Amer1/WTX couples Wnt-induced formation of PtdIns(4,5)P-2 to LRP6 phosphorylation

Published: EMBO JOURNAL 30, 1433-1443 Authors: Tanneberger, K., Pfister, AS., Brauburger, K., Schneikert, J., Hadjihannas, MV., Kriz, V., Schulte, G., Bryja, V., Behrens, J. Year: 2011

Abstract

Phosphorylation of the Wnt receptor low-density lipoprotein receptor-related protein 6 (LRP6) by glycogen synthase kinase 3b (GSK3 beta) and casein kinase 1 gamma (CK1 gamma) is a key step in Wnt/beta-catenin signalling, which requires Wnt-induced formation of phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P-2). Here, we show that adenomatous polyposis coli membrane recruitment 1 (Amer1) (also called WTX), a membrane associated PtdIns(4,5)P-2-binding protein, is essential for the activation of Wnt signalling at the LRP6 receptor level. Knockdown of Amer1 reduces Wnt-induced LRP6 phosphorylation, Axin translocation to the plasma membrane and formation of LRP6 signalosomes. Overexpression of Amer1 promotes LRP6 phosphorylation, which requires interaction of Amer1 with PtdIns(4,5)P-2. Amer1 translocates to the plasma membrane in a PtdIns(4,5)P-2-dependent manner after Wnt treatment and is required for LRP6 phosphorylation stimulated by application of PtdIns(4,5)P-2. Amer1 binds CK1 gamma, recruits Axin and GSK3 beta to the plasma membrane and promotes complex formation between Axin and LRP6. Fusion of Amer1 to the cytoplasmic domain of LRP6 induces LRP6 phosphorylation and stimulates robust Wnt/beta-catenin signalling. We propose a mechanism for Wnt receptor activation by which generation of PtdIns (4,5)P-2 leads to recruitment of Amer1 to the plasma membrane, which acts as a scaffold protein to stimulate phosphorylation of LRP6. The EMBO Journal (2011) 30, 1433-1443. doi:10.1038/emboj.2011.28; Published online 8 February 2011 Subject Categories: signal transduction