- Research article
- Open Access
Systems genetics analysis of body weight and energy metabolism traits in Drosophila melanogaster
© Jumbo-Lucioni et al; licensee BioMed Central Ltd. 2010
- Received: 9 January 2010
- Accepted: 11 May 2010
- Published: 11 May 2010
Obesity and phenotypic traits associated with this condition exhibit significant heritability in natural populations of most organisms. While a number of genes and genetic pathways have been implicated to play a role in obesity associated traits, the genetic architecture that underlies the natural variation in these traits is largely unknown. Here, we used 40 wild-derived inbred lines of Drosophila melanogaster to quantify genetic variation in body weight, the content of three major metabolites (glycogen, triacylglycerol, and glycerol) associated with obesity, and metabolic rate in young flies. We chose these lines because they were previously screened for variation in whole-genome transcript abundance and in several adult life-history traits, including longevity, resistance to starvation stress, chill-coma recovery, mating behavior, and competitive fitness. This enabled us not only to identify candidate genes and transcriptional networks that might explain variation for energy metabolism traits, but also to investigate the genetic interrelationships among energy metabolism, behavioral, and life-history traits that have evolved in natural populations.
We found significant genetically based variation in all traits. Using a genome-wide association screen for single feature polymorphisms and quantitative trait transcripts, we identified 337, 211, 237, 553, and 152 novel candidate genes associated with body weight, glycogen content, triacylglycerol storage, glycerol levels, and metabolic rate, respectively. Weighted gene co-expression analyses grouped transcripts associated with each trait in significant modules of co-expressed genes and we interpreted these modules in terms of their gene enrichment based on Gene Ontology analysis. Comparison of gene co-expression modules for traits in this study with previously determined modules for life-history traits identified significant modular pleiotropy between glycogen content, body weight, competitive fitness, and starvation resistance.
Combining a large phenotypic dataset with information on variation in genome wide transcriptional profiles has provided insight into the complex genetic architecture underlying natural variation in traits that have been associated with obesity. Our findings suggest that understanding the maintenance of genetic variation in metabolic traits in natural populations may require that we understand more fully the degree to which these traits are genetically correlated with other traits, especially those directly affecting fitness.
- Genetic Correlation
- Isofemale Line
- Gene Ontology Category
- Starvation Resistance
- Quantitative Genetic Analysis
Obesity is a condition characterized by an excess of adipose tissue that adversely affects human health . The clinical problem of excessive adipose tissue resides in its strong association with a number of chronic diseases, such as insulin resistance, type 2 diabetes mellitus (T2DM), coronary artery disease and stroke . In 2003-2004, 32.2% of the adults in the United States were obese . This estimate represents a significant increase in obesity prevalence over the past 20 years, and similar trends are being observed worldwide . As the rise in the incidence of obesity and related health problems continues, there is a considerable need to gain a better understanding of the etiology of obesity.
In humans, large twin, adoption, and family studies have firmly established that obesity-related traits, such as body mass index and measures of body composition (e.g., fat mass, lean mass, and percentage fat mass), are highly heritable [4–6]. Segregating variation in obesity-related traits has also been observed in natural populations of most other organisms, including invertebrates [7–9]. The general conclusion from these studies is that the genetic architecture of these traits is complex and affected by many loci, with numerous gene-by-gene interactions (e.g. epistasis) and extensive genotype-by-environment interactions reported in a diverse group of organisms [10–13]. In light of this complexity a growing body of research in humans and animal models has begun to take a more systems genetic approach with focus on identifying genetic networks that control body composition and energy metabolism traits [14–16]. Preliminary findings of such studies suggest an intricate interplay between body weight control, stress, and immune response [14, 15]. They also highlight a need for studying energy metabolism traits within a broader organismal context, integrating information on variation in traits influencing energy metabolism with information on variation in life history and other energetically demanding traits. This knowledge could help to explain the origin of trade-offs among these traits in natural populations. Organisms partition dietary resources acquired from the environment among the competing demands of growth, development, reproduction, maintenance and storage . Since these resources are limited, the way in which they are acquired and partitioned is critical to the fitness of the individual and often result in trade-offs between energetically demanding physiological functions . There is extensive empirical data on biochemical and physiological correlates of life-history variation and trade-offs within species [18, 19]. Yet little is known about genes and genetic networks responsible for generating correlations between energy metabolism and life history traits in natural populations . Such knowledge is not only important for understanding many central issues in life-history evolution , but could also elucidate the genetic basis of natural variation in human obesity.
In the present study we quantified genetic variation in wet body weight (BW), the content of three metabolites [glycogen (GLY), triacylglycerol (TAG), and glycerol (GLYC)], and metabolic rate (MR) in 40 wild-derived lines of D. melanogaster. We chose D. melanogaster as a model system because many of the genetic mechanisms controlling lipid metabolism and energy homeostasis are evolutionarily conserved between invertebrates and mammals (reviewed in [20–22]). Thus, insights about the genetics of body weight and energy metabolism gained from Drosophila may also apply to mammals. Additionally, D. melanogaster has long been a model for understanding the genetic basis of life history variation [17, 23–25]. The Drosophila lines used in this study were previously evaluated for several ecologically relevant traits, including longevity, resistance to starvation stress, chill-coma recovery, mating behavior, and competitive fitness, as well as for transcript abundance . This provided us with the opportunity to gain invaluable insights into the molecular mechanisms underlying the interrelationships among energy metabolism, behavioral, and life-history traits that have evolved in natural populations.
Natural variation in body weight and energy metabolism traits
Candidate genes for body weight and energy metabolism traits
Previously, we assessed variation in gene expression profiles among these wild-derived lines of D. melanogaster and identified 3,136 probes containing single feature polymorphisms (SFPs) and a total of 10,096 quantitative trait transcripts (QTTs) . To identify candidate genes that might regulate variability in each of the traits quantified in this study, we performed a genome-wide association screen to search for significant associations between SFPs or QTTs with each trait . At a P-value of 0.01, we found 93, 98, 131, 213, and 71 SFPs (see Additional file 2A: List of SFPs significantly correlated with body weight and energy metabolism traits) associated with BW, GLY, TAG, GLYC, and MR, respectively, in the analysis averaged across sexes. Because some genes were represented by 2 or more different SFPs, this analysis identified 65 independent genes for BW, 81 for GLY, 115 for TAG, 176 for GLYC, and 61 for MR. Given 3,136 SFPs, only 31 significant associations would be expected by chance at a P value of 0.01, thus the number of SFPs associated with each trait exceeded that expected by chance.
