Hypoxia-induced cell injury has been related to multiple pathological conditions. In order to render hypoxia-sensitive cells and tissues resistant to low O2 environment, in this current study, we used Drosophila melanogaster as a model to dissect the mechanisms underlying hypoxia-tolerance. A D. melanogaster strain that lives perpetually in an extremely low-oxygen environment (4% O2, an oxygen level that is equivalent to that over about 4,000 m above Mt. Everest) was generated through laboratory selection pressure using a continuing reduction of O2 over many generations. This phenotype is genetically stable since selected flies, after several generations in room air, survive at this low O2 level. Gene expression profiling showed striking differences between tolerant and naïve flies, in larvae and adults, both quantitatively and qualitatively. Up-regulated genes in the tolerant flies included signal transduction pathways (e.g., Notch and Toll/Imd pathways), but metabolic genes were remarkably down-regulated in the larvae. Furthermore, a different allelic frequency and enzymatic activity of the triose phosphate isomerase (TPI) was present in the tolerant versus naïve flies. The transcriptional suppressor, hairy, was up-regulated in the microarrays and its binding elements were present in the regulatory region of the specifically down-regulated metabolic genes but not others, and mutations in hairy significantly reduced hypoxia tolerance. We conclude that, the hypoxia-selected flies: (a) altered their gene expression and genetic code, and (b) coordinated their metabolic suppression, especially during development, with hairy acting as a metabolic switch, thus playing a crucial role in hypoxia-tolerance.
Hypoxia-induced injury has been related to multiple pathological conditions. In order to render mammalian cells and tissues resistant to low O2 environment, we wished to first understand the mechanisms underlying hypoxia-tolerance in resistant animals. Therefore, we generated a D. melanogaster strain that is tolerant to severe hypoxic conditions through long-term experimental selection. Several adaptive changes were identified in the hypoxia-selected flies that included up-regulation of multiple signal transduction pathways (such as Notch pathway, Insulin pathway, EGF receptor pathway, and Toll/Imd pathway), modulation of cellular respiration enzymes, and polymorphic differences in metabolic enzymes (such as TPI). While we believe that multiple pathways contribute to the hypoxia-tolerant trait in this Drosophila strain, we demonstrate that hairy-mediated metabolic suppression is a critical mechanism for reducing the mismatch between supply and demand of O2.
Citation: Zhou D, Xue J, Lai JCK, Schork NJ, White KP, Haddad GG (2008) Mechanisms Underlying Hypoxia Tolerance in Drosophila melanogaster: hairy as a Metabolic Switch. PLoS Genet 4(10): e1000221. doi:10.1371/journal.pgen.1000221
Editor: Eric Rulifson, University of California San Francisco, United States of America
Received: April 3, 2008; Accepted: September 10, 2008; Published: October 17, 2008
Copyright: © 2008 Zhou et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study was supported by NIH grants to GGH (RO1NS-037756 and PO1HD-032573); grants from the W.M. Keck Foundation, the Beckman Foundation and the NIH to KPW; a fellowship grant from Parker B. Francis foundation to JX; and a grant from American Heart Association to DZ.
Competing interests: The authors have declared that no competing interests exist.
Mammalian tissues experience a reduction in oxygen delivery at high altitude or during certain disease states, such as myocardial infarction and stroke. In order to survive, cells, tissues and organisms have developed various strategies to adapt to such O2 limited condition. There are indeed major differences between different organisms and cells in their ability to survive reduced environmental O2. For example, turtle neurons are very tolerant to low oxygen and can survive without O2 for hours and days ,. In contrast, mammalian neurons are very sensitive to reduced oxygen and cannot survive for even minutes under similar conditions. However, the mechanisms underlying survival in such extreme hypoxic conditions are not clear at present, in spite of the fact that there have been a number of interesting observations in this regard in the past few decades. For instance, it has been demonstrated that a number of hypoxia-tolerant animals (e.g. Pseudemys scripta and Crucian Carp) reduce their O2 consumption during hypoxia in such a way to minimize the mismatch between O2 supply and demand –. Similar phenomena was also observed in Drosophila melanogaster , and in newborn mammals ,. Many questions, however, remain unsolved. For instance, we do not have an adequate understanding of the mechanisms that are responsible for reducing metabolic rate during low O2 conditions; and similarly, the mechanisms that are responsible for coordinating the suppression of these metabolic processes are still largely unknown.
