- About this Journal
- Abstracting and Indexing
- Aims and Scope
- Article Processing Charges
- Articles in Press
- Author Guidelines
- Bibliographic Information
- Citations to this Journal
- Contact Information
- Editorial Board
- Editorial Workflow
- Free eTOC Alerts
- Publication Ethics
- Submit a Manuscript
- Subscription Information
- Table of Contents
The Scientific World Journal
Volume 2013 (2013), Article ID 685917, 14 pages
A Comparative Genomic Study in Schizophrenic and in Bipolar Disorder Patients, Based on Microarray Expression Profiling Meta-Analysis
1Neuropsychiatric Research Laboratory, Department of Clinical Medicine, Örebro University, 701 82 Örebro, Sweden
2Metabolic Engineering and Bioinformatics Program, Institute of Biology, Medicinal Chemistry and Biotechnology, National Hellenic Research Foundation, 48 Vassileos Constantinou Avenue, 11635 Athens, Greece
3Laboratory of Biotechnology, School of Chemical Engineering, National Technical University of Athens, 15780 Athens, Greece
Received 2 November 2012; Accepted 27 November 2012
Academic Editors: N. S. T. Hirata, M. A. Kon, and K. Najarian
Copyright © 2013 Marianthi Logotheti et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Schizophrenia affecting almost 1% and bipolar disorder affecting almost 3%–5% of the global population constitute two severe mental disorders. The catecholaminergic and the serotonergic pathways have been proved to play an important role in the development of schizophrenia, bipolar disorder, and other related psychiatric disorders. The aim of the study was to perform and interpret the results of a comparative genomic profiling study in schizophrenic patients as well as in healthy controls and in patients with bipolar disorder and try to relate and integrate our results with an aberrant amino acid transport through cell membranes. In particular we have focused on genes and mechanisms involved in amino acid transport through cell membranes from whole genome expression profiling data. We performed bioinformatic analysis on raw data derived from four different published studies. In two studies postmortem samples from prefrontal cortices, derived from patients with bipolar disorder, schizophrenia, and control subjects, have been used. In another study we used samples from postmortem orbitofrontal cortex of bipolar subjects while the final study was performed based on raw data from a gene expression profiling dataset in the postmortem superior temporal cortex of schizophrenics. The data were downloaded from NCBI's GEO datasets.
Schizophrenia (SZ) and bipolar disorder (BD) are approached and studied as diseases with aberrant functions of the neurotransmitter systems, as neurodevelopmental diseases or generally complex diseases caused by multiple genetic and environmental factors. Recently they have started to be studied as systemic diseases; thus a combination of disturbed biological systems and genes of small contribution is believed to cause their expression [1, 2].
Altered membrane composition of the cells, aberrant membrane phospholipid metabolism [3, 4], dysfunctional tyrosine, and other amino acid (AA) transport systems [5–11] evidence the systemic nature of SZ disease. Moreover, failure of niacin skin test implying reduced arachidonic acid (ARA) in cell membranes of schizophrenics  and abnormalities in muscle fibers  constitute such indications. The same holds for BD, which can also be considered a systemic disease. Aberrant tyrosine, and other AA transport systems, in cells from BD disorder patients [14, 15], aberrant signal transduction , and abnormal membrane composition and metabolism support the notion of BD being a systemic disease as well [17, 18].
Studying these disorders through this holistic approach, we presume the membrane phospholipid hypothesis, namely, that aberrant AA transport mechanisms and the disturbed cell membrane composition are highly correlated. AAs are transported though cell membranes with specific transporter/protein transport systems, which perform active transport of AAs from one side of the cell membrane to the other . These AA transporters are embedded in the cell membranes; thus their structure and functionality interact with the membrane composition and functionality, as well as with membrane fluidity and enzymatic activity [9, 20]. Particularly, a membrane defect would impact, for example, the functionality of the tyrosine transporters as well as the permeability of the membranes [2, 5].
The Membrane Theory
The membrane theory of mental diseases is related with two primary abnormalities: an increased rate of removal of essential fatty acids (EFA) from the membrane phospholipids, combined with a reduced rate of incorporation of fatty acids (FA) into membrane phospholipids . Some SZ study findings that relate the expression of the disease with the membrane hypothesis are studies based on postmortem and blood samples showing reduction of docosahexaenoic acid (DHA) and ARA in cell membranes independently of the disease state and magnetic resonance spectroscopy (MRS) studies revealing decreased levels of phosphomonoesters (phospholipid membrane synthesis precursors) and higher levels of phosphodiesters (phospholipid metabolism products) in SZ patients compared to control patients . Also, the niacin skin flush test is indicative of a membrane dysfunction resulting in an inflammatory dysfunction . In addition, phospholipase A2 (PLA) calcium (Ca) dependent type has been shown to have an increased activity and PLA Ca independent type a decreased activity. The latter is considered quite important finding, as the A2 enzyme catalyzes the breakdown of FA .
Similar findings suggest cell membrane dysfunction in BD. 31P-MRS magnetic resonance spectroscopy (MRS) measures phosphorus metabolites in the organs . Phosphomonoester levels are measured in BD depressed patients with MRS. Phosphomonoesters are measured as being higher in these patients compared to control subjects and lower in asymptomatic patients. Abnormal functionalities in signal transduction pathways are also repeated in several studies including overactivated phosphatidylinositol and G-protein pathways, as well as altered membrane protein kinase C and adenyl cyclase enzyme pathways. PLA enzyme activity and Ca release are involved in the membrane hypothesis of BD .
