Epigenetic organization of brain sex differences and juvenile social play behavior

被引:25
作者
Auger, Anthony P. [1 ]
Jessen, Heather M.
Edelmann, Michelle N.
机构
[1] Univ Wisconsin, Dept Psychol, Madison, WI 53706 USA
关键词
Epigentic; Methylation; Methyl-binding proteins; Sex differences; Juvenile social play; Corepressor; MeCP2; NCoR; Estrogen receptors; Amygdala; Preoptic area; THYROID-HORMONE RECEPTOR; DE-NOVO METHYLATION; NUCLEAR RECEPTOR; DNA METHYLATION; MATERNAL-CARE; N-COR; POSTNATAL-DEVELOPMENT; HISTONE DEACETYLASE; RAT HYPOTHALAMUS; MESSENGER-RNA;
D O I
10.1016/j.yhbeh.2010.06.017
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The study of epigenetic mechanisms is important for elucidating how gene-by-environment interactions can have lasting outcomes on brain function and behavior. In general, studies of epigenetic processes mainly focus on the methylation status of DNA. While methylation of DNA alone can interfere with gene transcription, it is the binding of methyl-CpG binding proteins to methylated DNA, and subsequent recruitment of nuclear corepressors and histone deacetylases, that results in more efficient gene repression. In this review, we will discuss sex differences in DNA methylation patterns, methyl binding proteins, and corepressor proteins that contribute to lasting differences in brain and juvenile behavior. Specifically, we will discuss new data on sex differences in ER alpha DNA promoter methylation patterns, and the role of MeCP2 and the nuclear corepressor, NCoR, on the organization of juvenile social play behavior. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:358 / 363
页数:6
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