- Open Access
Doxycycline-induced expression of sense and inverted-repeat constructs modulates phosphogluconate mutase (Pgm) gene expression in adult Drosophila melanogaster
© Allikian et al., licensee BioMed Central Ltd 2002
Received: 24 October 2001
Accepted: 8 March 2002
Published: 15 April 2002
A tetracycline-regulated (conditional) system for RNA interference (RNAi) would have many practical applications. Such a strategy was developed using RNAi of the gene for phosphogluconate mutase (Pgm). Pgm is a candidate lifespan regulator: PgmS allele frequency is increased by selection for increased lifespan, whereas PgmM and PgmF allele frequencies are decreased.
The Pgm alleles were cloned and sequenced and were found to differ by amino-acid substitutions consistent with the relative electrophoretic mobilities of the proteins. The 'tet-on' doxycycline-regulated promoter system was used to overexpress PgmS in a wild-type (PgmM) background. Enzyme activity increases of two- to five-fold were observed in five independent transgenic lines. Tet-on was also used to drive expression of an inverted-repeat fragment of Pgm coding region. The inverted-repeat transcript was expected to form a dsRNA hairpin, induce RNAi, and thereby reduce endogenous Pgm gene expression at the RNA level. Endogenous Pgm RNA levels in adult flies were found to be reduced or eliminated by doxycycline treatment in five independent inverted-repeat transgenic lines. Our results show that doxycycline-regulated expression of inverted-repeat constructs can cause a conditional reduction in specific gene expression. The effect of sense and inverted-repeat construct expression on lifespan was assayed in multiple transgenic lines. Under the conditions tested, altered Pgm gene expression had no detectable effect on adult Drosophila lifespan.
A system for conditional RNAi in Drosophila adults shows promise for assay of gene functions during aging. Our results indicate that Pgm does not have a simple strong effect on longevity.
Conditional gene expression systems such as promoters regulated by tetracycline or doxycycline (DOX) have several advantages for testing the effects of genes on aging and lifespan [1,2,3]. In the 'tet-on' system, feeding DOX to Drosophila melanogaster causes high levels of transgene expression in all tissues. By waiting until the young adult stage to administer DOX, all of pre-adult development is identical between control and experimental groups, and any difference in lifespan must be due to changes in the adult. Subtle differences in the genetic background of Drosophila strains can have significant effects on lifespan [4,5,6]. With the tet-on system, control and experimental animals have identical genetic backgrounds, and therefore any differences in lifespan must be due to DOX administration and transgene expression. DOX itself, and overexpression of control genes such as Escherichia coli lacZ, have no detectable effects on lifespan . In contrast, several genes have been identified for which DOX-regulated overexpression has negative effects on lifespan, and overexpression of the dGMII gene, encoding α-mannosidase II, was associated with slightly increased lifespan .
Expression of antisense RNA has long been known to be able to inhibit gene expression in Drosophila and other organisms [8,9,10,11,12]. Double-strand RNA (dsRNA) formed by hybridization of sense and antisense sequences is thought to initiate a pathway in which homologous RNA sequences are destroyed. This phenomenon has been referred to as post transcriptional gene silencing (PTGS) or RNA interference (RNAi). Expression of inverted-repeat constructs, where the transcript is expected to fold into a dsRNA hairpin, has been shown to be an efficient initiator of RNAi [13,14,15]. In experiments reported here, the tet-on system was used to drive expression of inverted-repeat constructs in Drosophila to determine if a conditional system for RNAi could be created.
In natural populations, lifespan and reproductive period are thought to co-evolve . The duration of the reproductive period is subject to natural selection, and lifespan is altered as a consequence. Significant experimental support for this model has come from laboratory selection experiments with D. melanogaster [17,18,19,20,21]. Genetically heterogeneous Drosophila populations have been selected over hundreds of generations for late-life reproduction. Such selection results in strains with increased lifespan relative to controls. Selection is thought to function by altering the frequency of gene alleles present in the starting population. Selected strains exhibit a number of correlated phenotypes. The correlated phenotypes can vary somewhat depending on the starting strains used; however, increased stress-resistance appears to be common to all or most long-lived strains [22,23,24,25,26]. In one well studied set of five replicate control (B) and long-lived (O) strains, lifespan was doubled and was correlated with increased stress-resistance and increased glycogen and lipid stores [27,28].