Based on the results of the quantitative genetic analyses described above, we also tested for association between SFPs and each trait using the data stratified by sex. The stratified analysis detected a reduced number of significant associations at a P-value of 0.01 (see Additional file 2B: List of SFPs significantly correlated with body weight and energy metabolism traits). The majority of these associations overlapped those identified by the analysis that used the average trait values across sexes for BW, GLYC, and TAG. However, several SFPs with sex-specific effects were detected for GLY and MR and this agrees with the moderate cross-sex correlations we observed for these traits reported above.
Our regression analyses identified 275, 130, 125, 389, and 93 QTTs significantly associated with variation in BW, GLY, TAG, GLYC, and MR, respectively, at a P value of 0.01 (see Additional file 3: List of transcripts significantly correlated with body weight and energy metabolism traits). In this case the number of transcripts associated with MR did not exceed chance expectation (100 significant associations would be expected); however the QTTs grouped into biologically meaningful modules as detailed below. Only few QTTs were also found as candidate genes by the SFP analyses.
We selected six candidate genes for TAG: rutabaga (rut), dead-box-1 (Ddx1), sugarless (sgl), Sirt7, RhoGAP71E, and GXIVsPLA. We found that four of the mutant alleles showed a significant difference in TAG compared to the control (see Additional file 4: Results of the screen of P-element insert lines for alterations in energy metabolites). While flies with a mutation in rut have more TAG than the control strain, flies with mutations in sgl, Sirt7, and GXIVsPLA have all less TAG than the controls (Figure 2B). rut encodes a Ca2+/calmodulin-responsive adenylyl cyclase that is involved in learning and memory  and also has a role in food choice behavior . Sgl encodes a homolog of mammalian UDP-glucose dehydrogenase, which is implicated in proteoglycan synthesis . P-element insertions within the sgl coding region have been previously reported to significantly impact fly energy stores . Sirt7 is a member of the Sirtuins or Sir2 (silent information regulator 2) histone deacetylase enzyme family, which has been shown to play a role in energy homeostasis and lifespan . Finally, GXIVsPLA2 encodes an enzyme involved in phospholipid metabolism .
We selected six candidate genes for GLYC: b4GalNAcTA, CG5946, CG8920, Gliotactin (gli), Glutamate dehydrogenase (Gdh), and tweety (tty). We found that four of the mutant alleles showed a significant difference in GLYC compared to the control (see Additional file 4: Results of the screen of P-element insert lines for alterations in energy metabolites). Flies with mutations in all four genes have more GLYC than the control strain (Figure 2C). CG8920 is predicted to encode a protein belonging to the Tudor domain family , which binds to RNA and single-strand DNA-associated complexes in the nucleus . Gdh encodes a nuclear-encoded mitochondrial enzyme with a role in utilization of metabolite pools for energy production . gli encodes a transmembrane protein transiently expressed in peripheral glia whose loss of function has been implicated in defects in axonal guidance and synaptogenesis . Finally, tty encodes a highly conserved calcium-activated chloride channel associated to flight behavioral abnormalities .
Together with our expression data, the findings using mutant and control stocks imply that the genes described above are candidates in the control of energy metabolites and motivate future studies to elucidate the mechanisms by which they influence metabolism.
Transcriptional networks associated with body weight and energy metabolism traits
We identified 13 modules of correlated transcripts associated with BW, ranging from 2 to 97 probe sets (see Additional file 5: Modules of correlated transcripts associated with body weight and energy metabolism traits). We used the EASE (Expression Analysis Systematic Explorer) analysis implemented in DAVID functional annotation tool http://david.niaid.nih.gov/david/ease.htm[41, 42] to analyze the candidate genes contained within each module for functional enrichment. Additional file 6 (see Additional file 6: Over-representation of Gene Ontology Categories, KEGG Pathways and Keywords for transcripts associated with body weight and energy metabolism traits) reports significant Gene Ontology categories. Two interesting patterns emerged from our analysis. First, after correction for multiple comparisons, we found that module 1 (P = 2.2E-2), module 2 (P = 2.3E-7), and module 13 (P = 1.2E-4) were enriched for genes involved in defense response categories. These results add to previous findings from systems genetics studies in mice showing that genes involved in immune function are involved in body weight regulation . Evidence for this link is also found in the evolutionarily conserved role that the Toll signaling pathway plays in mediating the insulin/insulin-like growth factor (IGF) signaling. Activation of the Toll-like receptors by adipose-derived inflammatory signals, such as free fatty acids and tumor necrosis factor-α, is critical in the development of systemic insulin resistance in obese rodents and humans . Recently, Diangelo et al.  reported that the activation of the immune Toll signaling pathway selectively in the fat body of D. melanogaster also suppresses insulin/IGF signaling leading to a decrease in both nutrient stores and growth. A major difference between flies and mammals is that while the effects on the insulin signaling in the latter are mediated by the c-Jun NH2 terminal kinase (JNK) branch of the mitogen-activated protein (MAPK) kinase signaling , this appears to not be the case in flies . Yet, JNK is a potent antagonist of insulin/IGF signaling in both Drosophila and mammals  and is required for the immune response to gram negative bacteria in Drosophila .
The second pattern observed in our analysis is that module 10 was enriched in genes involved in cell communication (P = 6.9E-7) and signal transduction (P = 2.5E-6) and two of its hub genes, g protein γ 1 (Ggamma1) and klingon (klg) (Figure 3B), are known to be involved in neuronal development [47, 48]. Tissue-specific expression patterns, based on data from FlyAtlas , showed that transcripts in this module are enriched in the adult brain, head, and the thoracicoabdominal ganglion, as well as in the larval central nervous system (CNS) (Figure 3C). Collectively, these findings suggest that the CNS plays a major part in regulating variation in BW in D. melanogaster. This is consistent with earlier reports on the genetic basis of rare monogenic forms of obesity in humans  and single-gene approaches in mammalian models [51, 52], which have long suggested involvement of the CNS in the regulation of mammalian body weight . Furthermore, recent genome-wide association studies (GWAS) in humans have mapped body weight-associated loci near genes that are highly expressed in the brain, particularly in the hypothalamus, and are involved in neuronal development and activity . Our results also corroborate emerging evidence showing that, as in mammals, the CNS of Drosophila integrates information regarding nutrient status and stores with visual, olfactory, and taste stimuli to elicit appropriate feeding behavior responses [22, 55–57]. For example, the hugin neuronal circuit modulates feeding behavior by interconnecting the gustatory sensillae to the protocerebrum, the ventral nerve cord, the ring gland, and the pharynx via the subesophageal ganglion . Consistent with this finding, we identified the hugin (hug) gene as a candidate regulating variation in BW among the Drosophila Raleigh lines. We also found that hug transcript abundance is highly correlated with Activating transcription factor-2 (Atf-2), which encodes a member of the ATF/cAMP response element-binding protein family of transcription factors and has been shown to regulate fat metabolism in the fat body , the fly equivalent of mammalian adipose/liver tissue.
