NGF/PI3K signaling-mediated epigenetic regulation of delta opioid receptor gene expression

Yulong L. Chen, Ping-Yee Law, Horace H Loh

Research output: Contribution to journalArticlepeer-review

28 Scopus citations

Abstract

The G protein-coupled delta opioid receptor gene (dor) has been associated with neuronal survival, differentiation, and neuroprotection. Our previous study identified PI3K/Akt/NF-κB signaling is a main downstream signaling pathway in nerve growth factor (NGF)-induced temporal expression of the dor gene in the PC12 cell model. It is still unknown how NGF/PI3K signaling regulates the expression of the dor gene in the nucleus. In the current study, we investigated how PI3K signaling affected epigenetic modifications of histone H3 Lys9 (H3K9) in the 5′-UTR region of the rat dor gene locus. NGF treatment resulted in the global reversal of H3K9 trimethylation in cells. Moreover, the locus-specific reversal of H3K9 trimethylation and acetylation of H3K9 were dependent upon NGF/PI3K signaling and temporally well correlated with NGF-induced gene expression. These results indicate the importance of epigenetic modifications of H3K9, particularly the reversal of trimethylated H3K9, in the regulation of NGF/PI3K-dependent genes during neuronal differentiation.

Original languageEnglish (US)
Pages (from-to)755-760
Number of pages6
JournalBiochemical and Biophysical Research Communications
Volume368
Issue number3
DOIs
StatePublished - Apr 11 2008

Bibliographical note

Funding Information:
This work was supported by National Institute of Health Grants DA-000546, DA-001583, DA-001806, DA07339, KO5-DA-70554 (HHL), K05-DA00513 (PYL), and by A. & F. Stark Fund of the Minnesota Medical Foundation.

Keywords

  • Akt
  • Chromatin remodeling
  • Delta opioid receptor
  • Histone modification
  • Lysine trimethylation
  • NF-κB
  • NGF
  • PI3K

Fingerprint

Dive into the research topics of 'NGF/PI3K signaling-mediated epigenetic regulation of delta opioid receptor gene expression'. Together they form a unique fingerprint.

Cite this