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
[51]   Meta-analysis of serotonin transporter polymorphisms and affective disorders [J].
Lotrich, FE ;
Pollock, BG .
PSYCHIATRIC GENETICS, 2004, 14 (03) :121-129
[52]   Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study [J].
Massat, I ;
Souery, D ;
Del-Favero, J ;
Nothen, M ;
Blackwood, D ;
Muir, W ;
Kaneva, R ;
Serretti, A ;
Lorenzi, C ;
Rietschel, M ;
Milanova, V ;
Papadimitriou, GN ;
Dikeos, D ;
Van Broeckhoven, C ;
Mendlewicz, J .
MOLECULAR PSYCHIATRY, 2005, 10 (06) :598-605
[53]  
MCMAHON FJ, 1995, AM J HUM GENET, V56, P1277
[54]   Whole genome amplification of sodium bisulfite-treated DNA allows the accurate estimate of methylated cytosine density in limited DNA resources [J].
Mill, Jonathan ;
Yazdanpanah, Simin ;
Guckel, Eva ;
Ziegler, Sigrid ;
Kaminsky, Zachary ;
Petronis, Arturas .
BIOTECHNIQUES, 2006, 41 (05) :603-607
[55]   Evidence for monozygotic twin (MZ) discordance in methylation level at two CpG sites in the promoter region of the catechol-O-methyltransferase (COMT) gene [J].
Mill, Jonathan ;
Dempster, Emma ;
Caspi, Avshalom ;
Williams, Benjamin ;
Moffitt, Terrie ;
Craig, Ian .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2006, 141B (04) :421-425
[56]   Microarrays in brain research: the good, the bad and the ugly [J].
Mirnics, K .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (06) :444-447
[57]   Diagnostic and Statistical Manual of Mental Disorders [J].
Mittal, Vijay A. ;
Walker, Elaine F. .
PSYCHIATRY RESEARCH, 2011, 189 (01) :158-159
[58]   Strategy for investigating interactions between measured genes and measured environments [J].
Moffitt, TE ;
Caspi, A ;
Rutter, M .
ARCHIVES OF GENERAL PSYCHIATRY, 2005, 62 (05) :473-481
[59]  
Murphy D L, 1975, Res Publ Assoc Res Nerv Ment Dis, V54, P277
[60]   Global mortality, disability, and the contribution of risk factors: Global Burden of Disease Study [J].
Murray, CJL ;
Lopez, AD .
LANCET, 1997, 349 (9063) :1436-1442