Starch-gel electrophoresis has been used to assay for changes in the frequency of enzyme electrophoretic alleles in the O and B lines. A change in the frequency of Cu/Zn-superoxide dismutase (Cu/ZnSOD) alleles was observed, with the more active allele enriched in the long-lived O strains . Consistent with this observation, overexpression of Cu/ZnSOD in transgenic Drosophila has been shown to be sufficient to cause significant increases in lifespan [30,31]. The most dramatic change in allele frequency in the O and B lines was observed for the gene for phosphogluconate mutase (Pgm) . Pgm exists in three electrophoretic forms: fast (PgmF), medium (PgmM) and slow (PgmS). PgmM predominates in the B strains, whereas PgmSallele frequency is on average ten-fold higher in the long-lived O strains relative to the B controls. When O strains were taken off selection for several generations (back-selection), lifespan decreased and PgmS allele frequency was reduced to levels more like those in B strains. These results suggest that Pgm or a closely linked gene is responding to selection, and make PgmS a candidate lifespan regulator.
Pgm encodes the enzyme phosphoglucomutase, which inter-converts glucose 1-phosphate and glucose 6-phosphate. Its activity is therefore important for both glycolysis and glycogen synthesis, and the altered Pgm allele frequency might therefore be relevant to the increased glycogen and lipid stores of the O strains. If the increased PgmS allele frequency is contributing to the unique phenotypes of the long-lived O strains, this might be because PgmS has increased or decreased enzyme activity, or enzyme activity has been altered in some way (perhaps by a change in its regulation). One way to begin to test these models experimentally is to engineer transgenic flies with increased or decreased Pgm expression and assay for effects on lifespan.
The northern blots were also hybridized with a Pgm-specific probe corresponding to Pgm coding-region sequences (+1 to +700) located outside the region used to create the inverted repeat. This probe is therefore specific for the endogenous Pgm transcript. Using this probe the smear of hybridization derived from the inverted-repeat construct was no longer detected, and the endogenous Pgm RNA levels were more readily observed and quantitated (Figure 3b). DOX induced expression of the inverted-repeat construct was found to cause a reduction of endogenous Pgm RNA levels. The decrease varied across the five transgenic lines, with reductions ranging from 1.3- to 24-fold. The inverted-repeat construct therefore appears to function as expected to induce RNAi and cause decreased expression of the endogenous Pgm gene. In the control strains where no transgene is expressed, DOX administration was found to have no effect on Pgm transcript levels (Figure 3c).
PGM enzyme activity
Enzyme activity (ΔOD/μg/min)
Percentage change (p-value)
0.1105 ± 0.014
0.5926 ± 0.089
0.1035 ± 0.004
0.5901 ± 0.070
0.1018 ± 0.013
0.4585 ± 0.010
0.1138 ± 0.014
0.5829 ± 0.018
0.0893 ± 0.010
0.4825 ± 0.014
0.1100 ± 0.020
0.6706 ± 0.085
0.1131 ± 0.007
0.4939 ± 0.048
0.0925 ± 0.012
0.2608 ± 0.060
0.1301 ± 0.003
0.3093 ± 0.047
0.1179 ± 0.0121
0.1162 ± 0.0069
0.0966 ± 0.0076
0.0625 ± 0.0049
0.1198 ± 0.0117
0.0810 ± 0.0070
0.0789 ± 0.0081
0.0852 ± 0.0047
0.1569 ± 0.0118
0.0723 ± 0.0077
0.0729 ± 0.0075
0.0736 ± 0.0041
0.2038 ± 0.0134
0.1241 ± 0.0077
0.1631 ± 0.0089
0.1179 ± 0.0054
0.2853 ± 0.014
0.1757 ± 0.002
0.1014 ± 0.0029
0.1019 ± 0.0093
0.0997 ± 0.0038
0.1118 ± 0.0038
Mean lifespan at 25°C
Mean lifespan (25°C)
Percentage change (p-value)
56.723 ± 0.763
56.048 ± 0.743
66.921 ± 0.746
64.955 ± 0.731
58.167 ± 0.777
54.140 ± 0.817
68.169 ± 0.686
67.966 ± 0.614
68.256 ± 0.845
65.236 ± 0.870
71.202 ± 0.730
67.268 ± 0.860
63.720 ± 0.844
67.568 ± 0.939