Amino Acid Transporters
The transport of AAs into the cell membranes of the blood brain barrier (BBB) is mediated by many transport systems. Three basic active transporters result in the AA flux from and into all types of cells (including brain cells). The primary active transport mechanism is an adenosine triphosphatase (ATPase) that exchanges sodium (Na) and potassium (K) ions, contributing in the maintenance of the ion gradients of the cells, known as sodium-potassium adenosine triphosphatase (Na,K-ATPase). These ion gradients in combination with other ions and gradients are utilized by the secondary active transport mechanisms for the influx of specific AAs into the cells. The secondary active transport through these AA influxes sets also an AA concentration gradient in the cells, which, in combination with Na+ exchange, is further utilized by the tertiary active transport mechanisms for transport of another group of AAs in and out of the cells. AAs may be transported via different AA transport mechanisms. An alteration in any of the active transport mechanisms could result in an aberrant AA transport into the cells [10, 25].
Aim of the Study
The aim of our meta-analysis was to interpret the results of comparative genomic profiling studies in schizophrenic patients as compared to healthy controls and in patients with BD and try to relate and integrate our results with an aberrant AA transport through cell membranes.
2. Materials and Methods
2.1. Microarray Datasets
Four human datasets were used, by downloading submitted raw data (Cel files) from corresponding studies, available at the Gene Expression Omnibus (GEO) database of National Center for Biotechnology Information (NCBI) .(1)The first study has the GEO Accession number GSE12654 and the microarrays preparation followed the guidelines of MIAME in the way it is described in . RNA from postmortem brain tissues (Brodmann’s Area 10) of 15 schizophrenic and 15 BD affected patients and 15 control healthy subjects was hybridized on Affymetrix HG-U95 Arrays. After quality control stage in this study, 11 schizophrenic, 11 BD and 15 control subjects were used for further bioinformatic analysis.(2)The second study has the GEO Accession number GSE5389, and the microarrays preparation followed the guidelines of MIAME in the way it is described in . RNA extracted from human postmortem brain tissue (Brodmann’s Area 11) from 15 adult subjects with BD and 15 healthy control subjects was hybridized to Affymetrix HG-U133A GeneChip to identify differentially expressed (DE) genes in the disease state. After quality control in this study, 10 BD and 11 control subjects were used for further bioinformatic analysis.(3)The third study has the GEO Accession number GSE21935, and the microarrays preparation followed the guidelines of MIAME in the way it is described in . 60 postmortem RNA samples derived from brain tissue (Brodmann’s Area 22) of schizophrenic and control patients were hybridized to the Affymetrix HG-U133 Plus 2.0 Array. After quality control stage samples from 19 control and 23 SZ subjects were subjected to bioinformatic analysis. (4)The fourth study has the GEO Accession number GSE12649, and the microarrays preparation followed the guidelines of MIAME in the way it is described in . RNA samples were extracted from postmortem brain tissue (Brodmann’s Area 46) of 35 BD subjects, 35 SZ subjects, and 35 healthy control subjects. The RNA was applied to the Affymetrix HG-U133A GeneChip. After quality control stage in this study, 35 SZ, 33 BD samples, and 34 control samples were finally subjected to bioinformatic analysis.
2.2. Analysis of Microarray Data
The raw signal intensity data of each study were imported into the Gene Automated and Robust MicroArray Data Analysis (Gene ARMADA) software tool  for versatile, microarray data analysis. In order to extract the signal intensities from the raw data, specific steps were followed: background correction was performed with the gcRMA method and was followed by Quantile normalization. The negative intensity values were treated with the minimum positive and noise method and then summarization followed with the Median Polish method. The data were transformed in values. In each analysis two experimental conditions were always selected: the disease condition and its corresponding control condition. Genes that were characterized as absent in more than 40% of the samples in each experimental condition were excluded from further analysis. The missing values were imputed using the k-nearest neighbor (k-NN) algorithm. All the steps of the microarray analysis were common for all the extracted datasets.
2.3. Statistical Analysis
The probe sets that were differentially expressed in the disease samples compared to the control healthy samples were selected by two-tailed Student’s t-test. The lists of the DE probe sets were defined by applying the following criteria in each dataset: (i) 1.3 or greater-fold change (FC) of the mean expression in all studies, except for the fourth study of BD samples compared to controls with (small number of DE genes with stricter cutoff) and (ii) value threshold below 0.05. The value distribution for each gene list was used to estimate the False Discovery Rate (FDR) levels. The final gene list corresponds to an . The statistical analysis was also performed in the Gene ARMADA software.
2.4. Prioritized Pathway/Functional Analysis of Differentially Expressed Genes
In order to derive better insight into the biological processes related to the DE genes, the lists of significant genes from each microarray analysis were subjected to statistical enrichment analysis using the Statistical Ranking Annotated Genomic Experimental Results (StRAnGER) web application . This bioinformatic tool is using gene ontology term (GOT) annotations and KEGG pathways as well as statistical overrepresentation tests further corrected by resampling methods, aiming to select in a prioritized fashion those GOTs and pathways related to the DE genes, that do not just have a high statistical enrichment score, but also bear a high biological information, in terms of differential expression. Specifically gene ontology (GO) based analysis and KEGG-based analysis result in a list of GO terms and KEGG pathways, respectively, based on hypergeometric tests with values <0.05, which have been reordered according to bootstrapping to correct for statistical distribution-related bias.
2.5. Prioritizations of Putative Disease Genes
In order to prioritize the gene list of interest according to the functional involvement of genes in various cellular processes, thus indicating candidate hubgenes, after inferring the theoretical topology of the GOT-gene interaction network delineated, we used the online tool GOrevenge  with the following settings: Aspect: BP (Biological Process), Distance: Resnik, Algorithm: BubbleGene, and Relaxation: 0.15. By adopting these settings we are able to exclude from the interaction network the bias relating to the presence of functionally redundant terms, describing the same cellular phenotypic trait, and thus assessing the centrality, namely, the correlation of the specific genes to certain biological phenotypes in an objective way.
Finally, BioGraph  is a data integration and data mining platform for the exploration and discovery of biomedical information. The platform offers prioritizations of putative disease genes, supported by functional hypotheses. BioGraph can retrospectively confirm recently discovered disease genes and identify potential susceptibility genes, without requiring prior domain knowledge, outperforming other text-mining applications in the field of biomedicine.
