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The Journal of Neuroscience, February 14, 2007, 27(7):1756-1768; doi:10.1523/JNEUROSCI.4164-06.2007

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Development/Plasticity/Repair
The Transcription Factor Nerve Growth Factor-Inducible Protein A Mediates Epigenetic Programming: Altering Epigenetic Marks by Immediate-Early Genes

Ian C. G. Weaver,1,2 Ana C. D'Alessio,3 Shelley E. Brown,3 Ian C. Hellstrom,1 Sergiy Dymov,2 Shakti Sharma,1 Moshe Szyf,2,3 and Michael J. Meaney1,2

1Douglas Hospital Research Center, Montréal, Québec, Canada H4H 1R3, and 2McGill Program for the Study of Behaviour, Genes, and Environment and 3Department of Pharmacology and Therapeutics, McGill University, Montréal, Québec, Canada H3G 1Y6

Correspondence should be addressed to either of the following: Michael Meaney, Douglas Hospital Research Centre, 6875 LaSalle Boulevard, Montréal, Québec, Canada H4H 1R3, Email: michael.meaney{at}mcgill.ca; or Moshe Szyf, Department of Pharmacology, McGill University, 3655 Drummond Street, Montréal, Québec, Canada H3G 1Y6, Email: moshe.szyf{at}mcgill.ca

Maternal care alters epigenetic programming of glucocorticoid receptor (GR) gene expression in the hippocampus, and increased postnatal maternal licking/grooming (LG) behavior enhances nerve growth factor-inducible protein A (NGFI-A) transcription factor binding to the exon 17 GR promoter within the hippocampus of the offspring. We tested the hypothesis that NGFI-A binding to the exon 17 GR promoter sequence marks this sequence for histone acetylation and DNA demethylation and that such epigenetic alterations subsequently influence NGFI-A binding and GR transcription. We report that (1) NGFI-A binding to its consensus sequence is inhibited by DNA methylation, (2) NGFI-A induces the activity of exon 17 GR promoter in a transient reporter assay, (3) DNA methylation inhibits exon 17 GR promoter activity, and (4) whereas NGFI-A interaction with the methylated exon 17 GR promoter is reduced, NGFI-A overexpression induces histone acetylation, DNA demethylation, and activation of the exon 17 GR promoter in transient transfection assays. Site-directed mutagenesis assays demonstrate that NGFI-A binding to the exon 17 GR promoter is required for such epigenetic reprogramming. In vivo, enhanced maternal LG is associated with increased NGFI-A binding to the exon 17 GR promoter in the hippocampus of pups, and NGFI-A-bound exon 17 GR promoter is unmethylated compared with unbound exon 17 GR promoter. Knockdown experiments of NGFI-A in hippocampal primary cell culture show that NGFI-A is required for serotonin-induced DNA demethylation and increased exon 17 GR promoter expression. The data are consistent with the hypothesis that NGFI-A participates in epigenetic programming of GR expression.

Key words: maternal behavior; rat; hippocampus; transcription factors; glucocorticoid receptor; DNA methylation


Received Sept. 22, 2006; revised Dec. 18, 2006; accepted Jan. 8, 2007.

Correspondence should be addressed to either of the following: Michael Meaney, Douglas Hospital Research Centre, 6875 LaSalle Boulevard, Montréal, Québec, Canada H4H 1R3, Email: michael.meaney{at}mcgill.ca; or Moshe Szyf, Department of Pharmacology, McGill University, 3655 Drummond Street, Montréal, Québec, Canada H3G 1Y6, Email: moshe.szyf{at}mcgill.ca


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