Transcriptional response to alcohol exposure in Drosophila melanogaster
© Morozova et al.; licensee BioMed Central Ltd. 2006
Received: 5 June 2006
Accepted: 20 October 2006
Published: 20 October 2006
Alcoholism presents widespread social and human health problems. Alcohol sensitivity, the development of tolerance to alcohol and susceptibility to addiction vary in the population. Genetic factors that predispose to alcoholism remain largely unknown due to extensive genetic and environmental variation in human populations. Drosophila, however, allows studies on genetically identical individuals in controlled environments. Although addiction to alcohol has not been demonstrated in Drosophila, flies show responses to alcohol exposure that resemble human intoxication, including hyperactivity, loss of postural control, sedation, and exposure-dependent development of tolerance.
We assessed whole-genome transcriptional responses following alcohol exposure and demonstrate immediate down-regulation of genes affecting olfaction, rapid upregulation of biotransformation enzymes and, concomitant with development of tolerance, altered transcription of transcriptional regulators, proteases and metabolic enzymes, including biotransformation enzymes and enzymes associated with fatty acid biosynthesis. Functional tests of P-element disrupted alleles corresponding to genes with altered transcription implicated 75% of these in the response to alcohol, two-thirds of which have human orthologues.
Expression microarray analysis is an efficient method for identifying candidate genes affecting complex behavioral and physiological traits, including alcohol abuse. Drosophila provides a valuable genetic model for comparative genomic analysis, which can inform subsequent studies in human populations. Transcriptional analyses following alcohol exposure in Drosophila implicate biotransformation pathways, transcriptional regulators, proteolysis and enzymes that act as metabolic switches in the regulation of fatty acid metabolism as important targets for future studies of the physiological consequences of human alcohol abuse.
The National Institute on Alcohol Abuse and Alcoholism has estimated that approximately 14 million people in the United States suffer from alcoholism . Genetic studies have demonstrated that the propensity for alcohol abuse is determined by multiple genes. Thus, vulnerability to alcohol abuse shows all the hallmarks of a quantitative trait, as it is polygenic and subject to genotype by environment interactions. Efforts to map chromosomal regions (quantitative trait loci (QTL)) that harbor genes responsible for alcohol-related traits have identified at least 24 QTL regions in the mouse genome . Although candidate genes have been identified within such QTL regions, including the multiple PDZ domain protein Mpdz on chromosome 4 , conclusive evidence that links candidate genes within QTL regions directly to the phenotype is often difficult to obtain. Quantitatively measuring alcohol dependence without confounding contributions of other psychiatric or social disorders is challenging with human subjects, although studies in ethnically defined populations have implicated alcohol dehydrogenase , the GABAA receptor complex , and the serotonin 1B receptor in alcohol sensitivity [6, 7].
Flies are naturally exposed to ethanol, as they feed on fermented food. Exposing flies to low concentrations of ethanol stimulates locomotor activity, whereas high concentrations of ethanol induce an intoxicated phenotype that shows marked similarities to human alcohol intoxication, characterized by locomotor impairments, loss of postural control, sedation [8, 9] and exposure-dependent development of tolerance . Alcohol sensitivity in Drosophila melanogaster can be quantified in an 'inebriometer', a 122 cm long vertical glass column, which contains a series of slanted mesh partitions to which flies can attach . Flies are introduced in the top of the column and exposed to ethanol vapors. As they lose postural control they fall through the column. The elution time from the column is used as a measure of sensitivity to alcohol intoxication. Following an initial exposure to alcohol, flies develop tolerance, manifested upon a second exposure by a shift in the elution profile . Tolerance peaks within hours after exposure and persists up to 24 hours in some individuals .
Here, we exploited the power of the Drosophila system to evaluate whole-genome transcriptional profiles that reflect alterations in gene expression upon exposure to alcohol and during development of tolerance, to gain insights into the underlying cellular and physiological mechanisms that respond to alcohol exposure. We then evaluated alcohol sensitivity and the development of tolerance in flies with mutations in 20 genes that were implicated by the analysis of differential transcript abundance, and identified 15 novel candidate genes affecting alcohol related phenotypes, 10 of which have human orthologues. Thus, whole genome transcriptional analysis following alcohol exposure in Drosophila can identify candidate genes and metabolic pathways that are relevant to alcohol abuse and its physiological consequences in people.
