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

J Cell Biol. 2022 Aug 1;221(8):e202110089. doi: 10.1083/jcb.202110089. Epub 2022 Jul 8.

Abstract

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.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Actins / metabolism*
  • Animals
  • COS Cells
  • Chlorocebus aethiops
  • Endoplasmic Reticulum / metabolism*
  • Endosomes / metabolism*
  • Humans
  • Microfilament Proteins / metabolism*
  • Nerve Growth Factors / genetics
  • Nerve Growth Factors / metabolism
  • Phosphate-Binding Proteins / metabolism
  • Protein Binding
  • rab7 GTP-Binding Proteins / metabolism

Substances

  • Actins
  • Microfilament Proteins
  • Nerve Growth Factors
  • Phosphate-Binding Proteins
  • rab7 GTP-Binding Proteins
  • rab7 GTP-binding proteins, human
  • coronin proteins