Gene expression in the prefrontal cortex during adolescence: implications for the onset of schizophrenia

被引:86
作者
Harris, Laura W. [1 ]
Lockstone, Helen E. [1 ]
Khaitovich, Phillipp [2 ]
Weickert, Cynthia Shannon [3 ]
Webster, Maree J. [4 ]
Bahn, Sabine [1 ]
机构
[1] Univ Cambridge, Inst Biotechnol, Cambridge, England
[2] Max Planck Inst Evolutionary Anthropol, Leipzig, Germany
[3] Univ New S Wales, Schizophrenia Res Inst, Prince Wales Med Inst, Sydney, NSW, Australia
[4] Stanley Lab Brain Res, Bethesda, MD USA
来源
BMC MEDICAL GENOMICS | 2009年 / 2卷
关键词
AGE-RELATED-CHANGES; MESSENGER-RNA; BRAIN-DEVELOPMENT; NEUROENDOCRINE BRAIN; PROTEIN EXPRESSION; BIPOLAR DISORDER; NERVOUS-SYSTEM; DNA MICROARRAY; MYELIN; NEUREGULIN-1;
D O I
10.1186/1755-8794-2-28
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Many critical maturational processes take place in the human brain during postnatal development. In particular, the prefrontal cortex does not reach maturation until late adolescence and this stage is associated with substantial white matter volume increases. Patients with schizophrenia and other major psychiatric disorders tend to first present with overt symptoms during late adolescence/early adulthood and it has been proposed that this developmental stage represents a "window of vulnerability". Methods: In this study we used whole genome microarrays to measure gene expression in post mortem prefrontal cortex tissue from human individuals ranging in age from 0 to 49 years. To identify genes specifically altered in the late adolescent period, we applied a template matching procedure. Genes were identified which showed a significant correlation to a template showing a peak of expression between ages 15 and 25. Results: Approximately 2000 genes displayed an expression pattern that was significantly correlated (positively or negatively) with the template. In the majority of cases, these genes in fact reached a plateau during adolescence with only subtle changes thereafter. These include a number of genes previously associated with schizophrenia including the susceptibility gene neuregulin I (NRGI). Functional profiling revealed peak expression in late adolescence for genes associated with energy metabolism and protein and lipid synthesis, together with decreases for genes involved in glutamate and neuropeptide signalling and neuronal development/plasticity. Strikingly, eight myelin-related genes previously found decreased in schizophrenia brain tissue showed a peak in their expression levels in late adolescence, while the single myelin gene reported increased in patients with schizophrenia was decreased in late adolescence. Conclusion: The observed changes imply that molecular mechanisms critical for adolescent brain development are disturbed in schizophrenia patients.
引用
收藏
页数:14
相关论文
共 89 条
[1]   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
[2]  
[Anonymous], 1967, Regional development of the brain in early life
[3]  
[Anonymous], 2005, R LANG ENV STAT COMP
[4]   Adolescence: Vulnerable period for stress-induced prefrontal cortical function? - Introduction to Part IV [J].
Arnsten, AFT ;
Shansky, RM .
ADOLESCENT BRAIN DEVELOPMENT: VULNERABILITIES AND OPPORTUNITIES, 2004, 1021 :143-147
[5]   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
[6]   Changes in the expression of the NR2B subunit during aging in macaque monkeys [J].
Bai, L ;
Hof, PR ;
Standaert, DG ;
Xing, YD ;
Nelson, SE ;
Young, AB ;
Magnusson, KR .
NEUROBIOLOGY OF AGING, 2004, 25 (02) :201-208
[7]   Schizophrenia: Breakdown in the well-regulated lifelong development and [J].
Bartzokis, G .
NEUROPSYCHOPHARMACOLOGY, 2002, 27 (04) :672-683
[8]   Age-related changes in frontal and temporal lobe volumes in men - A magnetic resonance imaging study [J].
Bartzokis, G ;
Beckson, M ;
Lu, PH ;
Nuechterlein, KH ;
Edwards, N ;
Mintz, J .
ARCHIVES OF GENERAL PSYCHIATRY, 2001, 58 (05) :461-465
[9]   GOstat: find statistically overrepresented Gene Ontologies within a group of genes [J].
Beissbarth, T ;
Speed, TP .
BIOINFORMATICS, 2004, 20 (09) :1464-1465
[10]   Discordant changes in cortical TrkC mRNA and protein during the human lifespan [J].
Beltaifa, S ;
Webster, MJ ;
Ligons, DL ;
Fatula, RJ ;
Herman, MM ;
Kleinman, JE ;
Weickert, CS .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2005, 21 (09) :2433-2444