Results and discussion
We collected flies either without exposure to ethanol, immediately after exposure to ethanol and passage through the inebriometer, or from a population that had developed tolerance two hours after the initial ethanol exposure (Figure 1b). We used 5 independent replicates of 30 3- to 5-day old males for each time point and generated cRNA for hybridization to high density oligonucleotide microarrays. Raw microarray data are given in Additional data file 1.
Probe sets with altered transcriptional regulation after ethanol exposure with q < 0.001
Probe set ID
Changes in expression
Transmission of nerve impulse; carbohydrate metabolism
Toll signaling pathway; defense response
Lipid metabolism; neurotransmitter secretion; transport
Olfactory behavior;response to chemical stimulus
Amino acid transport, metabolism
Negative regulation of transcription, DNA-dependent
Fatty acid biosynthesis; very-long-chain fatty acid metabolism
Ecdysone-inducible gene L2 (M,H)*
Long-term memory; circadian rhythm; signal transduction; negative regulation of transcription from RNA polymerase II promoter
Regulation of transcription from RNA polymerase II promoter; JNK cascade; autophagic cell death
Odorant-binding protein 99d
Transport; autophagic cell death
Extracellular transport; cation transport
Response to toxin; extracellular transport; defense response
antennal protein 10 (M,H)*
Sensory perception of chemical stimulus
antennal protein 5
Electron transport; steroid metabolism; lauric acid metabolism
Response to ethanol; sensory perception of smell; olfactory behavior
Regulation of transcription from RNA polymerase II promoter; determination of adult life span; gene silencing
Transmission of nerve impulse; cell adhesion
Pheromone-binding protein-related protein 1 (M)*
Signal transduction; sensory perception; response to pheromone
Signal transduction; response to pheromone; transport
Lipid transport; cell acyl-CoA homeostasis
Actin filament organization; bristle morphogenesis
Phosphate metabolism; extracellular transport; cation transport
We categorized the 582 significant probe sets as 'acutely' up- or down-regulated if transcript levels show sustained altered expression after the first exposure to ethanol; 'slowly' up-or down-regulated if transcript abundance only changes after the second exposure to alcohol; and 'transiently' up- or down-regulated if transcript levels are altered following the first exposure to ethanol, but are not sustained during the development of tolerance. We found 78 genes that show acute down-regulation and 77 genes that show acute up-regulation, In addition, 104 genes are slowly down-regulated, 258 genes are slowly up-regulated, 33 genes are transiently down-regulated, and 32 genes are transiently up-regulated.
Probe sets were annotated and compiled in Gene Ontology categories using Affymetrix software  and the FlyBase data base [15, 16] (Additional data files 3 and 4). Gene Ontology categories that are significantly more abundant among the probe sets than expected by chance include genes associated with olfactory function, which are acutely down-regulated, regulators of signal transduction, which are acutely up-regulated, metabolic enzymes, including peptidases, hydrolases and pigmentation genes, which are slowly down-regulated, and transcriptional regulators and circadian genes, which are slowly up-regulated (Additional data files 3 and 4). It is possible that the slow up-regulation of genes affecting circadian rhythm could be attributable to the two hour difference in sampling the control animals and those tested for tolerance.
