Prolyl isomerase Pin1 and protein kinase HIPK2 cooperate to promote cortical neurogenesis by suppressing Groucho/TLE:Hes1-mediated inhibition of neuronal differentiation

Cell Death Differ. 2014 Feb;21(2):321-32. doi: 10.1038/cdd.2013.160. Epub 2013 Nov 22.

Abstract

The Groucho/transducin-like Enhancer of split 1 (Gro/TLE1):Hes1 transcriptional repression complex acts in cerebral cortical neural progenitor cells to inhibit neuronal differentiation. The molecular mechanisms that regulate the anti-neurogenic function of the Gro/TLE1:Hes1 complex during cortical neurogenesis remain to be defined. Here we show that prolyl isomerase Pin1 (peptidyl-prolyl cis-trans isomerase NIMA-interacting 1) and homeodomain-interacting protein kinase 2 (HIPK2) are expressed in cortical neural progenitor cells and form a complex that interacts with the Gro/TLE1:Hes1 complex. This association depends on the enzymatic activities of both HIPK2 and Pin1, as well as on the association of Gro/TLE1 with Hes1, but is independent of the previously described Hes1-activated phosphorylation of Gro/TLE1. Interaction with the Pin1:HIPK2 complex results in Gro/TLE1 hyperphosphorylation and weakens both the transcriptional repression activity and the anti-neurogenic function of the Gro/TLE1:Hes1 complex. These results provide evidence that HIPK2 and Pin1 work together to promote cortical neurogenesis, at least in part, by suppressing Gro/TLE1:Hes1-mediated inhibition of neuronal differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / metabolism*
  • Carrier Proteins / metabolism*
  • Cell Differentiation / drug effects
  • Cell Line, Tumor
  • Cells, Cultured
  • Cerebral Cortex / cytology*
  • Cerebral Cortex / metabolism*
  • HEK293 Cells
  • Homeodomain Proteins / metabolism*
  • Humans
  • Mice
  • NIMA-Interacting Peptidylprolyl Isomerase
  • Naphthoquinones / pharmacology
  • Neural Stem Cells / cytology
  • Neural Stem Cells / drug effects
  • Neural Stem Cells / metabolism*
  • Neurogenesis*
  • Peptidylprolyl Isomerase / antagonists & inhibitors
  • Peptidylprolyl Isomerase / metabolism*
  • Protein Serine-Threonine Kinases / metabolism*
  • Repressor Proteins / metabolism*
  • Transcription Factor HES-1
  • Tretinoin / pharmacology

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Carrier Proteins
  • Homeodomain Proteins
  • NIMA-Interacting Peptidylprolyl Isomerase
  • Naphthoquinones
  • Repressor Proteins
  • Transcription Factor HES-1
  • HES1 protein, human
  • Tretinoin
  • HIPK2 protein, human
  • Protein Serine-Threonine Kinases
  • PIN1 protein, human
  • Peptidylprolyl Isomerase
  • Pin1 protein, mouse
  • juglone