Nucleotide degradation is a universal metabolic capability. Here we combine metabolomics, genetics and biochemistry to characterize the yeast pathway. Nutrient starvation, via PKA, AMPK/SNF1, and TOR, triggers autophagic breakdown of ribosomes into nucleotides. A protein not previously associated with nucleotide degradation, Phm8, converts nucleotide monophosphates into nucleosides. Downstream steps, which involve the purine nucleoside phosphorylase, Pnp1, and pyrimidine nucleoside hydrolase, Urh1, funnel ribose into the nonoxidative pentose phosphate pathway. During carbon starvation, the ribose‐derived carbon accumulates as sedoheptulose‐7‐phosphate, whose consumption by transaldolase is impaired due to depletion of transaldolase's other substrate, glyceraldehyde‐3‐phosphate. Oxidative stress increases glyceraldehyde‐3‐phosphate, resulting in rapid consumption of sedoheptulose‐7‐phosphate to make NADPH for antioxidant defense. Ablation of Phm8 or double deletion of Pnp1 and Urh1 prevent effective nucleotide salvage, resulting in metabolite depletion and impaired survival of starving yeast. Thus, ribose salvage provides means of surviving nutrient starvation and oxidative stress.
Metabolomics, genetics and biochemistry were combined to obtain the first complete map of the nucleotide degradation and ribose salvage pathway in yeast. This pathway promotes yeast survival in starvation and oxidative stress.
During carbon starvation, ribose salvage from nucleotides promotes yeast survival.
The salvage pathway requires the previously misannotated nucleotidase Phm8.
Ribose‐derived carbon accumulates as sedoheptulose‐7‐phosphate.
This carbon reserve enables rapid NADPH production in oxidative stress.
In natural environments, microbes face myriad environmental stressors including starvation for essential nutrients, such as carbon, nitrogen and phosphorous. Yeast has evolved metabolic responses to these stressors, which enable their survival and effective resumption of growth when conditions improve. Recent evidence suggests that these metabolic responses are substantially hardwired in metabolic enzymes themselves (Xu et al, 2012a, 2012b; Link et al, 2013). In parallel, with this intrinsic adaptation of metabolic network, proteins such as kinases sense metabolic conditions and activate signaling cascades to coordinate metabolism and overall cellular activity. Important examples of such signaling enzymes include protein kinase A (PKA, activated by glucose), AMP‐activated protein kinase (SNF1, repressed by glucose), and target of rapamycin (TOR, activated by abundant nitrogen) (Komeili et al, 2000; Wilson and Roach, 2002; Zaman et al, 2009; Ratnakumar and Young, 2010).
A particularly important function of these kinases is to control levels of ribosomes, which constitute about 10% of yeast dry weight. This is achieved through regulation both of ribosome production and of ribosome degradation via autophagy (ribophagy) (Ertugay and Hamamci, 1997; Martin et al, 2004; Lee et al, 2007; Yorimitsu et al, 2007; von der Haar, 2008; Stephan et al, 2009; Oliveira and Sauer, 2012). Ribosomes are composed of roughly equal amounts of protein and RNA (Ben‐Shem et al, 2011). Thus, their degradation yields both amino acids and nucleotides. Catabolism of nucleotides involves their dephosphorylation into nucleosides, and subsequent hydrolysis into ribose and bases (Tozzi et al, 2006). While many hydrolytic enzymes with nucleotidase and nucleosidase activities exist in various organisms (Lecoq et al, 2001; Kurtz et al, 2002; Mitterbauer et al, 2002; Nakanishi and Sekimizu, 2002; Canduri et al, 2004; Hunsucker et al, 2005), the ones that are actually responsible for nucleotide degradation in cells have remained undefined.
