4.6 Article

Molecular architecture of the C. elegans centriole

Journal

PLOS BIOLOGY
Volume 20, Issue 9, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pbio.3001784

Keywords

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Funding

  1. European Union [MCSA-IF 588594, 588459]
  2. Swiss National Science Foundation [310030_197749]
  3. NIH Office of Research Infrastructure Programs [P40 OD010440]
  4. Swiss National Science Foundation (SNF) [310030_197749] Funding Source: Swiss National Science Foundation (SNF)

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This study used U-Ex-STED microscopy and electron microscopy (EM) to reveal the molecular architecture of the C. elegans centriole in unprecedented detail. The researchers found that centriolar and PeriCentriolar Material (PCM) components exhibited a ring-like distribution with distinct diameters and often with a 9-fold radial symmetry. Additionally, they discovered the assembly location of the procentriole and its relationship with other components.
Uncovering organizing principles of organelle assembly is a fundamental pursuit in the life sciences. Caenorhabditis elegans was key in identifying evolutionary conserved components governing assembly of the centriole organelle. However, localizing these components with high precision has been hampered by the minute size of the worm centriole, thus impeding understanding of underlying assembly mechanisms. Here, we used Ultrastructure Expansion coupled with STimulated Emission Depletion (U-Ex-STED) microscopy, as well as electron microscopy (EM) and electron tomography (ET), to decipher the molecular architecture of the worm centriole. Achieving an effective lateral resolution of approximately 14 nm, we localize centriolar and PeriCentriolar Material (PCM) components in a comprehensive manner with utmost spatial precision. We found that all 12 components analysed exhibit a ring-like distribution with distinct diameters and often with a 9-fold radial symmetry. Moreover, we uncovered that the procentriole assembles at a location on the centriole margin where SPD-2 and ZYG-1 also accumulate. Moreover, SAS-6 and SAS-5 were found to be present in the nascent procentriole, with SAS-4 and microtubules recruited thereafter. We registered U-Ex-STED and EM data using the radial array of microtubules, thus allowing us to map each centriolar and PCM protein to a specific ultrastructural compartment. Importantly, we discovered that SAS-6 and SAS-4 exhibit a radial symmetry that is offset relative to microtubules, leading to a chiral centriole ensemble. Furthermore, we established that the centriole is surrounded by a region from which ribosomes are excluded and to which SAS-7 localizes. Overall, our work uncovers the molecular architecture of the C. elegans centriole in unprecedented detail and establishes a comprehensive framework for understanding mechanisms of organelle biogenesis and function.

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