Repeat sizes at CAG/CTG loci CTG18.1, ERDA1 and TGC13-7a in schizophrenia

被引:7
作者
Bowen, T
Guy, CA
Cardno, AG
Vincent, JB
Kennedy, JL
Jones, LA
Gray, M
Sanders, RD
McCarthy, G
Murphy, KC
Owen, MJ
O'Donovan, MC
机构
[1] Univ Wales Coll Cardiff, Coll Med, Div Psychol Med, Cardiff, S Glam, Wales
[2] Univ Wales Coll Cardiff, Coll Med, Div Med Genet, Cardiff, S Glam, Wales
[3] Univ Toronto, Ctr Addict & Mental Hlth, Neurogenet Sect, Clarke Div, Toronto, ON, Canada
关键词
schizophrenia; trinucleotide repeats; CTG18.1; ERDA; 1; TGC13-7a;
D O I
10.1097/00041444-200010010-00006
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A number of studies using the repeat expansion detection (RED) technique have suggested an association between unknown large CAG / CTG repeats and schizophrenia. The polymorphic CAG / CTG repeat loci CTG18.1 and ERDA1 have been reported to account for a high proportion (similar to 90%) of the large repeats detected by RED and may therefore be responsible for the cited association. The recently described locus TGC13-7a contains a highly polymorphic CTA/TAG and CAG / CTG composite repeat, and is thus another authentic candidate. In the present investigation, each locus was analysed for association with schizophrenia in a sample of 206 patients and 219 group-matched controls. No evidence for association of CTG18.1, ERDA1 and/or TGC13-7a with schizophrenia was found. The combined data accounted for only 54% of the CAG / CTG arrays of > 40 repeats found in our previous RED analysis. Psychiatr Genet 10:33-37 (C) 2000 Lippincott Williams & Wilkins.
引用
收藏
页码:33 / 37
页数:5
相关论文
共 22 条
[1]  
Bowen T, 1996, AM J HUM GENET, V59, P912
[2]   Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia [J].
Bowen, T ;
Guy, CA ;
Craddock, N ;
Cardno, AG ;
Williams, NM ;
Spurlock, G ;
Murphy, KC ;
Jones, LA ;
Gray', M ;
Sanders, RD ;
McCarthy, G ;
Chandy, KG ;
Fantino, E ;
Kalman, K ;
Gutman, GA ;
Gargus, JJ ;
Williams, J ;
McGuffin, P ;
Owen, MJ ;
O'Donovan, MC .
MOLECULAR PSYCHIATRY, 1998, 3 (03) :266-269
[3]   Linked polymorphisms upstream of exons 1 and 2 of the human cholecystokinin gene are not associated with schizophrenia or bipolar disorder [J].
Bowen, T ;
Norton, N ;
Jacobsen, NJO ;
Guy, C ;
Daniels, JK ;
Sanders, RD ;
Cardno, AG ;
Jones, LA ;
Murphy, KC ;
McGuffin, P ;
Craddock, N ;
O'Donovan, MC ;
Owen, MJ .
MOLECULAR PSYCHIATRY, 1998, 3 (01) :67-71
[4]   A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1 [J].
Breschel, TS ;
McInnis, MG ;
Margolis, RL ;
Sirugo, G ;
Corneliussen, B ;
Simpson, SG ;
McMahon, F ;
MacKinnon, DF ;
Xu, JF ;
Pleasant, N ;
Huo, Y ;
Ashworth, RG ;
Grundstrom, C ;
Grundstrom, T ;
Kidd, KK ;
DePaulo, JR ;
Ross, CA .
HUMAN MOLECULAR GENETICS, 1997, 6 (11) :1855-1863
[5]   Large CAG/CTG repeats are associated with childhood-onset schizophrenia [J].
Burgess, CE ;
Lindblad, K ;
Sidransky, E ;
Yuan, QP ;
Long, RT ;
Breschel, T ;
Ross, CA ;
McInnis, M ;
Lee, P ;
Ginns, EI ;
Lenane, M ;
Kumra, S ;
Jacobsen, L ;
Rapoport, JL ;
Schalling, M .
MOLECULAR PSYCHIATRY, 1998, 3 (04) :321-327
[6]   A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17q [J].
Ikeuchi, T ;
Sanpei, K ;
Takano, H ;
Sasaki, H ;
Tashiro, K ;
Cancel, G ;
Brice, A ;
Bird, TD ;
Schellenberg, GD ;
Pericak-Vance, MA ;
Welsh-Bohmer, KA ;
Clark, LN ;
Wilhelmsen, K ;
Tsuji, S .
GENOMICS, 1998, 49 (02) :321-326
[7]   An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8) [J].
Koob, MD ;
Moseley, ML ;
Schut, LJ ;
Benzow, KA ;
Bird, TD ;
Day, JW ;
Ranum, LPW .
NATURE GENETICS, 1999, 21 (04) :379-384
[8]  
Laurent C, 1998, AM J MED GENET, V81, P342, DOI 10.1002/(SICI)1096-8628(19980710)81:4<342::AID-AJMG12>3.0.CO
[9]  
2-L
[10]   Analysis of CAG/CTG repeat size in Chinese subjects with schizophrenia and bipolar affective disorder using the repeat expansion detection method [J].
Li, T ;
Vallada, HP ;
Liu, XH ;
Xie, T ;
Tang, XD ;
Zhao, JH ;
O'Donovan, MC ;
Murray, RM ;
Sham, PC ;
Collier, DA .
BIOLOGICAL PSYCHIATRY, 1998, 44 (11) :1160-1165