We identified 9 modules of correlated transcripts associated with GLY, ranging from 2 to 80 probe sets (see Additional file 5: Modules of correlated transcripts associated with body weight and energy metabolism traits). We found that modules 2 and 4 were enriched for genes involved in photoreceptor activity (P = 1.1E-3), and phospholipase A1 activity (P = 1.4E-3), respectively (see Additional file 6: Over-representation of Gene Ontology Categories, KEGG Pathways and Keywords for transcripts associated with body weight and energy metabolism traits).
Module 7 was enriched in genes mediating transmission of nerve impulse (P = 2.0E-4) and one of its major hub genes is Cbp53E (Figure 3D). Notably, Cbp53E had the highest correlation with CG10830, which is predicted to encode a homolog of the human potassium channel tetramerisation domain containing 12 (KCTD12) gene . A recent GWAS showed that a single nucleotide polymorphism in the human KCTD12 gene was associated with T2DM in a French population . Taken together with our findings, this proposes KCTD12 as a strong candidate for T2DM in humans.
Finally, it is worth mentioning that two of the genes in GLY module 6, puckered (puc) and hemipterous (hep), encode a MAP kinase phosphatase and a MAP kinase, respectively, that regulate the JNK signaling pathway . The mechanism by which changes in these genes regulate variation in GLY levels is not known, however, previous studies have shown that JNK represses Drosophila insulin-like peptide transcription in the neurosecretory cells of the brain that produce them . Thus, a plausible mechanism is that variation in puc and hep modulates GLY by regulating insulin-like peptide secretion via the JNK pathway. This hypothesis however needs to be tested in future studies.
We identified 5 modules of correlated transcripts associated with TAG, ranging from 1 to 71 probe sets (see Additional file 5: Modules of correlated transcripts associated with body weight and energy metabolism traits). Notably, seven of the genes in TAG module 4, death executioner Bcl-2 homologue (debcl), sex combs extra (Sce), viral iap-associated factor (viaf), Sirt7, CG7516, GXIVsPLA2, and Srp54, have human homologs, BOK, RING1, Pdcl3, SIRT7, NOL10, PLA2G12A, and SFRS12, respectively, whose transcript abundance has been associated with obesity in mice using a systems genetics analysis . Visualization of module 4 illustrates that two of these genes, Sirt7 and debcl, are hubs (Figure 3E). As discussed above, Sirt7 is involved in chromatin silencing and its mouse ortholog has been recently reported to play a role in the regulation of stress response of cardiomyocytes and to prevent apoptosis and inflammatory cardiomyopathy . debcl is a member of the evolutionarily conserved Bcl-2 family of protooncogenes that is composed of both pro- (e. g. bax and bak) and anti-apoptotic (e. g. bcl-2 and bcl-xL) proteins . Collectively, these data argue that variation in genes involved in apoptosis control TAG accumulation. As fatty acids destined for oxidation are in part derived from stored TAGs, our data are consistent with studies in mammals reporting that oxidation of fatty acids is inhibited by several mitogenic stimuli and increased by various agents of growth arrest and/or apoptosis . Our results not only suggest that the link between TAG accumulation and apoptosis is evolutionarily conserved, but also indicate that it extends to the transcriptional level.
We identified 13 modules associated with GLYC, ranging from 2 to 101 probe sets (see Additional file 5: Analysis of modules of correlated transcripts associated with body weight and energy metabolism traits). None of the modules associated with GLYC were found to be significantly enriched in specific functional categories after Benjamini correction. However, two points are worthy of mention. First, the most highly connected gene in module 11 was E2F transcription factor 2 (E2f2) (Figure 3F) that is critical for cell-cycle arrest . Since glycerol is an important intermediate in TAG metabolism, these latter findings corroborate the hypothesis of a link between cellular progression, apoptosis, and fatty acids oxidation discussed above. Second, among the genes included in module 12, there is Glycerol 3 phosphate dehydrogenase (Gpdh) that plays a major role in the metabolism of carbohydrates for insect flight .
We identified 6 modules of correlated transcripts associated with MR, ranging from 3 to 58 probe sets (see Additional file 5: Modules of correlated transcripts associated with body weight and energy metabolism traits). We found that transcripts associated with variation in MR were enriched for genes involved in hydrolase (module 2, P = 2.6E-3) and alpha-glucosidase (module 5, P = 6.8E-05) activities (see Additional file 6: Over-representation of Gene Ontology Categories, KEGG Pathways and Keywords for transcripts associated with body weight and energy metabolism traits). Transcripts associated with MR were also enriched for genes that are mainly expressed in the midgut and the Malpighian tubules (Figure 3G). The Malphighian tubules in insects are part of the excretory system responsible for absorbing water and nitrogenous wastes from the haemolymph and so critical for maintaining proper internal osmotic conditions. Because of their small size, insects and other terrestrial arthropods are susceptible to water loss by evaporation through the cuticle. One process that also promotes water loss in insects and thus increases the danger of desiccation is the respiratory gas exchange . Reduction in metabolic rate and the demand for oxygen has been proposed as a mechanism that can help the fly to conserve water . In addition, insect renal tubules constitute a cell-autonomous immune system that protects the organism against bacterial infection  and detoxification of xenobiotics . Thus, variation in gene expression in the gut and tubules could influence metabolic rate in a number of ways, through alterations in osmotic balance to changes in digestive efficiency. It will be important for future functional genetics studies to verify the phenotypic effects of variation in gene regulatory networks in these organs to elucidate their contribution to determining whole-body metabolic rates.
Genetic correlations between energy metabolism and life-history traits
Genetic correlations between energy metabolism and life-history traits averaged across sexes (A), for females (B), and for males (C).
