14-3-3 σ is a new target up-regulated by transforming growth factor-β1 through a Smad3-dependent mechanism

Biochem Biophys Res Commun. 2013 Mar 1;432(1):193-7. doi: 10.1016/j.bbrc.2012.12.123. Epub 2013 Jan 30.

Abstract

The seven members of the human 14-3-3 family play crucial roles in a diverse range of cellular responses including cell cycle progression, DNA damage checkpoint, and apoptosis. One particular isoform, 14-3-3 σ, the p53 target gene, is a unique tumor suppressor. We here report 14-3-3 σ as a transforming growth factor-beta (TGF-β) target gene. In mammary epithelial cells, TGF-β selectively induced expression of 14-3-3 σ at both mRNA and protein levels, and this induction was dependent on Smad3 not on p53. In addition, blockade of non-canonical Smad-independent pathways, including MAP kinases and Rho GTPases, did not affect the TGF-β1-induced 14-3-3 σ expression. Our data provides the first evidence that 14-3-3 σ is a Smad3-dependent target gene of TGF-β1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 14-3-3 Proteins / genetics*
  • Animals
  • Cell Line
  • Gene Expression Regulation*
  • Hep G2 Cells
  • Humans
  • Mice
  • Smad3 Protein / genetics
  • Smad3 Protein / metabolism*
  • Transforming Growth Factor beta1 / pharmacology*
  • Tumor Suppressor Protein p53 / metabolism
  • Up-Regulation

Substances

  • 14-3-3 Proteins
  • Sfn protein, mouse
  • Smad3 Protein
  • Smad3 protein, mouse
  • Transforming Growth Factor beta1
  • Tumor Suppressor Protein p53