70.610 ± 0.607
72.508 ± 0.803
89.660 ± 0.992
84.275 ± 0.806
58.568 ± 0.939
58.930 ± 0.938
59.957 ± 0.825
69.817 ± 0.547
66.428 ± 0.561
66.801 ± 0.640
55.415 ± 0.965
56.486 ± 1.014
69.061 ± 1.302
71.339 ± 1.253
71.111 ± 0.979
75.099 ± 1.100
75.958 ± 0.877
72.464 ± 0.917
59.855 ± 0.647
63.297 ± 0.656
83.443 ± 0.727
82.672 ± 0.948
74.312 ± 0.941
70.947 ± 0.810
Mean lifespan at 29°C
Mean lifespan (29°C)
Percentage change (p-value)
40.902 ± 0.834
43.910 ± 0.782
45.693 ± 0.581
44.663 ± 0.618
51.298 ± 0.626
53.989 ± 0.719
49.874 ± 0.541
48.681 ± 0.647
35.010 ± 0.470
36.030 ± 0.619
48.827 ± 0.404
48.568 ± 0.621
45.358 ± 0.606
47.726 ± 0.566
48.759 ± 0.647
51.646 ± 0.598
49.863 ± 0.583
51.826 ± 0.679
41.747 ± 0.499
39.539 ± 0.981
The phenomenon of RNAi (or PTGS) is of great interest for two reasons [9,10,11,12]. First, it represents an evolutionarily conserved pathway that probably has important functions in the regulation of gene expression and the control of transposable elements. Second, it provides a means for researchers to test gene functions by experimentally downregulating expression of specific genes under well controlled conditions. In Drosophila, RNAi can be initiated by injection of dsRNA into embryos, and this has allowed identification of novel phenotypes for genes during development . However, injection has limited potential application in the adult, as it is unlikely that the RNAi could be targeted to all tissues, or to specific tissues, and the trauma of injection is likely to have negative effects on phenotypes such as lifespan. Transgenic constructs have been used to cause RNAi in Drosophila, by using various promoters to drive expression of inverted-repeat fragments of gene coding regions [14,15]. Using the conditional tet-on promoter system to drive expression of an inverted-repeat provided conditional RNAi of the Pgm gene. This conditional system should have many applications, both in the study of the RNAi pathway itself and in the design of experiments where RNAi is used a research tool. Conditional RNAi should be particularly useful to study phenotypes in the adult such as aging and lifespan. Conditional gene-expression systems have previously been used to identify positive regulators of lifespan, such as Cu/ZnSOD and dGMII [7,31]. In addition, mutations have been used to identify several genes in Drosophila that act as negative regulators of lifespan, such as mth, INDY, InR and chico [35,36,37,38]. For mth and InR the null phenotype of the genes is lethality. Therefore it is only rare hypomorphic alleles or allele combinations that allow the animals to survive to adult stage where increased lifespan can be observed. Conditional RNAi should provide a powerful means to study these genes and other negative regulators of aging and lifespan. Inactivation or downregulation of the genes specifically in the adult using tet-on RNAi may allow increased lifespan without confounding effects on development. Lam and Thummel have recently reported the use of a heat-shock gene promoter to drive expression of dsRNA, and the efficient conditional inhibition of gene expression during larval and pupal stages of Drosophila development .
Genetic selection of Drosophila populations for late-life reproduction caused the correlated phenotype of increased lifespan and increased the frequency of the slow electrophoretic allele, PgmS, of the Pgm gene. If PgmS contributes to the increased lifespan phenotype of the selected strains, it might be because PgmS has increased activity, decreased activity or activity that is altered in some way such as through its regulation or subcellular localization. The Pgm alleles were cloned and sequenced and were found to differ by amino-acid substitutions consistent with the relative electrophoretic mobilities of the encoded enzymes.