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To gain insight into the molecular basis of the observed genetic correlations, we tested whether there was significant overlap of common transcripts between modules for the energy metabolism traits and life-history traits. We found substantial modular pleiotropy between BW, competitive fitness, and starvation resistance (see Additional file 7: Modular pleiotropy between energy metabolism and life history traits). In particular, we observed that transcript abundance of genes involved in innate immune response, such as Attacin-C (AttC), Cecropin C (CecC), and PGRP-SB1, were associated with variation in all three traits. Large energy investments are necessary for an adequate immune system to fight infections . As life-history theory predicts that the amount of energy available is finite , maintaining the cellular and molecular capabilities of mounting an efficient immune response may not be possible without cost to other energy demanding physiological functions. Indeed, trade-offs between immune function and other traits involving competition, specifically larval competitive ability in Drosophila, have been extensively reported [75, 76]. Based on these observations, we speculate that genotypic differences in the efficiency of the immune response among wild-derived lines of D. melanogaster may reflect differences in allocation of resources between traits associated with survival in a way that maximizes fitness. This view is consistent with evidence of an evolutionarily conserved link between immune function and the insulin/IGF signaling discussed above. These Drosophila lines are currently being assessed for variation in the efficacy of their immune response to infection which will allow us to test this hypothesis.
Our analysis also showed significant modular pleiotropy between BW, GLY, and competitive fitness (see Additional file 7: Modular pleiotropy between energy metabolism and life history traits). Three genes, nicotinic Acetylcholine Receptor beta 64B (nAcRβ-64B), Diuretic hormone 31 receptor 1 (Dh31-R1), and cAMP-dependent protein kinase 3 (Pka-C3) were associated with variation in all the traits. nAcRβ-64B and Dh31-R1 encode predicted G-protein coupled receptors that bind to the neurotransmitter acetylcholine and a diuretic hormone, respectively . Pka-C3 encodes a cAMP-dependent protein kinase  whose transcription is regulated by light . Furthermore, we found that two photosensory opsins, rhodopsin 4 (Rh4) and rhodopsin 6 (Rh6), were associated with variation in GLY and competitive fitness. In insects, the transcriptional coordination of circadian clocks has been implicated in affecting life-history traits by regulating physiological and behavioral rhythms , including feeding rhythms . Daily light/dark cycles may affect circadian rhythms by either entraining the clocks or via clock-independent molecular pathways and Drosophila circadian photoreception is mediated by cryptochrome in clock neurons and by rhodopsins in photic organs . Based on these observations, our findings confirm the interrelations among circadian photoreception, life-history traits, and energy metabolism and identify a key set of transcripts involved in this process.
The present study identified a large number of genes that varied both at the level of DNA sequence and at the level of gene expression to produce natural variation in BW, the content of GLY, TAG and GLYC, and MR among 40 wild-derived lines of D. melanogaster. Candidate genes identified based on sequence polymorphism generally differed from those identified based on variation in gene expression among lines. This suggests that phenotypic variation is the product of both alterations in gene expression as well as allelic variation at the sequence level. The relative importance of these two processes in producing phenotypic variation remains to be determined, but may vary depending on the trait and sampled population. Our gene expression data identified a number of modules of co-expressed genes affecting these traits with surprisingly little overlap. As these modules contain many genes of unknown function, their co-occurrence with genes with known function related to specific traits may be useful for annotation purposes. We did identify significant modular pleiotropy between BW, GLY, and competitive fitness and future studies will need to explore and validate the functional genetic basis of these interrelationships. Such knowledge would be useful not only in a practical sense to predict correlated changes in related traits given medical interventions to control body weight, but also from an evolutionary standpoint to elucidate the extent to which such pleiotropic modules might guide and constrain the evolution of the affected traits.
The 40 unrelated wild-type inbred lines of D. melanogaster were established from a sample of isofemale lines collected in the Raleigh Farmer's market (NC) and inbred to near-homozygosity by 20 generations of full-sib inbreeding . Mutants and their co-isogenic control lines were obtained from the Bloomington Drosophila Stock Center http://www.flybase.org.
We maintained each stock at constant parental density for at least two generations to minimize environmental effects. To control for larval density, we allowed the parents of the experimental flies to mate for 3 hours to generate egg collections on apple juice/agar medium in laying plates. After 24 hours, we picked groups of 100 first-instar larvae from the surface of the medium and put into replicate vials. For all assays, we used ten replicate vials per line, with each vial containing a group of 10 single-sexed individuals aged 3-5 days. We reared flies under the same experimental conditions described in Ayroles et al. , i.e. standard cornmeal, agar, molasses, and yeast medium, 25°C, 60-75% humidity, and 12 hr/12 hr light/dark cycle.
Body weight and metabolite measurements
We first starved the flies for one hour under non-dehydrating conditions to reduce the food-derived TAG and GLY present in the gut . We then weighed each group of flies to 0.1 mg accuracy with an analytical balance and stored them at -70°C. Finally, we homogenized each group using the protocol described in [7, 81] and measured TAG and GLYC spectrophotometrically using a commercially available kit (Sigma-Triglyceride Assay Kit) following the manufacturer's suggested protocol.
GLY was measured from the same homogenates using a modification of the protocol described in Clark et al. . Briefly, aliquots of 1.67 μl of homogenate were added to 250 μl of a reagent containing 0.1 U/ml of amyloglucosidase, 5 U/ml of glucose oxidase, 1 U/ml of peroxidase, and 0.04 mg/ml of O-dianisidine dihydrochloride. After 30-minute incubation period at 37°C, OD540 was measured. Concentration of GLY was determined from glucose and glycogen standards run with each replicate. Each sample was assayed twice and the mean used in the analysis. Previous studies have shown that this protocol accurately reflects glycogen concentration and that endogenous glucose present in the flies contributes only negligibly to the results .
Metabolic rate measurements
We measured MR as CO2 production using a flow-through respirometry system (Qubit System Research, Kingston, Ontario, Canada) and a modification of the method described in Van Voorhies et al. . Briefly, a pump is used to push air through a CO2 scrubber therefore providing CO2-free air to the system. The airstream is saturated with H2O by passing through a series of gas syringes filled with sterile H2O and cotton wool. Pressure in the line is controlled by a precision pressure regulator that sets the input pressure to the 4-channel mass flow meter/controller where the flow is divided into 4 gas streams and provided to the sample chambers. The flow rate entering the chamber was 30 ml/min. After leaving the sample chambers, air enriched in CO2 enters into the 4-channel gas switcher that directs the flow to either the analysis system or to waste (vented). For the determination of CO2, sample air was pulled through a drying column to remove H2O, a mass flow meter, and then the CO2 analyzer that has a range of 0-2000 ppm CO2 with a resolution of better than 1 ppm. We measured CO2 for 10 minutes/chamber with a 30 second flush period between measurements. The amount of CO2 produced by each group of flies was calculated using C950 Data Acquisition software (Qubit System Research, Kingston, Ontario, Canada).
