Altered gene expression in the superior temporal gyrus in schizophrenia
© Bowden et al; licensee BioMed Central Ltd. 2008
Received: 24 August 2007
Accepted: 29 April 2008
Published: 29 April 2008
The superior temporal gyrus (STG), which encompasses the primary auditory cortex, is believed to be a major anatomical substrate for speech, language and communication. The STG connects to the limbic system (hippocampus and amygdala), the thalamus and neocortical association areas in the prefrontal cortex, all of which have been implicated in schizophrenia.
To identify altered mRNA expression in the superior temporal gyrus (STG) in schizophrenia, oligonucleotide microarrays were used with RNA from postmortem STG tissue from 7 individuals with schizophrenia and 7 matched non-psychiatric controls. Overall, there was a trend towards down-regulation in gene expression, and altered expression of genes involved in neurotransmission, neurodevelopment, and presynaptic function was identified. To confirm altered expression identified by microarray analysis, the mRNA expression levels of four genes, IPLA2γ, PIK31R1, Lin-7b and ATBF1, were semi-quantitatively measured using relative real-time PCR. A number of genes with altered expression in the STG were also shown to have similar changes in expression as shown in our previous study of peripheral blood lymphocytes in schizophrenia.
This study has identified altered expression of genes in the STG involved in neurotransmission and neurodevelopment, and to a lesser extent presynaptic function, which further support the notion of these functions playing an integral role in the development of schizophrenia.
The introduction of cDNA microarrays has identified changes in the expression of hundreds of genes in post-mortem brain tissue from individuals with schizophrenia [1–14]. These studies have identified new genes with both altered expression in, and genetic association to schizophrenia. Many functional groups of genes have been reported to be altered in these studies including those involved in neurotransmission, presynaptic functioning, myelination, neurodevelopment and basic cellular processes such as cell-cycle regulation and intracellular signalling. The most studied region for gene expression analysis is the prefrontal cortex (PFC), with fewer comprehensive gene expression profiling studies reported for other cortical regions.
The superior temporal gyrus (STG), which encompasses the primary auditory cortex and is believed to be a major anatomical substrate for speech, language and communication . The STG connects to the limbic system (hippocampus and amygdala), the thalamus and neocortical association areas in the prefrontal cortex, all of which have been implicated in schizophrenia. Significant evidence suggests the STG plays an important role in the pathophysiology of some symptoms of schizophrenia. Structural MRI studies have consistently reported the left STG volume to be decreased in patients with schizophrenia compared to healthy controls [16–20], which was confirmed by a recent meta-analysis of 15 voxel-based morphometry studies . Other studies have reported a correlation between STG volume and the severity of auditory hallucinations [22, 23] and thought disorder . In addition, the STG is considered to be the generator of mismatch negativity (MMN), an auditory phenomenon, which is reduced in individuals with schizophrenia [24, 25].
There are limited reports of post mortem studies of the cytoarchitecture in the temporal cortex in schizophrenia. A reduction in the somal volume of deep layer 3 pyramidal cells in the temporal association cortex has been reported , however,  and colleagues reported no alteration of glial density or neuronal size and density in the Planum Temporale (PT), the posterior portion of the STG, in schizophrenia. With respect to neurotransmission, decreased density of muscarinic receptors  and increased density of GABAA receptors  have been reported in the STG. Despite evidence indicating functional disturbances of the auditory cortex and connections to most of the brain regions implicated in schizophrenia, the STG has to date been largely overlooked in large-scale gene expression, cellular composition and functional studies in schizophrenia.
In this study, oligonucleotide microarrays were used to identify altered gene expression in 7 age, gender, PMI and pH matched pairs of post-mortem STG tissue from individuals with schizophrenia and healthy controls. To confirm altered expression of 4 genes, an additional 6 matched pairs (n = 13) were included in relative real-time PCR confirmation studies. The expression of two previously reported putative genes for schizophrenia, RGS4 [30, 31] and RIMS2  was also measured. In addition, the genes found to be significantly altered in the STG were compared to those previously reported to be altered in peripheral blood lymphocytes (PBLs) . The findings of this study suggest that gene expression changes in the STG may be important in the pathophysiology of this disorder.
Altered gene expression in the STG from microarrays
Demographic data for matched pairs consisting of individuals with schizophrenia and non-psychiatric controls.
