Pygopus residues required for its binding to Legless are critical for transcription and development

J Biol Chem. 2004 Feb 13;279(7):5177-83. doi: 10.1074/jbc.M309722200. Epub 2003 Nov 11.

Abstract

Pygopus and Legless/Bcl-9 are recently discovered core components of the Wnt signaling pathway that are required for the transcriptional activity of Armadillo/beta-catenin and T cell factors. It has been proposed that they are part of a tri-partite adaptor chain (Armadillo>Legless>Pygopus) that recruits transcriptional co-activator complexes to DNA-bound T cell factor. Here, we identify four conserved residues at the putative PHD domain surface of Drosophila and mouse Pygopus that are required for their binding to Legless in vitro and in vivo. The same residues are also critical for the transactivation potential of DNA-tethered Pygopus in transfected mammalian cells and for rescue activity of pygopus mutant embryos. These residues at the Legless>Pygopus interface thus define a specific molecular target for blocking Wnt signaling during development and cancer.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Carrier Proteins / chemistry
  • Carrier Proteins / physiology*
  • Cell Line
  • Cloning, Molecular
  • DNA / chemistry
  • Drosophila
  • Drosophila Proteins / chemistry
  • Drosophila Proteins / physiology*
  • Escherichia coli / metabolism
  • Humans
  • Intracellular Signaling Peptides and Proteins*
  • Mice
  • Molecular Sequence Data
  • Mutation
  • Plasmids / metabolism
  • Protein Binding
  • Protein Structure, Tertiary
  • Proto-Oncogene Proteins / metabolism
  • Sequence Homology, Amino Acid
  • Signal Transduction
  • Transcription, Genetic*
  • Transcriptional Activation
  • Transfection
  • Wnt Proteins
  • Zebrafish Proteins*

Substances

  • Carrier Proteins
  • Drosophila Proteins
  • Intracellular Signaling Peptides and Proteins
  • Lgs protein, Drosophila
  • Proto-Oncogene Proteins
  • Wnt Proteins
  • Zebrafish Proteins
  • pygo protein, Drosophila
  • DNA