Association study on the DUSP6 gene, an affective disorder candidate gene on 12q23, performed by using fluorescence resonance energy transfer-based melting curve analysis on the LightCycler

被引:31
作者
Toyota, T
Watanabe, A
Shibuya, H
Nankai, M
Hattori, E
Yamada, K
Kurumaji, A
Karkera, JD
Detera-Wadleigh, SD
Yoshikawa, T
机构
[1] RIKEN, Brain Sci Inst, Lab Mol Psychiat, Wako, Saitama 3510198, Japan
[2] Tokyo Med & Dent Univ, Dept Neuropsychiat, Tokyo, Japan
[3] Natl Sanatorium Minami Hanamaki Hosp, Hanamaki, Iwate, Japan
[4] Tokyo Metropolitan Police Hosp, Dept Neuropsychiat, Tokyo, Japan
[5] NIMH, Intramural Res Program, Bethesda, MD 20892 USA
关键词
chromosome; 12q; genotyping; single nucleotide polymorphism (SNP); biallelic polymorphism; unipolar; bipolar;
D O I
10.1038/sj.mp.4000748
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
We introduced a new genotyping method, fluorescence resonance energy transfer-based melting curve analysis on the LightCycler, for the analysis of the gene, DUSP6(dual specificity MAP kinase phosphatase 6), in affective disorder patients. The DUSP6 gene is located on chromosome 12q22-23, which overlaps one of the reported bipolar disorder susceptibility loci. Because of its role in intracellular signalling pathways, the gene may be involved in the pathogenesis of affective disorders not only on the basis of its position but also of its function. We performed association analysis using a T>G polymorphism that gives rise to a missense mutation (Leu114Val), No evidence for a significant disease-causing effect was found in Japanese unipolars (n = 732) and bipolars (n = 122), when compared with controls (n = 299). More importantly, this study demonstrates that melting curve analysis on the LightCycler is an accurate, rapid and robust method for discriminating genotypes from biallelic markers. This strategy has the potential for use in high throughput scanning for and genotyping of single nucleotide polymorphisms (SNPs).
引用
收藏
页码:489 / 494
页数:6
相关论文
共 25 条
[1]  
Aslanidis C, 1999, CLIN CHEM, V45, P1094
[2]   HPA genotyping by PCR sequence-specific priming (PCR-SSP): A streamlined method for rapid routine investigations [J].
Cavanagh, G ;
Dunn, AN ;
Chapman, CE ;
Metcalfe, P .
TRANSFUSION MEDICINE, 1997, 7 (01) :41-45
[3]   ACTIVATION OF MAP KINASE KINASE IS NECESSARY AND SUFFICIENT FOR PC12 DIFFERENTIATION AND FOR TRANSFORMATION OF NIH 3T3 CELLS [J].
COWLEY, S ;
PATERSON, H ;
KEMP, P ;
MARSHALL, CJ .
CELL, 1994, 77 (06) :841-852
[4]   FAMILIAL COSEGREGATION OF MAJOR AFFECTIVE-DISORDER AND DARIERS-DISEASE (KERATOSIS-FOLLICULARIS) [J].
CRADDOCK, N ;
OWEN, M ;
BURGE, S ;
KURIAN, B ;
THOMAS, P ;
MCGUFFIN, P .
BRITISH JOURNAL OF PSYCHIATRY, 1994, 164 :355-358
[5]   LINKAGE STUDIES OF BIPOLAR DISORDER IN THE REGION OF THE DARIERS-DISEASE GENE ON CHROMOSOME 12Q23-24.1 [J].
DAWSON, E ;
PARFITT, E ;
ROBERTS, Q ;
DANIELS, J ;
LIM, L ;
SHAM, P ;
NOTHEN, M ;
PROPPING, P ;
LANCZIK, M ;
MAIER, W ;
REUNER, U ;
WEISSENBACH, J ;
GILL, M ;
POWELL, J ;
MCGUFFIN, P ;
OWEN, M ;
CRADDOCK, N .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 60 (02) :94-102
[6]   Significant linkage between bipolar affective disorder and chromosome 12q24 [J].
Ewald, H ;
Degn, B ;
Mors, O ;
Kruse, TA .
PSYCHIATRIC GENETICS, 1998, 8 (03) :131-140
[7]   Genomic analysis of DUSP6, a dual specificity MAP kinase phosphatase, in pancreatic cancer [J].
Furukawa, T ;
Yatsuoka, T ;
Youssef, EM ;
Abe, T ;
Yokoyama, T ;
Fukushige, S ;
Soeda, E ;
Hoshi, M ;
Hayashi, Y ;
Sunamura, M ;
Kobari, M ;
Horii, A .
CYTOGENETICS AND CELL GENETICS, 1998, 82 (3-4) :156-159
[8]   Applications of DNA chips for genomic analysis [J].
Hacia, JG ;
Brody, LC ;
Collins, FS .
MOLECULAR PSYCHIATRY, 1998, 3 (06) :483-492
[9]   No evidence for involvement of the leptin gene in anorexia nervosa, bulimia nervosa, underweight or early onset extreme obesity: identification of two novel mutations in the coding sequence and a novel polymorphism in the leptin gene linked upstream region [J].
Hinney, A ;
Bornscheuer, A ;
Depenbusch, M ;
Mierke, B ;
Tolle, A ;
Middeke, K ;
Ziegler, A ;
Roth, H ;
Gerber, G ;
Zamzow, K ;
Ballauff, A ;
Hamann, A ;
Mayer, H ;
Siegfried, W ;
Lehmkuhl, G ;
Poustka, F ;
Schmidt, MH ;
Hermann, H ;
Herpertz-Dahlmann, BM ;
Fichter, M ;
Remschmidt, H ;
Hebebrand, J .
MOLECULAR PSYCHIATRY, 1998, 3 (06) :539-543
[10]   ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes [J].
Jacobsen, NJO ;
Lyons, I ;
Hoogendoorn, B ;
Burge, S ;
Kwok, PY ;
O'Donovan, MC ;
Craddock, N ;
Owen, MJ .
HUMAN MOLECULAR GENETICS, 1999, 8 (09) :1631-1636