| Literature DB >> 25832671 |
Frankie D Heyward1, J David Sweatt2.
Abstract
The establishment of synaptic plasticity and long-term memory requires lasting cellular and molecular modifications that, as a whole, must endure despite the rapid turnover of their constituent parts. Such a molecular feat must be mediated by a stable, self-perpetuating, cellular information storage mechanism. DNA methylation, being the archetypal cellular information storage mechanism, has been heavily implicated as being necessary for stable activity-dependent transcriptional alterations within the CNS. This review details the foundational discoveries from both gene-targeted and whole-genome sequencing studies that have brought DNA methylation to our attention as a chief regulator of activity- and experience-dependent transcriptional alterations within the CNS. We present a hypothetical framework to resolve disparate experimental findings regarding distinct manipulations of DNA methylation and their effect on memory, taking into account the unique impact activity-dependent alterations in DNA methylation potentially have on both memory-promoting and memory-suppressing gene expression. And last, we discuss potential avenues for future inquiry into the role of DNA methylation during remote memory formation.Entities:
Keywords: DNA demethylation; DNA methylation; epigenetics; memory; synaptic plasticity
Mesh:
Year: 2015 PMID: 25832671 PMCID: PMC4770785 DOI: 10.1177/1073858415579635
Source DB: PubMed Journal: Neuroscientist ISSN: 1073-8584 Impact factor: 7.519