Age-related changes in Egr1 transcription and DNA methylation within the hippocampus

Hippocampus. 2016 Aug;26(8):1008-20. doi: 10.1002/hipo.22583. Epub 2016 Apr 4.

Abstract

Aged animals show functional alterations in hippocampal neurons that lead to deficits in synaptic plasticity and changes in cognitive function. Transcription of immediate-early genes (IEGs), including Egr1, is necessary for processes such as long-term potentiation and memory consolidation. Here, we show an age-related reduction in the transcription of Egr1 in the dentate gyrus following spatial behavior, whereas in the area CA1, Egr1 is reduced at rest, but its transcription can be effectively driven by spatial behavior to levels equivalent to those observed in adult animals. One mechanism possibly contributing to these aging-related changes is an age-associated, CpG site-specific change in methylation in DNA associated with the promoter region of the Egr1 gene. Our results add to a growing body of work demonstrating that complex transcriptional and epigenetic changes in the hippocampus significantly contribute to brain and cognitive aging. © 2016 Wiley Periodicals, Inc.

Keywords: aging; epigenetic modulation; memory; transcriptional regulation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / genetics
  • Aging / metabolism*
  • Aging / psychology
  • Animals
  • CA1 Region, Hippocampal / metabolism*
  • CpG Islands
  • DNA Methylation*
  • Dentate Gyrus / metabolism*
  • Early Growth Response Protein 1 / genetics
  • Early Growth Response Protein 1 / metabolism*
  • Male
  • Motor Activity / physiology
  • Promoter Regions, Genetic
  • RNA, Messenger / metabolism
  • Rats, Inbred F344
  • Spatial Memory / physiology
  • Transcription, Genetic

Substances

  • Early Growth Response Protein 1
  • Egr1 protein, rat
  • RNA, Messenger