A recent study reported the sequencing of several fast, medium and slow electrophoretic alleles of Pgm from a wild population of D. melanogaster . The sequences reported in that study (Verrelli alleles) are comparable to those reported here (Ives alleles) as follows: the medium Verrelli allele used for alignment is identical in amino-acid sequence to the Ives medium allele. The Verrelli fast alleles are identical to the Ives fast allele in each of the three amino-acid positions at which the Ives fast differs from the Ives medium (wild-type) allele. There are a number of differences between the Verrelli slow alleles and the Ives slow allele. The Verrelli slow alleles are not all identical to each other. The Ives slow allele differs from the Ives medium (wild-type) amino-acid sequence at two positions (amino-acid positions 6 (E → G) and 9 (A → T)). The amino-acid change in the Ives slow allele at position 6 (E → G) is not reflected in any of the Verrelli slow alleles. The second amino-acid change in the Ives slow allele (at position 9) is shared by two of the Verrelli slow alleles. In addition, the Verrelli slow alleles have ammo-acid substitutions that are not shared by the Ives slow allele. The data are consistent with the conclusion that Pgm is highly polymorphic and subject to selection in natural populations [40,41]. Consistent with this idea, Pgm haplotypes and glycogen content have been found to vary among flies at different latitudes .
The tet-on promoter system allowed a test of the hypothesis that increasing or decreasing Pgm gene expression would affect lifespan. PGM enzyme levels were increased two- to five-fold using a sense transgenic construct, and Pgm RNA levels were decreased 1.3- to 24-fold by driving expression of an inverted-repeat construct. No changes in lifespan were detected that were consistent across multiple transgenic lines or replicate experiments. The results indicate that simply increasing or decreasing Pgm gene expression does not significantly affect the lifespan of adult Drosophila, at least under the conditions tested.
The PgmS allele used in these experiments was cloned from the Ives strain, which is the progenitor of the long-lived selected strains and their controls. The high degree of polymorphism of Pgm makes it possible that the slow electrophoretic allele in the Ives strain could consist of multiple DNA sequence forms. The failure to observe effects on lifespan could therefore conceivably have resulted from overexpression of the wrong DNA sequence form of PgmS. However, PgmS was cloned and sequenced from four independent lines derived from the Ives strain and the clones had the same DNA sequence. The data therefore suggest that most, if not all, of the PgmS alleles in these strains have the same sequence, making sequence heterogeneity an unlikely explanation of the present results.
The results suggest several possibilities for the relationship of Pgm allele frequency to the increased lifespan of the selected strains. The first is that PgmS might in fact contribute to the increased lifespan of the selected strains as a result of an increased or decreased activity, but that the effect on lifespan is too small to be detected in these assays. The lifespan assay appears to have a variability with control strains of approximately -5% to +5%, as seen in the data presented here and elsewhere (G.L., D. Bhole and J.T., unpublished results). It is therefore unlikely that an effect much smaller than 10% could be identified. The second possibility is that Pgm allele frequencies are altered because of selection for an unknown linked gene, and this possibility cannot be ruled out at this time. The experiments presented here suggest that tet-on regulated overexpression and RNAi of genes near Pgm may be a promising approach.
Third, an interesting model is that PgmS contributes to increased lifespan of the selected strains because of an alteration in its regulation and/or subcellular localization. The sequence analysis of the Pgm alleles reveals a novel potential site in PgmS for phosphorylation by PKC; however, the potential significance of this change is unknown. The PgmS allele was used for the overexpression experiments presented here, and presumably the overexpressed enzyme should be subject to any regulation or localization characteristic of PgmS. However, the PgmS enzyme was overexpressed in a 'wild-type' PgmM background, and it may be that any phenotypic consequences of PgmS allele function are not apparent when PgmM is also present. Finally, another possible explanation for the absence of an effect on longevity is the method of assay. The selected O stocks were handled and assayed with males and females together, repeatedly mating during adult life. The present assay used segregated sexes, which is a different environment. This was done because the segregated-sexes assay is sensitive to even small changes in lifespan, and has been used successfully in the past to detect the effects of other genes on lifespan. It is possible that an effect of PGM on lifespan might be identified with different lifespan assay conditions. However, even if this explanation were to be true, the data still indicate that PGM does not have a simple strong effect on longevity. Further experiments will be required to distinguish between these interesting possibilities for the link between Pgm allele frequency and lifespan.
