Regulation of the pluripotency marker Rex-1 by Nanog and Sox2

J Biol Chem. 2006 Aug 18;281(33):23319-25. doi: 10.1074/jbc.M601811200. Epub 2006 May 21.

Abstract

Rex-1 (Zfp-42) is a known marker for undifferentiated embryonic stem cells and teratocarcinoma cells. However, the mechanism by which Rex-1 is regulated in pluripotent cells remains unresolved. Here we report that Nanog, an Nk-2 homeodomain protein known for its role in maintaining stem cell pluripotency, is a transcription activator for the Rex-1 promoter. Knockdown of Nanog in embryonic stem cells resulted in a reduction of Rex-1 expression, whereas forced expression of Nanog in P19 stimulated Rex-1 expression. Employing a Rex-1 reporter, we demonstrate that Nanog transactivates Rex-1 directly. Serial deletion studies mapped the Nanog-responsive element between -187 and -286 of the Rex-1 promoter. Although Oct-3/4 and Sox2 can both transactivate Rex-1 promoter, only Sox2 cooperates with Nanog in up-regulating Rex-1. Furthermore, we demonstrate that the C terminus of Nanog is responsible for transactivating the Rex-1 promoter, a function that can be substituted for by a viral transactivator Vp16 efficiently in NIH3T3 cells but less so in P19 cells. Taking these findings together, we conclude that Rex-1 is a direct target of Nanog, which is augmented by Sox2 and Oct-3/4.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Carrier Proteins / biosynthesis
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Cell Differentiation / genetics
  • Cell Line
  • Cell Line, Tumor
  • DNA-Binding Proteins / metabolism
  • DNA-Binding Proteins / physiology*
  • Homeodomain Proteins / metabolism
  • Homeodomain Proteins / physiology*
  • Humans
  • Kruppel-Like Transcription Factors
  • Mice
  • NIH 3T3 Cells
  • Nanog Homeobox Protein
  • Pluripotent Stem Cells / metabolism*
  • Promoter Regions, Genetic
  • Protein Binding / genetics
  • Response Elements
  • SOXB1 Transcription Factors
  • Trans-Activators / physiology*
  • Transcription Factors / biosynthesis
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • Biomarkers
  • Carrier Proteins
  • DNA-Binding Proteins
  • Homeodomain Proteins
  • Kruppel-Like Transcription Factors
  • Nanog Homeobox Protein
  • Nanog protein, mouse
  • Rex-1 protein, mouse
  • SOX2 protein, human
  • SOXB1 Transcription Factors
  • Sox2 protein, mouse
  • Trans-Activators
  • Transcription Factors
  • ZFP42 protein, human