Quantitative genetic analyses
All statistical analyses were performed using SAS version 9.1. We used a mixed model ANOVA to partition variation in each trait among the inbred lines according to the model, Y = μ + L + S + L × S + E, where μ is the overall mean; L and S are the main effects of Line (Random) and Sex (Fixed); LxS is the random effect of sex-by-line interaction; and E is the within-vial error variance. Reduced models by sex were also run. Broad-sense heritabilities (H 2 ) were computed as H2 = (σ L 2 + σ LS 2)/(σ L 2 + σ LS 2 + σ E 2) for the analyses pooled across sexes, where σ L 2 , σ LS 2 , and σ E 2 are the among line, sex-by-line and within line variance components, respectively. Cross-sex genetic correlations (r MF ) were also estimated as r MF = cov ♀♂ /(σ ♀ σ ♂ ), where cov ♀♂ is the covariance of line means between females and males, and σ ♀ and σ ♂ are the square roots of the among line variance components for females and males, respectively. Genetic correlations between traits were calculated as r GT = cov G12 /(σ G1 σ G2 ), where cov G12 is the covariance between traits among line means from the joint analysis, and σ G1 and σ G 2 are the square roots of the variances among lines from the analyses of each trait separately. We used sequential Bonferroni procedure to correct for multiple tests of significance of correlation coefficients among traits . The coefficients of genetic (CV G ) and environmental (CV E ) variances were calculated as CV G = 100σ G /μ and CV E = 100σ E /μ, respectively, where σ G and σ E are the square roots of the line and within line variance components, respectively.
Transcript-trait and SFP-trait associations
To identify transcripts associated (P < 0.01) with variation in each trait we performed a regression analysis as previously described . Briefly, regression models of the form Y = μ + S + T + S × T + ε, where S is sex, T is the trait, and ε is the error term were computed for each probe set. Similarly, SFPs associated (P < 0.01) with each trait were identified using the ANOVA model Y = μ + M + S + S × M + ε, where M is the presence or absence of the SFP, S is sex, and ε is the error term. Reduced models by sex were also run.
The genetic correlations between all transcripts significantly associated with each trait were computed after removing the correlation between these transcripts and the trait. This was achieved by fitting the model Y = μ + E + S + E × S + ε (Y is the trait, E is the covariate median log2 expression level, S is the sex effect and ε the residual error) and extracting the residuals to compute pair-wise transcript correlations for module construction . Modules of transcripts associated with each trait with coordinated patterns of expression across the 40 lines were then quantified as described previously  by transforming the pairwise genetic correlations among transcripts into Euclidean-like distances, which were used to construct an affinity matrix. The transcripts were partitioned into modules using a graph-theoretical approach that envisions the transcripts as nodes in an undirected graph whose edges are weighted by the entries of the affinity matrix. Transcriptional modules common to a metabolic trait as well as to other traits measured on the 40 wild-derived inbred lines  were identified by comparing the transcripts in each metabolic module to the transcripts in each module from the other traits and comparing whether the overlap between the modules exceed what is expected by chance using a Fischer's exact test.
We are grateful to Dr Brett McKinney for contributing with analytic tools. We thank two anonymous reviewers for their valuable suggestions. We also thank Dr Barbara Gower for her technical assistance in the metabolite measurements. Dr Gower's laboratory is supported, in part, by NIH Grants P30-DK56336 (NORC), P60-DK079626 (DRTC), and UL1RR025777 (CCTS). This study was supported by NIH Grants R01 DK084219 to MDL and JL and R01 GM 45146 to TFCM.
- Korner J, Woods SC, Woodworth KA: Regulation of energy homeostasis and health consequences in obesity. Am J Med. 2009, 122: S12-S18. 10.1016/j.amjmed.2009.01.003.PubMedView ArticleGoogle Scholar
- Ogden CL, Carroll MD, Curtin LR, McDowell MA, Tabak CJ, Flegal KM: Prevalence of overweight and obesity in the United States, 1999-2004. JAMA. 2006, 295: 1549-1555. 10.1001/jama.295.13.1549.PubMedView ArticleGoogle Scholar
- Obesity: preventing and managing the global epidemic. Report of a WHO consultation. World Health Organ Tech Rep Ser. 2000, 894: i-253.Google Scholar
- Stunkard AJ, Sorensen TI, Hanis C, Teasdale TW, Chakraborty R, Schull WJ: An adoption study of human obesity. N Engl J Med. 1986, 314: 193-198.PubMedView ArticleGoogle Scholar
- Schousboe K, Visscher PM, Erbas B, Kyvik KO, Hopper JL, Henriksen JE: Twin study of genetic and environmental influences on adult body size, shape, and composition. Int J Obes Relat Metab Disord. 2004, 28: 39-48. 10.1038/sj.ijo.0802524.PubMedView ArticleGoogle Scholar
- Arden NK, Spector TD: Genetic influences on muscle strength, lean body mass, and bone mineral density: a twin study. J Bone Miner Res. 1997, 12: 2076-2081. 10.1359/jbmr.1922.214.171.1246.PubMedView ArticleGoogle Scholar
- De Luca M, Yi N, Allison DB, Leips J, Ruden DM: Mapping quantitative trait loci affecting variation in Drosophila triacylglycerol storage. Obes Res. 2005, 13: 1596-1605. 10.1038/oby.2005.196.PubMedView ArticleGoogle Scholar
- Nowacka-Woszuk J, Szczerbal I, Fijak-Nowak H, Switonski M: Chromosomal localization of 13 candidate genes for human obesity in the pig genome. J Appl Genet. 2008, 49: 373-377.PubMedView ArticleGoogle Scholar
