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BiochemistrybioRxiv
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The conserved centrosomal motif, γTuNA, forms a dimer that directly activates microtubule nucleation by the γ-tubulin ring complex (γTuRC).

M. J. Rale, B. Romer, B. P. Mahon, S. M. Travis, S. Petry

Abstract

1.To establish the microtubule cytoskeleton, the cell must tightly regulate when and where microtubules are nucleated. This regulation involves controlling the initial nucleation template, the {gamma}-tubulin ring complex ({gamma}TuRC). Although {gamma}TuRC is present throughout the cytoplasm, its activity is restricted to specific sites including the centrosome and Golgi. The well-conserved {gamma}-tubulin nucleation activator ({gamma}TuNA) domain has been reported to increase the number of microtubules generated by {gamma}TuRCs. Here we utilize Xenopus egg extract and in vitro single molecule imaging assays to show that {gamma}TuNA activates microtubule nucleation in extract and directly activates {gamma}TuRC in vitro. Via mutation analysis, we find that {gamma}TuNA is an obligate dimer. Moreover, efficient dimerization as well as {gamma}TuNAs L70, F75, and L77 residues are required for binding to and activation of {gamma}TuRC. Finally, we find that {gamma}TuNAs activating effect opposes inhibitory regulation by stathmin. In sum, our study illuminates how {gamma}TuRC is controlled in space and time in order to build specific cytoskeletal structures.

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