3. Results and Discussion
3.1. Differentially Expressed Probesets
After the microarray analysis and the statistical selection, lists of DE probesets for each dataset occurred. From the first and fourth studies’ analysis, four lists of significantly differentiated probesets were generated: two after comparison of SZ and control subjects and two after comparison of BD and control subjects. The second study (comparison of BD patients to control subjects) resulted also in a list of DE probesets and the third study in another list of DE probesets (SZ subjects compared to control subjects). The differentiated probesets from each case are depicted in representative volcano plots (Figure 1).
3.1.1. Differentially Expressed Genes in Each Study
In postmortem studies the alterations in the gene expression are usually lower than twofold . For each study, transcripts of interest and of particular expression alterations are described in the following paragraphs. The lists of DE genes for each study are presented in Supplementary Tables 1–6 (available online at doi:10.1155/2013/685917). Information about the protein products arising from the DE genes has been provided mainly from the Reference Sequence (RefSeq) database of NCBI .
Statistical analysis of the gene expression profile of SZ and BD patients as compared to controls is summarized in Table 1. The number of DE genes is 196 and 134 respectively.
In SZ patients, transcripts related to the membrane hypothesis show altered expression. Lipases LPL and LIPA, downregulated phosphodiesterases ENPP2 and PDE8A, downregulated phosphoinositide PIK3R4, PNPLA4 phospholipase are related to membrane metabolic processes. ENPP2 and PDE8A dysregulation could also be related to previous MRS studies revealing different levels of phosphodiesters in SZ patients . Some genes encoding proteins of signal transduction pathways, for example, downregulated G protein-coupled receptors GPR37 and GPRC5B, downregulated kinase activity encoding genes PIK3R4 and AATK, or SST somatostatin and CX3CR1 chemokine receptor can also be related to membrane dysfunctions . Genes encoding ion homeostasis seem to be dysregulated as well. NPY, GRIN2A, and CACNA1C all annotated to Ca ion transport (provided by Gene Ontology Annotation UniProt Database) are DE. Also expression of manganese ion binding genes and copper ion binding genes (provided by Gene Ontology Annotation UniProt Database), such as MT1X, is affected. KCNQ2 encoding K voltage-gated channel is overexpressed.
In BD patients of the same study transcript ATP1A3, expressing Na,K-ATPase is downregulated. This ATPase is very important for the normal regulation of the primary active transport mechanism of the cells ; thus it affects indirectly the normal function of the AA active transport into the cells. Other dysregulated genes contribute to abnormal K binding and transport (provided by Gene Ontology Annotation UniProt Database): SLC12A5, KCNK3, and KCNK1 are downregulated. POLR2 K encoding phosphodiesterase 6D is upregulated. This fact complies with dysregulated membrane phospholipid metabolism, as phosphodiesters are products of this metabolic pathway . SLC7A8 gene is overexpressed. The importance of this gene relies on the fact that it is encoding transmembrane Na-independent AA transport proteins of the L system. LAT1 protein complex, which is specifically expressed from SL7A8 gene, is a tertiary active transporter and mediates tyrosine, tryptophan, and other neutral AA transport systems through cell membranes .
Statistical analysis of the gene expression profile of BD patients as compared to controls is summarized in Table 2. The number of DE genes is 1035.
Many transcripts regulating ion transport are shown to be downregulated in this study: SCN1A, KCNK1, TRPC1, ATP6V1A, and ATP5G3. Many metallothionein encoding genes (provided by Gene Ontology Annotation UniProt Database) (MT1X, MT2A, MT1E, MT1M, MT1H, MT3, MT1A, and MT1G) are overexpressed. The latter genes combined with downregulated genes COX11, PAM, and RNF7 seem to result in abnormal copper ion binding, because their protein products are involved in this pathway (provided by Gene Ontology Annotation UniProt Database). Genes, encoding ATPases related to Ca++ (ATP2B1, ATP2B2) and H+ (ATP5G3, ATP6AP2, ATP6V1A, ATP6V1D, ATP6V1G2) transporting (provided by Gene Ontology Annotation UniProt Database), are downregulated. The protein encoded by the overexpressed ATP1B1 gene is a member of the family of Na+/K+ and H+/K+ ATPases, as well as a member of the subfamily of responsible proteins for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membranes . PLA2G5 gene encodes an enzyme that belongs to PLA family. It catalyzes the membrane phospholipid hydrolysis to free FA, and in this study it is overexpressed. Overexpressed PLA2G4A also encodes an enzyme of A2 family. It hydrolyzes phospholipids to ARA (provided by RefSeq). ARA is subsequently metabolized into eicosanoids. Prostaglandins and leukotrienes belong to the eicosanoids, and they are lipid-based cell hormones that regulate inflammation pathways and cellular thermodynamics. The catalyzed hydrolysis also results in lysophospholipids that are further utilized as platelet-activating factors. High Ca++ levels and phosphorylation activate the enzyme (provided by RefSeq). 37 genes encoding proteins involved in magnesium ion binding (provided by Gene Ontology Annotation UniProt Database) show altered expression. Phosphoinositide-3-kinases encoded by downregulated genes PIK3C3, PIK3CB, and PIK3R1 encode phosphoinositide 3-kinases (PI3 K). These kinases are involved in signaling pathways, and their receptors are located on the outer cell membranes .
Statistical analysis of the gene expression profile of SZ patients as compared to controls is summarized in Table 3. The number of DE genes is 122.
The membrane-related protein encoded by the overexpressed ABCA1 gene is a member of ATP-binding cassette (ABC) transporter proteins superfamily. ABC proteins mediate transport of many molecules across extra- and intracellular membranes. ABC1 transporter subfamily’s substrate is cholesterol; thus its function is affecting the cellular lipid removal pathway. This gene is related to Tangier’s disease and familial high-density lipoprotein deficiency (provided by RefSeq). Apart from ABCA1 gene, also SLC27A3, HSD11B1, CHPT1, and GM2A genes encoding proteins associated with lipid metabolic processes (provided by Gene Ontology Annotation UniProt Database) present a different expression in SZ patients compared to controls. In the DE list CACNB2 is present as an overexpressed gene. This gene encodes a subunit of a voltage-dependent Ca channel protein which is a member of the voltage-gated Ca channel superfamily (provided by RefSeq). CACNA1B, encoding another Ca channel that regulates neuronal release of neurotransmitter, has been proved to be involved in BD and SZ (provided by RefSeq).