Expression of a suite of genes associated with odor recognition is acutely down-regulated, including genes that encode the odorant binding proteins lush, Obp19a, Pbprp1-5, the odorant receptor Or67d, and the ubiquitous odorant receptor Or83b, which is necessary for transport and insertion of odorant receptors in the chemosensory dendritic membranes of olfactory neurons  (Table 1 and Additional data file 2). Olfactory specific protein E and antennal proteins 5 and 10 are also acutely down-regulated (Table 1). This pattern of altered transcript abundance reflects acute down-regulation of olfactory function upon exposure to undiluted ethanol vapor. Expression of two olfactory proteins is up-regulated: Obp99d is slowly up-regulated and Pinocchio, a gene that encodes a protein implicated in removal of xenobiotics from the sensillar perilymph , is transiently up-regulated upon exposure to ethanol (Table 1). In addition, biotransformation enzymes, including those encoded by Cyp6a2 and Cyp6a13, and glutathione-S-transferase D5, are acutely up-regulated. Since Pinocchio is extensively expressed throughout the third antennal segment , it is unlikely that the observed reduction in expression of the subset of odorant binding proteins and odorant receptors is due to ethanol induced tissue damage.
Immediate up-regulation is also observed for transcripts involved in response to stress, including l(2)efl, Mpk2 and Hsp70Ab. Several transcriptional regulators are rapidly up-regulated, including cabut, Aly and Drop along with transcripts involved in protein ubiquitination (mib1, CG11414, CG40045 and TSG101). CG1516, which is orthologous to human pyruvate carboxylase is also acutely up-regulated after ethanol exposure (Additional data file 2).
During the two hour period in which tolerance culminates we observe modulation of transcription of a different set of genes. Sixteen genes that encode proteases are down-regulated along with six genes associated with lipid transport and fatty acid metabolism, including bubblegum, NLaz and Hmgs. Two biotransformation enzymes, encoded by Cyp12e1 and Cyp4ac1, are also down-regulated, as is the transcriptional regulator Sir2.
At the same time there is an extensive increase in expression of transcriptional regulators, proteases and metabolic enzymes. Nineteen transcription factors, eleven proteases and thirty enzymes associated with metabolism, including signal transduction components (protein kinase C δ, rdgA, G protein subunit γ1, fz2), enzymes associated with fatty acid biosynthesis and intermediary metabolism (for example, malic enzyme), and biotransformation enzymes (encoded by Cyp6a8, Cyp4e3, Cyp309a1, GstD1, GstE5, GstE7) are up-regulated (Additional data file 2). Thus, a single exposure to ethanol has the potential to elicit profound changes in the protein composition of the cell through altered transcriptional regulation and proteolysis aimed at rapidly adapting cellular metabolism to the consequences of alcohol intoxication.
Forty-six genes with altered transcript abundance on our microarrays correspond to murine orthologues implicated in altered transcriptional regulation in a recent meta-analysis study of alcohol drinking preference in mice  (Additional data file 2). Furthermore, several of the genes with changes in transcript levels have been associated previously with responses to alcohol exposure, including lush, which encodes a Drosophila odorant binding protein that interacts with short chain alcohols  and the contact pheromone cis-vaccenyl acetate , NLaz, which encodes an orthologue of human apolipoprotein D, which is preferentially expressed in prefrontal cortex of alcoholics , and period, a regulator of circadian activity that has been associated with alcohol consumption in mice and humans . In addition, Sorbitol dehydrogenase 2, CG1600 and v(2)k05816, which harbor alcohol dehydrogenase activity (Additional data file 2), also show altered transcript levels.
Mutant analysis has implicated a handful of other genes in sensitivity to ethanol. These include the cheapdate allele of amnesiac , which encodes a neuropeptide thought to activate the cyclic AMP signaling pathway ; the calcium/calmodulin-dependent adenylate cyclase encoded by the rutabaga (rut) gene ; the axonal migration and cell adhesion receptor, fasciclin II (Fas2) ; PkaR2, which encodes a cyclic AMP-dependent protein kinase ; the gene encoding the GABA-B receptor 1 ; and the genes encoding the Drosophila neuropeptide F (npf, a homolog of the mammalian neuropeptide Y) and its receptor . In addition, heat stress has been found to induce tolerance to a subsequent exposure to ethanol and implicated a nucleic acid binding zinc finger protein encoded by the hangover (hang) gene in both the response to heat stress and the induction of ethanol tolerance . Induction of ethanol tolerance was completely abolished in flies carrying both null mutations in hang and in the gene encoding tyramine β-hydroxylase (Tbh), which suggested that hang and the neurotransmitter octopamine mediate separate pathways involved in the induction of ethanol tolerance . Further, mutations in slowpoke, which encodes a large-conductance calcium-activated potassium channel, eliminate the capacity for rapid tolerance, defined as reduction of the duration of sedation on a second exposure to ethanol [31, 32].
