Epigenetic Mediation of Environmental Influences in Major Psychotic Disorders

被引:166
作者
Rutten, Bart P. F. [1 ]
Mill, Jonathan [2 ]
机构
[1] Maastricht Univ, Dept Psychiat & Neuropsychol, Sch Mental Hlth & Neurosci,Med Ctr, European Grad Sch Neurosci,S Limburg Mental Hlth, NL-6226 NB Maastricht, Netherlands
[2] Kings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Ctr, London WC2R 2LS, England
关键词
DNA methylation; histone modifications; development; schizophrenia; bipolar disorder; gene-environment interaction; MESSENGER-RNA EXPRESSION; PATERNAL AGE; BIPOLAR-DISORDER; DNA-METHYLATION; CANNABIS USE; PRENATAL EXPOSURE; GLUCOCORTICOID-RECEPTOR; CHROMATIN REGULATION; ADULT SCHIZOPHRENIA; MTHFR POLYMORPHISMS;
D O I
10.1093/schbul/sbp104
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
The major psychotic disorders schizophrenia and bipolar disorder are etiologically complex involving both heritable and nonheritable factors. The absence of consistently replicated major genetic effects, together with evidence for lasting changes in gene expression after environmental exposures, is consistent with the concept that the biologic underpinnings of these disorders are epigenetic in form rather than DNA sequence based. Psychosis-associated environmental exposures, particularly at key developmental stages, may result in long-lasting epigenetic alterations that impact on the neurobiological processes involved in pathology. Although direct evidence for epigenetic dysfunction in both schizophrenia and bipolar disorder is still limited, methodological technologies in epigenomic profiling have advanced. This means that we are at the exciting stage where it is feasible to start investigating molecular modifications to DNA and histones and examine the mechanisms by which environmental factors can act upon the genome to bring about epigenetic changes in gene expression involved in the etiology of these disorders. Given the dynamic nature of the epigenetic machinery and potential reversibility of epigenetic modifications, the understanding of such mechanisms is of key relevance for clinical psychiatry and for identifying new targets for prevention and/or intervention.
引用
收藏
页码:1045 / 1056
页数:12
相关论文
共 135 条
[1]   Hypomethylation of MB-COMT promoter is a major risk factor for schizophrenia and bipolar disorder [J].
Abdolmaleky, Hamid Mostafavi ;
Cheng, Kuang-hung ;
Faraone, Stephen V. ;
Wilcox, Marsha ;
Glatt, Stephen J. ;
Gao, Fangming ;
Smith, Cassandra L. ;
Shafa, Rahim ;
Aeali, Batol ;
Carnevale, Julie ;
Pan, Hongjie ;
Papageorgis, Panagiotis ;
Ponte, Jose F. ;
Sivaraman, Vadivelu ;
Tsuang, Ming T. ;
Thiagalingam, Sam .
HUMAN MOLECULAR GENETICS, 2006, 15 (21) :3132-3145
[2]   Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database [J].
Allen, Nicole C. ;
Bagade, Sachin ;
McQueen, Matthew B. ;
Ioannidis, John P. A. ;
Kavvoura, Fotini K. ;
Khoury, Muin J. ;
Tanzi, Rudolph E. ;
Bertram, Lars .
NATURE GENETICS, 2008, 40 (07) :827-834
[3]  
Allis CD., 2007, Epigenetics, P23
[4]   Causal association between cannabis and psychosis: examination of the evidence [J].
Arseneault, L ;
Cannon, M ;
Witton, J ;
Murray, RM .
BRITISH JOURNAL OF PSYCHIATRY, 2004, 184 :110-117
[5]   Substance use in a population-based clinic sample of people with first-episode psychosis [J].
Barnett, Jennifer H. ;
Werners, Ursula ;
Secher, Sandra M. ;
Hill, Katherine E. ;
Brazil, Rossa ;
Masson, Kim ;
Pernet, David E. ;
Kirkbride, James B. ;
Murray, Graham K. ;
Bullmore, Edward T. ;
Jones, Peter B. .
BRITISH JOURNAL OF PSYCHIATRY, 2007, 190 :515-520
[6]   GABAergic interneurons: Implications for understanding schizophrenia and bipolar disorder [J].
Benes, FM ;
Berretta, S .
NEUROPSYCHOPHARMACOLOGY, 2001, 25 (01) :1-27
[7]   The complex language of chromatin regulation during transcription [J].
Berger, Shelley L. .
NATURE, 2007, 447 (7143) :407-412
[8]   Effects of chronic exposure to cocaine are regulated by the neuronal protein Cdk5 [J].
Bibb, JA ;
Chen, JS ;
Taylor, JR ;
Svenningsson, P ;
Nishi, A ;
Snyder, GL ;
Yan, Z ;
Sagawa, ZK ;
Ouimet, CC ;
Nairn, AC ;
Nestler, EJ ;
Greengard, P .
NATURE, 2001, 410 (6826) :376-380
[9]   Reductions in frontal, temporal and parietal volume associated with the onset of psychosis [J].
Borgwardt, Stefan J. ;
McGuire, Philip K. ;
Aston, Jacqueline ;
Gschwandtner, Ute ;
Pflueger, Marlon O. ;
Stieglitz, Rolf-Dieter ;
Radue, Ernst-Wilhelm ;
Riecher-Roessler, Anita .
SCHIZOPHRENIA RESEARCH, 2008, 106 (2-3) :108-114
[10]   Decoding the Epigenetic Language of Neuronal Plasticity [J].
Borrelli, Emiliana ;
Nestler, Eric J. ;
Allis, C. David ;
Sassone-Corsi, Paolo .
NEURON, 2008, 60 (06) :961-974