Age (years) (sz/cntrl)
Medication (CPE) (mg/day)
Duration of Illness (years)
Cause of Death (sz/cntrl)
PMI (hours) (sz/cntrl)
ischaemic heart disease/ischaemic heart disease
cardiac arrhythmia/ischaemic heart disease
ischaemic heart disease/coronary thrombosis
Suicide/thrombotic coronary artery occlusion
Suicide/acute exacerbation of asthma
Suicide/atherosclerotic cardiovascular disease
ischaemic heart disease/cardiac arrest
Emphema/ischaemic heart disease
ischaemic heart disease/respiratory arrest
Coronary artery thrombosis/cardiac arrest
ischaemic heart disease/pulmonary thromboembolus
ischaemic heart disease/cardiovascular disease
cardiovascular disease/Cardiac atheroma
Means SZ Control
53.7 ± 13.0
54.5 ± 12.1
*637.9 ± 342.7
28.4 ± 13.2
27.4 ± 13.2
22.2 ± 8.7
6.4 ± 0.2
6.5 ± 0.2
Genes in schizophrenia linkage sites with significantly altered expression in the STG in schizophrenia.
SZ Linkage Site
# pairs changed/7
Average fold change
S100 calcium binding protein A1
S100 calcium binding protein A6 (calcyclin)
Mucin 1, transmembrane
Sorting nexin family member 27
Immunoglobulin superfamily, member 4B
RUN and SH3 domain containing 1
Hyperpolarization activated cyclic nucleotide-gated potassium channel 3
Hypothetical gene AK024293
Actin binding LIM protein family, member 3
Early B-cell factor
Transcriptional regulating factor 1
Leucine rich repeat and fibronectin type III domain containing 2
Dishevelled associated activator of morphogenesis 2
Zinc finger protein 193
HLA class II region expressed gene KE2
LEM domain containing 2
Proline-rich transmembrane protein 1
Ribonuclease P 21 kDa subunit
Histone 1, H2bn
Testis expressed sequence 27
Squamous cell carcinoma antigen recognized by T cells 2
RAB32, member RAS oncogene family
Farnesyltransferase, CAAX box, alpha
Myotubularin related protein 9
DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 26
Activating signal cointegrator 1 complex subunit 2
Ribosomal protein L3
Lectin, galactoside-binding, soluble, 1 (galectin 1)
Hypothetical protein MGC52010
NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 6
Genes with significantly altered expression in the STG in schizophrenia according to functional group.
# pairs changed/7
Average Fold Change
Glutamate receptor, ionotropic, N-methyl D-aspartate 2B
Glutamate receptor, ionotropic, N-methyl D-asparate-associated protein 1 (glutamate binding)
Glutamate receptor interacting protein 2
Solute carrier family 5 (choline transporter), member 7
Intracellular membrane-associated calcium-independent phospholipase A2 gamma*
Lin-7 homolog B (C. elegans)
Histamine receptor H3
Dynein, axonemal, heavy polypeptide 10
Acyl-CoA synthetase bubblegum family member 1*
Disabled homolog 1 (Drosophila)
AT-binding transcription factor 1
Neural precursor cell expressed, developmentally down-regulated 8
Phosphoinositide-3-kinase, regulatory subunit 1 (p85 alpha)
Contactin associated protein 1
Calcium channel, voltage-dependent, gamma subunit 2
FXYD domain containing ion transport regulator 1 (phospholemman)*
Other brain related illnesses
Amyloid beta (A4) precursor protein-binding, family A, member 2 (X11-like)
Fragile × mental retardation, autosomal homolog 2
Lupus brain antigen 1
Phosphoglycerate mutase 1 (brain)
Protein kinase C and casein kinase substrate in neurons 3
Regulator of G-protein signalling 4*
E2F transcription factor 1
Synapse defective 1, Rho GTPase, homolog 1 (C. elegans)
Olfactory receptor, family 7, subfamily E, member 47 pseudogene
Olfactory receptor, family 7, subfamily E, member 19 pseudogene
Relative real-time PCR confirmation of altered expression
Fold changes in gene expression in the STG from individuals with schizophrenia compared to non-psychiatric controls that were identified by microarrays and confirmed by relative real-time PCR.