The carbonaceous product of nucleotide degradation is ribose‐5‐phosphate, which must be converted into glycolytic intermediates in order to extract energy and generate anabolic precursors. Such conversion is carried out by the nonoxidative pentose phosphate pathway, a series of five reversible reactions whose net stoichiometry is 3 ribose‐5‐phosphate ←→2 fructose‐6‐phosphate (F6P)+1 glyceraldehyde‐3‐phosphate (Figure 1). Both F6P and glyceraldehyde‐3‐phosphate can be catabolized by glycolysis to yield NADH and ATP. In addition, F6P can isomerize into glucose‐6‐phosphate, which in turn can be catabolized by the oxidative pentose phosphate pathway (PPP) to generate NADPH, a key high energy electron donor required for reductive biosynthesis and redox defense (Grant, 2001; Ralser et al, 2007).
A central intermediate in the nonoxidative PPP is sedoheptulose‐7‐phosphate. When net flux is from ribose‐5‐phosphate towards glycolytic intermediates, S7P is produced by the enzyme transketolase and consumed by transaldolase. It was previously shown that, in the absence of transaldolase, xylose‐grown E. coli could also utilize the glycolytic enzyme phosphofructokinase (Pfk1) to phosphorylate S7P into SBP, which is further converted to erythrose‐4‐phosphate (E4P) and glycolytic intermediate dihydroxyacetone phosphate (Nakahigashi et al, 2009). No such reaction has been reported for wild‐type cells or other organisms, although it has recently been found that SBP can be produced in wild‐type yeast from E4P and dihydroxyacetone phosphate and subsequently dephosphorylated by the phosphatase Shb17 to yield S7P and thereby drive ribose production (Clasquin et al, 2011).
Here we use a combination of metabolomics, genetics and biochemistry to map the nucleotide degradation pathway in yeast (Figure 1), and to explore its regulation and physiological function. We show that during nutrient starvation, yeast accumulate both nucleosides and bases, indicating active nucleotide degradation. Surprisingly, during carbon starvation, they also accumulate S7P and SBP. By tracking the impact of gene deletions on the levels of these metabolites, we identify Phm8, which is currently annotated as a lysophosphatidic acid phosphatase (Reddy et al, 2008), as the main yeast nucleotidase. In addition, we determine the cause and physiological function of the S7P accumulation. We show that S7P accumulation and more generally nucleotide degradation enable metabolic homeostasis and survival of starving yeast.
Starvation triggers degradation of RNA into nucleosides, bases, and sedoheptulose‐7‐phosphate
To characterize the nucleotide degradation pathway, we first identified physiological conditions that robustly induced its activity. To evaluate whether nutrient starvation would do so, we used liquid chromatography—mass spectrometry (LC‐MS) to measure the changes in the metabolome profile of S. cerevisiae cells subjected to abrupt transition from complete minimal medium to media lacking carbon, nitrogen or phosphate. Nucleotide monophosphates (NMPs), the direct product of RNA degradation, increased only slightly. Nucleosides and bases, however, rapidly accumulated to greater than 10‐fold basal levels (Figure 2). Moreover, while sugar phosphates in upper glycolysis decreased by more than 10‐fold upon carbon starvation, PPP intermediates sedoheptulose‐7‐phosphate (S7P) and sedoheptulose‐1,7‐bisphosphate (SBP) accumulated, with S7P becoming the most abundant sugar phosphate in the cell (concentration ∼5 mM).
To explore the origin of the accumulating metabolites, we conducted a metabolomic experiment involving feeding of U‐13C‐glucose for 70 min followed by carbon starvation (Figure 3A). This regimen yields complete labeling of metabolic intermediates, including free nucleotides, but only partial labeling of macromolecule stores (protein, glycogen, RNA and DNA). Such transient labeling allowed us to determine the extent to which metabolites arise from macromolecule breakdown (Yuan and Rabinowitz, 2007). We found that the proportion of unlabeled nucleosides, bases and sedoheptulose species increased over time after carbon starvation (Figure 3B, closed symbols), indicating that these metabolites were predominantly derived from degradation of macromolecules. Consistent with those macromolecules being RNA, the total cellular RNA concentration decreased over the same time period (Supplementary Figure S1A).