Statistical analysis of the gene expression profiles of SZ and BD patients as compared to controls is summarized in Table 4. The number of DE genes is 216 and 205, respectively.
In SZ patients of these study genes ATP2B2 and ATP2B4 are downregulated and upregulated, respectively. These genes encode proteins that belong to the family of P-type ATPases. These enzymes regulate primary ion transport. These two specific ATPases are very important for the homeostasis of Ca in the cell, as they catalyze cellular efflux of bivalent Ca ions from cells against great concentration gradients (provided by RefSeq). Ca ion homeostasis and Ca ion transport (provided by Gene Ontology Annotation UniProt Database) are also dependent on some other genes dysregulated in this study, such as upregulated NPY, RYR3, and ITPR2 and downregulated CXCL12. Two metallothionein encoding genes MT1X and MT1H are overexpressed. After pathway analysis, these genes, in concert with the differentiated expression of several other genes, seem to affect zinc ion binding and copper ion binding (provided by Gene Ontology Annotation UniProt Database).
In BD patients of the fourth study ATP1A2 is overexpressed. The protein expressed by this gene is a member of P-type cation transport ATPases and belongs to the subfamily of Na,K-ATPases. It belongs to integral membrane proteins, responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane. These gradients are very important for osmoregulation, for Na-coupled transport of many organic and inorganic molecules, and for nerve and muscle electrical excitability. The catalytic subunit of Na,K-ATPase is encoded by multiple genes (provided by RefSeq). PLA2G16 is downregulated. The protein encoded by this gene belongs to a superfamily of PLA enzymes. PLA regulates adipocyte lipolysis and release of FA through a G-protein coupled pathway involving prostaglandin and prostaglandin receptors. It belongs to the phospholipase C enzymes that are activated by G-coupled regulatory pathways, such as serotoninergic 5-HT2 pathways (provided by RefSeq). Finally overexpressed metallothioneins MT1X, MT1M, MT1H, and MT1M may result in copper ion binding dysfunctions, as they are involved in this biological function (provided by Gene Ontology Annotation UniProt Database).
3.1.2. Common Differentially Expressed Genes in the Examined Studies
In the first and fourth study SZ gene expressions and BD gene expressions are compared to the same control gene expressions. Common DE genes in SZ and BD patients compared to the same control subjects, for example, in the first (Figure 2) and fourth (Figure 3) examined studies are depicted in Tables 5 and 6, respectively. The genes present in lists of statistical significant genes derived from SZ patients’ expression profiles are given in Table 8. The common genes in all DE genes of BD patients compared to control groups from all related studies are presented in Table 7. MT1X gene is overexpressed in all studies, in all gene expression comparisons, except for the second study, where it is not among the statistical significant genes as shown in Figure 4.
Among the common DE genes in BD and SZ patients of the first study HTR2C is an interesting gene. Serotonergic pathway is highly related to psychiatric disease expressions. The neurotransmitter serotonin (5-hydroxytryptamine, 5-HT) causes many physiological functions after binding to receptor subtypes, such as 5-HT2 family of seven-transmembrane-spanning, G-protein-coupled receptors. These receptors activate phospholipase C and D signaling pathways. This gene encodes the 2C subtype of serotonin receptor, and its RNA editing is predicted to alter AAs within the second intracellular loop of the 5-HT2C receptor and generate receptor isoforms that differ in their ability to interact with G proteins and the activation of phospholipase C and D signaling cascades, thus modulating serotonergic neurotransmission in the central nervous system. Studies in humans have reported abnormalities in patterns of 5-HT2C editing in depressed suicide victims. Three transcript variants encoding two different isoforms have been found for this gene. This gene is downregulated in both diseases . Serotonin neurotransmitter has been proved to play an important role in emotional, sexual, and eating behavior and in other symptoms of mental diseases, such as hallucinations. Many drugs used for the treatment of these diseases are serotonin agonists. Upregulated ADD2, GGRRF1, and MT1X encode proteins related to metal ion binding. HTR2C, DARC, and GRK5 products participate in signal transduction pathway.
The protein encoded by SDC4 gene is a transmembrane heparan sulfate proteoglycan that functions as a receptor in intracellular signaling. Downregulated KCNK1 gene encodes one of the members of the superfamily of K channel proteins, and it has been previously reported as dysregulated in BD patients . The downregulation of this gene may affect the passive transport of K into the cells.
NPY (neuropeptide) and GABA-system-related SST (somatostatin) are downregulated in two of our SZ studies. These genes have been reported in many studies as candidate psychosis genes . They have also been related to SZ. Earlier studies reveal also downregulation of these specific genes. Neuropeptide genes are involved in working memory functions . In psychiatric diseases working memory and neurodegeneration have been suggested as possible abnormal functions of the prefrontal cortex. These genes seem to be implicated in these functions . PALLD gene, myocardial infarction-related gene, has also been reported as dysregulated in SZ . The protein encoded by AQP4 gene is involved in the regulation of the water homeostasis. Upregulation of this gene has been already reported and has been related to white matter hyperintensity, observed in MRS studies of BD patients . Generally there are no common genes in all three SZ datasets. This could be explained by the fact that there are region-specific alterations in SZ, and our SZ raw data were extracted from different brain regions.
3.2. Pathway Analysis
The lists of statistical significant genes of each study were submitted to StrAnGER web application elucidating overrepresented GO terms. The results of GO-analysis for each dataset are presented in Supplementary Tables 7–12.