However, none of these genes exhibited significant alterations in transcript abundance following one or two exposures to ethanol in this study, at our false discovery rate threshold of q < 0.05. Several factors could account for this discrepancy. First, the genes may have low levels of expression in adult flies, such as amnesiac and GABA-B-1, which had absent calls and were consequently not included in the analysis. Second, the magnitude of the differences in expression may have been too small to be detected with our experimental design. Fas2, Pka-R2, rut, npf, hang and Tbh all exhibited changes in transcript abundance on exposure to ethanol, but the mean differences between treatments were not large enough to be significant. Third, differences in the definition of tolerance may be relevant. slowpoke expression in the nervous system is required for tolerance defined as reduced sedation on a second exposure to ethanol four hours after the initial exposure [31, 32] but the effects of reduced slowpoke expression have not been tested in our paradigm. Fourth, the mutational effects may be due to post-transcriptional regulation. Nevertheless, our results point at modulation of a complex genetic network upon alcohol exposure, in contrast to a simple linear model of two distinct and independent cellular pathways .
P[GT1]-element insertion lines with transposon insertions at genes with ethanol-dependent altered transcriptional regulation
P-element insertion site
Canton S* background
Mean elution time (min)† (1st exposure)
Time shift (between 1st and 2nd exposures)
In 1st intron
6.7 ± 0.25
2 min‡ ↑
410 bp in exon 1
Regulation of transcription, DNA-dependent; chromatin silencing
5.0 ± 0.2
2 min§ ↓
In 1st intron
Fatty acid metabolism
6.2 ± 0.21
0.5 min (NS) ↓
125 bp upstream of transcription initiation site of the longest transcript
Pyruvate metabolism; fatty acid biosynthesis
4.2 ± 0.12
1 min (NS) ↑
431 bp upstream of transcription initiation site
Negative regulation of translational initiation; response to stress; defense response
7.5 ± 0.11; R
2.5 min§ ↑
Pyruvate dehydrogenase kinase H
47 bp in exon 1
Pyruvate metabolism; tricarboxylic acid cycle; regulation of phosphate metabolism
7.4 ± 0.30; R
1 min‡ ↑
281 bp upstream of transcription initiation site
Fatty acid biosynthesis
6.1 ± 0.25
1 min (NS) ↑
elbow B H
888 bp upstream of transcription initiation site
Tracheal system development
6.8 ± 0.26
0.5 min (NS) ↓
Hormone receptor-like in 38
1,428 kb upstream of transcription initiation site
Regulation of transcription from RNA polymerase II promoter; intracellular signaling cascade
5.8 ± 0.22; S
1 min (NS) ↓
nuclear fallout H
In 4th intron
Actin cytoskeleton reorganization; microtubule-based process
6.6 ± 0.30
1 min (NS) ↓
136 bp upstream of transcription initiation site
4.8 ± 0.18
1.5 min‡ ↓
219 bp in exon 1 of the longest transcript
Regulation of transcription from RNA polymerase II promoter; peripheral nervous system development
5.8 ± 0.20
1 min§ ↑
50 bp in exon 1
6.1 ± 0.18
1.5 min§ ↓
In 1st intron
Nucleotide biosynthesis, metabolism
7.0 ± 0.16; R
0.5 min (NS) ↑
36 bp upstream of transcription initiation site
6.1 ± 0.26
2 min§ ↓
frizzled 2 H
147 bp in exon 1
Signal transduction; G-protein coupled receptor protein signaling pathway
5.9 ± 0.13; R
2 min§ ↑
Malic enzyme H
In 1st intron
Malate metabolism; tricarboxylic acid cycle
6.4 ± 0.15; R
6 min¶ ↑
73 bp in exon 1
7.6 ± 0.12; R
3.5 min§ ↑
spalt major H
154 bp upstream of transcription initiation site
Tracheal system development; sensory organ development; negative regulation of transcription
6.9 ± 0.18; R
0.5 min (NS) ↓
In 1st intron
Transmission of nerve impulse; regulation of transcription from RNA polymerase II promoter
6.1 ± 0.11; R
3 min§ ↑
In total, 15 P-element insertion lines (75%) show altered responsiveness to ethanol exposure compared to controls (Table 2); 6 of these lines had mutational effects on both initial response and tolerance; 6 affected only tolerance, and 3 affected only the initial response. This percentage is similar to a previous study in which 67% of co-regulated genes identified on expression microarrays of single P-element insert smell impaired mutations could be implicated in an epistatic network that mediates olfactory avoidance behavior . Thus, expression microarray analysis is an efficient method for identifying candidate genes affecting complex behavioral and physiological traits.