In the early 1990s, we discovered that the fruit fly, Drosophila melanogaster, is tolerant to acute anoxia (zero mmHg O2). Flies can sustain such environment for a few hours without any evidence of injury . Since a) Drosophila has been demonstrated to be a powerful genetic model for human diseases – and b) many biochemical and genetic pathways are highly conserved between Drosophila and mammals, we used Drosophila in the current study to explore the mechanisms underlying tolerance to long-term hypoxia. We first generated a Drosophila melanogaster strain that can live perpetually (i.e., from generation to generation) in severe, normally lethal, hypoxic conditions. To better understand the mechanisms underlying this remarkable hypoxia tolerance, we used cDNA microarrays containing 13,061 predicted or known genes (~90% genes in the genome) to examine the differences in gene expression profiles between the hypoxia-selected (AF) and naïve control (NF) flies –. We performed these studies in both larvae and adults to determine gene expression as a function of development. Furthermore, we used a combination of bioinformatic, molecular and genetic strategies to investigate the role of specific genes in hypoxia tolerance.
Experimental Selection of Hypoxia-Tolerant Drosophila melanogaster
Twenty-seven wild-type isogenic lines constituted the parental population that we used for long-term experimental selection of a Drosophila melanogaster strain. At baseline, there was significant variability in hypoxia tolerance among these 27 lines, as determined by eclosion rate under 5% O2 and recovery time from anoxic stupor . In order to determine the level of O2 at which to initiate the long-term selection experiment, we performed a pilot study by culturing F1 embryos of the parental flies under different levels of hypoxia (e.g., 8%, 6% or 4% O2) (Figure 1A). We found that their survival rate was reduced at 6% O2, and no adult flies were actually obtained at 4% O2. At 8% O2, however, the majority of embryos (>80%) completed their development and reached the adult stage. Therefore, hypoxia selection was initiated at 8% O2, an O2 level in which flies can develop throughout their life cycle. The O2 concentration was then gradually decreased by ~1% every 3 to 5 generations to maintain the selection pressure (except for the transition between 5% and 4% which necessitated a much longer time). By the 13th generation, flies were able to complete development and perpetually live in 5% O2; and by the 32nd generation, the AF flies could even live perpetually under a severer level (4% of O2), a lethal condition for NF. We hypothesized that this is due to, at least partially, newly occurring mutations or recombination and selection of favorable alleles in the AF population. To test this hypothesis, a subset of embryos obtained from selected flies were collected and cultured under normoxia for several consecutive generations. After 8 generations in normoxia, AF were re-introduced into the lethal hypoxic environment (4% O2), and again, the majority (>80%) of the flies completed their development and could be maintained in this extreme condition perpetually. This result strongly suggested that the hypoxia-tolerance in the selected flies is a heritable trait.
A) Survival rate of parental Drosophila melanogaster population in hypoxic conditions. The survival rates of the parental Drosophila melanogaster population were determined in hypoxic conditions, i.e., 8%, 6% and 4% oxygen. Data were presented as means±SD (* p<0.05, **p<0.01; student's t-test). The parental population survived well at 8% O2 but their survival rate was reduced at 6%; and 4% O2 was lethal. B) Lifespan of NF and AF. No significant alteration in lifespan was found in AF flies (p>0.05, student's t-test) at 25°C in normoxia. Survivorship curves were analyzed with GraphPad prism software (San Diego, CA) to calculate the mean lifespan. C) and D) Body size and weight in AF. The body size and weight of AF were significantly reduced, as compared to NF. Data were presented as means±SD (* p<0.05, **p<0.01; student's t-test).
Several remarkable phenotypic changes were observed in the hypoxia-selected flies (AF). As described previously , the AF flies have a shortened recovery time from anoxia-induced stupor , consume more oxygen in hypoxia, and show a significant reduction in body weight and size. We also demonstrated that this reduction in size is due to the reduction in both cell number and cell size . In the hypoxia chambers, at 5% O2 levels, adult flies had significantly decreased body weight: the decrease in male body weight was about 25% and was further reduced to about 40% under 4% O2 (Figure 1C and 1D). Interestingly, the reduction in body weight and size were reversed to normal when the AF embryos were grown under normoxia. Life span was also studied in our selected and naïve flies. Hypoxia-selection did not affect lifespan (Figure 1B).
Whole Genome Expression Profiles of Hypoxia-Selected Drosophila melanogaster
Global gene expression profiles were examined in hypoxia-selected Drosophila melanogaster in the 3rd instar larval stage and in adults using cDNA microarrays that contained 13,061 known or predicted genes of the Drosophila melanogaster genome ,. After analyzing the data sets with a significant cutoff of >1.5 fold difference and a false discovery rate (FDR) of <0.05 , 2749 genes (1534 up- and 1215 down-regulated) were significantly altered in the larval stage, but only 138 genes (~20 times less than those in larvae) met this criteria (95 up- and 43 down-regulated) in the adult. The complete list of differentially regulated genes is detailed in Tables S1 and S2. Among them, 51 genes were found to be altered in both larval and adult stages with 23 up-regulated and 7 down-regulated genes (Figure 2A). Interestingly, most of the commonly up-regulated genes encode proteins that are related to immunity, and the majority of the commonly down-regulated genes encode proteins that are related to metabolism.
