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

The Journal of cell biology (2022-07-09)
Jonathan F Striepen, Gia K Voeltz
ZUSAMMENFASSUNG

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.

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Sigma-Aldrich
Anti-GAPDH in Kaninchen hergestellte Antikörper, ~1 mg/mL, affinity isolated antibody, buffered aqueous solution
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Anti-Maus-IgG (Gesamtmolekül)-Peroxidase in Ziege hergestellte Antikörper, affinity isolated antibody, buffered aqueous solution
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Anti-Kaninchen-IgG-(Gesamtmolekül)-Peroxidase in Ziege hergestellte Antikörper, affinity isolated antibody, buffered aqueous solution
Sigma-Aldrich
Arp2/3-Komplex-Inhibitor I, CK-666, Arp2/3 Complex Inhibitor I, CK-666, CAS 442633-00-3, is a cell-permeable selective inhibitor of actin assembly mediated by actin-related protein Arp2/3 complex (IC50 = 4 uM in human).
Sigma-Aldrich
Anti-WASH-Komplex-Untereinheit-FAM21C-Antikörper, from rabbit