A likely mechanism of RNA degradation is via macroautophagy. We accordingly measured metabolite concentrations in the atg7 deletion strain, which fails to elicit macroautophagy upon starvation. Consistent with a requirement for macroautophagy in RNA catabolism, during carbon starvation the atg7 deletion strain did not accumulate nucleosides, bases and sedoheptulose species, as normally observed in a wild‐type strain (Figure 3C). Moreover, the deletion strain showed less increase in unlabeled species when transient feeding of 13C‐labeled glucose was followed by carbon starvation (Figure 3B, open symbols). Similarly, the increase in nucleosides and bases during nitrogen starvation was absent in the atg7 deletion strain (Supplementary Figure S1B). In contrast, their accumulation during phosphate starvation was not impaired by atg7 deletion, indicating that phosphate starvation activates RNA degradation via an alternative mechanism. Nonetheless, our results demonstrate that RNA degradation upon carbon and nitrogen starvation requires macroautophagy.
We examined whether the mechanism by which nutrient starvation triggers autophagy and subsequent nucleoside and base accumulation are through canonical nutrient‐sensing kinases, such as cyclic‐AMP dependent protein kinase (PKA), AMP‐activated protein kinase (SNF1), and target of rapamycin complex 1 (TORC1). PKA is an inhibitor of macroautophagy but is inactivated upon glucose removal (Yorimitsu et al, 2007; Stephan et al, 2009). SNF1 is active in the absence of glucose and is required for growth on most carbon sources other than glucose (Zaman et al, 2008; Broach, 2012). To test if ribophagy requires inactivation of PKA and/or activation of SNF1, we performed carbon starvation on a bcy1 deletion strain, which exhibits constitutively activated PKA activity, and on a snf1 deletion strain, which lacks SNF1 activity. Both strains had substantially decreased accumulation of nucleosides, bases, and sedoheptulose species (Figure 3D). Thus, both activation of SNF1 and inactivation of PKA are required for robust induction of autophagy in response to carbon starvation. TORC1 is an inhibitor of autophagy, which is inactivated upon nitrogen removal (Noda and Ohsumi, 1998). To test if TORC1 inactivation is sufficient to initiate RNA degradation, we treated wild‐type cells growing in the presence of nitrogen with rapamycin and analyzed metabolites over time following treatment. Rapamycin treatment resulted in accumulation of nucleosides and bases to an extent even higher than those observed following nitrogen starvation (Figure 3E). Thus, TORC1 inactivation is per se sufficient to activate autophagy.
Phm8 is the physiological yeast nucleotidase
The significant accumulation of nucleosides upon nutrient starvation or rapamycin addition indicates not only that starvation induces RNA degradation but also that the resulting nucleotides are dephosphorylated to nucleosides. The enzyme catalyzing the dephosphorylation step under physiological conditions has not been identified in any organism. Sdt1 has been proposed as the responsible enzyme in yeast, since Sdt1 dephoshorylates UMP and CMP into uridine and cytidine rapidly in vitro (Nakanishi and Sekimizu, 2002). Contrary to this expectation, our metabolomic analysis of an sdt1 strain subjected to carbon starvation did not reveal altered nucleotide salvage pathway metabolite concentrations (Figure 4A). The enzyme Phm8 is homologous to Sdt1 (42% amino‐acid sequence identity). Phm8 has been proposed to be a cytosolic lysophosphatidic acid (LPA) phosphatase involved in LPA hydrolysis in response to phosphate starvation (Reddy et al, 2008). Over‐expression of Phm8 decreased LPA in yeast but deletion of PHM8 did not markedly increase LPA levels, prompting the hypothesis that Phm8 is a minor LPA phosphatase. Interestingly, PHM8, but not SDT1, is expressed under various stress conditions including carbon, nitrogen and phosphate starvation (Gasch et al, 2000; Bradley et al, 2009; Klosinska et al, 2011) (Figure 4B). These expression data together with PHM8's sequence similarity to SDT1 suggested to us that it might serve as a nucleotidase in the ribose salvage pathway.