In the first study, StRAnGER analysis in the SZ-related DE gene list indicated that K ion binding and transport are two of the statistical significant altered GO terms. These processes are very important for the maintenance of K ion gradients in the cells. K ion transport regulates the fluxes of K ions from and into the cells via some transport proteins or pores [19, 25].
StRAnGER analysis in the BD-related DE gene list indicated altered synaptic pathways. Synaptic pathways and genes have been reported earlier as possible dysfunction factors in BD . G-protein pathways are also related to neurotransmitter receptors and particularly to serotonergic receptors, most studied in BD as part of serotonergic pathway . Ca transport, protein tyrosine kinase, and phosphoinositide binding are involved in signal transduction pathways. Several studies of BD patients have shown abnormalities in the phosphoinositol/protein kinase C (PKC) signaling system. One such study has demonstrated significantly higher concentrations of 4,5-bisphosphate (PIP2) in the platelet membranes of patients in the manic phase of BD; they also found that the levels of PIP2 increased when cycling from the euthymic state into the manic state. Additionally, the activity of platelet PKC was found elevated in patients, during a manic episode of BD. Additionally several independent studies have shown increased concentrations of the stimulatory alpha subunit (Gas) of G-protein in the brains of BD patients, specifically in the frontal, temporal, and occipital cortices. Other studies have suggested there is also increased presence/activity of G-proteins in the leukocytes of untreated manic patients and the mononuclear leukocytes of bipolar, but not unipolar, patients. Currently, there is no evidence to indicate that the increased concentration of Gas is caused by gene mutations; it has been suggested that they could be caused by a change in any of the biochemical pathways leading to the transcription and translation of the Gas gene . Copper ion binding belongs to the significant GOTs as well.
In the second study copper ion binding, magnesium ion binding, chloride channel activity, chloride transport, postsynaptic membrane, and inositol or phosphatidylinositol phosphatase activity represent significantly differentiated GOTs.
In study 3 and 4 defense response, immune response, and inflammatory response GOTs are present in the overrepresented GOTs. The inflammatory system is strongly related to these mental disorders, and the immune underlying mechanisms remain mainly obscure . Lipid metabolic process is also a statistically significant GOT altered in study 3.
Dysregulated neurotransmitter systems in the central nervous system of BD and SZ patients have been systematically reported [2, 4]; thus central nervous system development is among the GO terms resulting from pathway analysis of study 3 BD DE list. Copper ion binding, chloride ion binding, and signal transduction pathways seem to be affected.
Copper ion binding is present in almost all lists of significantly altered GO terms. Signaling pathways are among the KEGG pathways that appear more often as overrepresentative pathways (Supplementary Table 13).
We also performed GO analysis in the 68 genes, shown schematically in Figure 4, that were present in at least two of the BD or SZ DE lists. Table 9 summarizes the GO terms of this pathway analysis. ATP binding is essential for the maintenance of the ion gradients in the cell. ATP is universally an important coenzyme and enzyme regulator .
3.3. Identification of Candidate Hub Genes
In order to expand our knowledge regarding which genes have critical role among the common DE genes in BD datasets, we used the online tool GOrevenge , which performs prioritization of the gene list taking into consideration the centrality of each gene, as described in the GO tree. The 68 genes found differentiated in at least two BD- or SZ-related studies were submitted to GOrevenge, and the analysis was performed based on GO annotations for Homo sapiens as described in materials and methods section. A prioritized list of genes, containing candidate linker genes, that is, genes participating in many different cellular processes, was derived (Table 10). Among them, three genes, namely, APOE, RELA, and NPY, have also been found as statistically significantly differentiated in at least two of either SZ or BD DE gene lists.
3.4. Prioritizations of Putative Disease Genes
By setting SZ and BD as concept, the relation of each gene with the BD and SZ was assessed, and the 68 genes found differentiated in at least two BD- or SZ-related studies were prioritized by BioGraph algorithm as shown in Tables 11 and 12, respectively. The genes are prioritized according to their score which is a statistical enrichment measure of the relevance of each gene with the inquired context (here specified as either BD or SZ) to the total relations (references) of the gene in the universe of terms. In this way, the user can derive which of its genes are already associated and in what extent with a given disease or generally biological term and which of them represent novel findings with respect to the investigated pathological phenotype. APOE, RELA, and NPY have also high scores and are among the ten top genes related either to the BD or SZ after the prioritization of genes in BioGraph. These three genes have been shown to play a major role in the examined studies, after different bioinformatic analyses. NPY has been reported as a candidate psychosis gene, as aforementioned.
APOE regulates cholesterol of the central nervous system; thus any alteration in APOE levels may result in abnormal brain function. APOE has been mostly related to Alzheimer’s disease .
Genotyping studies and Western plot analysis have shown differences of APOE in SZ patients. Abnormal cholesterol metabolism has been associated with SZ as well. High levels of three different apolipoproteins in brains of patients with psychiatric disorders may indicate aberrant central nervous system lipid metabolism. Additionally, APOE has been implicated in inflammation pathways, after studies on mice revealing possible action of APOE as inflammatory response inhibitor. Inflammation pathways are considered candidate mechanisms responsible for the pathogenesis of several mental disorders and mainly of SZ .
RELA, v-rel reticuloendotheliosis viral oncogene homolog A (avian), is also involved in immune and inflammatory responses, as it encodes the main component of the NF-κB complex. NF-κB has been related indirectly to SZ, as it is highly correlated to SZ involved cytokines: interleukin-1β (IL-1β), IL-1 receptor antagonist (IL-1RA), IL-6, and tumor necrosis factor-α (TNF-α). NF-κB is a regulator of cytokines’ expression, and proinflammatory cytokines activate NF-κB. NF-κB is present in synaptic terminals and participates in regulation of neuronal plasticity. NF-κB regulates genes that encode subunits of N-methyl-D-aspartate receptors, voltage-dependent Ca channels and the Ca-binding protein calbindin, cell survival factors, including Bcl-2, Mn-SOD, and inhibitor of apoptosis proteins (IAPs) and cell death factors, including Bcl-x(S) and Bax. All these genes are related to neurotransmission, and altered expression of several of them has been reported in previous SZ postmortem brain studies .