Real-Time PCR results
Expression levels of putative schizophrenia genes using relative real-time PCR
The expression of a number of putative schizophrenia candidate genes was analysed using relative real-time PCR in the STG in the subjects with schizophrenia and compared to controls. RGS4 was present on the microarrays and displayed a 1.79 fold down-regulation which was significant by SAM analysis. The average expression level of RGS4 mRNA in this cohort measured by relative real-time PCR was previously reported  to be down-regulated by -2.06 fold (p = 0.03, df = 12, t = -2.33) in the schizophrenia subjects compared to the controls and there was no significant correlation of altered RGS4 expression and age (R2 = 0.27, p = 0.18), brain pH (R2 = 0.20, p = 0.32) or PMI (R2 = 0.15, p = 0.46). The decreased level of expression of RGS4 mRNA was present in 10 of the 13 matched pairs .
In addition, the RIMS2 mRNA expression level in the STG, a cytomatrix active zone gene, was investigated since it had been previously reported to be up-regulated in the amygdala . Relative real-time PCR analysis of the mRNA expression levels of RIMS2 was performed and detected in 12 of the 13 matched pairs using primers and real-time PCR conditions for RIMS2 as previously described . The control STG from pair 1 did not express RIMS2 at a detectable level in both microarray and real-time PCR analysis and so was excluded. The average expression level of RIMS2 mRNA detected by relative real-time PCR in the 12 matched pairs and normalized to 18s rRNA, was 1.56 × 10-4 in schizophrenia and 9.09 × 10-5 in the non-psychiatric controls. The resultant average fold change in expression of RIMS2 mRNA in the schizophrenia subjects compared to the controls was up-regulated by 1.72 fold (p = 0.03, df = 11, t = 2.15) and there was no significant correlation of altered RIMS2 expression and age (R2 = -0.07, p = 0.74), brain pH (R2 = -0.19, p = 0.36) or PMI (R2 = -0.11, p = 0.61). The up-regulation of RIMS2 mRNA was present in 9 of the 12 matched pairs. Pair 7, 12 and 13 displayed down-regulation of RIMS2 by 1.37, 1.52 and 2.56 fold, respectively. Although, RGS4 and RIMS2 were altered in 10 of 13 pairs and 9 of 12 pairs respectively, the pairs which did not have altered expression of RGS4 were not the same pairs as those which did not have altered RIMS2.
Consistent altered expression in PBLs and post-mortem STG
Genes with altered expression in post-mortem STG and PBLs from individuals with schizophrenia.
STG Pairs changed/7
Average STG fold change
PBLs Pairs changed/14
Average PBLs fold change
The use of high throughput tools such as microarrays has broadened the understanding of gene expression alterations in several brain regions in major mental illnesses such as schizophrenia. These regions include the PFC [1–4, 6, 8, 12, 13, 30], cerebellum , amygdala , hippocampus , as well as the cingulate , temporal [9, 11, 13], parietal , enterohinal  and occipital  cortices. Interestingly, the STG, a region reported to be dysfunctional in schizophrenia has the most pronounced changes in gene expression when compared to most of the other regions implicated in schizophrenia .
The number of genes expressed in the cerebral cortex has been largely unreported in previous gene expression studies of the PFC, temporal, parietal and occipital cortices. Although significantly altered gene expression has been reported for these areas, identifying the approximate number of genes expressed, and identifying similar expression patterns across regions, could lead to furthering our understanding of the functional and biological similarities and differences between cortical areas. In this study, 8737 of the 19000 genes tested were detectable in the STG in 4 or more of the 7 matched pairs studied, this is in contrast to our study of the amygdala, where only 5394 genes were detected using the same 19000 gene microarray . 4667 genes were expressed in both the amygdala and STG. Although the STG connects with the amygdala, the functions of the two regions are quite distinct which may be reflected in the difference in numbers of genes expressed. Mirnics and colleagues (2000) reported an average of 3735 genes expressed in the PFC of 9 individuals with schizophrenia, which is less than half that for the STG. However the microarray used by Mirnics and colleagues (2000) contained 7000 gene transcripts and the criteria to define genes that are expressed different from this study. Therefore, if tested using a larger gene set (e.g. 19000) the number of genes expressed in the PFC may be much higher.
One of the most consistent results across post-mortem brain studies is a trend towards overall down-regulation of genes in schizophrenia when compared to healthy controls [4, 9, 13, 14]. The average expression of the gene transcripts measured in this study showed an overall trend towards down-regulation in the 7 matched pairs of STG tissue which was similar to that previously reported for other brain regions in schizophrenia. This global down-regulation across many brain regions, particularly in the cerebral cortex including the STG, may contribute to the generalized deficiencies seen in individuals with schizophrenia, such as poor performance on cognitive tasks, reduced MMN, pre-pulse inhibition (PPI) and eye-tracking dysfunction. Although the biological cause underpinning these deficiencies is yet to be identified, overall down-regulation of gene expression in many brain regions may be the first steps towards explaining these phenomena.