A) Comparison of gene expression alterations in hypoxia-selected Drosophila melanogaster in the larva and adult fly. Expression levels of 2749 genes (1534 up- and 1215 down-regulated) in larvae and 138 genes (95 up- and 43 down-regulated) in the adult were significantly altered in AF (fold change>1.5 and q<0.05). Red: up-regulation; Green: down-regulation. B) Summary of significantly altered biological processes in larvae and adult hypoxia-selected Drosophila melanogaster (p<0.05).
The significantly altered genes were further analyzed, based upon the Gene Ontological categorizations (GO) , by GenMAPP and MAPPFinder ,. Less than half of the differentially expressed genes (~40%) encode for proteins whose functions have not been characterized; the remaining encode proteins that are involved in numerous biological functions, such as development, metabolism, defense mechanisms and signal transduction (Tables S3 and S4). More than 30 biological processes were found to be altered in both larvae and adult and these were mostly related to either defense (especially immune responses, p<0.05) or metabolism (especially carbohydrate and peptide metabolism, p<0.05) (Figure 2B). The most affected processes in larvae were related to metabolism (1044 genes, especially carbohydrate metabolism, 135 genes, p<0.01). In addition, multiple components of signal transduction pathways were identified to be significantly altered in larvae and these included EGF, insulin, Notch, and Toll/Imd signaling pathways (Figure 3, p<0.05). To confirm the changes obtained from microarrays, 10 differentially expressed genes were randomly chosen and their expression levels were determined by real-time qRT-PCR using specific primers in larval samples (Table S5). The microarray results and the real-time PCR gave similar trends (r = 0.85, Figure S1).
The expression levels of genes encoding five signal transduction pathways were significantly altered in hypoxia-selected Drosophila melanogaster (p<0.05). The majority of the changes was an up-regulation. Significantly altered genes encoding the components A) of EGF receptor pathway, B) of the Insulin receptor pathway, C) of the JNK cascade, D) of the Notch pathway, and E) of the Toll/Imd pathway.
Changes in Genes Encoding Cellular Respiratory Enzymes
Significant gene changes were identified in the family of genes regulating cellular respiration in AF, especially in larvae. The majority of these changes consisted of a down- rather than an up-regulation of gene expression (Table S3). Besides one pyruvate kinase isoform (CG12229), most of the genes encoding glycolytic enzymes were dramatically down-regulated (Figures 4A and 4B). Similarly, suppression was also found in the TCA cycle (Figures 4A and 4C), lipid β-oxidation, and respiratory chain complex genes in larvae (Figure 5). As shown in Figures 5B and 5C, among the 50 measured genes encoding components of the respiratory chain, 33 genes were down-regulated, and only 3 genes were up-regulated. Interestingly, the suppression of these metabolic genes occurred only in the larvae and not in the adult fly (Figure 5C).
A) Schematic illustration of the alterations in genes encoding glycolytic and TCA cycle enzymes (green: down-regulation, black: not significantly changed, red: up-regulation). B) Cluster map of changes in genes encoding glycolytic enzymes in NF and AF larvae. C) Cluster map of changes in genes encoding TCA cycle enzymes in NF and AF larvae. Each cluster contained 9 hybridizations of NF and 8 hybridizations of AF samples.
A) Cluster map of changes in gene expression encoding components of respiratory chain complexes in NF and AF larvae. Each cluster contained 9 hybridizations of NF and 8 hybridizations of AF samples. B) Summary of alterations in each respiratory chain complex measured in larvae. C) Comparison of gene expression changes in each respiratory chain complex between larvae and adult.
Coordinated Suppression of TCA Cycle Enzymes
Since many genes encoding metabolic enzymes were significantly down-regulated, we asked whether such down-regulation was coordinated at a transcriptional level. Therefore, the GenomatixSuite (GEMS) software was used to identify transcription factor binding elements in defined cis-regulatory regions of the TCA cycle, glycolysis and lipid β-oxidation genes. The TCA cycle related genes were separated into two groups, one containing the significantly down-regulated genes (down-regulated group, 16 genes) and the other containing those that were not significantly altered or up-regulated genes (reference group, 8 genes) (Table S6). The binding elements of the Drosophila transcriptional suppressor hairy were present in the regulatory region of the down-regulated genes (15 of 16 cis-regulatory regions, 0.88/kb) but not in the reference group (1 out of 7 cis-regulatory regions, 0.15/kb) (p<0.0001, CHI-Test) (Figure 6A). Of particular interest, the expression level of hairy was significantly up-regulated in AF (Figure 6B, Table S1). This result suggested that hairy, a key transcriptional suppressor, reduced the expression of the TCA cycle genes. No such specific transcription factor binding elements were found in genes encoding glycolysis or β-oxidation enzymes.
