Understanding the Pathology of Schizophrenia: The Impact of High-Throughput Screening of the Genome and Proteome in Postmortem CNS

被引:14
作者
Dean, Brian [1 ,2 ,3 ,4 ]
Keriakous, Dahlia [1 ]
Thomas, Elizabeth [1 ,5 ]
Scarr, Elizabeth [1 ,2 ]
机构
[1] Univ Melbourne, Mental Hlth Res Inst Victoria, Rebecca L Cooper Med Res Labs, Melbourne, Vic, Australia
[2] Monash Univ, Dept Psychiat, Clayton, Vic, Australia
[3] Monash Univ, Dept Pathol, Clayton, Vic, Australia
[4] Monash Univ, Dept Psychol Med, Clayton, Vic, Australia
[5] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
关键词
Postmortem; human; CNS; microarray; 2D electrophoresis; schizophrenia;
D O I
10.2174/1573400052953547
中图分类号
R749 [精神病学];
学科分类号
100205 [精神病与精神卫生学];
摘要
High-throughput screening technologies such as microarrays and 2D electrophoresis are powerful analytical tools particularly suited to investigating the pathologies of complex diseases. Schizophrenia is now widely recognised as a complex disorder resulting from the interplay between genetic predisposition to the illness and the effects of yet to be identified environmental factors. Based the hypothesis that the outcome of the interaction between genetic predisposition and environmental factors act to produce changes in protein expression in the CNS to cause schizophrenia, a number of studies have used postmortem CNS and high throughput screening technologies to identify potential pathological processes that might be involved in the pathology of the disorder. This review attempts to place the current findings on gene and protein expression data in postmortem CNS from subjects with schizophrenia into a perspective that allows hypotheses on the cause of the disorder to be formulated.
引用
收藏
页码:1 / 9
页数:9
相关论文
共 64 条
[1]
Microarray analysis of postmortem temporal cortex from patients with schizophrenia [J].
Aston, C ;
Jiang, LX ;
Sokolov, BP .
JOURNAL OF NEUROSCIENCE RESEARCH, 2004, 77 (06) :858-866
[2]
BENES FM, 1995, ARCH GEN PSYCHIAT, V52, P1015
[3]
Searching for schizophrenia genes [J].
Bray, NJ ;
Owen, MJ .
TRENDS IN MOLECULAR MEDICINE, 2001, 7 (04) :169-174
[4]
Positive association between synapsin II and schizophrenia [J].
Chen, Q ;
He, G ;
Wang, XY ;
Chen, QY ;
Liu, XM ;
Gu, ZZ ;
Liu, J ;
Li, KQ ;
Wang, SJ ;
Zhu, SM ;
Feng, GY ;
He, L .
BIOLOGICAL PSYCHIATRY, 2004, 56 (03) :177-181
[5]
Regulator of G-protein signaling 4 (RGS4) gene is associated with schizophrenia in Irish high density families [J].
Chen, XN ;
Dunham, C ;
Kendler, S ;
Wang, X ;
O'Neill, FA ;
Walsh, D ;
Kendler, KS .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2004, 129B (01) :23-26
[6]
cDNA array reveals differential gene expression following chronic neuroleptic administration: implications of synapsin II in haloperidol treatment [J].
Chong, VZ ;
Young, LT ;
Mishra, RK .
JOURNAL OF NEUROCHEMISTRY, 2002, 82 (06) :1533-1539
[7]
Association and linkage analyses of RGS4 polymorphisms in schizophrenia [J].
Chowdari, KV ;
Mirnics, K ;
Semwal, P ;
Wood, J ;
Lawrence, E ;
Bhatia, T ;
Deshpande, SN ;
K, TB ;
Ferrell, RE ;
Middleton, FA ;
Devlin, B ;
Levitt, P ;
Lewis, DA ;
Nimgaonkar, VL .
HUMAN MOLECULAR GENETICS, 2002, 11 (12) :1373-1380
[8]
COLLINS JOHN, 1957, MED JOUR AUSTRALIA II, V44, P467
[9]
Neuregulin 1-erbB signaling and the molecular/cellular basis of schizophrenia [J].
Corfas, G ;
Roy, K ;
Buxbaum, J .
NATURE NEUROSCIENCE, 2004, 7 (06) :575-580
[10]
Confirmation and refinement of an 'at-risk' haplotype for schizophrenia suggests the EST cluster, Hs.97362, as a potential susceptibility gene at the Neuregulin-1 locus [J].
Corvin, AP ;
Morris, DW ;
McGhee, K ;
Schwaiger, S ;
Scully, P ;
Quinn, J ;
Meagher, D ;
St Clair, D ;
Waddington, JL ;
Gill, M .
MOLECULAR PSYCHIATRY, 2004, 9 (02) :208-212