Among the 15 P-element  insertion lines that tag genes with differences in transcript abundance on exposure to ethanol, 10 have human orthologues (Table 2), including 5 enzymes associated with intermediary metabolism and fatty acid biosynthesis (CG1516, Pyruvate dehydrogenase kinase, Malic enzyme, bubblegum and v(2)k05816 with corresponding human orthologues pyruvate carboxylase (PC), Pyruvate dehydrogenase kinase, isoenzyme 3 (PDK3), Malic enzyme 1, NADP(+)-dependent (ME1), bubblegum related protein (BGR), and fatty acid synthase (FASN)), three transcription factors (elbow B, spalt major and frizzled 2 with corresponding human orthologues zinc finger protein 503 (ZNF503), sal-like1 (SALL1) and frizzled homolog 8 (FZD8)), CG9086 (with human orthologue Ubiquitin protein ligase E3 component n-recognin 2 (UBR2)), and nuclear fallout (with human orthologue RAB11 family interacting protein 4 (RAB11FIP4)).
Drosophila provides a powerful model for the identification of genes that respond to alcohol exposure. Dependent on their genetic background, flies can develop tolerance after an initial exposure, and transcriptional profiling shows that the development of tolerance is a process that is at least partially independent from initial sensitivity to alcohol. A significant fraction of genes implicated in the response to alcohol in flies have human orthologues and form part of conserved cellular and metabolic pathways. Whereas most studies on alcoholism in human populations have targeted genes associated with neurotransmission, our findings from the Drosophila model suggest that it might be fruitful to refocus some of these efforts on other targets, including (but not limited to) biotransformation pathways, transcriptional regulators, proteolysis and enzymes that act as metabolic switches in the regulation of fatty acid metabolism.
Materials and methods
Flies used for microarray experiments were in an isogenic Canton-S B genetic background. Homozygous P-element insertion lines contained P(GT1)-elements  in or near candidate genes in co-isogenic Canton S A, B, C, E or F backgrounds and were generated by Dr Hugo Bellen (Baylor College of Medicine, Houston, TX, USA) as part of the Berkeley Drosophila Genome Project . Behavioral assays were conducted between 9:00 am and 1:00 pm. Flies were not exposed to CO2 anesthesia for at least 24 h prior to the assay. All flies were reared on cornmeal/molasses/agar medium under standard culture conditions (25°C, 12:12 hour light/dark cycle).
Alcohol sensitivity and tolerance
To quantify alcohol sensitivity, we tested flies (5 replicates/genotype, N = 100/replicate) in an inebriometer  pre-equilibrated with ethanol vapor, from which they were eluted at one minute intervals. The mean elution time is a measure of alcohol sensitivity. To measure alcohol tolerance , we subjected flies to an initial exposure to ethanol, and recorded their elution profile as described above. We allowed the flies to recover for 2 h, and then repeated the assay with the same flies. The difference in the shift of modal elution times (5 replicates/genotype, N = 100/replicate) between the second and first assays is a measure of tolerance. We used analysis of variance to assess whether the sensitivity of P-element insertion lines differed significantly from the control, according to the model:
Y = μ + L + R(L) + ε
where μ is the overall mean, L is the fixed effect of line (P-element insertion versus control), R is the random effect of replicate, nested within line, and ε is the variance within replicates. We used t-tests to assess the significance of the difference in modal elution times between the first and second exposures.
