Microarray characterization of gene expression changes in blood during acute ethanol exposure
BMC Medical Genomics volume 6, Article number: 26 (2013)
As part of the civil aviation safety program to define the adverse effects of ethanol on flying performance, we performed a DNA microarray analysis of human whole blood samples from a five-time point study of subjects administered ethanol orally, followed by breathalyzer analysis, to monitor blood alcohol concentration (BAC) to discover significant gene expression changes in response to the ethanol exposure.
Subjects were administered either orange juice or orange juice with ethanol. Blood samples were taken based on BAC and total RNA was isolated from PaxGene™ blood tubes. The amplified cDNA was used in microarray and quantitative real-time polymerase chain reaction (RT-qPCR) analyses to evaluate differential gene expression. Microarray data was analyzed in a pipeline fashion to summarize and normalize and the results evaluated for relative expression across time points with multiple methods. Candidate genes showing distinctive expression patterns in response to ethanol were clustered by pattern and further analyzed for related function, pathway membership and common transcription factor binding within and across clusters. RT-qPCR was used with representative genes to confirm relative transcript levels across time to those detected in microarrays.
Microarray analysis of samples representing 0%, 0.04%, 0.08%, return to 0.04%, and 0.02% wt/vol BAC showed that changes in gene expression could be detected across the time course. The expression changes were verified by qRT-PCR.
The candidate genes of interest (GOI) identified from the microarray analysis and clustered by expression pattern across the five BAC points showed seven coordinately expressed groups. Analysis showed function-based networks, shared transcription factor binding sites and signaling pathways for members of the clusters. These include hematological functions, innate immunity and inflammation functions, metabolic functions expected of ethanol metabolism, and pancreatic and hepatic function. Five of the seven clusters showed links to the p38 MAPK pathway.
The results of this study provide a first look at changing gene expression patterns in human blood during an acute rise in blood ethanol concentration and its depletion because of metabolism and excretion, and demonstrate that it is possible to detect changes in gene expression using total RNA isolated from whole blood. The analysis approach for this study serves as a workflow to investigate the biology linked to expression changes across a time course and from these changes, to identify target genes that could serve as biomarkers linked to pilot performance.
As part of civil aviation safety research into aeromedical factors impacting flight safety, we have undertaken a time course study on the effects of acute ethanol exposure to the legal intoxication level of blood alcohol concentration (BAC), 0.08 g/dL (0.08% wt/vol), on human gene expression in non-chronic users. This is a novel study to identify gene expression patterns in whole blood messenger RNA and discover biomarkers linked to BAC.
Mandatory ethanol testing was implemented for U.S. commercial pilots in 1995. For the period 1995–2000 alcohol violations, occurrences of an alcohol level exceeding the Federal Aviation Administration (FAA) limit of ≥0.04%, were attributed to 0.13% of fatal aviation accidents . This number suggests that alcohol misuse is a relatively rare occurrence in the commercial aviation setting. To date, alcohol has not been implicated as the probable cause in any fatal crash involving a U.S. major airline; however, there are instances of commercial pilots reporting for duty impaired with BAC ≥0.04% [2, 3].
The current FAA regulations prohibit anyone from acting as a crewmember within eight hours of consuming alcohol or while having a BAC ≥0.04%. However, a number of reports addressing the carry-over effect of alcohol have shown a performance loss to remain after the BAC has returned to less than 0.02% . Communication performance decrement was still found eight hours post 0.08% BAC, and an ethanol effect on the vestibular and visual systems has been shown to persist for up to several days after BAC returned to zero (reviewed in ). Additionally, two studies [4, 6] found that testing at eight hours post 0.1 or 0.08% BAC showed variability in performance suggesting a range of susceptibility to ethanol. The authors suggested that an arbitrary eight hour flying prohibition does not take into account the amount consumed or individual differences in metabolism and recovery.
General (private) aviation accounts for more than 90% of all aviation accidents . For the period 1994–2000, 11.5% of alcohol-related general aviation crashes were linked to a pilot with a DWI (driving while intoxicated) history . No routine alcohol testing is required for general aviation pilots. The level of fatal general aviation crashes attributed to alcohol impairment has decreased from 30% of pilots with a BAC ≥0.04% in the early 1960s to 8% in the 1990s . However, a study of alcohol-related fatal crashes between 1985 and 2000 in Maryland, New Mexico, and North Carolina showed that 11% had positive BACs and 6% had BACs exceeding 0.04% . The FAA Toxicology and the Document Information Workflow System databases contain records of the 2391 certified pilots involved in fatal accidents for the period 2000–2007. These records show that 215 pilots tested positive post-mortem for alcohol and had drug or alcohol offenses. Twenty-three of the 215 were confirmed to have consumed ethanol prior to the fatal incident. In eleven of these cases, the National Transportation Safety Board linked the accident cause to alcohol impairment . These studies suggest that in general aviation, flight impairment due to alcohol consumption is still a safety concern.
FAA forensic toxicological testing detected ethanol above the legal cutoff of 0.04% in 7% of fatal general aviation accidents during 2000–2007 . To differentiate antemortem from postmortem alcohol in positive cases, the FAA (as of November, 2012) uses either the standard practice of tissue distribution ratios of alcohol present in blood, vitreous humor, and tissues or, if urine is available, the ratio of the serotonin metabolites, 5-HTOL and 5-HIAA [12, 13]. Unfortunately, in approximately 30% of ethanol-positive cases, distribution ratios are inconclusive and FAA toxicologists are unable to differentiate between ingested and other sources of the detected ethanol (R. Lewis, personal communication, November 14, 2012).
