Erk5 Is a Key Regulator of Naive-Primed Transition and Embryonic Stem Cell Identity

Cell Rep. 2016 Aug 16;16(7):1820-8. doi: 10.1016/j.celrep.2016.07.033. Epub 2016 Aug 4.

Abstract

Embryonic stem cells (ESCs) can self-renew or differentiate into any cell type, a phenomenon known as pluripotency. Distinct pluripotent states, termed naive and primed pluripotency, have been described. However, the mechanisms that control naive-primed pluripotent transition are poorly understood. Here, we perform a targeted screen for kinase inhibitors, which modulate the naive-primed pluripotent transition. We find that XMD compounds, which selectively inhibit Erk5 kinase and BET bromodomain family proteins, drive ESCs toward primed pluripotency. Using compound selectivity engineering and CRISPR/Cas9 genome editing, we reveal distinct functions for Erk5 and Brd4 in pluripotency regulation. We show that Erk5 signaling maintains ESCs in the naive state and suppresses progression toward primed pluripotency and neuroectoderm differentiation. Additionally, we identify a specialized role for Erk5 in defining ESC lineage selection, whereby Erk5 inhibits a cardiomyocyte-specific differentiation program. Our data therefore reveal multiple critical functions for Erk5 in controlling ESC identity.

MeSH terms

  • Animals
  • Benzodiazepinones / pharmacology
  • CRISPR-Cas Systems
  • Cell Differentiation
  • Cells, Cultured
  • DNA (Cytosine-5-)-Methyltransferases / genetics
  • DNA (Cytosine-5-)-Methyltransferases / metabolism
  • DNA Methyltransferase 3B
  • Embryoid Bodies / cytology
  • Embryoid Bodies / metabolism
  • Gene Editing
  • Gene Expression Regulation
  • Mice
  • Mitogen-Activated Protein Kinase 7 / antagonists & inhibitors
  • Mitogen-Activated Protein Kinase 7 / genetics*
  • Mitogen-Activated Protein Kinase 7 / metabolism
  • Mouse Embryonic Stem Cells / cytology
  • Mouse Embryonic Stem Cells / drug effects
  • Mouse Embryonic Stem Cells / metabolism*
  • Myocytes, Cardiac / cytology
  • Myocytes, Cardiac / metabolism
  • Nanog Homeobox Protein / genetics
  • Nanog Homeobox Protein / metabolism
  • Neural Plate / cytology
  • Neural Plate / metabolism
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • Pluripotent Stem Cells / cytology
  • Pluripotent Stem Cells / drug effects
  • Pluripotent Stem Cells / metabolism*
  • Protein Kinase Inhibitors / pharmacology
  • Signal Transduction
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism

Substances

  • Benzodiazepinones
  • Brd4 protein, mouse
  • Nanog Homeobox Protein
  • Nanog protein, mouse
  • Nuclear Proteins
  • Protein Kinase Inhibitors
  • Transcription Factors
  • DNA (Cytosine-5-)-Methyltransferases
  • Mitogen-Activated Protein Kinase 7