Pontin functions as an essential coactivator for Oct4-dependent lincRNA expression in mouse embryonic stem cells

Nat Commun. 2015 Apr 10:6:6810. doi: 10.1038/ncomms7810.

Abstract

The actions of transcription factors, chromatin modifiers and noncoding RNAs are crucial for the programming of cell states. Although the importance of various epigenetic machineries for controlling pluripotency of embryonic stem (ES) cells has been previously studied, how chromatin modifiers cooperate with specific transcription factors still remains largely elusive. Here, we find that Pontin chromatin remodelling factor plays an essential role as a coactivator for Oct4 for maintenance of pluripotency in mouse ES cells. Genome-wide analyses reveal that Pontin and Oct4 share a substantial set of target genes involved in ES cell maintenance. Intriguingly, we find that the Oct4-dependent coactivator function of Pontin extends to the transcription of large intergenic noncoding RNAs (lincRNAs) and in particular linc1253, a lineage programme repressing lincRNA, is a Pontin-dependent Oct4 target lincRNA. Together, our findings demonstrate that the Oct4-Pontin module plays critical roles in the regulation of genes involved in ES cell fate determination.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation
  • Chromatin / chemistry
  • Chromatin / metabolism
  • Chromatin Assembly and Disassembly
  • DNA Helicases / deficiency
  • DNA Helicases / genetics*
  • Epigenesis, Genetic*
  • Gene Expression Profiling
  • Genome-Wide Association Study
  • Mice
  • Mice, Knockout
  • Mouse Embryonic Stem Cells / cytology
  • Mouse Embryonic Stem Cells / metabolism*
  • Octamer Transcription Factor-3 / deficiency
  • Octamer Transcription Factor-3 / genetics*
  • Patched Receptors
  • Pluripotent Stem Cells / cytology
  • Pluripotent Stem Cells / metabolism
  • RNA, Long Noncoding / genetics*
  • RNA, Long Noncoding / metabolism
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism
  • Signal Transduction
  • Telomere-Binding Proteins / genetics
  • Telomere-Binding Proteins / metabolism
  • Tissue Inhibitor of Metalloproteinase-2 / genetics
  • Tissue Inhibitor of Metalloproteinase-2 / metabolism
  • Tropomyosin / genetics
  • Tropomyosin / metabolism

Substances

  • Chromatin
  • Octamer Transcription Factor-3
  • Patched Receptors
  • Pou5f1 protein, mouse
  • RNA, Long Noncoding
  • Receptors, Cell Surface
  • Rif1 protein, mouse
  • Telomere-Binding Proteins
  • Tpm1 protein, mouse
  • Tropomyosin
  • Tissue Inhibitor of Metalloproteinase-2
  • TIP48 protein, mouse
  • DNA Helicases