Regulated subset of G1 growth-control genes in response to derepression by the Wnt pathway

Proc Natl Acad Sci U S A. 2003 Mar 18;100(6):3245-50. doi: 10.1073/pnas.0330217100. Epub 2003 Mar 10.

Abstract

Pitx2 is a bicoid-related homeodomain factor that is required for effective cell type-specific proliferation directly activating a specific growth-regulating gene cyclin D2. Here, we report that Pitx2, in response to the Wntbeta-catenin pathway and growth signals, also can regulate c-Myc and cyclin D1. Investigation of molecular mechanisms required for Pitx2-dependent proliferation, in these cases, further supports a nuclear role for beta-catenin in preventing the histone deacetylase 1-dependent inhibitory functions of several DNA-binding transcriptional repressors, potentially including E2F4p130 pocket protein inhibitory complex, as well as lymphoid enhancer factor 1 and Pitx2, by dismissal of histone deacetylase 1 and loss of its enzymatic activity. Thus, beta-catenin plays a signal-integrating role in Wnt- and growth factor-dependent proliferation events in mammalian development by both derepressing several classes of repressors and by activating Pitx2, regulating the activity of several growth control genes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Line
  • Colonic Neoplasms / genetics
  • Colonic Neoplasms / metabolism
  • Cyclin D1 / metabolism
  • Cyclin D2
  • Cyclins / metabolism
  • Cytoskeletal Proteins / metabolism
  • G1 Phase / genetics*
  • G1 Phase / physiology
  • Genes, myc
  • Histone Deacetylase 1
  • Histone Deacetylases / metabolism
  • Homeobox Protein PITX2
  • Homeodomain Proteins / metabolism*
  • Humans
  • Mice
  • Mice, Knockout
  • Nuclear Proteins / metabolism
  • Nuclear Receptor Co-Repressor 1
  • Promoter Regions, Genetic
  • Proto-Oncogene Proteins / metabolism*
  • Repressor Proteins / metabolism
  • Signal Transduction
  • Trans-Activators / metabolism
  • Transcription Factors / metabolism*
  • Tumor Cells, Cultured
  • Wnt Proteins
  • Zebrafish Proteins*
  • beta Catenin

Substances

  • CCND2 protein, human
  • CTNNB1 protein, human
  • CTNNB1 protein, mouse
  • Ccnd2 protein, mouse
  • Cyclin D2
  • Cyclins
  • Cytoskeletal Proteins
  • Homeodomain Proteins
  • NCOR1 protein, human
  • Ncor1 protein, mouse
  • Nuclear Proteins
  • Nuclear Receptor Co-Repressor 1
  • Proto-Oncogene Proteins
  • Repressor Proteins
  • Trans-Activators
  • Transcription Factors
  • Wnt Proteins
  • Zebrafish Proteins
  • beta Catenin
  • Cyclin D1
  • HDAC1 protein, human
  • Histone Deacetylase 1
  • Histone Deacetylases