Materials and methods
Drosophilastocks and culture
All transgenic Drosophila stocks were generated by P-element germline transformation , using a modified microinjection technique . Transgenic lines are named as the construct, followed by the chromosome of insertion in parentheses, followed by a unique line designation. For example, PGMinvrpt(3)76 is PGMinvrpt construct inserted on chromosome 3, independent transgenic line 76. Cytological sites of insertion were not determined. Multiple strains homozygous for each of the PgmF, PgmM and PgmS alleles were generated by purifying third chromosomes from the Ives stock, which is the precursor to the O and B selection stocks . Homozygosity for a particular Pgm allele was confirmed by starch-gel electrophoresis assay, as previously described ( and data not shown). Other Drosophila strains are as described . All stocks were grown on standard cornmeal-agar medium  and were cultured at 25°C.
Strains homozygous for the transgenic constructs were crossed to rtTA(3)E2 strain, homozygous for the rtTA transactivator construct, to generate progeny heterozygous for both constructs . Control flies were rtTA(3)E2/+, that is, lacking a target construct. To obtain adult flies of defined age, the crosses were cultured at 25°C in urine specimen bottles. Before eclosion of the majority of pupae, bottles were cleared of adults and newly eclosed flies were allowed to emerge over the next 48 h. Most of the males will have mated during this time. The males only were then removed and were designated one day old, and were maintained at 25°C at 40 per vial in culture vials with food, and passaged to new vials every 48 h. For certain experiments the adult males were maintained at 29°C, as indicated. For certain experiments, female flies were used, as indicated. Those flies being fed DOX were kept on food vials supplemented with 250 μg/ml DOX.
All DNA sequencing reactions were done using the dideoxy chain-termination protocol and T7 Sequenase v2.0 (Amersham). Multiple clones were sequenced for each of the PgmF, PgmM and PgmS alleles. The clones were obtained by polymerase chain reaction (PCR) amplification of each allele using genomic DNA template isolated from strains homozygous for each allele. The primers used in each amplification are as follows. The primer locations were assigned on the basis of their relative distance from the A in the ATG start codon, which was defined as position +1.
Pgm 5'-end-2 (-27 to -4): 5'-AGCCAGCAGCCGGAAAACTCCAGT-3'; Pgm 3'-end (+1706 to +1727): 5'-GGATGGGTTGGTAATCTCAGTG-3'. Each PCR product was gel-purified and cloned into the EcoRV site of pBluescript KS+ (Stratagene). Predicted protein motifs were identified using Prosite software .
Phosphogluconate mutase enzyme activity assays
The activity assay was carried out essentially as described . Briefly, ten male flies were anesthetized with CO2 and placed in 200 μl ice-cold 0.1 M Tris buffer solution (pH 7.6). The flies were homogenized using a motorized mortar and pestle. An additional 200 μl Tris buffer was added for a total volume of 400 μl. The sample was centrifuged for 20 min at 12,000g at 4°C. Approximately 200-300 μl supernatant was removed, taking care to avoid a top layer of oil and debris. For the assay, 30-40 μl of this supernatant was used in a 3.1 ml assay mixture that contained: 1.5 mM MgCl2, 26 mM histidine solution (pH 7.6), 8 μM glucose-1,6-diphosphate, 0.45 U/ml glucose-6-phosphate dehydrogenase, and 0.2 mM NADP. This solution was mixed at room temperature and then 5 mM glucose 1-phosphate was added. The solution was mixed again and placed in a spectrophotometer. To insure that readings were being taken in the linear range of the enzyme activity, standard curves were generated with respect to both time and amount of protein added. Readings were taken at t = 6 min at OD340 and were expressed as ΔOD/μg/min. Protein concentrations were determined using the BioRad protein concentration solution using BSA as standard. All extracts were assayed in triplicate, and the averages and standard deviations are presented. Means were compared using unpaired, two-side t-tests and p-values are presented. The enzyme assay measures the conversion of NADP+ to NADPH rather than a direct measure of phosphoglucomutase itself. In other words, it is measuring a secondary, coupled reaction.
