Gene expression profiling in Brodmann's area 46 from subjects with schizophrenia

被引:65
作者
Dean, Brian
Keriakous, Dahlia
Scarr, Elizabeth
Thomas, Elizabeth A.
机构
[1] Univ Melbourne, Dept Pathol, Parkville, Vic 3052, Australia
[2] Univ Melbourne, Dept Psychiat, Parkville, Vic 3052, Australia
[3] Monash Univ, Dept Psychol Med, Melbourne, Vic 3168, Australia
[4] Mental Hlth Res Inst Victoria, Rebecca L Cooper Res Labs, Melbourne, Vic, Australia
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
bipolar; 1; disorder; disrupted in schizophrenia 1; muscleblind protein; protocadherin; 17; schizophrenia;
D O I
10.1080/00048670701213245
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: To identify altered gene expression in the dorsolateral prefrontal cortex obtained after death from subjects with schizophrenia. Method: Restriction fragment differential display (RFDD) was used to measure levels of mRNA in Brodmann area (BA) 46 from schizophrenia and control subjects. Findings on specific mRNA identified with RFDD were further investigated using real-time polymerase chain reaction (real-time PCR), PCR and western blotting. Results: Levels of mRNA for 63 of approximately 12 500 genes differed in BA 46 in schizophrenia. Subsequent real-time PCR has shown that mRNA for muscleblind protein 1 (MBNL1) and protocadherin 17 (PCDH17) are increased in BA 46 from subjects with schizophrenia of short, but not long, duration. Altered levels of mRNA for neither gene were present in BA 9 from subjects with schizophrenia or in either cortical area from subjects with bipolar 1 disorder. By contrast, both RFDD and real-time PCR failed to show altered expression of the schizophrenia candidate gene disrupted in schizophrenia 1 (DISC1) BA46 from any diagnostic cohort. Conclusion: The present study has identified genes that are differentially expressed in BA 46 in schizophrenia. Initial studies have shown that there is a need for a careful validation of genes shown to be affected in schizophrenia using high-throughput technologies. In addition the present study has shown that gene expression may vary considerably depending on the duration of schizophrenia. This raises the hypothesis that changing gene expression may be underlying the change in symptom profile that occurs with disease progression in some subjects with schizophrenia.
引用
收藏
页码:308 / 320
页数:13
相关论文
共 56 条
[1]   BCL6 gene translocation in follicular lymphoma:: a harbinger of eventual transformation to diffuse aggressive lymphoma [J].
Akasaka, T ;
Lossos, IS ;
Levy, R .
BLOOD, 2003, 102 (04) :1443-1448
[2]   Deficient hippocampal neuron expression of proteasome, ubiquitin, and mitochondrial genes in multiple schizophrenia cohorts [J].
Altar, CA ;
Jurata, LW ;
Charles, V ;
Lemire, A ;
Liu, P ;
Bukhman, Y ;
Young, TA ;
Bullard, J ;
Yokoe, H ;
Webster, MJ ;
Knable, MB ;
Brockman, JA .
BIOLOGICAL PSYCHIATRY, 2005, 58 (02) :85-96
[3]   The muscleblind gene participates in the organization of Z-bands and epidermal attachments of Drosophila muscles and is regulated by Dmef2 [J].
Artero, R ;
Prokop, A ;
Paricio, N ;
Begemann, G ;
Pueyo, I ;
Mlodzik, M ;
Perez-Alonso, M ;
Baylies, MK .
DEVELOPMENTAL BIOLOGY, 1998, 195 (02) :131-143
[4]   Gene expression profiling in the post-mortem human brain - no cause for dismay [J].
Bahn, S ;
Augood, S ;
Standaert, DG ;
Starkey, M ;
Emson, PC .
JOURNAL OF CHEMICAL NEUROANATOMY, 2001, 22 (1-2) :79-94
[5]  
Begemann G, 1997, DEVELOPMENT, V124, P4321
[6]   Longitudinal follow-up of neurochemical changes during the first year of antipsychotic treatment in schizophrenia patients with minimal previous medication exposure [J].
Bustillo, JR ;
Lauriello, J ;
Rowland, LM ;
Thomson, LM ;
Petropoulos, H ;
Hammond, R ;
Hart, B ;
Brooks, WM .
SCHIZOPHRENIA RESEARCH, 2002, 58 (2-3) :313-321
[7]   Effect of antipsychotic drugs on DISC1 and dysbindin expression in mouse frontal cortex and hippocampus [J].
Chiba, S. ;
Hashimoto, R. ;
Hattori, S. ;
Yohda, M. ;
Lipska, B. ;
Weinberger, D. R. ;
Kunugi, H. .
JOURNAL OF NEURAL TRANSMISSION, 2006, 113 (09) :1337-1346
[8]  
Dean B, 2000, AUST NZ J PSYCHIAT, V34, P560
[9]   Understanding the Pathology of Schizophrenia: The Impact of High-Throughput Screening of the Genome and Proteome in Postmortem CNS [J].
Dean, Brian ;
Keriakous, Dahlia ;
Thomas, Elizabeth ;
Scarr, Elizabeth .
CURRENT PSYCHIATRY REVIEWS, 2005, 1 (01) :1-9
[10]   Identification of polymorphisms within Disrupted in Schizophrenia 1 and Disrupted in Schizophrenia 2, and an investigation of their association with schizophrenia and bipolar affective disorder [J].
Devon, RS ;
Anderson, S ;
Teague, PW ;
Burgess, P ;
Kipari, TMJ ;
Semple, CAM ;
Millar, JK ;
Muir, WJ ;
Murray, V ;
Pelosi, AJ ;
Blackwood, DHR ;
Porteous, DJ .
PSYCHIATRIC GENETICS, 2001, 11 (02) :71-78