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Kinetic and structural roles for the surface in guiding SAS-6 self-assembly to direct centriole architecture

Author

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  • Niccolò Banterle

    (Swiss Federal Institute of Technology Lausanne (EPFL))

  • Adrian P. Nievergelt

    (Swiss Federal Institute of Technology Lausanne (EPFL)
    Max Planck Institute of Molecular Cell Biology and Genetics)

  • Svenja Buhr

    (Interdisciplinary Center for Scientific Computing (IWR) Heidelberg University
    Heidelberg Institute for Theoretical Studies, Heidelberg, Germany)

  • Georgios N. Hatzopoulos

    (Swiss Federal Institute of Technology Lausanne (EPFL))

  • Charlène Brillard

    (Swiss Federal Institute of Technology Lausanne (EPFL))

  • Santiago Andany

    (Swiss Federal Institute of Technology Lausanne (EPFL))

  • Tania Hübscher

    (Swiss Federal Institute of Technology Lausanne (EPFL))

  • Frieda A. Sorgenfrei

    (Heidelberg Institute for Theoretical Studies, Heidelberg, Germany
    Austrian Centre of Industrial Biotechnology c/o University of Graz, Institute of Chemistry, NAWI Graz, BioTechMed Graz)

  • Ulrich S. Schwarz

    (Interdisciplinary Center for Scientific Computing (IWR) Heidelberg University
    Heidelberg University, Institute for Theoretical Physics and BioQuant)

  • Frauke Gräter

    (Interdisciplinary Center for Scientific Computing (IWR) Heidelberg University
    Heidelberg Institute for Theoretical Studies, Heidelberg, Germany)

  • Georg E. Fantner

    (Swiss Federal Institute of Technology Lausanne (EPFL))

  • Pierre Gönczy

    (Swiss Federal Institute of Technology Lausanne (EPFL))

Abstract

Discovering mechanisms governing organelle assembly is a fundamental pursuit in biology. The centriole is an evolutionarily conserved organelle with a signature 9-fold symmetrical chiral arrangement of microtubules imparted onto the cilium it templates. The first structure in nascent centrioles is a cartwheel, which comprises stacked 9-fold symmetrical SAS-6 ring polymers emerging orthogonal to a surface surrounding each resident centriole. The mechanisms through which SAS-6 polymerization ensures centriole organelle architecture remain elusive. We deploy photothermally-actuated off-resonance tapping high-speed atomic force microscopy to decipher surface SAS-6 self-assembly mechanisms. We show that the surface shifts the reaction equilibrium by ~104 compared to solution. Moreover, coarse-grained molecular dynamics and atomic force microscopy reveal that the surface converts the inherent helical propensity of SAS-6 polymers into 9-fold rings with residual asymmetry, which may guide ring stacking and impart chiral features to centrioles and cilia. Overall, our work reveals fundamental design principles governing centriole assembly.

Suggested Citation

  • Niccolò Banterle & Adrian P. Nievergelt & Svenja Buhr & Georgios N. Hatzopoulos & Charlène Brillard & Santiago Andany & Tania Hübscher & Frieda A. Sorgenfrei & Ulrich S. Schwarz & Frauke Gräter & Geor, 2021. "Kinetic and structural roles for the surface in guiding SAS-6 self-assembly to direct centriole architecture," Nature Communications, Nature, vol. 12(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-26329-1
    DOI: 10.1038/s41467-021-26329-1
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    References listed on IDEAS

    as
    1. Jung-Eun Park & Liang Zhang & Jeong Kyu Bang & Thorkell Andresson & Frank DiMaio & Kyung S. Lee, 2019. "Phase separation of Polo-like kinase 4 by autoactivation and clustering drives centriole biogenesis," Nature Communications, Nature, vol. 10(1), pages 1-19, December.
    2. P. Guichard & V. Hamel & M. Le Guennec & N. Banterle & I. Iacovache & V. Nemčíková & I. Flückiger & K. N. Goldie & H. Stahlberg & D. Lévy & B. Zuber & P. Gönczy, 2017. "Cell-free reconstitution reveals centriole cartwheel assembly mechanisms," Nature Communications, Nature, vol. 8(1), pages 1-9, April.
    3. Shohei Yamamoto & Daiju Kitagawa, 2019. "Self-organization of Plk4 regulates symmetry breaking in centriole duplication," Nature Communications, Nature, vol. 10(1), pages 1-12, December.
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