| Literature DB >> 25977552 |
Jeffrey B Woodruff1, Oliver Wueseke1, Valeria Viscardi2, Julia Mahamid3, Stacy D Ochoa2, Jakob Bunkenborg4, Per O Widlund1, Andrei Pozniakovsky1, Esther Zanin2, Shirin Bahmanyar2, Andrea Zinke1, Sun Hae Hong5, Marcus Decker1, Wolfgang Baumeister3, Jens S Andersen6, Karen Oegema7, Anthony A Hyman8.
Abstract
The centrosome organizes microtubule arrays within animal cells and comprises two centrioles surrounded by an amorphous protein mass called the pericentriolar material (PCM). Despite the importance of centrosomes as microtubule-organizing centers, the mechanism and regulation of PCM assembly are not well understood. In Caenorhabditis elegans, PCM assembly requires the coiled-coil protein SPD-5. We found that recombinant SPD-5 could polymerize to form micrometer-sized porous networks in vitro. Network assembly was accelerated by two conserved regulators that control PCM assembly in vivo, Polo-like kinase-1 and SPD-2/Cep192. Only the assembled SPD-5 networks, and not unassembled SPD-5 protein, functioned as a scaffold for other PCM proteins. Thus, PCM size and binding capacity emerge from the regulated polymerization of one coiled-coil protein to form a porous network.Entities:
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Year: 2015 PMID: 25977552 PMCID: PMC5039038 DOI: 10.1126/science.aaa3923
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728