Direct Inhibition of GSK3β by the Phosphorylated Cytoplasmic Domain of LRP6 in Wnt/β-Catenin Signaling

• Published in: PloS one Vol. 3; no. 12; p. e4046
• Main Authors: Piao, Shunfu, Lee, Sun-Hye, Kim, Hyunjoon, Yum, Soohwan, Stamos, Jennifer L., Xu, Yongbin, Lee, Su-Jin, Lee, Jaewon, Oh, Sangtaek, Han, Jin-Kwan, Park, Bum-Joon, Weis, William I., Ha, Nam-Chul
• Format: Journal Article
• Language: English
• Published: San Francisco Public Library of Science 24-12-2008
• Subjects: Binding; Biochemistry/Cell Signaling and Trafficking Structures; Cell Biology/Cell Growth and Division; Cell Biology/Cell Signaling; Cloning; Clusters; Developmental biology; Drosophila; Embryos; Frizzled protein; Growth factors; Inhibition; Insects; Intracellular; Kinases; Life sciences; Microinjection; Molecular biology; Oncology/Gastrointestinal Cancers; Peptides; Pharmacy; Phosphorylation; Physiology; Proteins; Signal transduction; Signaling; Synthetic peptides; Wnt protein; Xenopus; Xenopus laevis; β-Catenin; United States > US; California
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0004046

Wnt/β-catenin signaling plays a central role in development and is also involved in a diverse array of diseases. Binding of Wnts to the coreceptors Frizzled and LRP6/5 leads to phosphorylation of PPPSPxS motifs in the LRP6/5 intracellular region and the inhibition of GSK3β bound to the scaffold protein Axin. However, it remains unknown how GSK3β is specifically inhibited upon Wnt stimulation. Here, we show that overexpression of the intracellular region of LRP6 containing a Ser/Thr rich cluster and a PPPSPxS motif impairs the activity of GSK3β in cells. Synthetic peptides containing the PPPSPxS motif strongly inhibit GSK3β in vitro only when they are phosphorylated. Microinjection of these peptides into Xenopus embryos confirms that the phosphorylated PPPSPxS motif potentiates Wnt-induced second body axis formation. In addition, we show that the Ser/Thr rich cluster of LRP6 plays an important role in LRP6 binding to GSK3β. These observations demonstrate that phosphorylated LRP6/5 both recruits and directly inhibits GSK3β using two distinct portions of its cytoplasmic sequence, and suggest a novel mechanism of activation in this signaling pathway.