The number of genes with altered expression in the STG identified by SAM and a 1.5 fold change cut-off in this study was remarkably similar to that reported by Katsel and colleagues (2005) using a high stringency criteria. This study identified 216 genes down-regulated and 85 genes up-regulated whereas Katsel and colleagues (2005) reported 185 genes down-regulated and 88 genes up-regulated in the same region in 22 schizophrenia and control samples. Although the genes identified in each study could not be directly compared.
The dysregulation of gene expression observed in the STG also highlighted a number of key cellular pathways including neurotransmission, particularly glutamate signaling, neurodevelopment and neuronal differentiation and presynaptic function. Indeed, there is building evidence for dysfunction of glutamate synapses in the STG and temporal lobe in general. For example, increased density of the N-methyl-D-aspartate (NMDA) glutamate receptor was reported by Nudmamud and colleagues  using ligand binding studies and Le Corre and colleagues  used in situ hybridization to show increased density of the NMDA NR1 subunit splice variant in the STG from subjects with schizophrenia. In addition, Eastwood and Harrison (2001)  reported that complexin II mRNA (expressed in excitatory neurons) was reduced in the dorsolateral PFC and the superior temporal cortex, and complexin I mRNA (expressed in inhibitory neurons) was decreased in the superior temporal cortex in schizophrenia. Furthermore, several of the schizophrenia candidate genes (e.g. glutamate receptor, metabotropic 3 (GRM3), G72, D-amino acid oxidase (DAAO), proline dehydrogenase oxidase 1 (PRODH), neuregulin 1 (NRG1) and protein phosphatase 3 catalytic subunit gamma isoform (PPP3CC)) are thought to be directly or indirectly linked with glutamatergic transmission via NMDA receptors [37, 38].
In this current study of the STG, the IPLA2γ gene was significantly up-regulated. IPLA2γ is an isoform of IPLA2 expressed in many tissue types, including the brain . IPLA2, a key enzyme for phospholipid degradation, is vital for the maintenance and formation of cellular membranes . IPLA2 is involved in neurotransmission via modulation of phosphorylation of the AMPA glutamate receptors. Endogenous IPLA2 activity limits phosphorylation on serine sites of the AMPA receptor GluR1 subunit, resulting in IPLA2 control over AMPA mediated synaptic transmission in the hippocampus [41, 42]. There are, however, limited reports of IPLA2 function in other brain regions and the control over AMPA-mediated transmission is yet to be studied in areas such as the STG. IPLA2 is thought to be involved in learning and memory via alterations in hippocampal plasticity , deficiencies of which are key indicators of schizophrenia. Contrary to most reports being related to hippocampal tissue, IPLA2 protein expression has previously been reported to be increased by up to 45% in post-mortem temporal cortex  and in blood serum of individuals with schizophrenia [45, 46], thus suggesting IPLA2 is worthy of further study.
Furthermore, the microarray analysis also showed that other genes involved in glutamate signaling were altered in the STG in patients with schizophrenia. These include, glutamate receptor, ionotropic, N-methyl D-aspartate 2B (GRIN2B) subunit, also known as NR2B, that had significantly up-regulated expression, and two glutamate receptor interacting proteins glutamate receptor N-methyl D-asparate-associated protein 1 (GRINA) and glutamate receptor interacting protein 2 (GRIP2) showing significant down-regulated expression in schizophrenia subjects. Furthermore, Lin-7b, which was downregulated in the STG of schizophrenia patients by microarray analysis, is highly enriched in post-synaptic densities (PSD) in association with PSD95/NMDA receptor complexes . More specifically, Lin-7b is a PSD-95/Dlg/ZO-1 (PDZ) domain containing protein, which increases the channel activity of the NR1-NR2B glutamate receptor . Thus, the evidence from this study supports dysfunction of glutamate transmission in the STG in the pathophysiology of schizophrenia.