We measured the enzymatic activity of purified Phm8 against 90 different phosphorylated compounds. Of these, the preferred substrates were nucleotide monophosphates (specific activity >500 nmol/mg/min for AMP, GMP, CMP, and UMP) (Figure 4C). In contrast, the activity toward LPA was only ∼2 nmol/mg/min (Reddy et al, 2008). Thus, Phm8's primary enzymatic activity is as a nucleotidase. Kinetic characterization of Phm8 and Sdt1 toward their most preferred substrate CMP shows that Phm8 has higher kcat and lower Km (Figure 4D); thus, Phm8 is more active than Sdt1. To evaluate Phm8's physiological role, we measured metabolite levels in the phm8 strain upon carbon starvation. Although nucleosides and bases still increased, phm8 deletion blocked the increase in S7P and SBP levels (Figure 4A). Thus, while other nucleotidases can apparently partially substitute for Phm8, Phm8 is required to maintain sufficient nucleotide catabolic flux to elevate S7P and SBP.
Nucleosides are converted into ribose‐5‐phosphate by Pnp1, Urh1, and Pgm3
Nucleosides are cleaved into nucleic bases and ribose moieties via either a phosphorylase, which yields ribose‐1‐phosphate, or a hydrolase, which yields unphosphorylated ribose. In yeast, purine nucleoside phosphorylase (Pnp1) and pyrimidine uridine hydrolase (Urh1) have been shown to catalyze these reactions (Lecoq et al, 2001; Kurtz et al, 2002). To investigate if Pnp1 and Urh1 are required for ribose salvage, we examined strains deleted for PNP1 or URH1 or both. Following carbon starvation, the pnp1 strain accumulated more of the nucleosides, inosine and guanosine and less of the bases hypoxanthine and guanine than did wild‐type cells; similarly urh1 accumulated more uridine and cytidine and less uracil (Figure 5). Adenosine did not accumulate in the pnp1 strain, consistent with the previous finding that Pnp1 exhibits no activity with adenosine. In addition, guanine, cytosine and cytidine concentrations were markedly lower than xanthine, uracil and uridine, presumably due to the activities of guanine, cytosine and cytidine deaminases Gud1, Fcy1 and Cdd1 respectively (Supplementary Figure S2A). Strains with individual deletions of PNP1 or URH1 exhibited decreased S7P and SBP levels upon carbon starvation compared to wild type, indicating that both enzymes contribute to ribose salvage. The double deletion strain accumulated all nucleosides and depleted all bases, and exhibited decreased S7P and SBP levels following carbon starvation to an extent similar as the phm8 deletion. Thus, Pnp1 and Urh1 work in concert to convert purine and pyrimidine nucleosides into bases and ribose or ribose‐1‐phosphate.
Further metabolism of ribose‐1‐phosphate requires its conversion to ribose‐5‐phosphate. Phosphoglucomutase 3 (Pgm3) has been proposed to be a phosphoribomutase capable of catalyzing this conversion (Walther et al, 2012). Consistent with this proposal, we found that deletion of PGM3, but not PGM1 or PGM2, led to accumulation of ribose‐1‐phosphate and upstream purines in the ribose salvage pathway (Figure 5). Thus, Pgm3 is the physiological phosphoribomutase required for ribose salvage from purines. We accordingly refer to the gene by the new name PRM15.
The enzyme responsible for the phosphorylation of ribose generated from pyrimidine degradation remains, however, undefined. An open reading frame (Rbk1) has been annotated as a ribokinase due to its similarity to ribokinases in other organisms. While S. cerevisiae cannot utilize ribose as the sole carbon source, in the absence of glucose, it did assimilate extracellular ribose, albeiet at a slow rate (Supplementary Figure S2C, D). Rbk1 deletion only slightly slows extracellular ribose assimilation and does not alter S7P or SBP accumulation during carbon starvation (Supplementary Figure S2B–D). Thus, another enzyme presumably phosphorylates the ribose produced by pyrimidine nucleoside degradation. As no other yeast enzyme exhibits strong homology to known ribokinases, it is possible that an annotated hexokinase might fulfill this role.
Sedoheptulose species accumulate due to substrate limitation of transaldolase
To confirm that the sedoheptulose species accumulating during carbon starvation derive from ribose phosphate produced from RNA degradation, we deleted both transketolase isozymes (TKL1/TKL2), preventing conversion of pentose phosphates into sedoheptulose7‐phosphate. Unlike wild‐type, the tkl1/tkl2 strain did not accumulate S7P and SBP upon carbon starvation (Figure 6A and B). Thus, ribose salvage requires a functional nonoxidative PPP.