A) Genomic localization of hairy binding elements in the cis-regulatory region of genes encoding TCA cycle enzymes. Arrowheads indicate consensus hairy binding sites and arrows indicate transcriptional start sites. B) Significant up-regulation of hairy expression in hypoxia-selected AF populations (p<0.01). C) Chromatin immunoprecipitation assay of gene l(1)G0030, SdhB and CG12344 under normoxia or hypoxia.
To confirm that hairy directly binds to the cis-regulatory regions of these candidate TCA cycle genes, chromatin immunoprecipitation (ChIP) assay was performed using a specific antibody to hairy in Drosophila Kc cells. The candidate hairy binding targets were tested using specific primers in both hypoxia and normoxia (Table S5). For a negative control, we included a cis-regulatory region of another TCA cycle gene (i.e., CG6629) that was up-regulated in AF and had no hairy binding elements detected. We found that hairy did bind to the cis-regulatory region of gene l(1)G0030 in hypoxia but not in normoxia. Similarly, hairy was also found to bind to the cis-regulatory region of gene SdhB under both hypoxic and normoxic conditions, and its binding activity was significantly higher in hypoxia than in normoxia. Such hypoxia-induced increase in hairy binding did not occur in CG12344, a hairy target gene, which encodes for a non-metabolic gene (i.e., an isoform of GABA-A receptor). This result demonstrates that the down-regulated TCA cycle genes are direct targets of hairy, and hairy specifically suppresses their expression under hypoxia. Furthermore, such hypoxia-induced suppression of TCA cycle genes was abolished in the hairy loss-of-function mutants, h1 or h1j3 (Figure 7A). To further evaluate the role of hairy in hypoxia tolerance, we determined the survival rate of these two hairy loss-of-function mutants at 6% of O2. This mild level of O2 was used since it is sufficient to show differences between the mutants and controls. As shown in Figure 7B, both hairy loss-of-function mutants exhibited much lower survival rate (p<0.0001, CHI-Test) as compared to controls, proving the contribution of hairy to hypoxia tolerance in flies.
A) Abolished suppression of genes encoding TCA cycle enzymes in hairy loss-of-function mutants. The differences in gene expression were measured in yw control and hairy mutants using real-time PCR. Individual genes encoding TCA cycle enzymes had a significantly higher expression level in all hairy mutants than those in control except gene CG10219. Data were presented as means±SD (p<0.01). Gene description: l(1)G0030: citrate synthase; Idh: isocitrate dehydrogenase; l(1)G0156: isocitrate dehydrogenase; CG6439: isocitrate dehydrogenase; SdhB: succinate dehydrogenase; CG10219: succinate dehydrogenase; CG6666: succinate dehydrogenase; l(1)G0255: fumarase. B) Significant reduction in hypoxia survival in hairy loss-of-function mutants. Embryos from loss-of-function hairy mutants (h1 and h1j3) and controls (Canton-S and yw) were cultured at normoxic or 6% O2 hypoxic condition. The ratio of adult flies to pupae was determined as survival rate of each stock. The loss-of-function hairy mutants exhibited a significantly reduced rate of hypoxia survival. Data were presented as means±SD (** p<0.01).
Differences in DNA Sequence between AF and NF
Since some of the current experiments suggested that hypoxia tolerance was a heritable trait in the AF population, we studied these flies further to determine the genetic basis of this heritability. Two types of experiments were performed. First, we examined the activity levels of 2 key glycolytic enzymes, triose phosphate isomerase (TPI) and pyruvate kinase (PK) in NF and AF. We argued that, if there was a genetic basis for the change in enzyme activity, such activity level would be altered not only in the hypoxia-cultured flies but also in those cultured in normoxia, i.e., the enzyme activity would be different from that in NF, whether in hypoxia or normoxia. As shown in Figures 8A and 8B, the activity of TPI in AF was indeed reduced when these flies were cultured in either normoxia or hypoxia. When PK activity was assessed, however, AF had a higher level activity under hypoxia and stayed at the same level in normoxia without a significant increase as compared to NF. Second, the genomic locus encoding TPI was sequenced to determine whether there were any differences between AF and NF. We chose to sequence the TPI locus, because, unlike PK, TPI is encoded by a single gene. As expected, a number of significant polymorphic differences were identified in the AF population that included 3 SNPs (−77T/C, −53A/G, −51A/T) and 1 indel (−74 to −66) in the cis-regulatory region, 1 synonymous SNP (1051A/G) in the coding region, 1 SNP (1480A/G) in the 3′-untranslated region, and 1 SNP (1662C/T) in the downstream region (Figure 8C, Table S7), demonstrating significant genetic differences in the AF population (p<0.001, CHI-Test).
