Mest/Peg1 inhibits Wnt signalling through regulation of LRP6 glycosylation

Biochem J. 2011 Jun 1;436(2):263-9. doi: 10.1042/BJ20101512.

Abstract

Mest (mesoderm-specific transcript)/Peg1 (paternally expressed gene 1) is an imprinted gene that plays important roles in embryo development, although its biochemical role has not been determined. Ectopic expression of Mest/Peg1 inhibited Wnt-mediated reporter activity by enhancing the ubiquitination of β-catenin. The maturation and plasma membrane localization of the Wnt co-receptor LRP6 [LDLR (low-density lipoprotein receptor)-related protein 6], which are both necessary for Wnt signalling, were blocked by the expression of Mest/Peg1. Mest/Peg1 inhibited maturation of LRP6 by controlling the glycosylation of LRP6. Knockdown of Mest/Peg1, which might enhance Wnt signalling, blocked adipogenic differentiation of 3T3-L1 cells. Overall, our results suggest that Mest/Peg1 is a novel regulator of Wnt/β-catenin signalling during adipogenic differentiation.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipogenesis / physiology
  • Animals
  • Glycosylation
  • HEK293 Cells
  • Humans
  • LDL-Receptor Related Proteins / antagonists & inhibitors
  • LDL-Receptor Related Proteins / biosynthesis
  • LDL-Receptor Related Proteins / metabolism*
  • Low Density Lipoprotein Receptor-Related Protein-6
  • Mice
  • Proteins / physiology*
  • Signal Transduction / physiology*
  • Wnt Proteins / antagonists & inhibitors*
  • Wnt Proteins / physiology*

Substances

  • LDL-Receptor Related Proteins
  • LRP6 protein, human
  • Low Density Lipoprotein Receptor-Related Protein-6
  • Lrp6 protein, mouse
  • Proteins
  • Wnt Proteins
  • mesoderm specific transcript protein