Alteration to neurodevelopment and neuronal differentiation in the STG is supported by the significant up-regulation of ATBF1 by microarray and real-time PCR analysis in the STG tissue from individuals with schizophrenia compared to the non-psychiatric controls. This gene is highly expressed in the central nervous system, in particular dopaminergic neurons during neuronal differentiation . The expression of ATBF1 results in suppression of the nestin gene and activation of the Neurogenic differentiation 1 (NEUROD1) gene, which are responsible for specific neuronal differentiation . NEUROD1 was up-regulated in a gene expression study of the middle temporal gyrus (MTG) in schizophrenia , which may be a direct result of ATBF1 up-regulation similar to that observed in this study. Overexpression of ATBF1 in neuroblastoma cell lines produces cell cycle arrest, which is thought to occur in vivo as the result of nuclear localization of ATBF1 in differentiating neurons . Therefore, overexpression of ATBF1 in the STG of patients with schizophrenia might reflect deficits in neuronal differentiation and neurodevelopment
There have been a number of reports indicating dysregulation of presynaptic function genes . Indeed, our previous study of the amygdala  highlighted dysfunction of the genes coding for proteins in the cytomatrix active zone, a specialized region of the synapse involved in the regulation of vesicle release. RIMS2 codes for a protein that forms part of the cytomatrix of the active zone of synapses and was observed to be upregulated in the amygdala in schizophrenia . The STG directly connects to the limbic system, of which the amygdala is a constituent. In this study RIMS2 was significantly up-regulated by 1.72 fold, similar to the 2.37 fold change reported in the amygdala. In contrast, Mirnics et al (2001a) reported a downregulation of presynaptic function genes, although those genes were not investigated in this study. RIMS2 modulates Ca2+-triggered exocytosis and may be overexpressed in the STG as a compensatory mechanism to overcome other presynaptic function deficiencies.
Regulator of G-protein signaling 4 (RGS4) is a schizophrenia candidate gene that was identified by Mirnics and colleagues [30, 51] and has subsequently been reported in linkage  and convergent functional genomics studies . The relative expression level of RGS4 mRNA in the STG from the cohort used in this study has been previously reported as significantly down-regulated by an average fold change of -1.93 by relative real-time PCR , which was confirmed in the current study as a significant down-regulation of -1.79 fold by microarray analysis. This down-regulation of RGS4 expression in the STG is in accordance with the decreased expression previously reported in the PFC, motor and visual cortices in schizophrenia  further establishing RGS4 as a schizophrenia candidate gene.
Changes in gene expression in PBLs are emerging as biological reflections of altered expression in the brain as described in . Consistent with previous studies  3 genes, MTMR9, EWSR1 and NFκβα were altered in the same direction in the post-mortem STG tissue and the peripheral blood lymphocytes (PBLs) from a separate cohort of individuals with schizophrenia identified in a previous study . Whether this may lead to the use of PBLs in the development of a biological basis for identifying individuals with schizophrenia awaits further investigation.
The findings of this study and previous gene expression studies involving post-mortem brain tissue are limited by the availability of tissue and the potential of mRNA expression alterations being due to mRNA degradation from variables such as brain pH and PMI . To control for this potential bias in this study, post-mortem brain tissue from individuals with schizophrenia and non-psychiatric controls were carefully screened and matched for brain pH and PMI in addition to brain hemisphere, age and gender. The tissue pH for pairs 3, 8 and 10 were not as closely matched as the remaining pairs, however there was no correlation between lower pH in the patients, numbers of genes expressed, levels of gene expression on the microarrays or in the relative levels of gene expression measured by real-time PCR. Even though all the variables thought to influence RNA integrity and gene expression were controlled for as much as possible in this study, one cannot rule out the possibility that differences in pH could cause changes in gene expression in post-mortem brain tissue.
In addition to this, another variable which may influence post-mortem tissue gene expression is anti-psychotic medication. The large range of chlorpromazine equivalents (CPE) dosages across the cohort as well as the medication history of one individual being unknown resulted in the inability to perform correlation analyses between anti-psychotic medications and altered gene expression, therefore the influence of anti-psychotic medications on the genes with altered expression in the STG requires further investigation.
This study has shown altered expression via microarrays and real-time PCR of genes in the STG involved in neurotransmission (particularly glutamate transmission), neurodevelopment, and to a lesser extent presynaptic function. These alterations in gene expression particularly involving glutamate-related transcripts, are likely to have dramatic consequences for neurotransmission in the STG in schizophrenia.
Characteristics of subjects
This study was approved by the University of Newcastle Human Research Ethics Committee, Australia. Blocks of coronally sectioned post-mortem STG tissue (1 cm thick) were sourced from the NSW Tissue Resource Centre, The University of Sydney, Australia. Tissue from 13 pairs of individuals with schizophrenia and controls were matched for gender, age, brain hemisphere, post-mortem interval (PMI) and pH (Table 1). Differences in the age, PMI and pH of the schizophrenia and control groups were not statistically significant (paired 2 tailed t-test). Pairs 1–7 were used for microarray analysis, whilst all 13 pairs were used for the relative real-time PCR studies. These cases were the same cohort used in a previous study of RGS4 expression .