A) Enzymic activity and hypoxia response of TPI in AF and NF. TPI activity was measured in 3rd instar larvae of AF and NF cultured under either normoxia or hypoxia. AF had a significantly reduced enzymic activity than NF under both hypoxic and normoxic conditions. In contrast to the effect of hypoxia in NF, hypoxia did not induce a significant reduction on enzyme activity in AF. Data were presented as means±SD (* p<0.05, #p>0.05). B) Enzymic activity and hypoxia response of PK in AF and NF. The enzymic activity of PK was measured in 3rd instar larvae of NF and AF cultured under either normoxia or hypoxia. There was no significant difference in PK activity between AF and NF cultured under normoxia. Hypoxia induced a significant reduction of PK activity in NF but not in AF. Data were presented as means±SD (* p<0.05, #p>0.05). C) Comparison of allelic frequency in the genomic region of TPI gene between AF and NF. The genomic locus encoding TPI gene was amplified by high fidelity PCR using specific primers. The PCR products were purified and cloned into pCR4-TOPO plasmid to create a plasmid library for the TPI alleles of AF and NF populations. Ten clones from the AF or NF TPI allele library were sequenced and compared by using ClustalW2 software and DnaSP 4.0. The statistical power for the comparison was calculated by GPower software 3.0.3. Seven significant polymorphic differences were identified in the AF population that included 3 SNPs (−77T/C, −53A/G, −51A/T) and 1 indel (−74 to −66) in the cis-regulatory region, 1 synonymous SNP (1051A/G) in the coding region, 1 SNP (1480A/G) in the 3′-untranslated region, and 1 SNP (1662C/T) in the downstream region (p<0.001, CHI-Test).
The current laboratory selection experiments have shown that the hypoxia-selected flies have garnered, with ongoing generations, a spectacular ability to survive extremely low O2 conditions. To put this ability in perspective, these flies live perpetually now at an oxygen level that is equivalent to that above Mount Everest by ~4,000 meters. This phenotypic breakthrough occurred after 32 generations of selection. One of the most profound phenotypic abnormalities is a reduction in body size in the AF flies. This substantial decrease in body size was presumably of physiologic relevance, which is likely related to shorten the O2 diffusion distances for improved survival. It is very interesting to note that, though we show evidence of heritability of the hypoxia survival trait in the selected flies, the change of body size and weight did not seem to be heritable, as body size was reverted to normal, even after a single generation in room air.
The goal of the current study was to determine the genetic and molecular basis of adaptation to long-term (i.e., over generations) hypoxic environments. Since survival under long term hypoxia is a complex trait, we expected this adaptation to be controlled by a number of pathways and genes. Indeed, our microarray and genetic analyses have shown that the survival of both larvae and adult flies was accompanied by alterations in a number of major signaling pathways, such as EGF, Insulin, Notch and Toll/Imd pathways. In this regard, there are a number of interesting observations made from our studies. First, the number of significantly altered genes was much larger in larvae than in the adults. More than 20% of all measured genes were significantly altered in the larval samples whereas only ~1% changed in the adults, using the same statistical criteria. This major difference between larvae and adults may have a number of explanations, including the fact that larval cells undergo rapid growth, proliferation and differentiation as compared to adults. Second, although adaptive changes were found in both larvae and adult flies, it is possible that these changes were induced through both genetic and/or epigenetic physiologic regulation. Since we found that a) the hypoxia-selected flies could live for a number of generations in normoxia and survive again when introduced back in 4% hypoxia, b) some glycolytic enzymes maintained their activity in the AF population at a lower (or higher) level not only during hypoxia but also in normoxia (e.g., TPI and PK), and c) a number of polymorphic changes existed in AF as compared to NF, our data provided direct evidence for actual genetic alterations that were responsible for, at least in part, tolerance to severe hypoxia. Third, several signal transduction pathways were altered in the selected flies, i.e., EGF, Insulin, Notch and Toll/Imd pathway, which have also been found to be activated by hypoxic stimuli in mammalian tissues/cells –. For example, we and others have shown that the Notch receptor and its targets were altered in mouse heart  and cultured cells , following chronic hypoxia. Such similarities in hypoxia responses demonstrated that some of the mechanisms underlying hypoxia-tolerance are conserved across species. Fourth, previous studies have demonstrated an enhancement of glycolytic activity as a major metabolic response in cells/tissues following acute (in minutes or hours) hypoxia, in contrast, our present data showed that many genes encoding glycolytic enzymes were down-regulated in the AF. Moreover, no significant lactate accumulation was found in the AF flies (unpublished observations from our laboratory). Finally, although hypoxia-tolerance is a complex trait, a single gene alteration, such as that of hairy, can remarkably make a significant difference in terms of survival.