The aim of the study was to interpret the results of comparative genomic profiling studies in schizophrenic patients as compared to healthy controls and in patients with BD and try to relate and integrate our results with an aberrant AA transport through cell membranes. Starting from genomewide expression data, the analysis focused on genes and mechanisms involved in AA transport through cell membranes. We performed transcriptomic computational analysis on raw data derived from four different studies. Moreover, a multistage, translational bioinformatic computational framework is employed, previously utilized for the molecular analysis of transcriptomic data of atherosclerotic mice models , exploiting different methods in order to identify critical altered molecular mechanisms and important central players. In this way, the results derived here do not rely solely on a single stage of significance. They are complying to a systematic screening of the results, exploiting various statistical measures, in a unified analysis pipeline. These measures either exploit the stringent FDR estimations at the single gene level, further filtered to keep those common in between diseases or studies comparisons. Moreover, the consensus gene lists thus derived are corrected through a rigorous, bootstrapping framework, applied in the statistical enrichment analysis of the significant biological processes. Moreover, critical regulatory genes, prioritized by their total number of GO annotations, to the resulting significant GOTs list, are highlighted. It is also examined, whether these genes have been associated with the disease phenotypes of SZ or BD in the broader biomedical literature. The results were eventually analyzed, complying with a meta-analysis context, giving emphasis on common functional patterns mined amid the various studies.
Our bioinformatic analyses of the downloaded datasets demonstrate genes and GOTs associated with ion transport dysregulation (K, Na, Ca, and other ion transports and bindings) resulting in a disturbed primary active transport, suggesting a deficit in transmembrane Na+ and K+ gradients maintenance. Characteristic downregulation of Na+ and K+ transporting ATPases, enzymes responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane, is indicated in the DE gene lists of two of our datasets. They are also upregulated in one dataset (BD patients’ expression profiles). Also downregulation of P-type ATPases is reported in the datasets. Altered distribution of specific ions in the cells may affect distributions of other ion groups. A statistical integration of many studies has previously related published data of Na,K-ATPase activity in erythrocytes of BD patients with the expression of the disease . Decreased activity of Na,K-ATPase has been also related to SZ in previous studies . The disturbed primary active transport observed in our study indicates difficulty in maintaining transmembrane ion gradients. This fact should result in disrupted, secondary, active AA transporter Systems A, X-AG, N, and y+, as they couple AA transport to the electrical and chemical gradients initiated by primary active transport. AA exchangers, systems ASC, y+L and L, that transport AAs by antiport mechanisms, may suffer from a deficit of secondary, actively transported AAs they need for the exchange, resulting in a disrupted transport of AAs mainly transported through this third mechanism.
Genes and pathways related to Ca transport agree with abnormalities in Ca signaling, that have been implicated in BD; findings show elevated intracellular Ca concentrations in the platelets, lymphocytes, and neutrophils of BD patients. Ca is very important in most intracellular signaling pathways and in the regulation of neurotransmitter synthesis and release .
Phospholipase activity may be dysregulated in BD and SZ diseases, as indicated by altered expression of the genes encoding this enzyme in this study. This alteration has obvious impacts on the phospholipid metabolism of the membrane, as it is a crucial enzyme in this metabolic pathway .
A consistent upregulation of MT1X and generally of metallothionein genes is consistent in different datasets. The functional role of metallothioneins in the brain has not been very well characterized . The main function of metallothioneins is to protect neurons from pathological stressing factors. Abnormal expression of genes encoding these proteins may indicate an endogenous reaction to constant oxidative stress . Several studies have suggested involvement of metallothioneins in functions of the central nervous system, such as neuroprotection, regeneration, and cognitive function. Other studies reported that metallothioneins are involved in cellular response, immunoregulation, cell survival, and brain functional restoration. Metallothioneins are mainly produced in astrocytes. Metallothionein overexpression has been also reported as a contributing factor in brain pathologies, such as excitotoxic injury, amyotrophic lateral sclerosis, Alzheimer’s disease, and Parkinson’s disease. Animal studies have associated substance dependences and learning procedures with metallothioneins. Other prefrontal cortex (PFC) studies have revealed overexpression of metallothioneins in SZ patients. All these studies indicate involvement of metallothioneins in neuroprotection and cognitive functions. A possible neurodegenerative function in the PFC may affect cognitive function in BD and SZ patients. Overexpression of these genes could then be a defense mechanism against these adverse processes. Metallothioneins have also been proposed as possible medical treatment as they have been tested in animal models and have been proved nontoxic .
The observed small number of common DE genes among the different studies reflects heterogeneity among the datasets analyzed, which could be explained by both biological and technical reasons. The brain area under study, the microarray platform used, and the selection of patients and controls could contribute to the heterogeneity and should be taken into consideration and duly addressed, ideally at the stage of the experimental design, whenever analogous meta-analysis tasks are envisioned. Highlighting genes that present different expression in different cases, but in the context of a multitiered systematic framework, like the one presented here, could result in molecular interactions, linked with causative, universal, and molecular pathways in mental disorders.
|ARMADA:||Automate Robust Microarray Data Analysis|
|EFA:||Essential fatty acids|
|FDR:||False discovery rate|
|GEO:||Gene expression omnibus|
|GOT:||Gene ontology term|
|MRS:||Magnetic resonance spectroscopy|
|NCBI:||National Center for Biotechnology Information|
|Na,K-ATPase:||Sodium-potassium adenosine triphosphatase|
|StRAnGER:||Statistical Ranking Annotated Genomic Experimental Results|
|Gas:||alpha subunit of G protein|
- A. Sawa and S. H. Snyder, “Schizophrenia: diverse approaches to a complex disease,” Science, vol. 296, no. 5568, pp. 692–695, 2002.
