Age-related changes in the expression of schizophrenia susceptibility genes in the human prefrontal cortex

被引:46
作者
Colantuoni, Carlo [1 ,2 ]
Hyde, Thomas M. [1 ]
Mitkus, Shruti [1 ]
Joseph, Andrew [1 ]
Sartorius, Leah [1 ]
Aguirre, Claudia [1 ]
Creswell, Johanna [1 ]
Johnson, Elizabeth [2 ]
Deep-Soboslay, Amy [1 ]
Herman, Mary M. [1 ]
Lipska, Barbara K. [1 ]
Weinberger, Daniel R. [1 ]
Kleinman, Joel E. [1 ]
机构
[1] NIMH, Clin Brain Disorders Branch, Genes Cognit & Psychosis Program, IRP,NIH, Bethesda, MD 20892 USA
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Biostat, Baltimore, MD 21205 USA
关键词
aging; disease onset; schizophrenia; gene expression; susceptibility; postmortem; prefrontal cortex;
D O I
10.1007/s00429-008-0181-5
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The molecular basis of complex neuropsychiatric disorders most likely involves many genes. In recent years, specific genetic variations influencing risk for schizophrenia and other neuropsychiatric disorders have been reported. We have used custom DNA microarrays and qPCR to investigate the expression of putative schizophrenia susceptibility genes and related genes of interest in the normal human brain. Expression of 31 genes was measured in Brodmann's area 10 (BA10) in the prefrontal cortex of 72 postmortem brain samples spanning half a century of human aging (18-67 years), each without history of neuropsychiatric illness, neurological disease, or drug abuse. Examination of expression across age allowed the identification of genes whose expression patterns correlate with age, as well as genes that share common expression patterns and that possibly participate in common cellular mechanisms related to the emergence of schizophrenia in early adult life. The expression of GRM3 and RGS4 decreased across the entire age range surveyed, while that of PRODH and DARPP-32 was shown to increase with age. NRG1, ERBB3, and NGFR show expression changes during the years of greatest risk for the development of schizophrenia. Expression of FEZ1, GAD1, and RGS4 showed especially high correlation with one another, in addition to the strongest mean levels of absolute correlation with all other genes studied here. All microarray data are available at http://www.ncbi.nlm.nih.gov/geo/ (accession #: TBA).
引用
收藏
页码:255 / 271
页数:17
相关论文
共 99 条
[1]   GAD1 (2q31.1), which encodes glutamic acid decarboxylase (GAD67), is associated with childhood-onset schizophrenia and cortical gray matter volume loss [J].
Addington, AM ;
Gornick, M ;
Duckworth, J ;
Sporn, A ;
Gogtay, N ;
Bobb, A ;
Greenstein, D ;
Lenane, M ;
Gochman, P ;
Baker, N ;
Balkissoon, R ;
Vakkalanka, RK ;
Weinberger, DR ;
Rapoport, JL ;
Straub, RE .
MOLECULAR PSYCHIATRY, 2005, 10 (06) :581-588
[2]   Evidence for decreased DARPP-32 in the prefrontal cortex of patients with schizophrenia [J].
Albert, KA ;
Hemmings, HC ;
Adamo, AIB ;
Potkin, SG ;
Akbarian, S ;
Sandman, CA ;
Cotman, CW ;
Bunney, WE ;
Greengard, P .
ARCHIVES OF GENERAL PSYCHIATRY, 2002, 59 (08) :705-712
[3]   Age of onset in familial and sporadic schizophrenia [J].
Alda, M ;
Ahrens, B ;
Lit, W ;
Dvorakova, M ;
Labelle, A ;
Zvolsky, P ;
Jones, B .
ACTA PSYCHIATRICA SCANDINAVICA, 1996, 93 (06) :447-450
[4]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[5]   GENDER DIFFERENCES IN AGE AT ONSET OF SCHIZOPHRENIA - AN OVERVIEW [J].
ANGERMEYER, MC ;
KUHN, L .
EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE, 1988, 237 (06) :351-364
[6]   Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia [J].
Badner, JA ;
Gershon, ES .
MOLECULAR PSYCHIATRY, 2002, 7 (04) :405-411
[7]   White matter development during childhood and adolescence: A cross-sectional diffusion tensor imaging study [J].
Barnea-Goraly, N ;
Menon, V ;
Eckert, M ;
Tamm, L ;
Bammer, R ;
Karchemskiy, A ;
Dant, CC ;
Reiss, AL .
CEREBRAL CORTEX, 2005, 15 (12) :1848-1854
[8]   Disrupted in Schizophrenia 1 and Nudel form a neurodevelopmentally regulated protein complex: implications for schizophrenia and other major neurological disorders [J].
Brandon, NJ ;
Handford, EJ ;
Schurov, I ;
Rain, JC ;
Pelling, M ;
Duran-Jimeniz, B ;
Camargo, LM ;
Oliver, KR ;
Beher, D ;
Shearman, MS ;
Whiting, PJ .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2004, 25 (01) :42-55
[9]   Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22 [J].
Brzustowicz, LM ;
Simone, J ;
Mohseni, P ;
Hayter, JE ;
Hodgkinson, KA ;
Chow, EWC ;
Bassett, AS .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (05) :1057-1063
[10]   Neuregulin and ErbB receptor signaling pathways in the nervous system [J].
Buonanno, A ;
Fischbach, GD .
CURRENT OPINION IN NEUROBIOLOGY, 2001, 11 (03) :287-296