Epigenetic Mechanisms: Critical Contributors to Long-Term Memory Formation

被引:60
|
作者
Lubin, Farah D. [1 ]
Gupta, Swati [1 ]
Parrish, R. Ryley [1 ]
Grissom, Nicola M. [1 ]
Davis, Robin L. [1 ]
机构
[1] Univ Alabama Birmingham, Dept Neurobiol, Evelyn F McKnight Brain Inst, Birmingham, AL 35294 USA
来源
NEUROSCIENTIST | 2011年 / 17卷 / 06期
关键词
epigenetics; NF-kappa B; histone acetylation; histone methylation; DNA methylation; memory formation; hippocampus; amygdala; HDAC; NF-KAPPA-B; HISTONE DEACETYLASE INHIBITORS; FAMILY TRANSCRIPTION FACTOR; MESSENGER-RNA EXPRESSION; DNA METHYLATION; SYNAPTIC PLASTICITY; REGULATES MEMORY; LYSINE METHYLATION; CHROMATIN REGULATION; BDNF TRANSCRIPTION;
D O I
10.1177/1073858411386967
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Recent advances in chromatin biology have identified a role for epigenetic mechanisms in the regulation of neuronal gene expression changes, a necessary process for proper synaptic plasticity and memory formation. Experimental evidence for dynamic chromatin remodeling influencing gene transcription in postmitotic neurons grew from initial reports describing posttranslational modifications of histones, including phosphorylation and acetylation occurring in various brain regions during memory consolidation. An accumulation of recent studies, however, has also highlighted the importance of other epigenetic modifications, such as DNA methylation and histone methylation, as playing a role in memory formation. This present review examines learning-induced gene transcription by chromatin remodeling underlying long-lasting changes in neurons, with direct implications for the study of epigenetic mechanisms in long-term memory formation and behavior. Furthermore, the study of epigenetic gene regulation, in conjunction with transcription factor activation, can provide complementary lines of evidence to further understanding transcriptional mechanisms subserving memory storage.
引用
收藏
页码:616 / 632
页数:17
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