Molecular studies of major depressive disorder: the epigenetic perspective

被引:214
作者
Mill, J. [1 ]
Petronis, A. [1 ]
机构
[1] Ctr Addit & Mental Hlth, Krembil Fam Epigenet Lab, Toronto, ON M5T 1R8, Canada
基金
英国医学研究理事会;
关键词
depression; epigenetics; methylation; genetics; environment; sex-effects;
D O I
10.1038/sj.mp.4001992
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Major depressive disorder (MDD) is a common and highly heterogeneous psychiatric disorder encompassing a spectrum of symptoms involving deficits to a range of cognitive, psychomotor and emotional processes. As is the norm for aetiological studies into the majority of psychiatric phenotypes, particular focus has fallen on the interplay between genetic and environmental factors. There are, however, several epidemiological, clinical and molecular peculiarities associated with MDD that are hard to explain using traditional gene and environment-based approaches. Our goal in this study is to demonstrate the benefits of looking beyond conventional DNA+environment' and 'DNA x environment' aetiological paradigms. Epigenetic factors - inherited and acquired modifications of DNA and histones that regulate various genomic functions occurring without a change in nuclear DNA sequence - offer new insights about many of the non-Mendelian features of major depression, and provide a direct mechanistic route via which the environment can interact with the genome. The study of epigenetics, especially in complex diseases, is a relatively new field of research, and optimal laboratory techniques and analysis methods are still being developed. Incorporating epigenetic research into aetiological studies of MDD thus presents a number of methodological and interpretive challenges that need to be addressed. Despite these difficulties, the study of DNA methylation and histone modifications has the potential to transform our understanding about the molecular aetiology of complex diseases.
引用
收藏
页码:799 / 814
页数:16
相关论文
共 117 条
[91]   Epigenetics and the environment [J].
Sutherland, JE ;
Costa, M .
EPIGENETICS IN CANCER PREVENTION: EARLY DETECTION AND RISK ASSESSMENT, 2003, 983 :151-160
[92]   Fragile-X syndrome and myotonic dystrophy:: parallels and paradoxes [J].
Tapscott, SJ ;
Klesert, TR ;
Widrow, RJ ;
Stöger, R ;
Laird, CD .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1998, 8 (02) :245-253
[93]   Sex-specific association between bipolar affective disorder in women and GPR50, an X-linked orphan G protein-coupled receptor [J].
Thomson, PA ;
Wray, NR ;
Thomson, AM ;
Dunbar, DR ;
Grassie, MA ;
Condie, A ;
Walker, MT ;
Smith, DJ ;
Pulford, DJ ;
Muir, W ;
Blackwood, DHR ;
Porteous, DJ .
MOLECULAR PSYCHIATRY, 2005, 10 (05) :470-478
[94]   Analysis and quantification of multiple methylation variable positions in CpG islands by Pyrosequencing™ [J].
Tost, J ;
Dunker, J ;
Gut, IG .
BIOTECHNIQUES, 2003, 35 (01) :152-+
[95]   Nonshared environment: A theoretical, methodological, and quantitative review [J].
Turkheimer, E ;
Waldron, M .
PSYCHOLOGICAL BULLETIN, 2000, 126 (01) :78-108
[96]   Fidelity of the methylation pattern and its variation in the genome [J].
Ushijima, T ;
Watanabe, N ;
Okochi, E ;
Kaneda, A ;
Sugimura, T ;
Miyamoto, K .
GENOME RESEARCH, 2003, 13 (05) :868-874
[97]  
Vaillant GE, 2005, AUST NZ J PSYCHIAT, V39, P730
[98]   Polymorphisms of the glucocorticoid receptor gene and major depression [J].
van Rossum, EFC ;
Binder, EB ;
Majer, M ;
Koper, JW ;
Ising, M ;
Modell, S ;
Salyakina, D ;
Lamberts, SWJ ;
Holsboer, F .
BIOLOGICAL PSYCHIATRY, 2006, 59 (08) :681-688
[99]   In psychosis, cortical interneurons overexpress DNA-methyltransferase 1 [J].
Veldic, M ;
Guidotti, A ;
Maloku, E ;
Davis, JM ;
Costa, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (06) :2152-2157
[100]   Rural-urban differences in the prevalence of major depression and associated impairment [J].
Wang, JL .
SOCIAL PSYCHIATRY AND PSYCHIATRIC EPIDEMIOLOGY, 2004, 39 (01) :19-25