TGF-β control of stem cell differentiation genes

FEBS Lett. 2012 Jul 4;586(14):1953-8. doi: 10.1016/j.febslet.2012.03.023. Epub 2012 Apr 10.

Abstract

The canonical TGF-β/Smad signaling pathway was delineated in the mid 90s and enriched over the past decade with many findings about its specificity, regulation, networking, and malfunctions in disease. However, a growing understanding of the chromatin status of a critical class of TGF-β target genes - the genes controlling differentiation of embryonic stem cells - recently prompted a reexamination of this pathway and its critical role in the regulation of stem cell differentiation. The new findings reveal master regulators of the pluripotent state set the stage for Smad-mediated activation of master regulators of the next differentiation stage. Furthermore, a novel branch of the TGF-β/Smad pathway has been identified in which a chromatin-reading Smad complex makes the master differentiation genes accessible to canonical Smad complexes for transcriptional activation. These findings provide exciting new insights into the global role of TGF-β signaling in the regulators of stem cell fate.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cell Differentiation
  • Cell Lineage
  • Chromatin / metabolism
  • Embryonic Stem Cells / cytology
  • Gene Expression Regulation, Developmental*
  • Humans
  • Ligands
  • Mice
  • Models, Biological
  • Signal Transduction
  • Smad2 Protein / metabolism
  • Smad3 Protein / metabolism
  • Smad4 Protein / metabolism
  • Stem Cells / cytology*
  • Transcription Factors / metabolism
  • Transcriptional Activation
  • Transforming Growth Factor beta / metabolism*

Substances

  • Chromatin
  • Ligands
  • Smad2 Protein
  • Smad3 Protein
  • Smad4 Protein
  • TRIM33 protein, human
  • Transcription Factors
  • Transforming Growth Factor beta