- Diament AL, Fisler JS, Warden CH: Studies of natural allele effects in mice can be used to identify genes causing common human obesity. Obes Rev. 2003, 4: 249-255. 10.1046/j.1467-789X.2003.00113.x.PubMedView ArticleGoogle Scholar
- Montooth KL, Marden JH, Clark AG: Mapping determinants of variation in energy metabolism, respiration and flight in Drosophila. Genetics. 2003, 165: 623-635.PubMed CentralPubMedGoogle Scholar
- Ankra-Badu GA, Pomp D, Shriner D, Allison DB, Yi N: Genetic influences on growth and body composition in mice: multilocus interactions. Int J Obes (Lond). 2009, 33: 89-95. 10.1038/ijo.2008.215.View ArticleGoogle Scholar
- Dong C, Li WD, Li D, Price RA: Interaction between obesity-susceptibility loci in chromosome regions 2p25-p24 and 13q13-q21. Eur J Hum Genet. 2005, 13: 102-108. 10.1038/sj.ejhg.5201292.PubMedView ArticleGoogle Scholar
- Silventoinen K, Hasselbalch AL, Lallukka T, Bogl L, Pietilainen KH, Heitmann BL: Modification effects of physical activity and protein intake on heritability of body size and composition. Am J Clin Nutr. 2009, 90: 1096-1103. 10.3945/ajcn.2009.27689.PubMed CentralPubMedView ArticleGoogle Scholar
- Ghazalpour A, Doss S, Sheth SS, Ingram-Drake LA, Schadt EE, Lusis AJ: Genomic analysis of metabolic pathway gene expression in mice. Genome Biol. 2005, 6: R59-10.1186/gb-2005-6-7-r59.PubMed CentralPubMedView ArticleGoogle Scholar
- Dobrin R, Zhu J, Molony C, Argman C, Parrish ML, Carlson S: Multi-tissue coexpression networks reveal unexpected subnetworks associated with disease. Genome Biol. 2009, 10: R55-10.1186/gb-2009-10-5-r55.PubMed CentralPubMedView ArticleGoogle Scholar
- Voy BH, Aronow BJ: Embrace diversity! Systems genetics-enabled discovery of disease networks. Physiol Genomics. 2009, 39: 169-171. 10.1152/physiolgenomics.00158.2009.PubMedView ArticleGoogle Scholar
- Roff DA, Fairbairn DJ: The evolution of trade-offs: where are we?. J Evol Biol. 2007, 20: 433-447. 10.1111/j.1420-9101.2006.01255.x.PubMedView ArticleGoogle Scholar
- Harshman LG, Zera AJ: The cost of reproduction: the devil in the details. Trends Ecol Evol. 2007, 22: 80-86. 10.1016/j.tree.2006.10.008.PubMedView ArticleGoogle Scholar
- Zera AJ, Harshman LG: The physiology of life-history trade-oofs in animals. Annu Rev Ecol Syst. 2001, 32: 95-126. 10.1146/annurev.ecolsys.32.081501.114006.View ArticleGoogle Scholar
- Schlegel A, Stainier DY: Lessons from "lower" organisms: what worms, flies, and zebrafish can teach us about human energy metabolism. PLoS Genet. 2007, 3: e199-10.1371/journal.pgen.0030199.PubMed CentralPubMedView ArticleGoogle Scholar
- Leopold P, Perrimon N: Drosophila and the genetics of the internal milieu. Nature. 2007, 450: 186-188. 10.1038/nature06286.PubMedView ArticleGoogle Scholar
- Buch S, Pankratz MJ: Making metabolic decisions in Drosophila. Fly (Austin). 2009, 3: 74-77.View ArticleGoogle Scholar
- Knight GR, Robertson A: Fitness as a Measurable Character in Drosophila. Genetics. 1957, 42: 524-530.PubMed CentralPubMedGoogle Scholar
- Prout T: The Relation between Fitness Components and Population Prediction in Drosophila. I: The Estimation of Fitness Components. Genetics. 1971, 68: 127-149.PubMed CentralPubMedGoogle Scholar
- Charlesworth B, Hughes KA: Age-specific inbreeding depression and components of genetic variance in relation to the evolution of senescence. Proc Natl Acad Sci USA. 1996, 93: 6140-6145. 10.1073/pnas.93.12.6140.PubMed CentralPubMedView ArticleGoogle Scholar
- Ayroles JF, Carbone MA, Stone EA, Jordan KW, Lyman RF, Magwire MM: Systems genetics of complex traits in Drosophila melanogaster. Nat Genet. 2009, 41: 299-307. 10.1038/ng.332.PubMed CentralPubMedView ArticleGoogle Scholar
- Fontaine E, Savard R, Tremblay A, Despres JP, Poehlman E, Bouchard C: Resting metabolic rate in monozygotic and dizygotic twins. Acta Genet Med Gemellol (Roma). 1985, 34: 41-47.Google Scholar
- Reed DR, Bachmanov AA, Tordoff MG: Forty mouse strain survey of body composition. Physiol Behav. 2007, 91: 593-600. 10.1016/j.physbeh.2007.03.026.PubMed CentralPubMedView ArticleGoogle Scholar
- Sadowska ET, Labocha MK, Baliga K, Stanisz A, Wroblewska AK, Jagusiak W: Genetic correlations between basal and maximum metabolic rates in a wild rodent: consequences for evolution of endothermy. Evolution. 2005, 59: 672-681.PubMedView ArticleGoogle Scholar
- Iyengar VK, Eisner T: Heritability of body mass, a sexually selected trait, in an arctiid moth (Utetheisa ornatrix). Proc Natl Acad Sci USA. 1999, 96: 9169-9171. 10.1073/pnas.96.16.9169.PubMed CentralPubMedView ArticleGoogle Scholar
- Mackay TF, Stone EA, Ayroles JF: The genetics of quantitative traits: challenges and prospects. Nat Rev Genet. 2009, 10: 565-577. 10.1038/nrg2612.PubMedView ArticleGoogle Scholar
- Harbison ST, Carbone MA, Ayroles JF, Stone EA, Lyman RF, Mackay TF: Co-regulated transcriptional networks contribute to natural genetic variation in Drosophila sleep. Nat Genet. 2009, 41: 371-375. 10.1038/ng.330.PubMed CentralPubMedView ArticleGoogle Scholar
- Edwards AC, Ayroles JF, Stone EA, Carbone MA, Lyman RF, Mackay TF: A transcriptional network associated with natural variation in Drosophila aggressive behavior. Genome Biol. 2009, 10: R76-10.1186/gb-2009-10-7-r76.PubMed CentralPubMedView ArticleGoogle Scholar
- Morozova TV, Ayroles JF, Jordan KW, Duncan LH, Carbone MA, Lyman RF: Alcohol sensitivity in Drosophila: translational potential of systems genetics. Genetics. 2009, 183: 733-12SI. 10.1534/genetics.109.107490.PubMed CentralPubMedView ArticleGoogle Scholar