For more than three decades, physiologists have debated the importance of down-regulation of metabolism in hypoxia tolerance in some tolerant animals such as the turtle. For example, Hochachka and others have argued that anoxia-tolerant organisms depress their metabolism in order to minimize the mismatch between supply and demand –. While this idea, based on metabolic data, is intuitively appealing, there is no information about how various metabolic enzymes could be coordinated in order to survive severe long lasting hypoxia. Our current work provides the first evidence showing that such coordination can be achieved at a transcriptional level by a seemingly metabolic switch, i.e., hairy, which is a transcriptional suppressor. This notion is supported by a number of observations from current study: a) expression of hairy was up-regulated in AF, b) hairy-binding region was presented in the cis-regulatory regions of the down-regulated genes but not others, c) the functional ChIP analysis led us to believe that the down-regulation of these metabolic genes is based on the changes of hairy, especially that its binding was not increased for other, non-metabolic target genes, e.g., CG12344, and d) hairy loss-of-function mutations abolished the suppression on the expression of TCA cycle genes and significantly reduced hypoxia survival in Drosophila. This decreased survival in flies carrying the hairy mutation is particularly important since these experiments strongly demonstrate that hairy contributes to hypoxia tolerance through the regulation of TCA cycle enzymes. While it is possible that the decreased survival is not related to the role that hairy plays in metabolic regulation but due to an inherent weakness of the hairy mutants, this is much less likely because a) we have studied in the past different mutation alleles in flies and they do not necessarily behave differently in hypoxia , and b) we chose two different mutants of hairy and they have similar effects.
Another interesting observation in this work is related to the enzymatic activities of triose-phosphate isomerase (TPI) and pyruvate kinase (PK) in AF. We hypothesized that, if there is a genetic basis for the change in enzyme activity, we should be able to detect the alterations in AF flies that were cultured in both hypoxia and normoxia, and the enzyme activity should maintain different from those in NF, whether in hypoxia or normoxia. Indeed, as expected, we found that the expression level and enzymatic activity of TPI were significantly lower in AF than those in NF in both hypoxia and normoxia. In addition, we identified 7 polymorphic differences in the genomic locus of the TPI gene in AF which demonstrated a genetic modification of this locus in AF strain. In contrast, the activity of PK in AF did not differ from that of NF in normoxia, although its activity was significantly higher in AF under hypoxia (Figure 8B). This result demonstrated that there was an inhibition of this enzyme in NF under hypoxia, and such hypoxia-induced inhibition was abolished in AF. On the surface, this result might weaken our argument, a potential explanation for such a difference between PK and TPI is that the regulation of PK is much more complicated. Indeed, there are 7 genes encoding PK in D. melanogaster. In AF, we found that 1 gene (i.e., Pyk) was down-regulated and another gene (i.e., CG12229) was up-regulated. Therefore, in addition to possible genetic rearrangements, other factors may play a role to keep higher activity of PK in AF under hypoxia and to minimize the difference between AF and NF in normoxia.
If the changes that led to enhanced survival in extremely low O2 levels in the AF population are genetic in nature, as we demonstrated in this work, it is important to note that the breakthroughs in survival to lower and lower O2 levels took place after a relatively small number of generations in the Drosophila. This relatively small number of generations was also found when previous investigators were studying other phenomena such as geotaxis . If translated into human years, the 32 generations that were needed to alter the phenotype and genotype in Drosophila can be approximated to about a thousand years. Although changes in the DNA code with selection pressure could take a much longer period of time (potentially thousands and millions of years in “Darwinian time”), this work demonstrated that such changes in DNA and phenotype could proceed at a much faster rate, presumably because of the trait itself or the selection pressure applied.
In summary, we have generated a Drosophila melanogaster strain that is very tolerant to severe hypoxic conditions through long-term experimental selection. Several adaptive changes have been identified in the hypoxia-selected AF flies that include up-regulation of multiple signal transduction pathways, modulation of cellular respiration enzymes, and polymorphic differences in metabolic enzymes such as TPI. While we believe that multiple pathways contribute to hypoxia-tolerant trait in this Drosophila strain, we demonstrate that hairy-mediated metabolic suppression is an important one. The adaptive mechanisms identified in this hypoxia-tolerant Drosophila model may also play a crucial role in protecting mammals from hypoxia injury.
