Transcriptional regulation by Smads: crosstalk between the TGF-beta and Wnt pathways

J Bone Joint Surg Am. 2001;83-A Suppl 1(Pt 1):S31-9.

Abstract

Background: Several studies have shown that cooperation between transforming growth factor beta (TGF-beta) and Wnt/wingless signaling pathways plays a role in controlling certain developmental events. These factors elicit their biological effects through distinct pathways in which TGF-beta and Wnt signaling induce activation of the transcriptional regulators Smads and lymphoid enhancer binding factor/T-cell-specific factor (LEF/TCF), respectively. To understand the mechanism for cooperativity between these pathways, we have investigated the molecular mechanism for this synergistic effect.

Methods: Transcriptional assays were conducted by transient transfection of HepG2 cells with use of luciferase reporter constructs. Protein/protein interaction studies were conducted in vitro with the use of glutathione-S-transferase pull-down assays and in intact cells by immunoprecipitation and immunoblotting.

Results: We show that Smads physically interact with LEF1/TCF transcription factors and that specific DNA binding sites in the Xenopus twin promoter are required for synergistic activation by TGF-beta and Wnt pathways. In addition, we demonstrate that TGF-beta-dependent activation of LEF1/TCF target genes can occur independently of beta-catenin, an essential component of the Wnt signaling pathway.

Conclusions: TGF-beta and Wnt signaling pathways can independently or cooperatively regulate LEF1/TCF target genes. This suggests that the cooperation between these pathways may be important for the specification of cell fates during development.

Publication types

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

MeSH terms

  • Animals
  • Cells, Cultured
  • Cytoskeletal Proteins / physiology
  • DNA-Binding Proteins / physiology*
  • Gene Expression Regulation*
  • Humans
  • Promoter Regions, Genetic
  • Protein-Tyrosine Kinases / physiology*
  • Proto-Oncogene Proteins / physiology*
  • Signal Transduction / physiology*
  • Smad Proteins
  • Trans-Activators / physiology*
  • Transcription Factors / physiology
  • Transcription, Genetic*
  • Transfection
  • Transforming Growth Factor beta / physiology*
  • Wnt Proteins
  • Zebrafish Proteins*
  • beta Catenin

Substances

  • CTNNB1 protein, human
  • Cytoskeletal Proteins
  • DNA-Binding Proteins
  • Proto-Oncogene Proteins
  • Smad Proteins
  • Trans-Activators
  • Transcription Factors
  • Transforming Growth Factor beta
  • Wnt Proteins
  • Zebrafish Proteins
  • beta Catenin
  • Protein-Tyrosine Kinases