The nonoxidative PPP should in principle be capable of converting ribose phosphate entirely into glycolytic intermediates. Thus, the cause of S7P and SBP accumulation under carbon starvation conditions is unclear. In the canonical nonoxidative PPP, S7P is synthesized from two pentose phosphates by transketolase, and then converted by transaldolase by condensation with glyceraldehyde‐3‐phosphate (GAP) into F6P and E4P. Indeed, genetic inactivation of both transaldolase isozymes (tal1/nqm1) led to chronic S7P accumulation (Figure 6C). Accordingly, depletion of GAP during carbon starvation might prevent S7P consumption by transaldolase and thus lead to S7P accumulation. Although we could not directly measure GAP due to its low abundance, it is in rapid exchange with DHAP, which decreased more than 20‐fold in carbon starvation.
To explore whether GAP depletion underlies the S7P accumulation, in lieu of complete carbon starvation, we transferred cells from minimal media containing glucose as the sole carbon source to minimal media containing dihydroxyacetone (DHA) as sole carbon source. DHA can be transported into yeast cells and phosphorylated into DHAP, which then forms GAP. These reactions can support yeast growth, but only after several days of adaptation (Molin et al, 2003). In the shorter time scale of our experiments, we found that the switch to DHA produces the same metabolite concentration changes as overt starvation, with only three exceptions: DHAP was two‐fold higher and S7P and SBP decreased rather than increased (Figure 6D). Thus, during carbon starvation, GAP depletion precludes S7P catabolism by transaldolase and consequently results in S7P accumulation.
The results from the above experiments present a conundrum regarding the source of SBP. Previous studies have shown that SBP is produced in yeast via a reversible reaction catalyzed by FBP aldolase, whose substrates are DHAP+E4P (Clasquin et al, 2011). However, DHAP decreases substantially under carbon starvation. Moreover, as evident from Figures 2, 4, and 5, S7P and SBP concentrations are highly correlated. We also observed that, after feeding yeast with different labeled forms of glucose, S7P and SBP always exhibited identical labeling patterns during subsequent carbon starvation (Supplementary Figure S3). Accordingly, we explored the possibility that SBP can also be formed from S7P.
E. coli phosphofructokinase can phosphorylate S7P to SBP (Nakahigashi et al, 2009). To test whether this can occur in yeast, we created strains lacking either phosphofructokinases isozyme, Pfk1 or Pfk2, and measured metabolites following carbon starvation. The pfk1 but not pfk2 deletion strain had lower SBP and higher S7P (Figure 6E and Supplementary Figure S4), indicating that Pfk1 phosphorylates S7P to SBP, perhaps selectively during carbon starvation when the S7P/F6P ratio (reflected by S7P/G6P ratio, as G6P and F6P are linked via a single reversible reaction) greatly increases (Figure 2). As the pfk1 strain exhibited lower DHAP compared to the wild‐type strain upon carbon starvation, SBP is presumably degraded by aldolase into DHAP, providing an alternative route into glycolysis.
Ribose salvage is essential for yeast's survival in starvation and oxidative stress
The identification of the enzymes of ribose salvage provided us the opportunity to investigate the pathway's physiological role. Ribose salvage could serve to maintain energy charge and levels of key metabolites during nutrient starvation. We confirmed this hypothesis by metabolomic analysis of the ribose salvage mutants phm8 and pnp1/urh1 (Figure 7A). Specifically, there was a marked impairment in energy charge in carbon starvation; glutamine abundance (a hallmark of nitrogen availability, Crespo et al, 2002; Zaman et al, 2008) in nitrogen starvation, and ATP abundance (a hallmark of phosphate availability, Boer et al, 2010) in phosphate starvation. These metabolite concentration changes were also associated with altered cell growth and viability: While the phm8 and pnp1/urh1 deletion strains grew identically to wild type on complete minimal media, they were less effective than wild type at sustaining growth when nitrogen or phosphorous was removed (Figure 7B). All strains ceased growth immediately upon carbon starvation. However, phm8 and pnp1/urh1 strains exhibited substantially slower initiation of gluconeogenesis if switched from glucose to glycerol+ethanol (Figure 7D), presumably due to the inferior carbon supply in the interval between fermentative and respiratory growth. The phm8 and pnp1/urh1 strains also exhibited decreased viability in long‐term starvation (Figure 7C). These findings indicate that nucleotide degradation and ribose salvage are essential for yeast's growth and survival under nutrient deprivation.
