Myosin-Va is required for preciliary vesicle transportation to the mother centriole during ciliogenesis

Nat Cell Biol. 2018 Feb;20(2):175-185. doi: 10.1038/s41556-017-0018-7. Epub 2018 Jan 15.

Abstract

Primary cilia play essential roles in signal transduction and development. The docking of preciliary vesicles at the distal appendages of a mother centriole is an initial/critical step of ciliogenesis, but the mechanisms are unclear. Here, we demonstrate that myosin-Va mediates the transportation of preciliary vesicles to the mother centriole and reveal the underlying mechanism. We also show that the myosin-Va-mediated transportation of preciliary vesicles is the earliest event that defines the onset of ciliogenesis. Depletion of myosin-Va significantly inhibits the attachment of preciliary vesicles to the distal appendages of the mother centriole and decreases cilia assembly. Myosin-Va functions upstream of EHD1- and Rab11-mediated ciliary vesicle formation. Importantly, dynein mediates myosin-Va-associated preciliary vesicle transportation to the pericentrosomal region along microtubules, while myosin-Va mediates preciliary vesicle transportation from the pericentrosomal region to the distal appendages of the mother centriole via the Arp2/3-associated branched actin network.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin-Related Protein 2 / genetics
  • Actins / genetics
  • Animals
  • Biological Transport / genetics
  • Centrioles / genetics
  • Centrioles / metabolism
  • Cilia / genetics*
  • Cilia / metabolism
  • Humans
  • Mice
  • Microtubules / genetics
  • Microtubules / metabolism
  • Myosin Heavy Chains / antagonists & inhibitors
  • Myosin Heavy Chains / genetics*
  • Myosin Type V / antagonists & inhibitors
  • Myosin Type V / genetics*
  • NIH 3T3 Cells
  • Primary Cell Culture
  • Retinal Pigment Epithelium / cytology
  • Retinal Pigment Epithelium / growth & development
  • Retinal Pigment Epithelium / metabolism
  • Signal Transduction
  • Vesicular Transport Proteins / genetics*
  • rab GTP-Binding Proteins / genetics*

Substances

  • Actin-Related Protein 2
  • Actins
  • EHD1 protein, human
  • Vesicular Transport Proteins
  • MYO5A protein, human
  • Myosin Type V
  • rab11 protein
  • Myosin Heavy Chains
  • rab GTP-Binding Proteins