- Drysdale RA, Crosby MA: FlyBase: genes and gene models. Nucleic Acids Research. 2005, 33: D390-D395. 10.1093/nar/gki046.PubMed CentralPubMedView ArticleGoogle Scholar
- Kohyama-Koganeya A, Kim YJ, Miura M, Hirabayashi Y: A Drosophila orphan G protein-coupled receptor BOSS functions as a glucose-responding receptor: loss of boss causes abnormal energy metabolism. Proc Natl Acad Sci USA. 2008, 105: 15328-15333. 10.1073/pnas.0807833105.PubMed CentralPubMedView ArticleGoogle Scholar
- Motosaka K, Koganezawa M, Narikawa S, Furuyama A, Shinozaki K, Isono K: Cyclic AMP-dependent memory mutants are defective in the food choice behavior of Drosophila. J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2007, 193: 279-283. 10.1007/s00359-006-0200-z.PubMedView ArticleGoogle Scholar
- Harbison ST, Sehgal A: Quantitative genetic analysis of sleep in Drosophila melanogaster. Genetics. 2008, 178: 2341-2360. 10.1534/genetics.107.081232.PubMed CentralPubMedView ArticleGoogle Scholar
- Hipkiss AR: Energy metabolism, altered proteins, sirtuins and ageing: converging mechanisms?. Biogerontology. 2008, 9: 49-55. 10.1007/s10522-007-9110-x.PubMed CentralPubMedView ArticleGoogle Scholar
- Ponting CP: Tudor domains in proteins that interact with RNA. Trends Biochem Sci. 1997, 22: 51-52. 10.1016/S0968-0004(96)30049-2.PubMedView ArticleGoogle Scholar
- Dennis G, Sherman BT, Hosack DA, Yang J, Gao W, Lane HC: DAVID: Database for Annotation, Visualization, and Integrated Discovery. Genome Biol. 2003, 4: 3-10.1186/gb-2003-4-5-p3.View ArticleGoogle Scholar
- Huang DW, Sherman BT, Lempicki RA: Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc. 2009, 4: 44-57. 10.1038/nprot.2008.211.View ArticleGoogle Scholar
- Zeyda M, Stulnig TM: Obesity, inflammation, and insulin resistance--a mini-review. Gerontology. 2009, 55: 379-386. 10.1159/000212758.PubMedView ArticleGoogle Scholar
- Diangelo JR, Bland ML, Bambina S, Cherry S, Birnbaum MJ: The immune response attenuates growth and nutrient storage in Drosophila by reducing insulin signaling. Proc Natl Acad Sci USA. 2009, 106: 20853-20858. 10.1073/pnas.0906749106.PubMed CentralPubMedView ArticleGoogle Scholar
- Karpac J, Jasper H: Insulin and JNK: optimizing metabolic homeostasis and lifespan. Trends Endocrinol Metab. 2009, 20: 100-106. 10.1016/j.tem.2008.11.004.PubMed CentralPubMedView ArticleGoogle Scholar
- Delaney JR, Stoven S, Uvell H, Anderson KV, Engstrom Y, Mlodzik M: Cooperative control of Drosophila immune responses by the JNK and NF-kappaB signaling pathways. EMBO J. 2006, 25: 3068-3077. 10.1038/sj.emboj.7601182.PubMed CentralPubMedView ArticleGoogle Scholar
- Fuse N, Hisata K, Katzen AL, Matsuzaki F: Heterotrimeric G proteins regulate daughter cell size asymmetry in Drosophila neuroblast divisions. Curr Biol. 2003, 13: 947-954. 10.1016/S0960-9822(03)00334-8.PubMedView ArticleGoogle Scholar
- Butler SJ, Ray S, Hiromi Y: klingon, a novel member of the Drosophila immunoglobulin superfamily, is required for the development of the R7 photoreceptor neuron. Development. 1997, 124: 781-792.PubMedGoogle Scholar
- Chintapalli VR, Wang J, Dow JA: Using FlyAtlas to identify better Drosophila melanogaster models of human disease. Nat Genet. 2007, 39: 715-720. 10.1038/ng2049.PubMedView ArticleGoogle Scholar
- Farooqi IS, O'Rahilly S: Monogenic human obesity syndromes. Recent Prog Horm Res. 2004, 59: 409-424. 10.1210/rp.59.1.409.PubMedView ArticleGoogle Scholar
- Chen Y, Hu C, Hsu CK, Zhang Q, Bi C, Asnicar M: Targeted disruption of the melanin-concentrating hormone receptor-1 results in hyperphagia and resistance to diet-induced obesity. Endocrinology. 2002, 143: 2469-2477. 10.1210/en.143.7.2469.PubMedView ArticleGoogle Scholar
- Chung WK, Belfi K, Chua M, Wiley J, Mackintosh R, Nicolson M: Heterozygosity for Lep(ob) or Lep(rdb) affects body composition and leptin homeostasis in adult mice. Am J Physiol. 1998, 274: R985-R990.PubMedGoogle Scholar
- Morton GJ, Cummings DE, Baskin DG, Barsh GS, Schwartz MW: Central nervous system control of food intake and body weight. Nature. 2006, 443: 289-295. 10.1038/nature05026.PubMedView ArticleGoogle Scholar
- Hofker M, Wijmenga C: A supersized list of obesity genes. Nat Genet. 2009, 41: 139-140. 10.1038/ng0209-139.PubMedView ArticleGoogle Scholar
- Ryuda M, Tsuzuki S, Tanimura T, Tojo S, Hayakawa Y: A gene involved in the food preferences of larval Drosophila melanogaster. J Insect Physiol. 2008, 54: 1440-1445. 10.1016/j.jinsphys.2008.08.006.PubMedView ArticleGoogle Scholar
- Melcher C, Pankratz MJ: Candidate gustatory interneurons modulating feeding behavior in the Drosophila brain. PLoS Biol. 2005, 3: e305-10.1371/journal.pbio.0030305.PubMed CentralPubMedView ArticleGoogle Scholar
- Melcher C, Bader R, Pankratz MJ: Amino acids, taste circuits, and feeding behavior in Drosophila: towards understanding the psychology of feeding in flies and man. J Endocrinol. 2007, 192: 467-472. 10.1677/JOE-06-0066.PubMedView ArticleGoogle Scholar
- Okamura T, Shimizu H, Nagao T, Ueda R, Ishii S: ATF-2 regulates fat metabolism in Drosophila. Mol Biol Cell. 2007, 18: 1519-1529. 10.1091/mbc.E06-10-0909.PubMed CentralPubMedView ArticleGoogle Scholar
- Cauchi S, Proenca C, Choquet H, Gaget S, De GF, Marre M: Analysis of novel risk loci for type 2 diabetes in a general French population: the D.E.S.I.R. study. J Mol Med. 2008, 86: 341-348. 10.1007/s00109-007-0295-x.PubMedView ArticleGoogle Scholar
- Karpac J, Hull-Thompson J, Falleur M, Jasper H: JNK signaling in insulin-producing cells is required for adaptive responses to stress in Drosophila. Aging Cell. 2009, 8: 288-295. 10.1111/j.1474-9726.2009.00476.x.PubMed CentralPubMedView ArticleGoogle Scholar
