| Literature DB >> 28575670 |
Jeffrey B Woodruff1, Beatriz Ferreira Gomes2, Per O Widlund3, Julia Mahamid4, Alf Honigmann2, Anthony A Hyman5.
Abstract
Centrosomes are non-membrane-bound compartments that nucleate microtubule arrays. They consist of nanometer-scale centrioles surrounded by a micron-scale, dynamic assembly of protein called the pericentriolar material (PCM). To study how PCM forms a spherical compartment that nucleates microtubules, we reconstituted PCM-dependent microtubule nucleation in vitro using recombinant C. elegans proteins. We found that macromolecular crowding drives assembly of the key PCM scaffold protein SPD-5 into spherical condensates that morphologically and dynamically resemble in vivo PCM. These SPD-5 condensates recruited the microtubule polymerase ZYG-9 (XMAP215 homolog) and the microtubule-stabilizing protein TPXL-1 (TPX2 homolog). Together, these three proteins concentrated tubulin ∼4-fold over background, which was sufficient to reconstitute nucleation of microtubule asters in vitro. Our results suggest that in vivo PCM is a selective phase that organizes microtubule arrays through localized concentration of tubulin by microtubule effector proteins.Entities:
Keywords: Centrosome; Polo Kinase; SPD-5; TPX2; XMAP215; microtubule-organizing center; pericentriolar material; phase separation; scaffold
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Year: 2017 PMID: 28575670 DOI: 10.1016/j.cell.2017.05.028
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582