The pluripotency factor Nanog regulates pericentromeric heterochromatin organization in mouse embryonic stem cells

Genes Dev. 2016 May 1;30(9):1101-15. doi: 10.1101/gad.275685.115. Epub 2016 Apr 28.

Abstract

An open and decondensed chromatin organization is a defining property of pluripotency. Several epigenetic regulators have been implicated in maintaining an open chromatin organization, but how these processes are connected to the pluripotency network is unknown. Here, we identified a new role for the transcription factor NANOG as a key regulator connecting the pluripotency network with constitutive heterochromatin organization in mouse embryonic stem cells. Deletion of Nanog leads to chromatin compaction and the remodeling of heterochromatin domains. Forced expression of NANOG in epiblast stem cells is sufficient to decompact chromatin. NANOG associates with satellite repeats within heterochromatin domains, contributing to an architecture characterized by highly dispersed chromatin fibers, low levels of H3K9me3, and high major satellite transcription, and the strong transactivation domain of NANOG is required for this organization. The heterochromatin-associated protein SALL1 is a direct cofactor for NANOG, and loss of Sall1 recapitulates the Nanog-null phenotype, but the loss of Sall1 can be circumvented through direct recruitment of the NANOG transactivation domain to major satellites. These results establish a direct connection between the pluripotency network and chromatin organization and emphasize that maintaining an open heterochromatin architecture is a highly regulated process in embryonic stem cells.

Keywords: embryonic stem cells; heterochromatin; nuclear organization; pluripotency.

MeSH terms

  • Animals
  • Cell Line
  • Chromatin / metabolism
  • Chromatin Assembly and Disassembly / genetics
  • Down-Regulation
  • Gene Deletion
  • Heterochromatin / genetics*
  • Heterochromatin / metabolism*
  • Mice
  • Mouse Embryonic Stem Cells / physiology*
  • Nanog Homeobox Protein / genetics
  • Nanog Homeobox Protein / metabolism*
  • Protein Domains
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • Chromatin
  • Heterochromatin
  • Nanog Homeobox Protein
  • Nanog protein, mouse
  • Sall1 protein, mouse
  • Transcription Factors