- M. L. Persson, J. Johansson, R. Vumma et al., “Aberrant amino acid transport in fibroblasts from patients with bipolar disorder,” Neuroscience Letters, vol. 457, no. 1, pp. 49–52, 2009.
- D. F. Horrobin, “Schizophrenia as a membrane lipid disorder which is expressed throughout the body,” Prostaglandins Leukotrienes and Essential Fatty Acids, vol. 55, no. 1-2, pp. 3–7, 1996.
- T. M. Du Bois, C. Deng, and X. F. Huang, “Membrane phospholipid composition, alterations in neurotransmitter systems and schizophrenia,” Progress in Neuro-Psychopharmacology and Biological Psychiatry, vol. 29, no. 6, pp. 878–888, 2005.
- F. A. Wiesel, J. L. R. Andersson, G. Westerberg et al., “Tyrosine transport is regulated differently in patients with schizophrenia,” Schizophrenia Research, vol. 40, no. 1, pp. 37–42, 1999.
- F. A. Wiesel, G. Edman, L. Flyckt et al., “Kinetics of tyrosine transport and cognitive functioning in schizophrenia,” Schizophrenia Research, vol. 74, no. 1, pp. 81–89, 2005.
- R. Vumma, F. A. Wiesel, L. Flyckt, L. Bjerkenstedt, and N. Venizelos, “Functional characterization of tyrosine transport in fibroblast cells from healthy controls,” Neuroscience Letters, vol. 434, no. 1, pp. 56–60, 2008.
- E. Olsson, F. A. Wiesel, L. Bjerkenstedt, and N. Venizelos, “Tyrosine transport in fibroblasts from healthy volunteers and patients with schizophrenia,” Neuroscience Letters, vol. 393, no. 2-3, pp. 211–215, 2006.
- L. Flyckt, N. Venizelos, G. Edman, L. Bjerkenstedt, L. Hagenfeldt, and F. A. Wiesel, “Aberrant tyrosine transport across the cell membrane in patients with schizophrenia,” Archives of General Psychiatry, vol. 58, no. 10, pp. 953–958, 2001.
- L. Flyckt, G. Edman, N. Venizelos, and K. Borg, “Aberrant tyrosine transport across the fibroblast membrane in patients with schizophrenia -indications of maternal inheritance,” Journal of Psychiatric Research, vol. 45, no. 4, pp. 519–525, 2011.
- C. N. Ramchand, M. Peet, A. E. Clark, A. E. Gliddon, and G. P. Hemmings, “Decreased tyrosine transport in fibroblasts from schizophrenics: implications for membrane pathology,” Prostaglandins Leukotrienes and Essential Fatty Acids, vol. 55, no. 1-2, pp. 59–64, 1996.
- P. E. Ward, J. Sutherland, E. M. T. Glen, and A. I. M. Glen, “Niacin skin flush in schizophrenia: a preliminary report,” Schizophrenia Research, vol. 29, no. 3, pp. 269–274, 1998.
- L. Flyckt, J. Borg, K. Borg et al., “Muscle biopsy, macro EMG, and clinical characteristics in patients with schizophrenia,” Biological Psychiatry, vol. 47, no. 11, pp. 991–999, 2000.
- R. Vumma, J. Johansson, T. Lewander, and N. Venizelos, “Tryptophan Transport in human fibroblast cells: a functional characterization,” International Journal of Tryptophan Research, vol. 4, pp. 19–27, 2011.
- D. Raucoules, J. M. Azorin, A. Barre, and R. Tissot, “Plasma levels and red blood cell membrane transports of L-tyrosine and L-tryptophan in depressions. Assessment at baseline and recovery,” Encephale, vol. 17, no. 3, pp. 197–201, 1991.
- Y. Bezchlibnyk and L. T. Young, “The neurobiology of bipolar disorder: focus on signal transduction pathways and the regulation of gene expression,” Canadian Journal of Psychiatry, vol. 47, no. 2, pp. 135–148, 2002.
- P. M. Kidd, “Bipolar disorder as cell membrane dysfunction. Progress toward integrative management,” Alternative Medicine Review, vol. 9, no. 2, pp. 107–135, 2004.
- D. F. Horrobin and C. N. Bennett, “Depression and bipolar disorder: relationships to impaired fatty acid and phospholipid metabolism and to diabetes, cardiovascular disease, immunological abnormalities, cancer, ageing and osteoporosis. Possible candidate genes,” Prostaglandins Leukotrienes and Essential Fatty Acids, vol. 60, no. 4, pp. 217–234, 1999.
- R. Hyde, P. M. Taylor, and H. S. Hundal, “Amino acid transporters: roles in amino acid sensing and signalling in animal cells,” Biochemical Journal, vol. 373, no. 1, pp. 1–18, 2003.
- L. Bjerkenstedt, L. Farde, L. Terenius, G. Edman, N. Venizelos, and F. A. Wiesel, “Support for limited brain availability of tyrosine in patients with schizophrenia,” International Journal of Neuropsychopharmacology, vol. 9, no. 2, pp. 247–255, 2006.
- D. F. Horrobin, “The membrane phospholipid hypothesis as a biochemical basis for the neurodevelopmental concept of schizophrenia,” Schizophrenia Research, vol. 30, no. 3, pp. 193–208, 1998.
- A. Chatziioannou and P. Moulos, “Exploiting statistical methodologies and controlled vocabularies for prioritized functional analysis of genomic experiments: the StRAnGER web application,” Frontiers in Neuroscience, vol. 5, pp. 1–14, 2011.
- D. L. Scott, S. P. White, Z. Otwinowski, W. Yuan, M. H. Gelb, and P. B. Sigler, “Interfacial catalysis: The mechanism of phospholipase A2,” Science, vol. 250, pp. 1541–1546, 1990.