The above results provide a clear physiological role for the ribose salvage pathway. They do not, however, clarify the function of the S7P accumulation during carbon starvation. Motivated by our observation that S7P can be consumed if GAP is available, we looked for a stress condition under which DHAP and GAP might accumulate. Since oxidative stress inhibits GAP dehydrogenase in yeast (Shenton and Grant, 2003), carbon stored as S7P could be released by a transient increase in GAP triggered by oxidative stress. Moreover, conversion of S7P to F6P could in turn lead to production of glucose‐6‐phosphate by phosphoglucose isomerase and NADPH production by the oxidative PPP. Subsequent consumption of NADPH to regenerate reduced glutathione could promote survival of oxidative stress. To test this possibility, we added H2O2 to carbon‐starved wild type, phm8 and pnp1/urh1 yeast cells (Figure 8A and B). Indeed, DHAP, which is in rapid exchange with GAP, accumulated immediately upon oxidative stress, mirrored by a rapid decrease in S7P and rise in G6P in the wild‐type cells (Figure 8C). The phm8 and pnp1/urh1 deletion strains, in contrast, exhibited lower G6P, NADPH/NADP+ ratio, reduced glutathione, and viability (Figure 8D and E). Thus, S7P accumulated during short‐term carbon starvation enables rapid NADPH production in response to oxidative stress.
Our characterization of nucleotide degradation in yeast represents the most comprehensive metabolomic investigation to date, in any organism, of the pathway from nucleotide monophosphates to central metabolism. Such investigation has substantially clarified the enzymatic steps of the pathway. Because degradative pathways, unlike biosynthetic pathways, are inessential for growth, they cannot be readily mapped by purely genetic approaches relying on overt phenotypes such as dependence on a particular added nutrient (auxotrophy). Moreover, many degradation enzymes have promiscuous activity against a diversity of substrates, rendering their functions difficult to determine from biochemistry alone (Saghatelian and Cravatt, 2005b). For example, in E. coli, various enzymes have been putatively identified as nucleotidases (Innes et al, 2001; Proudfoot et al, 2004; Kuznetsova et al, 2006) and nucleosidases (Jensen and Nygaard, 1975; Petersen and Moller, 2001; Dandanell et al, 2005), but which one(s) are physiologically important remains unknown. Mammalian nucleotide degradation and ribose salvage are yet more complex and less well defined (Tozzi et al, 2006).
To analyze the physiological function of nucleotide degradation enzymes in yeast, we employed metabolomic analysis of targeted deletion strains (Fraenkel, 1992; Raamsdonk et al, 2001; Fiehn, 2002; Forster et al, 2002; Allen et al, 2003; Saghatelian and Cravatt, 2005a), and examined the metabolic response to a perturbation that strongly induces the degradation pathway. This allowed us to identify the physiologically relevant enzyme for all but one reaction of the pathway. The significance of this effort is highlighted by its rectifying multiple different misannotations in the current genome‐scale yeast metabolic model, including clarifying the lack of Pnp1 activity against adenosine (Figure 5), the specificity of Urh1 to pyrimidines (Figure 5), the phosphoribomutase activity of Pgm3 (now Prm15) (Figure 5), and most importantly identifying the physiological yeast nucleotidase to be Phm8 (Figure 4), a gene of the haloacid dehalogenase‐like hydrolase family. Intriguingly, the strongest metabolic response to PHM8 deletion occurred in S7P and SBP levels, which are more sensitive to flux through the ribose salvage pathway than are Phm8's direct substrates and products. Measurement of these more distal metabolites was a key benefit of metabolomics over a more targeted analytical approach.
