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A distal centriolar protein network controls organelle maturation and asymmetry

Author

Listed:
  • Lei Wang

    (New York University School of Medicine)

  • Marion Failler

    (New York University School of Medicine)

  • Wenxiang Fu

    (New York University School of Medicine
    University of Basel)

  • Brian D. Dynlacht

    (New York University School of Medicine)

Abstract

A long-standing mystery in the centrosome field pertains to the origin of asymmetry within the organelle. The removal of daughter centriole-specific/enriched proteins (DCPs) and acquisition of distal appendages on the future mother centriole are two important steps in the generation of asymmetry. We find that DCPs are recruited sequentially, and their removal is abolished in cells lacking Talpid3 or C2CD3. We show that removal of certain DCPs constitutes another level of control for distal appendage (DA) assembly. Remarkably, we also find that Talpid3 forms a distal centriolar multi-functional hub that coordinates the removal of specific DCPs, DA assembly, and recruitment of ciliary vesicles through distinct regions mutated in ciliopathies. Finally, we show that Talpid3, C2CD3, and OFD1 differentially regulate the assembly of sub-distal appendages, the CEP350/FOP/CEP19 module, centriolar satellites, and actin networks. Our work extends the spatial and functional understanding of proteins that control organelle maturation and asymmetry, ciliogenesis, and human disease.

Suggested Citation

  • Lei Wang & Marion Failler & Wenxiang Fu & Brian D. Dynlacht, 2018. "A distal centriolar protein network controls organelle maturation and asymmetry," Nature Communications, Nature, vol. 9(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-06286-y
    DOI: 10.1038/s41467-018-06286-y
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    Cited by:

    1. Ting-Jui Ben Chang & Jimmy Ching-Cheng Hsu & T. Tony Yang, 2023. "Single-molecule localization microscopy reveals the ultrastructural constitution of distal appendages in expanded mammalian centrioles," Nature Communications, Nature, vol. 14(1), pages 1-15, December.

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