Ethanol ingestion impacts human metabolism, lowering blood glucose by stimulating the glucose-stimulated insulin early secretion response, which can result in a transient hypoglycemia . Metabolism of ethanol occurs primarily in the liver and results in production of intermediate acetaldehyde and then acetate, which can be utilized by other tissues. This oxidation results in a decrease in the NAD+/NADH ratio (reviewed in ). Ethanol exposure increases the level of reactive oxygen species (ROS) in part because of the shift in NAD+/NADH ratio and the action of cytochromes p450 and CYP2E1 .
The impact of acute ethanol consumption on the innate immune system and inflammation is well-documented and includes suppression of proinflammatory cell activation in a dose-dependent manner . Nuclear factor κB (NF-κB) is a central mediator of the innate immune response  whose activity is reduced in the presence of ethanol, in turn affecting levels of pro-inflammatory cytokines, TNF and IL-1B at the transcription level [19, 20].
A major kinase signaling cascade is anchored by the p38 mitogen activated protein kinase (MAPK). It is activated by a variety of stressors and inflammatory cytokines . p38 MAPK regulates a diverse set of downstream transcription factors, pathways, and cell functions including cytokine production, cell proliferation, differentiation, and apoptosis including transcription activity of NF-κB. Acute ethanol exposure has a negative affect on p38 MAPK activity, leading to decreased NF-κB transcriptional activity, lower levels of TNF and of proinflammatory cytokine production [22, 23], and, ultimately, neutrophil and granulocyte migration to sites of inflammation . Conversely, ethanol induces oxidative stress by increasing levels of ROS ( that can enhance p38 MAPK activity. p38 MAPK phosphorylates p300, which in turn acetylates the RelA component, increasing NF-κB transcription activity . Cytochrome C and calcium are inter-organellar messengers of apoptosis (reviewed in ). The p38 MAPK pathway is linked to apoptosis through ROS, mediating mitochondrial dysfunction, triggering the release of cytochrome C, followed by calcium release from the ER .
Transcription factor STAT3 phosphorylation increases in the presence of acute ethanol because of increased activity of Src kinases . IL-10, an anti-inflammatory cytokine, is a target of the src-STAT3 pathway and shows an increase in transcription in the presence of acute ethanol . STAT3 also is an activator of Suppressor of Cytokine Signaling 3 (SOCS3), and SOCS1, negative regulators of cytokine signaling . Additionally, acute ethanol exposure has been shown to have a reproducible and negative affect on the ability of both monocytes and dendritic cells to stimulate T-cell antigen presentation function .
Our approach for this study was to evaluate changes in gene expression levels, using RNA extracted from whole blood, across a five-point time course as ethanol entered the blood system, reached a level of 0.08 g/dL (0.08% BAC), and returned to 0.02% BAC, the lowest concentration of breathalyzer detection. By microarray analysis, we examined gene expression changes and evaluated the resulting genes of interest (GOIs) for ethanol-related biological relevance, identifying sets of genes to serve as potential biomarkers for alcohol-related effects.
Nine age-matched subjects for the ethanol study were recruited by D. L. Strayer, Department of Psychology, University of Utah, Salt Lake City UT. Institutional Review Board approval to perform research on human subjects was gained from boards at both the University of Utah and the FAA Civil Aerospace Medical Institute (CAMI). The study was conducted at the Department of Psychology, Salt Lake City, Utah. Informed consent was obtained by investigators at the Department of Psychology. The control experiment to establish the effects of drinking orange juice only was conducted at the CAMI. Five age-matched male subjects were recruited at the University of Central Oklahoma. Institutional Review Board approval was granted from boards at both the University of Central Oklahoma and the CAMI. Informed consent was obtained by investigators at the CAMI for the five subjects.
Sample collection and preparation
Subjects drank 125 mL of an orange juice and 80 proof vodka mixture calculated to achieve a blood alcohol concentration of 0.08% wt/vol . Blood Alcohol Concentrations (BACs) were verified using infrared spectrometry breath analysis (Intoxilyzer 5000, CMI Inc; Ownsboro, KY, ). Blood samples were collected into PAXgene™ Blood RNA tubes (Cat. # 762165, Qiagen US; Valencia, CA) at five time points corresponding to BAC, baseline = BAC1, 0.04% = BAC2, 0.08% = BAC3, 0.04% = BAC4 during recovery, and 0.02% = BAC5, this last point being the lower limit of quantitation by the Intoxilyzer. Control experiment samples were collected from subjects at time points corresponding to the average collection time for the alcohol group: T1 was taken prior to drinking 125 mL of orange juice (OJ), T2 at 90 minutes; T3 at 2 hours, 49 minutes; T4 at 5 hours, 8 minutes; and T5 at 7 hours, 8 minutes.
For the alcohol group, two blood samples were collected at each timepoint. Total RNA was purified using the PAXgene™ RNA purification system with the optional on-column DNase treatment (Cat # 762164; Qiagen; Hilden, Germany) , and stored at −80°C. A modification in the manufacturer’s published protocol pooled the two samples from each subject timepoint at the column binding step such that total RNA was purified from one PAXgene™ column. A single blood sample was obtained from each control group subject for each timepoint in a PAXgene™ Blood RNA tube and purified according to the manufacturer’s published protocol with the on-column DNase step.