- A. Klemm, R. Rzanny, R. Fünfstück et al., “31P-Magnetic resonance spectroscopy (31P-MRS) of human allografts after renal transplantation,” Nephrology Dialysis Transplantation, vol. 13, no. 12, pp. 3147–3152, 1998.
- S. Bröer, “Adaptation of plasma membrane amino acid transport mechanisms to physiological demands,” Pflügers Archiv. European Journal of Physiology, vol. 444, no. 4, pp. 457–466, 2002.
- T. Barrett, D. B. Troup, S. E. Wilhite et al., “NCBI GEO: archive for high-throughput functional genomic data,” Nucleic Acids Research, vol. 37, no. 1, pp. D885–D890, 2009.
- K. Iwamoto, C. Kakiuchi, M. Bundo, K. Ikeda, and T. Kato, “Molecular characterization of bipolar disorder by comparing gene expression profiles of postmortem brains of major mental disorders,” Molecular Psychiatry, vol. 9, no. 4, pp. 406–416, 2004.
- M. M. Ryan, H. E. Lockstone, S. J. Huffaker, M. T. Wayland, M. J. Webster, and S. Bahn, “Gene expression analysis of bipolar disorder reveals downregulation of the ubiquitin cycle and alterations in synaptic genes,” Molecular Psychiatry, vol. 11, no. 10, pp. 965–978, 2006.
- M. R. Barnes, J. Huxley-Jones, P. R. Maycox et al., “Transcription and pathway analysis of the superior temporal cortex and anterior prefrontal cortex in schizophrenia,” Journal of Neuroscience Research, vol. 89, no. 8, pp. 1218–1227, 2011.
- K. Iwamoto, M. Bundo, and T. Kato, “Altered expression of mitochondria-related genes in postmortem brains of patients with bipolar disorder or schizophrenia, as revealed by large-scale DNA microarray analysis,” Human Molecular Genetics, vol. 14, no. 2, pp. 241–253, 2005.
- A. Chatziioannou, P. Moulos, and F. N. Kolisis, “Gene ARMADA: an integrated multi-analysis platform for microarray data implemented in MATLAB,” BMC Bioinformatics, vol. 10, article 1471, p. 354, 2009.
- K. Moutselos, I. Maglogiannis, and A. Chatziioannou, “GOrevenge: a novel generic reverse engineering method for the identification of critical molecular players, through the use of ontologies,” IEEE Transactions on Bio-Medical Engineering, vol. 58, no. 12, pp. 3522–3527, 2011.
- A. M. L. Liekens, J. De Knijf, W. Daelemans, B. Goethals, P. De Rijk, and J. Del-Favero, “Biograph: unsupervised biomedical knowledge discovery via automated hypothesis generation,” Genome Biology, p. R57, 2011.
- K. D. Pruitt, T. Tatusova, W. Klimke, and D. R. Maglott, “NCBI reference sequences: current status, policy and new initiatives,” Nucleic Acids Research, vol. 37, no. 1, pp. D32–D36, 2009.
- N. Matigian, L. Windus, H. Smith et al., “Expression profiling in monozygotic twins discordant for bipolar disorder reveals dysregulation of the WNT signalling pathway,” Molecular Psychiatry, vol. 12, no. 9, pp. 815–825, 2007.
- K. H. Choi, M. Elashoff, B. W. Higgs et al., “Putative psychosis genes in the prefrontal cortex: combined analysis of gene expression microarrays,” BMC Psychiatry, vol. 8, article 87, 2008.
- T. Hashimoto, D. Arion, T. Unger et al., “Alterations in GABA-related transcriptome in the dorsolateral prefrontal cortex of subjects with schizophrenia,” Molecular Psychiatry, vol. 13, no. 2, pp. 147–161, 2008.
- N. Petronijević, D. Mićić, B. Duricić, D. Marinković, and V. R. Paunović, “Substrate kinetics of erythrocyte membrane Na, K-ATPase and lipid perosides in schizophrenia,” Progress in Neuro-Psychopharmacology & Biological Psychiatry, vol. 27, no. 3, pp. 431–440, 2003.
- C. A. Ogden, M. E. Rich, N. J. Schork et al., “Candidate genes, pathways and mechanisms for bipolar (manic-depressive) and related disorders: an expanded convergent functional genomics approach,” Molecular Psychiatry, vol. 9, no. 11, pp. 1007–1029, 2004.
- H. K. Manji and R. H. Lenox, “The nature of bipolar disorder,” Journal of Clinical Psychiatry, vol. 61, no. 13, pp. 42–57, 2000.
- S. Hope, I. Melle, P. Aukrust et al., “Similar immune profile in bipolar disorder and schizophrenia: selective increase in soluble tumor necrosis factor receptor I and von Willebrand factor,” Bipolar Disorders, vol. 11, no. 7, pp. 726–734, 2009.
- E. A. Thomas and J. G. Sutcliffe, “The neurobiology of apolipoproteins in psychiatric disorders,” Molecular Neurobiology, vol. 26, no. 2-3, pp. 369–388, 2002.
- R. Hashimoto, K. Ohi, Y. Yasuda et al., “Variants of the RELA gene are associated with schizophrenia and their startle responses,” Neuropsychopharmacology, vol. 36, no. 9, pp. 1921–1931, 2011.
- O. Papadodima, A. Sirsjö, F. N. Kolisis, and A. Chatziioannou, “Application of an integrative computational framework in trancriptomic data of atherosclerotic mice suggests numerous molecular players,” Advances in Bioinformatics, vol. 2012, Article ID 453513, 9 pages, 2012.
- S. W. Looney and R. S. Ei-Mallakh, “Meta-analysis of erythrocyte Na, K-ATPase activity in bipolar illness,” Depression and Anxiety, vol. 5, no. 2, pp. 53–65, 1997.
- E. Mocchegiania, C. Bertoni-Freddarib, F. Marcellinic, and M. Malavolta, “Brain, aging and neurodegeneration: role of zinc ion availability,” Progress in Neurobiology, vol. 75, pp. 367–390, 2005.