- Vakhrusheva O, Smolka C, Gajawada P, Kostin S, Boettger T, Kubin T: Sirt7 increases stress resistance of cardiomyocytes and prevents apoptosis and inflammatory cardiomyopathy in mice. Circ Res. 2008, 102: 703-710. 10.1161/CIRCRESAHA.107.164558.PubMedView ArticleGoogle Scholar
- Galindo KA, Lu WJ, Park JH, Abrams JM: The Bax/Bak ortholog in Drosophila, Debcl, exerts limited control over programmed cell death. Development. 2009, 136: 275-283. 10.1242/dev.019042.PubMed CentralPubMedView ArticleGoogle Scholar
- Ockner RK: Nutrient and Energy Metabolism in Cell Proliferation. Integration of metabolism, energetics, and signal transduction: unifying foundations in cell growth and death, cancer, atherosclerosis, and Alzheimer disease. 2004, New York: Klumer Academic/Plenum Publishers, 19-40.Google Scholar
- Ambrus AM, Nicolay BN, Rasheva VI, Suckling RJ, Frolov MV: dE2F2-independent rescue of proliferation in cells lacking an activator dE2F1. Mol Cell Biol. 2007, 27: 8561-8570. 10.1128/MCB.01068-07.PubMed CentralPubMedView ArticleGoogle Scholar
- Colgan DJ: Glycerol-3-phosphate dehydrogenase isozyme variation in insects. Biological Journal of the Linnean Society. 2008, 47: 37-47. 10.1111/j.1095-8312.1992.tb00654.x.View ArticleGoogle Scholar
- Lehmann FO: Matching spiracle opening to metabolic need during flight in Drosophila. Science. 2001, 294: 1926-1929. 10.1126/science.1064821.PubMedView ArticleGoogle Scholar
- Gibbs AG, Matzkin LM: Evolution of water balance in the genus Drosophila. J Exp Biol. 2001, 204: 2331-2338.PubMedGoogle Scholar
- McGettigan J, McLennan RK, Broderick KE, Kean L, Allan AK, Cabrero P: Insect renal tubules constitute a cell-autonomous immune system that protects the organism against bacterial infection. Insect Biochem Mol Biol. 2005, 35: 741-754. 10.1016/j.ibmb.2005.02.017.PubMedView ArticleGoogle Scholar
- Yang J, McCart C, Woods DJ, Terhzaz S, Greenwood KG, ffrench-Constant RH: A Drosophila systems approach to xenobiotic metabolism. Physiol Genomics. 2007, 30: 223-231. 10.1152/physiolgenomics.00018.2007.PubMedView ArticleGoogle Scholar
- Holm S: A simple sequentially rejective multiple test procedure. Scandinavian Journal of Statistics. 1979, 6: 65-70.Google Scholar
- Djawdan M, Chippindale AK, Rose MR, Bradley TJ: Metabolic reserves and evolved stress resistance in Drosophila melanogaster. Physiol Zool. 1998, 71: 584-594.PubMedView ArticleGoogle Scholar
- Rion S, Kawecki TJ: Evolutionary biology of starvation resistance: what we have learned from Drosophila. J Evol Biol. 2007, 20: 1655-1664. 10.1111/j.1420-9101.2007.01405.x.PubMedView ArticleGoogle Scholar
- Hoffmann AA, Hallas R, Sinclair C, Mitrovski P: Levels of variation in stress resistance in drosophila among strains, local populations, and geographic regions: patterns for desiccation, starvation, cold resistance, and associated traits. Evolution. 2001, 55: 1621-1630.PubMedView ArticleGoogle Scholar
- Bonneaud C, Mazuc J, Gonzalez G, Haussy C, Chastel O, Faivre B: Assessing the cost of mounting an immune response. Am Nat. 2003, 161: 367-379. 10.1086/346134.PubMedView ArticleGoogle Scholar
- Fellowes MD, Kraaijeveld AR, Godfray HC: Trade-off associated with selection for increased ability to resist parasitoid attack in Drosophila melanogaster. Proc Biol Sci. 1998, 265: 1553-1558. 10.1098/rspb.1998.0471.PubMed CentralPubMedView ArticleGoogle Scholar
- Vijendravarma RK, Kraaijeveld AR, Godfray HC: Experimental evolution shows Drosophila melanogaster resistance to a microsporidian pathogen has fitness costs. Evolution. 2009, 63: 104-114. 10.1111/j.1558-5646.2008.00516.x.PubMedView ArticleGoogle Scholar
- Wijnen H, Naef F, Boothroyd C, Claridge-Chang A, Young MW: Control of daily transcript oscillations in Drosophila by light and the circadian clock. PLoS Genet. 2006, 2: e39-10.1371/journal.pgen.0020039.PubMed CentralPubMedView ArticleGoogle Scholar
- Xu K, Zheng X, Sehgal A: Regulation of feeding and metabolism by neuronal and peripheral clocks in Drosophila. Cell Metab. 2008, 8: 289-300. 10.1016/j.cmet.2008.09.006.PubMed CentralPubMedView ArticleGoogle Scholar
- Hanai S, Ishida N: Entrainment of Drosophila circadian clock to green and yellow light by Rh1, Rh5, Rh6 and CRY. Neuroreport. 2009, 20: 755-758. 10.1097/WNR.0b013e32832a7c4e.PubMedView ArticleGoogle Scholar
- Wong R, Piper MD, Blanc E, Partridge L: Pitfalls of measuring feeding rate in the fruit fly Drosophila melanogaster. Nat Methods. 2008, 5: 214-215. 10.1038/nmeth0308-214.PubMed CentralPubMedView ArticleGoogle Scholar
- Clark AG, Keith LE: Variation among extracted lines of Drosophila melanogaster in triacylglycerol and carbohydrate storage. Genetics. 1988, 119: 595-607.PubMed CentralPubMedGoogle Scholar
- Van Voorhies WA, Khazaeli AA, Curtsinger JW: Testing the "rate of living" model: further evidence that longevity and metabolic rate are not inversely correlated in Drosophila melanogaster. J Appl Physiol. 2004, 97: 1915-1922. 10.1152/japplphysiol.00505.2004.PubMedView ArticleGoogle Scholar
- Stone EA, Ayroles JF: Modulated modularity clustering as an exploratory tool for functional genomic inference. PLoS Genet. 2009, 5: e1000479-10.1371/journal.pgen.1000479.PubMed CentralPubMedView ArticleGoogle Scholar
- Chintapalli VR, Wang J, Dow JA: Using FlyAtlas to identify better Drosophila melanogaster models of human disease. Nat Genet. 2007, 39: 715-720. 10.1038/ng2049.PubMedView ArticleGoogle Scholar
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