TY - JOUR
T1 - Golgi-Resident Gαo Promotes Protrusive Membrane Dynamics
AU - Solis, Gonzalo P.
AU - Bilousov, Oleksii
AU - Koval, Alexey
AU - Lüchtenborg, Anne Marie
AU - Lin, Chen
AU - Katanaev, Vladimir L.
N1 - Publisher Copyright:
© 2017 Elsevier Inc.
PY - 2017/8/24
Y1 - 2017/8/24
N2 - To form protrusions like neurites, cells must coordinate their induction and growth. The first requires cytoskeletal rearrangements at the plasma membrane (PM), the second requires directed material delivery from cell's insides. We find that the Gαo-subunit of heterotrimeric G proteins localizes dually to PM and Golgi across phyla and cell types. The PM pool of Gαo induces, and the Golgi pool feeds, the growing protrusions by stimulated trafficking. Golgi-residing KDELR binds and activates monomeric Gαo, atypically for G protein-coupled receptors that normally act on heterotrimeric G proteins. Through multidimensional screenings identifying > 250 Gαo interactors, we pinpoint several basic cellular activities, including vesicular trafficking, as being regulated by Gαo. We further find small Golgi-residing GTPases Rab1 and Rab3 as direct effectors of Gαo. This KDELR → Gαo → Rab1/3 signaling axis is conserved from insects to mammals and controls material delivery from Golgi to PM in various cells and tissues.
AB - To form protrusions like neurites, cells must coordinate their induction and growth. The first requires cytoskeletal rearrangements at the plasma membrane (PM), the second requires directed material delivery from cell's insides. We find that the Gαo-subunit of heterotrimeric G proteins localizes dually to PM and Golgi across phyla and cell types. The PM pool of Gαo induces, and the Golgi pool feeds, the growing protrusions by stimulated trafficking. Golgi-residing KDELR binds and activates monomeric Gαo, atypically for G protein-coupled receptors that normally act on heterotrimeric G proteins. Through multidimensional screenings identifying > 250 Gαo interactors, we pinpoint several basic cellular activities, including vesicular trafficking, as being regulated by Gαo. We further find small Golgi-residing GTPases Rab1 and Rab3 as direct effectors of Gαo. This KDELR → Gαo → Rab1/3 signaling axis is conserved from insects to mammals and controls material delivery from Golgi to PM in various cells and tissues.
KW - Drosophila melanogaster
KW - G protein coupled receptors
KW - Golgi apparatus
KW - Gαo interactome
KW - heterotrimeric G proteins
KW - KDEL receptor
KW - neurite outgrowth
KW - protrusion formation
KW - Rab1/3 GTPases
KW - vesicular trafficking
UR - http://www.scopus.com/inward/record.url?scp=85028047396&partnerID=8YFLogxK
U2 - 10.1016/j.cell.2017.07.015
DO - 10.1016/j.cell.2017.07.015
M3 - Article
C2 - 28803726
AN - SCOPUS:85028047396
SN - 0092-8674
VL - 170
SP - 939-955.e24
JO - Cell
JF - Cell
IS - 5
ER -