relevant tubulins were not available. Here, we show that tubulins purified from two closely related frogs, Xenopus laevis and Xenopus tropicalis, have surprisingly different microtubule dynamics in vitro. X. laevis microtubules combine very fast
growth and infrequent catastrophes. In contrast, X. tropicalis microtubules grow slower and catastrophe
more frequently. We show that spindle length and microtubule mass can be controlled by titrating the ratios
of the tubulins from the two frog species. Furthermore, we combine our in vitro reconstitution assay and egg
extract experiments with computational modeling to show that differences in intrinsic properties of different
tubulins contribute to the control of microtubule mass and therefore set steady-state spindle length.
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Current Biology
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Open Access
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CC BY-NC-ND license
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2099-12-30
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