The molecular logic of Nanog-induced self-renewal in mouse embryonic stem cells

Nat Commun. 2019 Mar 7;10(1):1109. doi: 10.1038/s41467-019-09041-z.

Abstract

Transcription factor networks, together with histone modifications and signalling pathways, underlie the establishment and maintenance of gene regulatory architectures associated with the molecular identity of each cell type. However, how master transcription factors individually impact the epigenomic landscape and orchestrate the behaviour of regulatory networks under different environmental constraints is only partially understood. Here, we show that the transcription factor Nanog deploys multiple distinct mechanisms to enhance embryonic stem cell self-renewal. In the presence of LIF, which fosters self-renewal, Nanog rewires the pluripotency network by promoting chromatin accessibility and binding of other pluripotency factors to thousands of enhancers. In the absence of LIF, Nanog blocks differentiation by sustaining H3K27me3, a repressive histone mark, at developmental regulators. Among those, we show that the repression of Otx2 plays a preponderant role. Our results underscore the versatility of master transcription factors, such as Nanog, to globally influence gene regulation during developmental processes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cell Self Renewal / genetics
  • Cell Self Renewal / physiology*
  • Enhancer Elements, Genetic
  • Gene Expression Regulation
  • Gene Regulatory Networks
  • Histone Code / genetics
  • Leukemia Inhibitory Factor / genetics
  • Leukemia Inhibitory Factor / metabolism
  • Mice
  • Mouse Embryonic Stem Cells / cytology*
  • Mouse Embryonic Stem Cells / metabolism*
  • Nanog Homeobox Protein / genetics
  • Nanog Homeobox Protein / metabolism*
  • Otx Transcription Factors / genetics
  • Otx Transcription Factors / metabolism

Substances

  • Leukemia Inhibitory Factor
  • Lif protein, mouse
  • Nanog Homeobox Protein
  • Nanog protein, mouse
  • Otx Transcription Factors
  • Otx2 protein, mouse