RNA quality was assessed on an Agilent Bioanalyzer 2100 (Agilent; Santa Clara, CA) using the Agilent RNA 6000 Nano Series II kit following manufacturer’s directions with 1 μL of sample and the 2100 Expert software (ver. B.02.03.SI307). Yield and A260/280 was determined on a Nanodrop 1000 spectrophotometer (Thermo Scientific; Waltham, MA) (Additional file 1).
Samples from six male subjects (S8, S13, S15, S17, S18, and S19) were used in the ethanol microarray study and samples from one female (S1) and 5 male subjects (S5, S10, S13, S17, S19) were used for qRT-PCR validation of microarray results.
Microarray target material was made using the One-cycle IVT kit (P/N 900431; Affymetrix Inc.; Santa Clara, CA) and the resulting amplified cRNA hybridized to Affymetrix HGU133plus2.0 GeneChips® according to the manufacturer’s instructions. One sample, S18-BAC4 was excluded from further analysis due to a low percent present call with MAS5.0 (Affymetrix Inc.; Santa Clara, CA) and insufficient RNA to repeat the amplification/hybridization leaving 29 samples and arrays.
Total RNA from the five orange juice (OJ) Control subjects was used to derive target material using the Ovation 3’ kit (P/N 2200, NuGen Technologies; San Carlos, CA) according to the manufacturer’s protocol and hybridized to Affymetrix HGU133plus2.0 GeneChips®.
Data handling and analysis
To assess quality and variability in the microarray data, CEL files underwent standard QC analysis using the Affymetrix™ GeneChip Operating Software, GCOS (Affymetrix Inc.; Santa Clara, CA), including a percent present determination using MAS5.0 (Affymetrix Inc.; Santa Clara, CA) as noted in the section above. For the ethanol subjects, CEL files were imported into S + ArrayAnalyzer™, version 2.1.1 (Tibco Software Inc.; Palo Alto CA), summarized and quantile normalized using both RMA  and GCRMA  algorithms. RMA summarized data was filtered for log2 (RMA expression) >6 in at least six arrays; GCRMA, summarized data were filtered for log2 (GCRMA expression) >5 in at least six arrays. The Local Pooled Error T-test, LPE,  was used to test for significance of differential gene expression across all possible pairwise comparisons in both sets of summarized data. Probe sets with p < 0.05 after False Discovery Rate correction by the method of Benjamini and Hochberg  were further filtered for a fold change greater than 1.25 in at least one pairwise comparison.
RMA summarized data were used for analysis using Extraction and Analysis of Differential Gene Expression, EDGE  and the timecourse package  in Bioconductor . The EDGE output was filtered for probe sets with q < 0.02, the EDGE-specified cutoff. From the timecourse analysis, the ranked T2 test scores were visualized as a histogram. Based on a leveling off of the histogram as scores reached 50, probe sets with ≥50 were considered the Timecourse50 list. This list was added to the lists derived from LPE testing and EDGE for further analysis. Duplicate probe sets and those with the Affymetrix x_at designation were removed and where a gene was represented by multiple probe sets, the probe set with the greatest fold change was retained.
CEL files from OJ Control samples were analyzed using the same three methods: LPE, EDGE and timecourse. Since the control subjects were not the same as the ethanol subjects, to generate a comprehensive list of genes and functional pathways responding to orange juice alone thereby minimizing false positives in the alcohol-responsive gene list, a significance score of T2 ≥ 25 was applied to the timecourse analyzed control data. Probe sets found on both the ethanol and OJ lists were removed from the alcohol list.
qRT-PCR validation of genes across a range of fold-changes was used to refine endpoint settings for all three analysis methods (Results and see below). Cutoff limits were set at 1.53 fold-change for LPE derived genes, q ≤ 0.0017 EDGE derived genes and T2 > 82.83 for timecourse derived genes resulting in a list of 203 probe sets for further analysis. To cluster probe sets by temporal expression pattern, Z-transformed expression values for the probe sets were used as input for K-means fuzzy-clustering .
The entire probe set list and the individual expression pattern-clustered probe sets, were analyzed with Ingenuity Pathway Analysis, IPA (version 8.7, Ingenuity® Systems, Inc., http://www.ingenuity.com; Redwood City, CA) and the Database for Annotation, Visualization, and Integrated Discovery, DAVID . The BioGPS database was used to evaluate tissue-specific gene expression using the Human U133A/GNF1H Gene Atlas dataset, (GEO-GSE1133, [41, 42] ). The BIOBASE  ExPlain™  Mammalian Module 3.0 was used with the application Match™ to examine the promoter regions of the cluster genes for transcription factor binding matrices using the BIOBASE TRANSFAC® database. The RMA summarized data set filtered for average log2 (expression) > 6 and with the 203 candidate genes removed was used for the No-set (background). The vertebrate_h0.01 profile was used. High-specific matrices with cut-offs minFP were used for a 1200 base promoter window from −1000 to 200. Both cut-off and window position were optimized with a p-value threshold of 0.001. The Match matrix output was filtered for a Yes/No ratio of >1.5, P-value <0.01 and Matched promoters P-value <0.01. The weight matrices profile was used to create a transcription factor gene set and filtered for human specific factors. The gene set was mapped on canonical pathways using the BIOBASE Transpath application using P-value <0.01, minimal hits to group of two. A Transpath gene set linking the transcription factors to pathways was generated for each cluster. The resulting output was examined for signaling pathways and transcription factors predicted to affect genes on our list. Figure 1 shows the analysis pipeline.
