Foxd3 suppresses NFAT-mediated differentiation to maintain self-renewal of embryonic stem cells

EMBO Rep. 2014 Dec;15(12):1286-96. doi: 10.15252/embr.201438643. Epub 2014 Nov 6.

Abstract

Pluripotency-associated transcription factor Foxd3 is required for maintaining pluripotent cells. However, molecular mechanisms underlying its function are largely unknown. Here, we report that Foxd3 suppresses differentiation induced by calcineurin-NFAT signaling to maintain the ESC identity. Mechanistically, Foxd3 interacts with NFAT proteins and recruits co-repressor Tle4, a member of the Tle repressor family highly expressed in undifferentiated ESCs, to suppress NFATc3's transcriptional activities. Furthermore, global transcriptome analysis shows that Foxd3 and NFATc3 co-regulate a set of differentiation-associated genes in ESCs. Collectively, our study establishes a molecular and functional link between a pluripotency-associated factor and an important ESC differentiation-inducing pathway.

Keywords: Foxd3; NFAT; embryonic stem cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / genetics
  • Cell Differentiation / physiology
  • Cell Line
  • Electrophoretic Mobility Shift Assay
  • Embryonic Stem Cells / cytology*
  • Embryonic Stem Cells / metabolism*
  • Forkhead Transcription Factors / genetics
  • Forkhead Transcription Factors / metabolism*
  • Mice
  • Models, Theoretical
  • NFATC Transcription Factors / genetics
  • NFATC Transcription Factors / metabolism*
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*

Substances

  • Forkhead Transcription Factors
  • Foxd3 protein, mouse
  • NFATC Transcription Factors
  • Repressor Proteins