Developmental downregulation of histone posttranslational modifications regulates visual cortical plasticity

Neuron. 2007 Mar 1;53(5):747-59. doi: 10.1016/j.neuron.2007.02.007.

Abstract

The action of visual experience on visual cortical circuits is maximal during a critical period of postnatal development. The long-term effects of this experience are likely mediated by signaling cascades regulating experience-dependent gene transcription. Developmental modifications of these pathways could explain the difference in plasticity between the young and adult cortex. We studied the pathways linking experience-dependent activation of ERK to CREB-mediated gene expression in vivo. In juvenile mice, visual stimulation that activates CREB-mediated gene transcription also induced ERK-dependent MSK and histone H3 phosphorylation and H3-H4 acetylation, an epigenetic mechanism of gene transcription activation. In adult animals, ERK and MSK were still inducible; however, visual stimulation induced weak CREB-mediated gene expression and H3-H4 posttranslational modifications. Stimulation of histone acetylation in adult animals by means of trichostatin promoted ocular dominance plasticity. Thus, differing, experience-dependent activations of signaling molecules might be at the basis of the differences in experience-dependent plasticity between juvenile and adult cortex.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation / drug effects
  • Age Factors
  • Animals
  • Critical Period, Psychological
  • Cyclic AMP Response Element-Binding Protein / metabolism
  • Dominance, Cerebral / physiology
  • Down-Regulation / genetics
  • Epigenesis, Genetic / physiology
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Gene Expression Regulation / physiology
  • Histones / genetics
  • Histones / metabolism*
  • Hydroxamic Acids / pharmacology
  • MAP Kinase Signaling System / physiology
  • Mice
  • Mice, Inbred C57BL
  • Neuronal Plasticity / physiology*
  • Phosphorylation
  • Photic Stimulation
  • Protein Processing, Post-Translational / physiology*
  • Protein Synthesis Inhibitors / pharmacology
  • Ribosomal Protein S6 Kinases, 90-kDa / metabolism
  • Visual Cortex / cytology
  • Visual Cortex / growth & development
  • Visual Cortex / physiology*

Substances

  • Creb1 protein, mouse
  • Cyclic AMP Response Element-Binding Protein
  • Histones
  • Hydroxamic Acids
  • Protein Synthesis Inhibitors
  • trichostatin A
  • Ribosomal Protein S6 Kinases, 90-kDa
  • mitogen and stress-activated protein kinase 1
  • Extracellular Signal-Regulated MAP Kinases