Integrative genome-wide association analysis of cytoarchitectural abnormalities in the prefrontal cortex of psychiatric disorders

被引:26
|
作者
Kim, S. [1 ]
Webster, M. J. [1 ]
机构
[1] Stanley Med Res Inst, Stanley Brain Res Lab, Rockville, MD 20850 USA
关键词
GABAergic neuron; oligodendrocyte; SNP; expression profile; schizophrenia; bipolar disorder; GENE-EXPRESSION; BIPOLAR DISORDER; NMDA RECEPTORS; SCHIZOPHRENIA; BRAIN; OLIGODENDROCYTES; CALCIUM; DEATH; RISK;
D O I
10.1038/mp.2010.23
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cytoarchitectural abnormalities have been described in the prefrontal cortex (PFC) of subjects with psychiatric disorders. We explored the possible genetic causalities that may underlie the cytoarchitectural abnormalities of calbindin-containing gamma-aminobutyric acid (GABA)ergic neurons and perineuronal oligodendrocytes in the PFC of subjects with psychiatric disorders by converging results from genome-wide single-nucleotide polymorphism (SNP) scans for the traits and expression SNP (eSNP) associations. In the initial genome-wide scans, we identified several development- and apoptosis-related genes associated with the cytoarchitectural traits. Moreover, the susceptibility gene for bipolar disorder, PPP2R2C, was found to be associated with the number of perineuronal oligodendrocytes. Further eSNP analyses indicated that two novel candidate genes, RAB2A and SLC38A1, were associated with the density of calbindin-positive neurons and the number of perineuronal oligodendrocytes, respectively. Our findings may provide novel insights into the genetic causalities associated with cytoarchitectural abnormalities in the PFC of subjects with major psychiatric disorders as well as into the etiology of such disorders. Molecular Psychiatry (2011) 16, 452-461; doi:10.1038/mp.2010.23; published online 23 March 2010
引用
收藏
页码:452 / 461
页数:10
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