Materials and Methods
Drosophila melanogaster Stocks, Hypoxia Selection, and Phenotypic Assays
Twenty-seven isogenic Drosophila melanogaster lines (kindly provided by Dr. Andrew Davis) were used as parental stocks for the long-term hypoxia-selection experiment as described previously . Briefly, embryos collected from the parental population were divided into 6 groups, 3 groups of them were subjected to long-term hypoxia-selection, and 3 other groups were maintained under normoxia as controls. Both hypoxia-selection and control experiments were performed in specially designed population chambers (26 cm×16 cm×16 cm). These chambers were connected to either O2 at certain concentrations (balanced with N2, for the hypoxia-selection experiments) or to room air (21% O2, for the control experiments). The humidity in the chambers was maintained by passing the gas through water prior to going into the chambers. The flow speed was monitored by 565 Glass Tube Flowmeter (Concoa, Virginia Beach, VA), and the O2 level within the chamber was monitored with Diamond General 733 Clark Style Electrode (Diamond General Development Corp., Ann Arbor, MI). The selection was started at 8% O2 and this concentration was gradually decreased by 1% each 3 to 5 generations to keep the selection pressure. Embryos, 3rd instar larvae and adult flies were collected from each generation and stored at −80°C for analyses. The results presented in the current study were derived from expression arrays using larval and adult samples.
The body weight of hypoxia-selected flies was determined at each generation. Male flies (n = 100) from hypoxia or control chambers were collected, weighed and used as the index of body weight.
The hairy loss-of-function mutants (h1 and h1j3) were obtained from Drosophila Stock Center (Bloomington, IN). The survival rate of these stocks in hypoxia was determined by culturing them in a 6% O2 environment. After 3 weeks in culture, the number of live adult flies and pupae were counted. The ratio between live adult flies to the total number of pupae was calculated and presented as survival rate. The statistical significance of survival between hairy mutants and controls was calculated by CHI-test.
cDNA Microarray Analysis
cDNA microarrays containing 13,061 known or predicted genes of the D. melanogaster genome were processed according to previous descriptions ,. Nine larval samples from AF or NF, 6 adult samples from AF or NF were included in this analysis. Each larval sample contained a pool of 25 3rd instar larvae, and each adult sample contained 25 male and 25 female adult flies from each individual population. Total RNA was extracted from the samples using TRIzol (Invitrogen, Carlsbad, CA) followed by a clean-up with RNeasy kit (Qiagen, Valencia, CA). Three µg of total RNA from each sample was amplified with an in vitro transcription-based strategy . A common reference design was applied for the hybridizations, and the reference RNA sample was created using a balanced pool of 3rd instar larvae (for the larval samples) or adult flies (for the adult samples) from each parental line. This reference was chosen so that relative abundance of each transcript could be calculated individually, and the relative levels of each transcript among biological replicates could be compared. A total of 30 arrays were included in this analysis, and the hybridizations were done in different days using arrays printed from different batches. Microarray images were acquired by GenePix 4000 microarray scanner using GenePix Pro 3 microarray analysis software (Axon Instruments, Sunnyvale, CA, USA). The statistical significance (q-value, i.e., false discover rate (FDR)) and the ratio of the changes in expression was calculated using Significance Analysis of Microarray (SAM) software  following LOWESS normalization. The fold changes were presented as ratios, if up-regulated, or −1/ratio, if down-regulated. The gene ontology (GO) based analyses were performed using GenMAPP software . The microarray data can be retrieved using access number GSE8803 in the GEO database at http://www.ncbi.nlm.nih.gov/geo.
Semi-Quantitative Real-Time RT-PCR
Semi-quantitative real-time RT-PCR was used to evaluate the result of microarrays and to determine the differences in expression levels of genes encoding TCA cycle enzymes between the hairy mutants and control. All specific primers were designed by Primer 3 software  and synthesized at ValueGene (San Diego, CA) (Table S5). First strand cDNA was synthesized using SuperScriptII reverse transcriptase and Oligo-(dT) primer. Real-time PCR amplification was performed using ABI Prism 7900HT Sequence Detection System (Applied Biosystems, Foster City, CA). For each reaction, 10 µl of 2× SYBR green PCR master mix (Applied Biosystems, Foster City, CA) and 0.5 µM of both forward and reverse primers along with 100 ng of each appropriate cDNA samples were mixed (total reaction volume: 20 µl). Melting curves were determined and the final products were isolated with 4% agarose gel to ensure specificity of the reaction. The relative expression level was calculated using 2−ΔΔCt method, as described previously –. Drosophila melanogaster β-actin was used as internal control. The final results were presented as fold change of AF over NF or hairy mutants over yw control. All experiments were done in triplicate.
Enzyme Activity Assays
The enzymatic activity of Triose Phosphate Isomerase (TPI) and Pyruvate Kinase (PK) were determined as previously described with modifications . Briefly, the assay samples were extracted from 3rd instar larvae cultured under either normoxic or hypoxic condition (4% O2). 0.2 ml (100 mg wet weight/ml) of isolation medium (0.25 M sucrose,1 mM EDTA-K, 5 mM HEPES-Tris, pH 7.4, with protease inhibitors) was added and the suspension of larval tissue in isolation medium was transferred into a 2 ml all glass homogenizer. 10% (v/v) Triton X-100 was added to this suspension making the final concentration of Triton X-100 0.5% (v/v). Then the tissue was homogenized with the B (i.e., tight) pestle. Aliquots of this homogenate were employed for enzymatic activity measurements. The enzymatic activities of TPI or PK were determined using 10, 20, or 30 µl of the homogenate with proper substrates. The dynamic of color formation was recorded using Beckman Coulter DU800 Spectrophotometer at selected wave length for each substrate. The kinetic parameters of the reaction were calculated by curve fitting.
