The dysbindin gene (DTNBP1) and schizophrenia:: No support for an association in the Korean population

被引:23
作者
Joo, Eun-Jeong
Lee, Kyu-Young
Jeong, Seong Hoon
Ahn, Yong-Min
Koo, Young Jin
Kim, Yong Sik
机构
[1] Seoul Natl Univ, Coll Med, Seoul Natl Univ Hosp, Dept Psychiat & Behav Sci, Seoul 110744, South Korea
[2] Seoul Natl Univ, Coll Med, Seoul Natl Univ Hosp, Inst Human Behav Med, Seoul 110744, South Korea
[3] Eulji Univ, Sch Med, Dept Neuropsychiat, Eulji Gen Hosp, Seoul 139711, South Korea
[4] Seoul Natl Univ Hosp, Clin Res Inst, Seoul 110744, South Korea
[5] Dongguk Univ, Coll Med, Dept Psychiat, Dongguk Univ Int Hosp, Goyang Si 411773, Gyeonggi Do, South Korea
关键词
association; DTNBP1; dysbindin; gene; Korean; schizophrenia; SNP;
D O I
10.1016/j.neulet.2006.08.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The dysbindin gene (DTNBP1) is located in chromosome 6p22.3, one of the regions of positive linkage for schizophrenia. A strong genetic association between DTNBP1 and schizophrenia has been replicated through many recent studies. In particular, dysbindin protein has been found to play a role in the glutamate neural transmission in the brain. In this study, we attempted to replicate the previously reported positive association between DTNBP1 and schizophrenia in the Korean population. Our sample included 194 patients with schizophrenia based on DSM-IV and 351 normal controls. We genotyped five SNPs including SNP A in promoter region of DTNBP1. The allele and genotype association were analyzed and the simulated haplotype was investigated as well. As the result, we could not find a significant association of DTNBP1 with schizophrenia in this Korean sample. Additional analysis of the subgroup of schizophrenia having familial loading of major psychiatric disorders did not show association. either. In summary, DTNBP1 is not likely to be a major susceptibility gene for schizophrenia in this Korean population. This result of no association also implies possible genetic heterogeneity of schizophrenia. Further studies with more dense SNPs of the whole gene sequence for various populations will be necessary to understand the genetic contribution of DTNBP1 for the development of schizophrenia. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:101 / 106
页数:6
相关论文
共 31 条
[11]   Korean version of the diagnostic interview for genetic studies: Validity and reliability [J].
Joo, EJ ;
Joo, YH ;
Hong, JP ;
Hwang, S ;
Maeng, SJ ;
Han, JH ;
Yang, BH ;
Lee, YS ;
Kim, YS .
COMPREHENSIVE PSYCHIATRY, 2004, 45 (03) :225-229
[12]  
JOO EJ, 2005, PSYCHIAT INVEST, V3, P14
[13]   Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria [J].
Kirov, G ;
Ivanov, D ;
Williams, NM ;
Preece, A ;
Nikolov, I ;
Milev, R ;
Koleva, S ;
Dimitrova, A ;
Toncheva, D ;
O'Donovan, MC ;
Owen, MJ .
BIOLOGICAL PSYCHIATRY, 2004, 55 (10) :971-975
[14]   Linkage disequlibrium in the DTNBP1 (Dysbindin) gene region and on chromosome 1p36 among psychotic patients from a genetic isolate in israel:: Findings from identity by descent haplotype sharing analysis [J].
Kohn, Y ;
Danilovich, E ;
Filon, D ;
Oppenheim, A ;
Karni, O ;
Kanyas, K ;
Turetsky, N ;
Korner, M ;
Lerer, B .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2004, 128B (01) :65-70
[15]   Genome scan meta-analysis of schizophrenia and bipolar disorder, part II:: Schizophrenia [J].
Lewis, CM ;
Levinson, DF ;
Wise, LH ;
DeLisi, LE ;
Straub, RE ;
Hovatta, I ;
Williams, NM ;
Schwab, SG ;
Pulver, AE ;
Faraone, SV ;
Brzustowicz, LM ;
Kaufmann, CA ;
Garver, DL ;
Gurling, HMD ;
Lindholm, E ;
Coon, H ;
Moises, HW ;
Byerley, W ;
Shaw, SH ;
Mesen, A ;
Sherrington, R ;
O'Neill, FA ;
Walsh, D ;
Kendler, KS ;
Ekelund, J ;
Paunio, T ;
Lönnqvist, J ;
Peltonen, L ;
O'Donovan, MC ;
Owen, MJ ;
Wildenauer, DB ;
Maier, W ;
Nestadt, G ;
Blouin, JL ;
Antonarakis, SE ;
Mowry, BJ ;
Silverman, JM ;
Crowe, RR ;
Cloninger, CR ;
Tsuang, MT ;
Malaspina, D ;
Harkavy-Friedman, JM ;
Svrakic, DM ;
Bassett, AS ;
Holcomb, J ;
Kalsi, G ;
McQuillin, A ;
Brynjolfson, J ;
Sigmundsson, T ;
Petursson, H .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (01) :34-48
[16]   Identifying potential risk haplotypes for schizophrenia at the DTNBP1 locus in Han Chinese and Scottish populations [J].
Li, T ;
Zhang, F ;
Liu, X ;
Sun, X ;
Sham, PC ;
Crombie, C ;
Ma, X ;
Wang, Q ;
Meng, H ;
Deng, W ;
Yates, P ;
Hu, X ;
Walker, N ;
Murray, RM ;
St Clair, D ;
Collier, DA .
MOLECULAR PSYCHIATRY, 2005, 10 (11) :1037-1044
[17]   Mutation analysis of the human dystrobrevin-binding protein 1 gene in schizophrenic patients [J].
Liao, HM ;
Chen, CH .
SCHIZOPHRENIA RESEARCH, 2004, 71 (01) :185-189
[18]   PowerMarker: an integrated analysis environment for genetic marker analysis [J].
Liu, KJ ;
Muse, SV .
BIOINFORMATICS, 2005, 21 (09) :2128-2129
[19]   Single nucleotide polymorphism detection:: allelic discrimination using TaqMan [J].
McGuigan, FEA ;
Ralston, SH .
PSYCHIATRIC GENETICS, 2002, 12 (03) :133-136
[20]   No evidence for association of the dysbindin gene [DTNBP1] with schizophrenia in an Irish population-based study [J].
Morris, DW ;
McGhee, KA ;
Schwaiger, S ;
Scully, P ;
Quinn, J ;
Meagher, D ;
Gill, M ;
Corvin, AP .
SCHIZOPHRENIA RESEARCH, 2003, 60 (2-3) :167-172