Effects of MAOA promoter methylation on susceptibility to paranoid schizophrenia

被引:42
作者
Chen, Yanbo [1 ,2 ]
Zhang, Jiexu [1 ,2 ]
Zhang, Li [3 ]
Shen, Yan [1 ,2 ]
Xu, Qi [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Inst Basic Med Sci, Natl Lab Med Mol Biol, Beijing 100005, Peoples R China
[2] Peking Union Med Coll, Beijing 100005, Peoples R China
[3] MOH, Hlth Human Resources Dev Ctr, Beijing, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
MONOAMINE-OXIDASE-A; BIPOLAR DISORDER; MONOZYGOTIC TWINS; GENE-EXPRESSION; DNA; ASSOCIATION; BEHAVIOR; RISK; HYPOMETHYLATION; TRANSCRIPTION;
D O I
10.1007/s00439-011-1131-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
This study was undertaken to analyze DNA methylation profiling at the monoamine oxidase A (MAOA) locus, in order to determine whether abnormal DNA methylation is involved in the development of schizophrenia. We recruited a total of 371 patients with paranoid schizophrenia (199 males and 172 females) and 288 unrelated control subjects (123 males and 165 females) for analysis of DNA methylation. Diagnosis was made based on the Structured Clinical Interview for DSM-VI. Genomic DNA extracted from peripheral blood was chemically modified using bisulfite, and DNA methylation profiles of the MAOA promoter were determined by BSP-sequencing. DNA methylation ratios of individual CpG residues and overall methylation ratios were measured on each subject. The results showed that there was no significant difference in overall DNA methylation ratios between patients and controls either in the female group (P = 0.42) or in the male group (P = 0.24). Of 15 CpG residues that showed significant differences in DNA methylation status between the patient group and the control group in females, eight of which had an increased level and seven, a decreased level, with a combined P value of 1 (df = 160). In male subjects, however, six individual CpG residues showed an increased methylation level with a combined P value of 5.80E-35 (df = 158). In conclusion, abnormalities of DNA methylation at the MAOA promoter may be associated with schizophrenia in males.
引用
收藏
页码:1081 / 1087
页数:7
相关论文
共 41 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]   Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 [J].
Amir, RE ;
Van den Veyver, IB ;
Wan, M ;
Tran, CQ ;
Francke, U ;
Zoghbi, HY .
NATURE GENETICS, 1999, 23 (02) :185-188
[3]  
APA A.P. A., 2000, Diagnostic and statistical manual of mental disorders: DSM-IV, V4th
[4]   CDNA CLONING OF HUMAN-LIVER MONOAMINE OXIDASE-A AND OXIDASE-B - MOLECULAR-BASIS OF DIFFERENCES IN ENZYMATIC-PROPERTIES [J].
BACH, AWJ ;
LAN, NC ;
JOHNSON, DL ;
ABELL, CW ;
BEMBENEK, ME ;
KWAN, SW ;
SEEBURG, PH ;
SHIH, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (13) :4934-4938
[5]   ABNORMAL-BEHAVIOR ASSOCIATED WITH A POINT MUTATION IN THE STRUCTURAL GENE FOR MONOAMINE OXIDASE-A [J].
BRUNNER, HG ;
NELEN, M ;
BREAKEFIELD, XO ;
ROPERS, HH ;
VANOOST, BA .
SCIENCE, 1993, 262 (5133) :578-580
[6]  
BRUNNER HG, 1993, AM J HUM GENET, V52, P1032
[7]   X-inactivation profile reveals extensive variability in X-linked gene expression in females [J].
Carrel, L ;
Willard, HF .
NATURE, 2005, 434 (7031) :400-404
[8]   AGGRESSIVE-BEHAVIOR AND ALTERED AMOUNTS OF BRAIN-SEROTONIN AND NOREPINEPHRINE IN MICE LACKING MAOA [J].
CASES, O ;
SEIF, I ;
GRIMSBY, J ;
GASPAR, P ;
CHEN, K ;
POURNIN, S ;
MULLER, U ;
AGUET, M ;
BABINET, C ;
SHIH, JC ;
DEMAEYER, E .
SCIENCE, 1995, 268 (5218) :1763-1766
[9]   Methylation analysis of the fragile X syndrome by PCR [J].
Das, S ;
Kubota, T ;
Song, M ;
Daniel, R ;
Berry-Kravis, EM ;
Prior, TW ;
Popovich, B ;
Rosser, L ;
Arinami, T ;
Ledbetter, DH .
GENETIC TESTING, 1997, 1 (03) :151-155
[10]   A GENOMIC SEQUENCING PROTOCOL THAT YIELDS A POSITIVE DISPLAY OF 5-METHYLCYTOSINE RESIDUES IN INDIVIDUAL DNA STRANDS [J].
FROMMER, M ;
MCDONALD, LE ;
MILLAR, DS ;
COLLIS, CM ;
WATT, F ;
GRIGG, GW ;
MOLLOY, PL ;
PAUL, CL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (05) :1827-1831