The microarray data is publicly accessible and has been assigned series number GSE20489 in the Gene Expression Omnibus (GEO)  and can be freely accessed from their website.
Fifty nanograms of total RNA from each of six ethanol subjects, S1, S5, S10, S13, S17, and S19, were reversed transcribed and amplified for use with qRT-PCR with the Ovation 3’ amplification kit (P/N 2200, NuGen Technologies; San Carlos, CA) according to the manufacturer’s protocol. Candidate GOIs for qRT-PCR were chosen from the EDGE-generated list (IMPA2, TMEM8 and CDA) and from the pooled LPE list (ANKRD28, EVI2A, FKBP5, LR8). The final GOI, RNF11, was on both lists.
Candidate normalizer genes were filtered from RMA-summarized, non-normalized microarray expression data with coefficient of variance < 0.2 and average log2 expression >5.5 across all 29 chips and further refined with the analysis tools NormFinder  and geNorm . geNorm pairwise variation showed that three normalizers were sufficient for the study. The three genes selected, ITGA5, SCAMP2, and PLCG2, had NormFinder stability rankings in the top 20% of the candidates, 0.045, 0.045 and 0.048, respectively, and are functionally non-redundant. Genes with better stability rankings were not good candidates for primer design.
Primers for both normalizer genes and GOIs were designed for detection by SYBR-Green using Beacon Designer 7.0 (PremierBiosoft; Palo Alto, CA) (Additional file 2) and obtained from Integrated DNA Technologies (Coralville, IA). Primer pairs were rigorously screened for qRT-PCR reaction efficiency greater than or equal to 93% and the presence of a single product by electrophoresis on a Bioanalyzer DNA 1000 chip (Agilent; Santa Clara, CA). qRT-PCR was performed on a MX3005P cycler (Stratagene; La Jolla, CA) using Platinum SYBR-Green qRT-PCR SuperMix UDG (P/N 11733046, Invitrogen; Carlsbad, CA) in 25 μL reactions according to the enzyme manufacturer’s recommendations and optimal primer annealing temperature for each primer pair. A noRT experiment with TMEM8 revealed all samples had 10 Cts or greater difference compared to the experimental samples. Differential expression analysis of qRT-PCR data was performed with REST2009  after normalization to the geometric mean of normalizer expression values.
Results and discussion
Microarray data analysis and candidate gene list derivation
We report microarray derived gene expression changes over a BAC profile to a maximum of 0.08% after ingestion of an alcohol cocktail of orange juice (OJ) and vodka. A control group was administered only orange juice to distinguish genes and biological pathways responding to the OJ from those responding to the alcohol. Five samples were taken from each subject (BAC1-5), a baseline sample and then at BAC levels, or for the control group, the time matched equivalent, of 0.04%, 0.08%, and recovery samples at 0.04% and 0.02%, the lowest concentration detectable by breathalyzer (Methods).
Because the experimental conditions were performed with different groups of subjects, we used a conservative analysis model that included three microarray data analysis tools - LPE t-test , EDGE  and timecourse  (Methods) - to identify candidate genes. The LPE t-test was applied across all 10 possible pairwise timepoint comparisons and the lists of significant probe sets pooled. From the ethanol data, the LPE list contained 171 probe sets, the EDGE list 63 probe sets, and the Timecourse50 list 452 probe sets.
When applied to the OJ data, the LPE t-test found 22 differentially expressed probe sets, one of which was in common with the ethanol list. The EDGE analysis found no significantly changing probe sets. In the timecourse analysis, 23 probe sets above the test score cutoff of 25 were found in common with the ethanol list. These 24 probe sets were removed from the ethanol list. The 19 genes represented by these probe sets were examined in DAVID and IPA to determine pathways responding to OJ. GO_FAT results from DAVID showed that eight genes are involved in translation and translation elongation. Therefore, the “protein translation” biological process was not considered in further analysis of the ethanol data.
Quantitative PCR validation and establishment of cut-off values
qRT-PCR was used to validate the microarray results for direction and fold-change across the experiment. Four genes were selected from the LPE list: ANKRD28, EVI2A, FKBP5, LR8, and the EDGE list: IMPA2, TMEM8, CDA and RNF11 (Table 1). Only ANKRD28 and LR8 were not on the Timecourse50 list. ITGA5, SCAMP2 and PLCG2 were selected as normalizers based on microarray expression data across all 29 chips (Methods).
Comparisons across all 10 possible pair-wise BAC contrasts were performed using Relative Expression Software Tool, REST (, Methods). The direction of change was found to be the same for the microarray and qRT-PCR results with the single exception of the BAC 4 versus 5 contrast for ANKRD28, where the microarray results showed an increase rather than the decrease seen in the qRT-PCR comparison (Table 2); however, this was not a statistically significant contrast in the LPE t-test (Table 1).
With two exceptions, all other statistically significant contrasts from microarray data were validated by qRT-PCR. LR8, significant in a single contrast at a fold-change level of 1.25 (Table 1), could not be confirmed, and EVI2A could not be confirmed at one of its three significant contrasts (BAC2 vs. 5, Table 1). Therefore, for further characterization of the biological response to ethanol, the limit of detection for genes coming from the LPE analysis was set at a fold change of 1.53, based on confirmation of FKBP5 (Tables 1 and 2). Likewise, based on the observation that the largest q-value from the EDGE analysis that could be validated by qRT-PCR was 0.0017, the gene list was filtered to remove EDGE-list genes above that level. Similarly, the lowest validated timecourse score was 82.83, based on IMPA2 (Table 1). Genes below this level were removed. The resulting merged list from the three analyses contained 203 GOIs.
