Epigenetic regulation of estrogen receptor α contributes to age-related differences in transcription across the hippocampal regions CA1 and CA3

被引:15
|
作者
Ianov, Lara [1 ,2 ]
Kumar, Ashok [1 ]
Foster, Thomas C. [1 ,2 ]
机构
[1] Univ Florida, Dept Neurosci, McKnight Brain Inst, POB 100244, Gainesville, FL 32610 USA
[2] Univ Florida, Genet Inst, Genet & Genom Program, Gainesville, FL USA
关键词
Aging; Estrogen receptor alpha; Hippocampus; Transcription; DNA methylation; DNA METHYLATION; GENE-EXPRESSION; BETA; PROMOTER; INHIBITION; HORMONE; BRAIN; REPRESSION; CORTEX; ESR1;
D O I
10.1016/j.neurobiolaging.2016.09.013
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The expression of estrogen receptor alpha (ER alpha) varies across brain regions and changes with age and according to the previous history of estradiol exposure. ERa is regulated by a number of mechanisms including the level of mRNA (Esr1) expression. For this study, we took advantage of regional differences in hippocampal ERa expression to investigate DNA ERa promoter methylation at CpG dinucleotide sites as a potential epigenetic mechanism for regulating gene expression. Young and aged female Fischer 344 rats were ovariectomized, and Esr1 expression and ERa promoter methylation were examined in hippocampal regions CA1 and CA3, either 3 or 14 weeks following surgery. The results indicate that reduced Esr1 expression in region CA1 relative to CA3 was associated with an increase in DNA methylation in region CA1, particularly for the first CpG site. Additionally, differential methylation of distal CpG sites, 11-17, was associated with altered Esr1 expression during aging or following long-term hormone deprivation. The results support the idea that methylation of site 1 may be the primary regulatory region for cross-regional patterns in ERa expression, while distal sites are modifiable across the life span and may act as a feedback mechanism for ERa activity. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:79 / 85
页数:7
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