We initiated our study of the ribose salvage pathway to explore an initial observation that, during starvation, mutants defective in nutrient signaling (bcy1 and snf1) exhibited a distinct pattern of PPP metabolites (Figure 3D) (Xu et al, 2012b). This suggested that nutrient signaling kinases might regulate metabolic enzymes of the PPP through direct phosphorylation. Similar to our recent observations regarding control of glycolytic enzymes upon glucose removal and re‐feeding (Xu et al, 2012b), however, we do not find evidence that direct enzyme phosphorylation is controlling PPP metabolite concentrations or fluxes. Rather, the nutrient‐signaling kinases serve to coordinate metabolism and cell ribosome contents through regulation of autophagy. The effect of these kinases on the ribose salvage pathway intermediates thus arises from mass action as a consequence of the increased production of nucleotide monophosphates via ribophagy.
Beyond being a marker of nucleotide degradation flux, S7P accumulation during carbon starvation provides a potentially useful nutrient reserve of carbon and phosphate. We find that this reserve helps carbon‐starved yeast to respond to an acute oxidative stressor. The initial cause of the S7P accumulation in carbon starvation is depletion of glyceraldehyde‐3‐phosphate, which, when present, reacts with S7P to produce F6P and E4P. Oxidative stress blocks the glycolytic consumption of GAP (Shenton and Grant, 2003), thereby providing the substrate required to react with S7P. The resulting F6P production in turn drives NADPH production via the oxidative PPP and subsequent glutathione reduction.
The accumulation of S7P during carbon starvation is reminiscent of similar accumulation of PEP upon glucose removal. We have recently shown that the increase in PEP is caused by rapid depletion of fructose‐1,6‐bisphosphate (FBP), an essential activator of the PEP‐consuming enzyme pyruvate kinase. The elevated PEP provides a readily accessible reserve of high‐energy phosphate bonds, which facilitate fast uptake of glucose if it becomes re‐available (Xu et al, 2012a, 2012b). Analogously, S7P accumulation is caused by depletion of FBP's product glyceraldehyde‐3‐phosphate, a substrate of the S7P‐consuming enzyme transaldolase. Like the elevated PEP, the increased S7P prepares the cell for a possible subsequent event, oxidative stress in this case, a major threat for microbes growing on plants (Baker and Orlandi, 1995). In both cases, intrinsic properties of the metabolic network result, during carbon starvation, in carbonaceous metabolite accumulation to provide energy reserves for quick response to further environmental changes.
Beyond the specific role of the S7P accumulation in stress protection, we find that nucleotide degradation is critical to metabolic homeostasis and thus survival of starving yeast. In previous work, during the transient period following glucose upshift when ATP consumption by hexokinase and phosphofructokinase precedes ATP generation by lower glycolysis, AMP degradation was found to help maintain energy charge (Walther et al, 2010). In starvation, the goal is not elimination of AMP, but access to the carbon, nitrogen and phosphorous within it and other nucleotide monophosphates. That such constituents would be fed into central metabolism via nucleotide degradation is not unexpected. The significance of their contribution to starvation survival is nevertheless surprising, given that proteins are more copious and carbohydrate stores more accessible. The strikingly lower energy charge, altered metabolite levels and poor survival in the phm8 deletion strain, however, show that nucleotide salvage plays an indispensable role. This can be rationalized based on the abundance of ribosomes, which are needed in large amounts only during rapid growth (Mager and Planta, 1991; Bremer and Dennis, 1996; Scott et al, 2010). Thus they may be preferentially used as fuel during the transition from fast growth to slow growth or stationary phase.
Building from careful mapping of the nucleotide degradation pathway, we have been able to demonstrate an important role of the pathway in starvation survival of yeast. Orthologs of Phm8 are found in most fungi and plants, and some bacteria and animals but not humans (http://yeast‐phylogroups.princeton.edu/). In organisms where Phm8 orthologs are present, our results may directly facilitate mapping of their nucleotide degradation pathways. In other organisms, the approach laid out here may translate even though the gene product does not. For example, although mammalian cells are not normally subject to acute starvation, autophagy is essential for survival of the neonatal period (Kuma et al, 2004; Efeyan et al, 2012) and contributes to the growth of Ras‐driven tumors (Guo et al, 2011; Mathew and White, 2011; Yang et al, 2011). The latter observation raises the intriguing possibility that a more complete understanding of nucleotide degradation in humans would reveal new drug targets for treatment of aggressive cancers.
