TY - JOUR
T1 - ABP1 Mediates Auxin Inhibition of Clathrin-Dependent Endocytosis in Arabidopsis
AU - Robert, Stephanie
AU - Kleine-Vehn, Juergen
AU - Barbez, Elke
AU - Sauer, Michael
AU - Paciorek, Tomasz
AU - Baster, Pawel
AU - Vanneste, Steffen
AU - Zhang, Jing
AU - Simon, Sibu
AU - Covanova, Milada
AU - Hayashi, Kenichiro
AU - Dhonukshe, Pankaj
AU - Yang, Zhenbiao
AU - Bednarek, Sebastian Y.
AU - Jones, Alan M.
AU - Luschnig, Christian
AU - Aniento, Fernando
AU - Zazimalova, Eva
AU - Friml, Jiri
PY - 2010
Y1 - 2010
N2 - Spatial distribution of the plant hormone auxin regulates multiple aspects of plant development. These self-regulating auxin gradients are established by the action of PIN auxin transporters, whose activity is regulated by their constitutive cycling between the plasma membrane and endosomes. Here, we show that auxin signaling by the auxin receptor AUXIN-BINDING PROTEIN 1 (ABP1) inhibits the clathrin-mediated internalization of PIN proteins. ABP1 acts as a positive factor in clathrin recruitment to the plasma membrane, thereby promoting endocytosis. Auxin binding to ABP1 interferes with this action and leads to the inhibition of clathrin-mediated endocytosis. Our study demonstrates that ABP1 mediates a nontranscriptional auxin signaling that regulates the evolutionarily conserved process of clathrin-mediated endocytosis and suggests that this signaling may be essential for the developmentally important feedback of auxin on its own transport.
AB - Spatial distribution of the plant hormone auxin regulates multiple aspects of plant development. These self-regulating auxin gradients are established by the action of PIN auxin transporters, whose activity is regulated by their constitutive cycling between the plasma membrane and endosomes. Here, we show that auxin signaling by the auxin receptor AUXIN-BINDING PROTEIN 1 (ABP1) inhibits the clathrin-mediated internalization of PIN proteins. ABP1 acts as a positive factor in clathrin recruitment to the plasma membrane, thereby promoting endocytosis. Auxin binding to ABP1 interferes with this action and leads to the inhibition of clathrin-mediated endocytosis. Our study demonstrates that ABP1 mediates a nontranscriptional auxin signaling that regulates the evolutionarily conserved process of clathrin-mediated endocytosis and suggests that this signaling may be essential for the developmentally important feedback of auxin on its own transport.
UR - https://res.slu.se/id/publ/87467
U2 - 10.1016/j.cell.2010.09.027
DO - 10.1016/j.cell.2010.09.027
M3 - Journal article
C2 - 20887896
SN - 0092-8674
VL - 143
SP - 111
EP - 121
JO - Cell
JF - Cell
IS - 1
ER -