Identification of Transcription Factor Binding Element in cis-Regulatory Region
The common transcription factor binding sites in the defined promoter regions of candidate genes were analyzed using GenomatixSuite (Genomatix Software GmbH, Germany). The genes encoding TCA cycle or β-oxidation enzymes were separated into down-regulated or reference groups. The genome DNA sequences from 2000 bp upstream of the first transcription starting site (TSS) to 500 bp downstream of the last TSS of each gene was downloaded and used as cis-regulatory region of the gene (Drosophila genome R5.2) . These sequences were subjected to GEMS analysis to identify common transcription factor binding elements . The statistical significance of the transcription factor binding element frequency in the AF and NF population was analyzed by CHI-test.
Chromatin immunoprecipitation and PCR detection of hairy binding in the cis-regulatory regions of genes encoding TCA cycle enzymes were performed in cultured Drosophila Kc cells (obtained from Dr. Amy Kiger, UCSD) ,. The Kc cells were treated with 0.5% O2 for 4 hours. About 106 cells were used in each ChIP experiment. Chromatin immunoprecipitation was carried out using ChIP assay kit (Upstate, Temecula, CA) according to the manufacture's instructions. The immunoprecipitation was performed overnight at 4°C with 2 µg of hairy antibody (Abcam, Cambridge, MA). DNA fragments were purified with phenol:chloroform (Invitrogen, Carlsbad, CA). For PCR, 2 µl of a 25 µl DNA extraction was amplified with specific primers (Table S5).
DNA Sequencing and Analysis
Genomic DNA was extracted from 15 male AF or NF adult flies. The samples were ground in 400 µl of homogenate buffer (100 mM Tris/HCl, 100 mM EDTA, 100 mM NaCl and 0.5% SDS, pH7.5) and incubated at 65°C for 30 min. Genomic DNA was extracted by adding in 800 µl extraction solution (1 2.5 (v/v) of 5 M KAc and 6 M LiCl). After 15 min of centrifugation at 13,000 rpm, the supernatant was transferred into a new tube and the genomic DNA was precipitated by adding 600 µl of isopropanol. The DNA pellet was washed with 70% of ethanol and dissolved in TE buffer.
The genomic locus encoding TPI gene was amplified by PCR using specific primers (forward primer: GTTTAAGGTCCGCAGAGGTG, and reverse primer: ATTTTGGCAAGCCTGTTGAT). All the coding exons and intronic flanking regions were amplified by polymerase chain reaction (PCR) using the high fidelity proofreading DNA polymerase, Platinum Pfx DNA Polymerase (Invitrogen, Carlsbad, CA). The PCR products were purified and cloned into pCR4-TOPO plasmid to create the plasmid library for TPI alleles of the AF and NF population. Cycle sequencing was performed on an ABI automated sequencer (Applied Biosystems, Foster City, CA) by Eton Biosciences, Inc. (San Diego, CA). Ten clones from AF or NF TPI allele library were sequenced and compared by using ClustalW2 software  (http://www.ebi.ac.uk/Tools/clustalw2/) and DnaSP 4.0 . The statistical power for the comparison was calculated by GPower software 3.0.3 .
Correlation between Microarray and qRT-PCR Results.
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List of Significantly Altered Genes in Hypoxia-Selected Drosophila melanogaster at Larval Stage.
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List of Significantly Altered Genes in Hypoxia-Selected Drosophila melanogaster at Adult Stage.
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List of Significantly Altered Biological Processes in Hypoxia-Selected Drosophila melanogaster at Larval Stage.
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List of Significantly Altered Biological Processes in Hypoxia-Selected Drosophila melanogaster at Adult Stage.
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Primers for qRT-PCR and ChIP-PCR Assays.
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Summary of Genomic Locations of hairy Transcription Repressor Binding Elements in the cis-Regulatory Regions of Genes Encoding TCA Cycle Enzymes.
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Comparison of the TPI Genomic Locus between NF and AF with Multiple Sequence Alignment.
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We thank Orit Gavrialov, Juan Wang, Jenna Lau, Nuny Morgan and Ying Lu-Bo for technical assistance.
Conceived and designed the experiments: DZ KPW GGH. Performed the experiments: DZ JCKL. Analyzed the data: DZ JX JCKL NJS. Contributed reagents/materials/analysis tools: NJS KPW. Wrote the paper: DZ JX GGH.
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