All inserts for microinjection were cloned into a derivative of the 7T40 construct  called USC1.0. USC1.0 was generated as follows: First, 7T40 was digested with EcoRI, thus liberating the Hsp70 polyadenylation signal sequence. The construct was then religated and transformed. Next, the PstI site in polylinker 1 was destroyed by partial PstI digestion followed by T4 DNA polymerase fill-in and ligation. Clones were screened for destruction of the correct PstI site to generate USC1.0 (Figure 2a). All inserts were cloned into the unique PstI to EcoRI sites of USC1.0.
The Pgm sense construct was made as follows. The reverse transcription was carried out on total RNA isolated from a strain of flies homozygous for the PgmS allele, using the following primer: dTBIBO: 5'-TAACCCGGGTCTACAAAGTGATACTGCGTAACTGACTATATTTTTTTTTTTTTTTTT-3'. A nested PCR strategy was then used to amplify the PgmS cDNA using the following primers: First primer set: BI: 5'-TAACCCGGGTCTACAAAGTG-3'. Pgm 5'-end-2 (-27 to -4): 5'-AGCCAGCAGCCGGAAAACTCCAGT-3'. Second (nested) primer set: BO: 5'-ATACTGCGTAACTGACTATA-3'. 5B6 (+1,520 to +1,534): 5'-CTGGAAGCTCGGGAG-3'. The resulting PCR product was cloned into the EcoRV site of pBluescript KS+ and clones were screened for the correct orientation. The PgmS cDNA was then liberated by EcoRI complete digest followed by PstI partial digest and cloned into the EcoRI to PstI sites of USC1.0 to generate construct PGMsense (Figure 2b).
The PGMinvrpt construct was made as follows: because the final insert would be a large inverted repeat, PgmS was PCR-amplified in two pieces, in opposite orientations. The two sets of primers used for the amplifications were: First set: Pgm-sense (3') (+1,773 to +1,794): 5'-AGCTGAATTCCACAAACTTTAATAAATCCGAAAC-3'. Pgm-anti Not (+711 to +731):5'-AGCTGCGGCCGCCCTGAACCGGTTGGGTGCCAC-3'. Second set: Pgm-anti Not (+711 to +731): 5'-AGCTGCGGCCGCCCTGAACCGGTTGGGTGCCAC-3'. Pgm-anti Pst (+1,773 to +1,794): 5'-AGCTCTGCAGCACAAACTTTAATAAATCCGAAAC-3'. Each of these PCR products was cloned individually into the EcoRV site of pBluescript KS+, and then restriction digested with EcoRI and NotI (first-set fragment) or NotI and PstI (second-set fragment). Each of the liberated fragments was gel purified and triple-ligated into the PstI to EcoRI sites of USC1.0 to generate construct PGMinvrpt (Figure 2c).
RNA was extracted using Trizol reagent (Gibco BRL) and the amount of RNA was quantitated by UV spectrophotometry. Approximately 5-10 μg RNA per lane was resolved on a 1.0% agarose gel. RNA markers (Gibco BRL) were used to determine the sizes of bands. After blotting, the RNA was fixed to Genescreen nylon membrane (Dupont) using a UV crosslinker (Stratagene). Probes were 32P-labeled using the Prime-It II kit (Stratagene). To determine fold increases/decreases, northern blots were exposed onto a phosphor screen and results were analyzed using a phosphorimager (ImageQuaNT, Molecular Dynamics). Ribosomal protein 49 gene (Rp49)  was used as a loading control, and all Pgm northern data is normalized to Rp49 RNA levels.
M.J.A. was supported by a pre-doctoral training grant from the National Institute on Aging (AG00093). This research was supported by a grant from the Department of Health and Human Services to J.T. (AG11644).
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