TY - JOUR
T1 - Gene expression profiling of the dorsolateral and orbital prefrontal cortex in schizophrenia
AU - Mladinov, Mihovil
AU - Sedmak, Goran
AU - Fuller, Heidi R.
AU - Babić Leko, Mirjana
AU - Mayer, Davor
AU - Kirincich, Jason
AU - Štajduhar, Andrija
AU - Borovečki, Fran
AU - Hof, Patrick R.
AU - Šimić, Goran
N1 - Publisher Copyright:
© 2016 Mihovil Mladinov et al., published by De Gruyter Open 2016.
PY - 2016/1/1
Y1 - 2016/1/1
N2 - Schizophrenia is a complex polygenic disorder of unknown etiology. Over 3,000 candidate genes associated with schizophrenia have been reported, most of which being mentioned only once. Alterations in cognitive processing - working memory, metacognition and mentalization - represent a core feature of schizophrenia, which indicates the involvement of the prefrontal cortex in the pathophysiology of this disorder. Hence we compared the gene expression in postmortem tissue from the left and right dorsolateral prefrontal cortex (DLPFC, Brodmann's area 46), and the medial part of the orbitofrontal cortex (MOFC, Brodmann's area 11/12), in six patients with schizophrenia and six control brains. Although in the past decade several studies performed transcriptome profiling in schizophrenia, this is the first study to investigate both hemispheres, providing new knowledge about possible brain asymmetry at the level of gene expression and its relation to schizophrenia. We found that in the left hemisphere, twelve genes from the DLPFC and eight genes from the MOFC were differentially expressed in patients with schizophrenia compared to controls. In the right hemisphere there was only one gene differentially expressed in the MOFC. We reproduce the involvement of previously reported genes TARDBP and HNRNPC in the pathogenesis of schizophrenia, and report seven novel genes: SART1, KAT7, C1D, NPM1, EVI2A, XGY2, and TTTY15. As the differentially expressed genes only partially overlap with previous studies that analyzed other brain regions, our findings indicate the importance of considering prefrontal cortical regions, especially those in the left hemisphere, for obtaining disease-relevant insights.
AB - Schizophrenia is a complex polygenic disorder of unknown etiology. Over 3,000 candidate genes associated with schizophrenia have been reported, most of which being mentioned only once. Alterations in cognitive processing - working memory, metacognition and mentalization - represent a core feature of schizophrenia, which indicates the involvement of the prefrontal cortex in the pathophysiology of this disorder. Hence we compared the gene expression in postmortem tissue from the left and right dorsolateral prefrontal cortex (DLPFC, Brodmann's area 46), and the medial part of the orbitofrontal cortex (MOFC, Brodmann's area 11/12), in six patients with schizophrenia and six control brains. Although in the past decade several studies performed transcriptome profiling in schizophrenia, this is the first study to investigate both hemispheres, providing new knowledge about possible brain asymmetry at the level of gene expression and its relation to schizophrenia. We found that in the left hemisphere, twelve genes from the DLPFC and eight genes from the MOFC were differentially expressed in patients with schizophrenia compared to controls. In the right hemisphere there was only one gene differentially expressed in the MOFC. We reproduce the involvement of previously reported genes TARDBP and HNRNPC in the pathogenesis of schizophrenia, and report seven novel genes: SART1, KAT7, C1D, NPM1, EVI2A, XGY2, and TTTY15. As the differentially expressed genes only partially overlap with previous studies that analyzed other brain regions, our findings indicate the importance of considering prefrontal cortical regions, especially those in the left hemisphere, for obtaining disease-relevant insights.
KW - Brain asymmetry
KW - Dorsolateral prefrontal cortex
KW - Gene expression
KW - Orbitofrontal cortex
KW - Schizophrenia
KW - Transcriptomics
UR - http://www.scopus.com/inward/record.url?scp=85007589286&partnerID=8YFLogxK
U2 - 10.1515/tnsci-2016-0021
DO - 10.1515/tnsci-2016-0021
M3 - Article
AN - SCOPUS:85007589286
SN - 2081-3856
VL - 7
SP - 139
EP - 150
JO - Translational Neuroscience
JF - Translational Neuroscience
IS - 1
ER -