DEDD negatively regulates transforming growth factor-beta1 signaling by interacting with Smad3

FEBS Lett. 2010 Jul 16;584(14):3028-34. doi: 10.1016/j.febslet.2010.05.043. Epub 2010 May 27.

Abstract

Transforming growth factor-beta1 (TGF-beta1) regulates a wide variety of cellular responses, such as proliferation, differentiation, migration and apoptosis. Here we report that death effector domain-containing DNA-binding protein (DEDD) physically interacts with Smad3. The inhibition of Smad3 by DEDD resulted in a reduction in TGF-beta1/Smad3-mediated transcription. DEDD inhibited the functions of Smad3 by preventing Smad3 phosphorylation, which led to the reduced expression of TGF-beta1/Smad3-targeted genes. TGF-beta1 inhibited DEDD expression, and DEDD inhibited TGF-beta1-mediated invasion. Therefore, our findings suggest that through its interaction with Smad3, DEDD is a novel negative regulator of the TGF-beta1 signaling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Cell Differentiation / genetics
  • DNA-Binding Proteins
  • Death Domain Receptor Signaling Adaptor Proteins
  • Mice
  • Phosphorylation
  • Signal Transduction / genetics
  • Signal Transduction / physiology*
  • Transforming Growth Factor beta1 / genetics
  • Transforming Growth Factor beta1 / metabolism*

Substances

  • DEDD protein, human
  • DNA-Binding Proteins
  • Death Domain Receptor Signaling Adaptor Proteins
  • Transforming Growth Factor beta1