Whole genome expression analysis
To assess transcriptional regulation after ethanol exposure, we used 3 to 5 day old Canton-S B males. We collected five replicates of pools of 30 flies with 0, 1 or 2 exposures to ethanol. For each replicate, we began with two groups of >100 flies. A total of 15 flies from each group was not exposed to ethanol (control flies; Figure 1b) and were pooled and frozen immediately on dry ice. We passed the remaining flies from each group through the inebriometer, and collected individuals that eluted at 3 to 5 minutes (the peak elution time for the first exposure; Figure 1b). A total of 15 of these flies from each group was pooled and frozen immediately on dry ice. The remaining flies were kept on standard fly food for 2 h. They were then passed once again through the inebriometer in 2 groups, and 15 flies from each group that eluted at 7 to 10 minutes (the peak elution time for the 2nd exposure; Figure 1b) were collected, pooled, and frozen.
Total RNA was extracted from the 15 samples (three treatments × five replicates/treatment) using the Trizol reagent (Gibco BRL, Gaithersburg MD, USA). Biotinylated cRNA probes were hybridized to high density oligonucleotide microarrays (Drosophila GeneChip 2.0, Affymetrix Inc., Santa Clara, CA, USA) and visualized with a streptavidin-phycoerythrin conjugate, as described in the Affymetrix GeneChip Expression Analysis Technical Manual (2000), using internal references for quantification.
The quantitative estimate of expression of each probe set is the Signal (Sig) metric, as described in the Affymetrix Microarray Suite, Version 5.0. The 18,769 probe sets on the Affymetrix Drosophila GeneChip 2.0 are represented by 14 perfect-match (PM) and 14 mismatch (MM) pairs. The Sig metric is computed using the weighted log(PM-MM) intensity for each probe set, and was scaled to a median intensity of 500. A detection call of Present, Absent, or Marginal is also reported for each probe set. We excluded all probe sets with samples called 'Absent' from the analysis. On the remaining probe sets, we conducted one-way fixed effect ANOVAs of the Signal metric using the GLM procedure in SAS , with the following model:
Y = μ + T + ε
where Y is the observed value for each treatment, μ is the overall mean value, T is the fixed effect of treatment and ε is the error variance between replicate arrays. We corrected the p values for multiple tests by calculating the false positive discovery rate q-value, which estimates the proportion of false positives among all terms declared significant  and used a confidence level of q < 0.05 as measure of statistical significance. We identified 582 probe sets with altered transcriptional regulation at q < 0.05 (Additional data file 2) and performed further analysis by post hoc Tukey tests using the MEANS procedure in SAS  to identify the direction (up- or down-regulation) of expression between treatment groups (control, 1st exposure, and 2nd exposure) at the p < 0.05 level. Gene ontology categories were annotated using Affymetrix  and FlyBase [15, 16] compilations. We conducted χ2 tests to determine which categories are over- or under-represented by probe sets that are significantly up- or down-regulated between treatment groups compared to the expected number of genes in each category based on its representation on the microarray (Additional data files 3 and 4). The microarray data discussed in this publication have been deposited in NCBIs Gene Expression Omnibus  and are accessible through GEO Series number GSE5382 .
Additional data files
The following additional data are available with the online version of this paper. Additional data file 1 contains raw microarray data without any analysis. Additional data file 2 is a list of all probe sets differentially expressed between treatment groups with q < 0.05. Additional data file 3 contains biological process gene ontology categories of the genes listed in Additional data file 2. Additional data file 4 contains molecular function gene ontology categories of genes listed in Additional data file 2. Additional data file 5 lists information regarding influences of different genetic backgrounds on ethanol sensitivity and tolerance development.
We thank RF Lyman for advice with data analysis. This work was supported by grants from the National Institutes of Health (to RRHA and TFCM). This is a publication of the WM Keck Center for Behavioral Biology.
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