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Coronin 1C restricts endosomal branched actin to organize ER contact and endosome fission.

Jonathan F StriepenGia K Voeltz
Published in: The Journal of cell biology (2022)
ER contact sites define the position of endosome bud fission during actin-dependent cargo sorting. Disrupting endosomal actin structures prevents retrograde cargo movement; however, how actin affects ER contact site formation and endosome fission is not known. Here we show that in contrast with the WASH complex, actin, its nucleator ARP2/3, and COR1C form a contained structure at the bud neck that defines the site of bud fission. We found that actin confinement is facilitated by type I coronins. Depletion of type I coronins allows actin to extend along the length of the bud in an ARP2/3-dependent manner. We demonstrate that extension of branched actin prevents ER recruitment and stalls buds before fission. Finally, our structure-function studies show that the COR1C's coiled-coil domain is sufficient to restore actin confinement, ER recruitment, and endosome fission. Together, our data reveal how the dynamics of endosomal actin and activity of actin regulators organize ER-associated bud fission.
Keyphrases
  • cell migration
  • breast cancer cells
  • estrogen receptor
  • endoplasmic reticulum
  • magnetic resonance
  • mass spectrometry
  • electronic health record