RNA was extracted as described in . Briefly, a hole punch of grey matter, excluding white matter, was taken from the outer edge of the block of STG from the most caudal coronal brain slice (1 cm thick) containing the STG (Brodmann's Area 22). Total RNA was extracted using TRIzol reagent (Gibco-BRL, USA) as described previously . Briefly, approximately 50–60 mg tissue was added to 1 ml TRIzol reagent and total RNA was prepared according to manufacturer's instructions. RNA integrity was assessed by A260/A280 ratios (> 1.8 and < 2.1) and visualisation of 18s and 28s ribosomal bands by electrophoresis with formaldehyde denaturing 1% agarose gel.
The microarray procedure used in this study was essentially as described in . Briefly, Compugen Version 2 19 K oligonucleotide spotted glass microarrays (Clive and Vera Ramaciotti Centre for Gene Function Analysis and the Adelaide Microarray Facility, Australia) were used to compare the amount of fluorescence (Cy3/Cy5) of each matched pair on a single slide. Matched pairs were analysed in duplicate with a dye swap for the second microarray to reduce the effects of dye incorporation bias. Indirect labeling of the cDNA was performed using the CyScribe Post-Labelling Kit (Amersham Biosciences, UK) as per manufacturer's instructions. Briefly, total RNA (25 μg) was reverse transcribed, using an oligo-dT primer, into cDNA incorporating an amino-allyl modified d-UTP, which was then labelled with either Cy5 or Cy3 fluorescent dyes and hybridised to the microarray for 16 h at 42-C. Post-hybridisation, the microarrays were washed in increasingly stringent solutions of SDS and SSC (1 × SSC and 0.1% SDS at 50°C through to 0.1 × SSC at room temperature) and then dried using centrifugation. Microarrays were scanned with the Axon GenePix 4000B microarray scanner (Molecular Devices, California, USA), the images were then analysed using the GenePix Pro 3.0 software. Areas of the microarray that were affected by background were excluded from further analyses.
Microarray data analysis
GeneSpring 5.0 (Silicon genetics, USA) was used to normalize per spot and per array (Lowess curve) and to a 50th percentile. To determine the fold change corresponding to a 5% error rate for this microarray platform a sample of control human brain RNA was split in two and labelled with Cy3 and Cy5 and hybridised in duplicate to a glass microarray similar to those used throughout this study. To identify significantly altered genes in the STG, one-class significance analysis of microarrays (SAM) was performed on Log 2 transformed expression data, with 128 permutations using SAM version 2.0 .
Relative real-time PCR
Relative real-time PCR was performed essentially as described previously . Briefly, 100 ng total RNA was treated with DNAse 1 (Invitrogen, USA) and reverse transcribed using oligo dT primers and Superscript II reverse transcriptase (200U/μl) (Invitrogen, USA) as per manufacturer's instructions. Relative Real-time PCR using SYBR green Mastermix (PE Applied Biosystems, UK) and an ABI prism 7900 sequence detection system (PE Applied Biosystems, UK) was performed in triplicate to identify relative changed expression of IPLA2G, PIK31R1, Lin-7b and ATBF1 compared to the housekeeping genes β-actin and 18s rRNA. The statistical significance of the altered expression was tested by a paired two-tailed t-test (p < 0.05), the reported p values were calculated using the relative expression levels compared to 18s RNA. Bivariate correlation analysis was performed to determine if there was any correlation between the altered expression and the age, pH or PMI. Correlation analysis could not be performed for medication as many of the individuals with schizophrenia had large ranges of reported dosage and the medication history of one individual was unknown.
This work was supported by:
Neuroscience Institute of schizophrenia and Allied Disorders (NISAD) and The Hunter Medical Research Institute (HMRI) utilising infrastructure funding from NSW Health.
HMRI Adamstown Lions Club Young Investigator Award.
School of Biomedical Sciences RIBG and the University of Newcastle Strategic Reserve.
None of the funding bodies contributed to study design, experimentation and data analysis or the writing of the manuscript.
Tissues were received from the NSW Tissue Resource Centre, which is supported by The University of Sydney, NISAD, National Institute of Alcohol Abuse and Alcoholism and NSW Department of Health.
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