Functional analysis of the genes of interest (GOIs)
To obtain an overall picture of pathways that respond to ethanol ingestion, the complete list of 203 GOIs was assessed using IPA. Functional categories included immune and inflammatory response, hematological system development and function, hepatic system disease, carbohydrate metabolism, cell death, cell-cell signaling, and nucleic acid and amino acid metabolism. Using DAVID, the GOIs clustered into functional categories including immune system development, protein catabolism, and S100A EF hand proteins. An examination for over-represented GO terms from DAVID in the candidate gene list identified 21 genes with immune response, 16 with defense response and eight with innate immune response.
To further examine the temporal response to ethanol exposure, we clustered the GOIs by expression pattern. Seven clusters were formed by 199 of the genes; four were unclustered. The seven clusters were analyzed using IPA, BIOBASE, and BioGPS (Figure 1 and Methods).
Genes in this cluster exhibit a decreased expression level at BAC4 followed by a sharp increase at BAC5 (Figure 2), suggesting that these genes constitute a late response of increased expression well after alcohol levels begin to decrease. Of the 23 genes in Cluster 1, IPA created a single network from 14 members with the top biological functions of Infectious Disease, Cell Signaling, and Small Molecule Biochemistry (Table 3).
Interactions within the network include RIOK3, a GOI that regulates NF-κB , which in turn interacts with the GOIs BAX, a blood exclusive, stress-induced proapoptotic factor , UBR5 the E3 ubiquitin ligase linked to apoptosis , and KLF3, a hematopoietic transcription factor important in apoptosis and the inflammatory response . Transcription regulator TP53 levels are regulated by the GOIs UBE2D3, an E2 ligase , BAX, and the proteoglycan VCAN, important in cell adhesion . Other GOIs in the network include the lysosomal marker LAMP1, important for protein trafficking , ACTR2, essential for cell shape , the cytokine regulator CNPY3 , PF4V1, a hematopoietic chemokine and histone methylation factor , and MPHOSPH8 a transcription regulator involved in DNA methylation .
Transcription Factor Binding Site (TFBS) analysis with BIOBASE found binding sites for NF-κB in BAX, KLF3, UBE2D3, and PF4V1. LAMP1, ACTR2, and the poorly annotated genes TMEM165 and MGC2752 contain binding sites for the ETS protein SPI-1, important in lymphoid and B-cell development ([60, 61]. The BIOBASE analysis reinforces the NF-κB link detected in IPA and implicates the p38 MAPK pathway and its regulation of NF-κB (Figures 3 and 4).
Cluster 2 genes increase expression at BAC 3, 4, and 5 from BAC 1 or 2 with no return to baseline (Figure 2). IPA created a single network that includes 40 of the 44 genes in the expression cluster. Top network functions are Cellular Assembly and Organization, DNA Replication, Recombination and Repair, and Cell Cycle (Table 3). Insulin, a key sensor of glucose levels, is found in this network with connections to the GOI PDP1, an activator of pyruvate dehydrogenase , and PIKFYVE, a member of the inositol phosphate metabolism pathway under positive regulation by insulin . Pro-inflammatory cytokine, IL-6, is a central non-GOI member of the network linked to insulin and regulating GOIs TBC1D9, a GTPase factor expressed in dendritic cells , BMI1, a factor in stem-cell pluripotency  and PARP8, involved in post-translational modification . The heterotrimeric GTPase subunit GNAQ impacts the ERK and Akt signaling pathways. HNF4A, a non-GOI transcription factor regulating genes involved in glucose metabolism and homeostasis , has direct protein-DNA interaction with the GOIs SEC23A, an ER-Golgi trafficking molecule  known to be positively regulated by insulin , TMEM30A, also involved in protein exit from the ER , NEK7, a mitotic regulator , the TGFB1 receptor, TGFBR1 and BMI1. NF-κB, another central non-GOI in this expression cluster, interacts with or regulates the GOIs, BMI1, GNAQ, the ER-aminopeptidase, ERAP2, and TGFBR1 (Figure 4). The non-GOI cytokine TGFB1 interacts with the aforementioned receptor TGFBR1, and BMI1.
BIOBASE TFBS analysis found seven genes carrying the binding matrix for ATF2 and/or CREB1. Phosphorylation of both is regulated by p38 MAPK [70, 71]. Three blood or dendritic cell-specific genes carry a matrix binding only CREB1 (, Figure 3). This analysis also identified four GOIs which bind interferon regulatory factors 3 and 7 (IRF3 and IRF7), members of the Toll-like receptor 4 (TLR4) pathway (Figure 3). In summary, genes in Cluster 2 are influenced by insulin and co-regulated by factors in the p38 MAPK signaling pathway.
