PCAF-dependent epigenetic changes promote axonal regeneration in the central nervous system

Nat Commun. 2014 Apr 1:5:3527. doi: 10.1038/ncomms4527.


Axonal regenerative failure is a major cause of neurological impairment following central nervous system (CNS) but not peripheral nervous system (PNS) injury. Notably, PNS injury triggers a coordinated regenerative gene expression programme. However, the molecular link between retrograde signalling and the regulation of this gene expression programme that leads to the differential regenerative capacity remains elusive. Here we show through systematic epigenetic studies that the histone acetyltransferase p300/CBP-associated factor (PCAF) promotes acetylation of histone 3 Lys 9 at the promoters of established key regeneration-associated genes following a peripheral but not a central axonal injury. Furthermore, we find that extracellular signal-regulated kinase (ERK)-mediated retrograde signalling is required for PCAF-dependent regenerative gene reprogramming. Finally, PCAF is necessary for conditioning-dependent axonal regeneration and also singularly promotes regeneration after spinal cord injury. Thus, we find a specific epigenetic mechanism that regulates axonal regeneration of CNS axons, suggesting novel targets for clinical application.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Animals
  • Axons / enzymology*
  • Central Nervous System / physiology*
  • Epigenesis, Genetic*
  • Female
  • Histones / metabolism
  • Humans
  • Male
  • Mice
  • Mice, Knockout / genetics
  • Nerve Regeneration*
  • Spinal Cord Injuries / enzymology*
  • Spinal Cord Injuries / genetics
  • Spinal Cord Injuries / physiopathology
  • p300-CBP Transcription Factors / genetics
  • p300-CBP Transcription Factors / metabolism*


  • Histones
  • p300-CBP Transcription Factors
  • p300-CBP-associated factor

Associated data

  • GEO/GSE55514