| Literature DB >> 26999736 |
Manuel Hilbert1, Akira Noga2, Daniel Frey1, Virginie Hamel3, Paul Guichard3, Sebastian H W Kraatz1, Moritz Pfreundschuh4, Sarah Hosner1, Isabelle Flückiger3, Rolf Jaussi1, Mara M Wieser1, Katherine M Thieltges1, Xavier Deupi1,5, Daniel J Müller4, Richard A Kammerer1, Pierre Gönczy3, Masafumi Hirono2, Michel O Steinmetz1.
Abstract
Centrioles are critical for the formation of centrosomes, cilia and flagella in eukaryotes. They are thought to assemble around a nine-fold symmetric cartwheel structure established by SAS-6 proteins. Here, we have engineered Chlamydomonas reinhardtii SAS-6-based oligomers with symmetries ranging from five- to ten-fold. Expression of a SAS-6 mutant that forms six-fold symmetric cartwheel structures in vitro resulted in cartwheels and centrioles with eight- or nine-fold symmetries in vivo. In combination with Bld10 mutants that weaken cartwheel-microtubule interactions, this SAS-6 mutant produced six- to eight-fold symmetric cartwheels. Concurrently, the microtubule wall maintained eight- and nine-fold symmetries. Expressing SAS-6 with analogous mutations in human cells resulted in nine-fold symmetric centrioles that exhibited impaired length and organization. Together, our data suggest that the self-assembly properties of SAS-6 instruct cartwheel symmetry, and lead us to propose a model in which the cartwheel and the microtubule wall assemble in an interdependent manner to establish the native architecture of centrioles.Entities:
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Year: 2016 PMID: 26999736 DOI: 10.1038/ncb3329
Source DB: PubMed Journal: Nat Cell Biol ISSN: 1465-7392 Impact factor: 28.824