The expression patterns of Clusters 2 and 3 are similar; Cluster 3 exhibits an immediate-early decrease in expression from BAC1 to BAC2 not seen in Cluster 2 (Figure 2), followed by increasing expression levels through BAC5. IPA analysis of genes in Cluster 3 resulted in a network containing 36 of the 47 members (Table 3). Transcription factor HNF4A seen in the Cluster 2 network is found here linked to six GOIs, RASA1, which promotes cell migration and adhesion , RORA, a T-cell specific factor , CUL5, a cullin expressed in lymphocytes , DCK, expressed in whole blood and lymphocytes , GFM1, a mitochondrial translation elongation factor , and PKA, a cellular effector of cAMP . The network also includes the two GOI integrins positively regulated by calcium ion and TGFB1, ITGA4, and ITGB1, components of the innate immune response (reviewed in ).
BIOBASE analysis associated six Cluster 3 GOIs with the p38 pathway through JUN and two transcription factors detected in Cluster 2, CREB1 and ATF2, which can heterodimerize with JUN (Table 4). These GOIs include ZNF12, a transcriptional repressor of AP-1 , DNAJB14, RORA, CUL5, LYRM7, and PRKACB.
Transcription factor SPI-1, an effector of p38 MAPK signaling (, Table 4), regulates seven Cluster 3 GOIs, RORA, DNAJB14, DOCK10, a factor induced by IL-4 in B lymphocytes , SP4 a transcription factor that regulates NF-κB , two ubiquitination factors, USP1 and RNF6, and vacuolar protein VPS13C.
Binding sites for E2F family transcription factors are found in FECH, which catalyses the last step in heme biosynthesis , MBNL1, linked to insulin receptor splicing , UBE2J1 a dendritic cell-specific  ubiquitin conjugating enzyme HLTF, a transcription factor regulating cytokine production , PRKD3 a B cell protein kinase , FAM46C and FAM3C cytokine-like factors  and SP4, DOCK10, ITGB1, ITGA4 and RORA, five factors mentioned previously. Fifteen Cluster 3 GOIs contain TCF/LEF binding sites. This Wnt-regulated group includes three factors involved with mRNA maturation, RASA1, SFRS7, NUDT21, and three involved with protein modification or degradation, ZDHHC2, MGAT4A, and YOD1.
These nine genes exhibit an immediate-early response, sharply decreasing in expression from baseline to BAC2, and then moderately increasing at BAC3 (Figure 2). Two of these genes have not been characterized (Additional file 3). The remaining seven genes form a single IPA network with functions including Cell Growth and Proliferation, and Small Molecule Biochemistry that contains TP53 and NF-κB as central non-GOIs. Within this cluster, the NF-κB inhibitor, NFKBIA, and the pro-inflammatory calcium-binding protein S100A12 are found highlighting the delicate interplay in regulatory control of NF-κB activity. Also in this cluster are MED6, a member of the Mediator complex , and PADI4, a gene that plays a role in granulocyte and macrophage development in inflammation and the immune response .
From BIOBASE, p38 MAPK is implicated in the regulation of Cluster 4 immediate-early response genes through binding sites for the JUN/ATF2 heterodimer in the PADI4 and S100A12 genes, and ELK1 binding to PHC2, NFKBIA, and MED6. In addition, BIOBASE also associated Cluster 4 GOIs PHC2, MED6, GPSM3, PADI4, NFKBIA with the apoptosis signaling pathway through binding matrices for ELK-1, FOXO3 and 4, and MYC (Table 4), of which four are shared with p38 MAPK signaling (Figure 3). PHC2 is highly expressed in whole blood and can associate with BMI1 a GOI factor in Cluster 2 associated with cell division in hematopoietic stem cells . GPSM3 is unique in containing only a FOXO3 binding site.
This is the largest expression cluster, containing 67 early response GOIs with a distinctive decrease in expression from BAC2 to BAC5 (Figure 2). Due to computational limitations in network size, IPA created two networks that could be merged. Examination of the merged network reveals central non-GOIs that include NF-κB, p38 MAPK, insulin, IL-1, -6, and −12, TNF, TGFB1, and d-glucose as an activation agent. The functions assigned to the individual networks include for Network 1: Immune Cell Trafficking, Hematological System Function, and Apoptosis and for Network 2: Cell Growth, Proliferation and Development, Gene Expression, and Carbohydrate Metabolism (Table 3).
Cluster 5 contains three members of the pentose phosphate pathway (PGLS, TALDO1, TKT), which is inhibited in the presence of ethanol . GOI IMPA2 is important in phosphatidylinositol and insulin signaling . Four members of the S100A calcium binding family are members of Cluster 5 and are network targets of TGFB1. Additionally in the network, S100A4 is regulated by the NF-κB complex, ERK and AP-1; S100A9 is regulated by P38 MAPK, and S100A6 is linked to activation of JNK, which in turn is integral to IL-1 and IL-12 signaling .
BIOBASE analysis linked 44 Cluster 5 genes to the p38 MAPK signaling pathway through binding sites for transcription factors ELK-1, CREB1, NF-κB, and SPI-1 (Figure 3). Most have binding sites for more than one of these factors. However, seventeen of the 44 contain only SPI-1 binding sites and function in defense response, the pentose phosphate shunt, inositol phosphate signaling, and S100A signaling.
These four genes constitute a late-response cluster specific to falling ethanol levels with an expression spike at BAC4 and return to baseline at BAC5 (Figure 2). IPA put two of the four members, HLA-DQA1 and HLA-DQB1, the subunits of the DQ heterodimer and components of major histocompatibility complex CII  in an immune response network. GIMAP2 and MXRA7 were not assigned to a network. GIMAP2 is uniquely expressed in whole blood and T-cells , and is a GTPase in the immunity-associated protein family . MXRA7 is a ubiquitously expressed gene with unknown function.
