Analysis of protocadherin alpha gene deletion variant in bipolar disorder and schizophrenia

被引:19
作者
Lachman, Herbert M. [1 ]
Petruolo, Oriana A. [1 ]
Pedrosa, Erika [1 ]
Novak, Tomas [3 ]
Nolan, Karen [2 ]
Stopkova, Pavla [3 ]
机构
[1] Albert Einstein Coll Med, Dept Psychiat & Behav Sci, Basic Res Div, Bronx, NY 10461 USA
[2] Nathan S Kline Inst Psychiat Res, Dept Psychiat, Orangeburg, NY 10962 USA
[3] Prague Psychiat Ctr, Prague, Czech Republic
关键词
bipolar disorder; cadherin; copy number variant; copy number variation; protocadherin; schizophrenia;
D O I
10.1097/YPG.0b013e3282fa1838
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objectives The cell adhesion proteins protocadherins and cadherins, through their effects on guiding neurons during development neuronal differentiation, and synaptogenesis, are feasible targets to consider in schizophrenia (SZ) and bipolar disorder (BD) pathogenesis. Thus, allelic variation occurring in protocadherin and cadherin encoding genes that map to regions of the genome targeted in SZ and BD linkage studies are particularly strong candidates to consider as underlying susceptibility factors. One such set of candidate genes is the 5q31-linked PCDH family. A polymorphic copy number variation in this locus, a 16.7-kb deletion affecting PCDH-alpha exons 8-10 (alpha 8-alpha 10 Delta), was analyzed in this study as a potential candidate variant in SZ and BD. Methods The frequency of the alpha 8-alpha 10 Delta variant was determined in a cohort of Caucasian patients with SZ from the United States and a cohort of patients with BD from the Czech Republic, and corresponding controls by amplifying DNA with deletion specific primers followed by gel electrophoresis. Results No significant difference was observed in the frequency of the alpha 8-alpha 10 Delta variant in patients with SZ or BD compared with their respective controls. Conclusion Although the results of this study were negative, theoretical considerations and linkage studies suggest that the 5q31-linked PCDH family should be analyzed as a potential locus underlying SZ and BD susceptibility. Psychiatr Genet 18:110-115 (c) 2008 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:110 / 115
页数:6
相关论文
共 62 条
[1]   A genome-wide association study implicates diacylglycerol kinase η (DGKH) and several other genes in the etiology of bipolar disorder [J].
Baum, A. E. ;
Akula, N. ;
Cabanero, M. ;
Cardona, I. ;
Corona, W. ;
Klemens, B. ;
Schulze, T. G. ;
Cichon, S. ;
Rietschel, M. ;
Noethen, M. M. ;
Georgi, A. ;
Schumacher, J. ;
Schwarz, M. ;
Abou Jamra, R. ;
Hoefels, S. ;
Propping, P. ;
Satagopan, J. ;
Detera-Wadleigh, S. D. ;
Hardy, J. ;
McMahon, F. J. .
MOLECULAR PSYCHIATRY, 2008, 13 (02) :197-207
[2]   Evidence for shared susceptibility in bipolar disorder and schizophrenia [J].
Berrettini, W .
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2003, 123C (01) :59-64
[3]   Positional cloning, association analysis and expression studies provide convergent evidence that the cadherin gene FAT contains a bipolar disorder susceptibility allele [J].
Blair, IP ;
Chetcuti, AF ;
Badenhop, RF ;
Scimone, A ;
Moses, MJ ;
Adams, LJ ;
Craddock, N ;
Green, E ;
Kirov, G ;
Owen, MJ ;
Kwok, JBJ ;
Donald, JA ;
Mitchell, PB ;
Schofield, PR .
MOLECULAR PSYCHIATRY, 2006, 11 (04) :372-383
[4]   Screening the human protocadherin 8 (PCDH8) gene in schizophrenia [J].
Bray, NJ ;
Kirov, G ;
Owen, RJ ;
Jacobsen, NJ ;
Georgieva, L ;
Williams, HJ ;
Norton, N ;
Spurlock, G ;
Jones, S ;
Zammit, S ;
O'Donovan, MC ;
Owen, MJ .
GENES BRAIN AND BEHAVIOR, 2002, 1 (03) :187-191
[5]   Genome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of Palau [J].
Devlin, B ;
Bacanu, SA ;
Roeder, K ;
Reimherr, F ;
Wender, P ;
Galke, B ;
Novasad, D ;
Chu, A ;
TCuenco, K ;
Tiobek, S ;
Otto, C ;
Byerley, W .
MOLECULAR PSYCHIATRY, 2002, 7 (07) :689-694
[6]   Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders [J].
Durand, CM ;
Kappeler, C ;
Betancur, C ;
Delorme, R ;
Quach, H ;
Goubran-Botros, H ;
Melke, J ;
Nygren, G ;
Chabane, N ;
Bellivier, F ;
Szoke, A ;
Schurhoff, F ;
Rastam, M ;
Anckarsäter, H ;
Gillberg, C ;
Leboyer, M ;
Bourgeron, T .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2006, 141B (01) :67-70
[7]   Widening the spectrum of human genetic variation [J].
Eichler, EE .
NATURE GENETICS, 2006, 38 (01) :9-11
[8]  
ENDICOTT J, 1978, ARCH GEN PSYCHIAT, V35, P837
[9]   Monoallelic yet combinatorial expression of variable exons of the protocadherin-α gene cluster in single neurons [J].
Esumi, S ;
Kakazu, N ;
Taguchi, Y ;
Hirayama, T ;
Sasaki, A ;
Hirabayashi, T ;
Koide, T ;
Kitsukawa, T ;
Hamada, S ;
Yagi, T .
NATURE GENETICS, 2005, 37 (02) :171-176
[10]   Protocadherins [J].
Frank, M ;
Kemler, R .
CURRENT OPINION IN CELL BIOLOGY, 2002, 14 (05) :557-562