Literature DB >> 21094887

Genetic and epigenetic underpinnings of sex differences in the brain and in neurological and psychiatric disease susceptibility.

Irfan A Qureshi1, Mark F Mehler.   

Abstract

There are numerous examples of sex differences in brain and behavior and in susceptibility to a broad range of brain diseases. For example, gene expression is sexually dimorphic during brain development, adult life, and aging. These differences are orchestrated by the interplay between genetic, hormonal, and environmental influences. However, the molecular mechanisms that underpin these differences have not been fully elucidated. Because recent studies have highlighted the key roles played by epigenetic processes in regulating gene expression and mediating brain form and function, this chapter reviews emerging evidence that shows how epigenetic mechanisms including DNA methylation, histone modifications, and chromatin remodeling, and non-coding RNAs (ncRNAs) are responsible for promoting sexual dimorphism in the brain. Differential profiles of DNA methylation and histone modifications are found in dimorphic brain regions such as the hypothalamus as a result of sex hormone exposure during developmental critical periods. The elaboration of specific epigenetic marks is also linked with regulating sex hormone signaling pathways later in life. Furthermore, the expression and function of epigenetic factors such as the methyl-CpG-binding protein, MeCP2, and the histone-modifying enzymes, UTX and UTY, are sexually dimorphic in the brain. ncRNAs are also implicated in promoting sex differences. For example, X inactivation-specific transcript (XIST) is a long ncRNA that mediates X chromosome inactivation, a seminal developmental process that is particularly important in brain. These observations imply that understanding epigenetic mechanisms, which regulate dimorphic gene expression and function, is necessary for developing a more comprehensive view of sex differences in brain. These emerging findings also suggest that epigenetic mechanisms are, in part, responsible for the differential susceptibility between males and females that is characteristic of a spectrum of neurological and psychiatric disorders.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 21094887      PMCID: PMC4465286          DOI: 10.1016/B978-0-444-53630-3.00006-3

Source DB:  PubMed          Journal:  Prog Brain Res        ISSN: 0079-6123            Impact factor:   2.453


  125 in total

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Journal:  Science       Date:  2008-03-28       Impact factor: 47.728

5.  Epigenetic gene silencing by the SRY protein is mediated by a KRAB-O protein that recruits the KAP1 co-repressor machinery.

Authors:  Hongzhuang Peng; Alexey V Ivanov; Hyun J Oh; Yun-Fai C Lau; Frank J Rauscher
Journal:  J Biol Chem       Date:  2009-12-18       Impact factor: 5.157

6.  The histone demethylase UTX enables RB-dependent cell fate control.

Authors:  Jordon K Wang; Miao-Chih Tsai; Gino Poulin; Adam S Adler; Shuzhen Chen; Helen Liu; Yang Shi; Howard Y Chang
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  35 in total

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Review 3.  Disruption of fetal hormonal programming (prenatal stress) implicates shared risk for sex differences in depression and cardiovascular disease.

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Review 4.  Neurobiological Mechanisms of Stress Resilience and Implications for the Aged Population.

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Review 5.  Disorders of Sexual Development: Current Status and Progress in the Diagnostic Approach.

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6.  Chronic Ethanol Exposure Alters DNA Methylation in Neural Stem Cells: Role of Mouse Strain and Sex.

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Journal:  Mol Neurobiol       Date:  2019-08-14       Impact factor: 5.590

Review 7.  Sexually selected traits: a fundamental framework for studies on behavioral epigenetics.

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Journal:  ILAR J       Date:  2012

8.  Sex differences of gray matter morphology in cortico-limbic-striatal neural system in major depressive disorder.

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Journal:  J Psychiatr Res       Date:  2013-03-01       Impact factor: 4.791

9.  Influence of developmental lead exposure on expression of DNA methyltransferases and methyl cytosine-binding proteins in hippocampus.

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