These five genes show a delayed response, increasing in expression levels at BAC4 and 5 as ethanol levels decrease. Four of the five genes appear in an IPA network with gene expression as the top function. HMGB1(amphoterin), is a cytokine mediator of inflammation  through RAGE (, Figure 4). Also in this network are UBA6, regulated by TNF and INF-gamma , RGS18, a whole blood-specific  G-protein signaling attenuator , PPP4R2, involved in the maturation of splicosomal snRNPs . EVI2A is an uncharacterized factor not included in the IPA network with blood-specific expression . Cluster 7 members regulate a range of cellular mechanisms, including protein recycling , signal transduction , immuno-modulation , and transcript maturation .
BIOBASE analysis showed that HMGB1 carries binding sites for STAT1, 3 or 5A. STAT1 can form homo- or heterodimers  with STAT3, which is also upregulated by acute ethanol exposure as part of the Src pathway . STAT5a, an antiapoptotic factor , shows cell-specific response to ethanol, is up-regulated in T cells and down-regulated in NK cells and induced by a number of cytokines . HMGB1 is an antiapoptotic factor that binds RAGE to elicit release of cytokines [100, 101].
To identify potential gene expression markers and increase our understanding of the biological response to acute ethanol ingestion, we used a microarray and qRT-PCR-based approach on whole-blood RNA samples collected from human subjects administered orange juice with and without ethanol.
Our microarray data analysis revealed biases in the three analysis methods used. At the qRT-PCR-validated significance limits used, the LPE- and EDGE-lists share only one gene. Timecourse was more comprehensive; this list shared 13 genes with the LPE-derived list and 17 genes with the EDGE-derived list. This observation extended to the expression patterns detected upon clustering of the genes. The LPE t-test uniquely identified 42 of 44 genes in Cluster 2 and 38 of 47 Cluster 3 genes, whereas in Cluster 5, 39 of 67 genes were identified only by EDGE. All of the Cluster 4 and unclustered genes were from the Timecourse50 list. The explanation of the bias is likely rooted in the nature of the relative expression change patterns; for example, LPE was the analysis method that detected the majority of genes increasing in expression across the experimental time course. Most importantly all three methods identified genes that were confirmed by qRT-PCR as differentially expressed (Tables 1 and 2).
Certain biological regulatory motifs emerged from our analysis, key among them, calcium flux, the influence of NF-κB and p38 MAPK.
There are 16 calcium binding genes in the ethanol GOIs, as characterized by DAVID (Additional file 3). Notably, six are members of the S100A family. This is a group of more than 25 small, acidic, EF-hand (calcium-binding) proteins. They can form homo- or heterodimers leading to complex calcium signaling dependent on the available S100A populations . Four, S100A4, -6, -9, and −11, are found in Cluster 5, an early response cluster with decreased expression. S100A12 belongs to Cluster 4 and has an immediate early decreased expression profile. The unclustered S100A8 has an early decrease in expression but returns to baseline at BAC5. Taken together, the known decrease in NF-κB mediated inflammation from ethanol  could be the result of decreased S100A4, -6, -11, and −12 binding to the pro-inflammatory RAGE ([102, 93], Figure 4).
Five calcium binding genes showed increased expression as members of the early response Cluster 2 and immediate early Cluster 3 (Figure 2). Cluster 2 includes TBC1D9, linked to hepatic disease , PDP1, a regulator of pyruvate levels, GALNT7, a member of the O-glycosylation pathway , and the mannose hydrolase MAN1A1. Cluster 3 contains ITGA4, an integrin highly expressed in blood and leukocytes linked to recruitment of leukocytes to sites of inflammation .
It is known that levels of ionized calcium in the blood decrease in the presence of acute ethanol exposure, and in rats, the level and duration of the decrease is correlated with the concentration of ethanol . Decreased calcium would further modulate inflammation through decreased S100 protein oligomerization. It is known that in T-cell activation, ionized calcium regulates entry into the cell cycle through the induction of gene transcription by reversing Rb1 inhibition of E2F factors . We found that E2F factors were linked to Cluster 3 expression (Table 4) suggesting that the known ethanol-dependent reduction of ionized calcium levels  is acting at the transcription level to inhibit, then release entry into the cell-cycle.
NF-κB as central regulator
NF-κB is a central regulator appearing in all but one of the cluster function analyses (Figure 4), indicating a level of co-regulation linking ethanol ingestion to innate immunity and the inflammatory response. Combining temporal expression patterns with direct and indirect molecular interactions defined by pathway analysis, we hypothesize that NF-κB-regulated inflammation is down-regulated early and moderates as blood ethanol levels decrease. The decreasing inflammatory response results from lower levels of S100A proteins and their effect on RAGE induction of NF-κB, and RORA activation of NFKBIA. BMI1 is induced in an immediate early response and may counter the decreased inflammatory response. Evidence for the return to normal levels of NF-κB activity is in the late increase in expression of S100A8 and Cluster 1 genes KLF3, UBE2D3, and PF4V1, and may be a result of increased expression of Cluster 7 gene, HMGB1 (Figure 4) and subsequent activation of RAGE (reviewed in ). Modulating the late increase in NF-κB activity is BAX, another Cluster 1 gene. NF-κB acts as both an enhancer and suppressor in the MHC CII promoter , suggesting NF-κB regulation of the expression spike in the two Cluster 6 MHC CII components.
Signaling pathway membership
BIOBASE is a powerful tool that complements the IPA analysis by looking for conserved transcription factor binding sites in the GOIs and moving upstream to identify significant signaling pathways. Within a 1200 bp window, several transcription factors were found to bind to GOI promoters across more than one cluster. SPI-1, ATF2, and CREB1 are each binding within genes in multiple but not the same clusters, (Table 4A). ATF2 and JUN are both found in Clusters 3 and 4, which have differing expression patterns overall, but share a marked decrease in expression from BAC1 to BAC2. The shared ATF2/CREB binding site is found in Clusters 2 and 3 which have similar expression patterns, especially from BAC2 to BAC5.
The p38 MAPK pathway was identified as a central regulatory pathway for clusters 1, 2, 3, 4, and 5 (Figure 3). These clusters have diverse expression patterns likely reflecting the heterogeneity of cells in whole blood, interactions with various other signaling molecules or transcription factors, and the variability of post-translational modification, none of which can be detected by BIOBASE. The p38-regulated functional categories predicted by BIOBASE include the innate and inflammatory immune responses, ubiquitination, apoptosis, and energy metabolism.
Unique signaling pathways that may modulate p38 MAPK were predicted by BIOBASE within three clusters (Figure 3). GOIs within Cluster 2 contain binding sites for IRF3 and IRF7, which are linked to TLR4 signaling. TLR4 signaling activates the p38 MAPK pathway and is especially sensitive to ethanol exposure, exhibiting a dose-dependent response curve .
Binding sites for ETF2 are found within 12 genes in Cluster 3; these GOIs are involved in ubiquitination and cytokine production. The binding site for LEF/TCF is found within 13 GOIs in Cluster 3, in which are also found binding sites for transcription factors from multiple signaling pathways that regulate hemoglobin biosynthesis and immune response regulation. The apoptosis network regulated through FOXO3 and 4, and MYC binding, in concert with p38 MAPK signaling through ELK1, is unique to Cluster4. Unlinked to p38 MAPK signaling is STAT signaling found in the delayed response Cluster 7 (Table 4B) and known to be up-regulated in response to acute ethanol [19, 26].
Conceptually, markers for ethanol consumption could be of two types, actual BAC, or impairment. Expression patterns of the clustered genes neither positively nor negatively correlate to ethanol concentration; however, two unclustered genes correlate to BAC more closely, CRISPLD2 and NUDT4. These two genes have opposite patterns of expression exhibiting their most extreme variation from baseline to 0.08% BAC and returning to baseline expression at 0.02% BAC, the last collection point in this study and are potentially useful markers for BAC.
For forensic toxicology, impairment is the least understood but most important metric. Here, we have shown that most of our 203 genes do not return to baseline at 0.02% BAC, suggesting that further efforts should concentrate on correlating cognition to expression patterns, thereby capturing the “hangover” effect. Specifically, several genes in Clusters 2 such as PDP1, GNAQ and TGFBR1, and Cluster 5 members like S100A4, -6, and −8 and the three pentose phosphate shunt members TALDO1, TKT and PGLS, exhibit expression patterns consistently increasing or decreasing over the entire experimental time-course, suggesting that they may return to baseline as cognition recovers. Further effort to determine at what cognitive level they returned to baseline would be informative. Likewise, the delayed response genes in Cluster 7 (Figure 2) may be indicative of cognitive impairment.
We determined patterns of gene expression related to acute exposure to ethanol. Our analysis suggests that we could detect significant gene expression changes related to imbibed ethanol using RNA isolated from blood. We found that members of each cluster were linked by common biological processes, signaling pathways, and functions including:
– protein synthesis and modification
– hematological and immune functions, especially innate immunity
– p38 MAPK and NF-κB signaling
central metabolism and small molecule metabolism
Additionally, our findings support the workflow described here for selecting candidate biomarker genes for future studies. Those studies would correlate performance limitations to ETOH-dependent gene expression patterns and, using currently available toxicological tests to monitor BAC, must extend beyond the breathalyzer limit of detection of 0.02%, to capture cognitive “hangover effects”. A gene expression-based test for ingested ethanol would provide additional sensitivity in those forensic instances where standard toxicological tests cannot discriminate between ingestion and post-mortem ethanol sources. We further expect that understanding gene expression changes and their correlation to human performance metrics will facilitate modification of flight regulations based on increased understanding of ethanol’s impact on performance independent of blood alcohol concentration.
Blood alcohol concentration
Civil aerospace medical institute
Driving while intoxicated
Grams per liter
Grams per deciliter
Gene of interest
Genes of interest
Orange juice control
Quantitative polymerase chain reaction
Reactive oxygen species
RNA integrity number
Transcription factor binding site.
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The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1755-8794/6/26/prepub
The authors declare that they have no competing interests.
DMK performed qRT-PCR, and carried out analysis of GOIs. VW collected blood samples, performed RNA isolation and microarray hybridization. DLS and DC recruited subjects and collected blood samples. DB recruited subjects, performed informatics analysis, and supervised the study. DMK and DB wrote and reviewed the manuscript. All authors read and approved the final manuscript.
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Kupfer, D.M., White, V.L., Strayer, D.L. et al. Microarray characterization of gene expression changes in blood during acute ethanol exposure. BMC Med Genomics 6, 26 (2013). https://doi.org/10.1186/1755-8794-6-26
- Gene expression