Materials and methods
Yeast strains and media
Yeast strains were derived from prototrophic S288C or W303. Prototrophic deletions were created by homologous recombination using the allele amplified by PCR from the synthetic genetic analysis (SGA) deletion set (Tong et al, 2001). Double deletion strains were made by sporulation and tetrad dissection. Cells were grown in minimal media comprising 6.7 g/l Difco Yeast nitrogen base without amino acids plus 2% (w/v) glucose. For nitrogen and phosphate starvation, cells were grown in nitrogen or phosphate‐limited media (Supplementary Table S2) before nutrient deprivation to deplete the otherwise large intracellular store of these two nutrients.
Yeast culture conditions and extraction
The metabolome of Saccharomyces cerevisiae was characterized as described previously (Xu et al, 2012b). Briefly, saturated overnight cultures were diluted 1:30 and grown in liquid media in a shaking flask to A600 of ∼0.6. A portion of the cells (3 ml) were filtered onto a 50 mm nylon membrane filter (Millipore, Billerica, MA), which was immediately transferred into −20°C extraction solvent (40:40:20 acetonitrile/methanol/water). For nutrient removal, 100 ml of cell culture at A600 of ∼0.6 was poured onto a 100‐mm cellulose acetate membrane filter (Sterlitech, Kent, WA) resting on a vacuum filter holder with a 1000‐ml funnel (Kimble Chase, Vineland, NJ) and was washed with 100 ml prewarmed (30°C) starvation liquid medium lacking the indicated nutrient. Immediately after the wash media went through, the filter was taken off the holder and the cells were washed into a new flask containing 100 ml prewarmed (30°C) starvation medium. Samples were then taken at the indicated time points after nutrient removal and filtered and quenched as described above.
For RNA extraction and quantitation, yeast cells were grown in the same condition as for metabolomics experiments. Total RNA was extracted using the hot acid phenol method followed by ethanol precipitation (Spellman et al, 1998). The resulting sample was dissolved in water and total RNA concentration was measured by a fluorometer (Qubit; Invitrogen, Carlsbad, CA).
For cell viability assay, 200 μl of culture were diluted in a 10‐fold series, spread onto YPD agar plates and incubated for 24 h. The percentage of cells that survived under a stress was calculated by dividing the number of colonies formed after a stress exposure by the number of colonies formed under the same growth condition but without the stress exposure.
Cell extracts were analyzed by reversed phase ion‐pairing liquid chromatography (LC) coupled by electrospray ionization (ESI) (negative mode) to a high‐resolution, high‐accuracy mass spectrometer (Exactive; Thermo Fisher Scientific, Waltham, MA) operated in full scan mode at 1 s scan time, 105 resolution, with compound identities verified by mass and retention time match to authenticated standard (Rabinowitz et al, 2010). Isomers are reported separately only where they are fully chromatographically resolved. Absolute intracellular metabolite concentrations in steadily growing S. cerevisiae were determined as described previously (Bennett et al, 2008). Metabolite concentrations after perturbations were computed based on fold‐change in ion counts relative to steadily‐growing cells (grown and analyzed in parallel) multiplied by the known absolute concentration in the steadily growing cells, as determined using an isotope ratio‐based approach (Bennett et al, 2009). Energy charge was calculated as ([ATP]+0.5[ADP])/([ATP]+[ADP]+[AMP]) (Chapman and Atkinson, 1977).
Protein purification and enzymatic assays
The genes encoding Phm8 (Yer037w) and Sdt1 (Ygl224c) were amplified by PCR using S. cerevisiae genomic DNA. The amplified fragments were cloned into a modified pET15b vector (Novagen, Darmstadt, Germany) and overexpressed in the E. coli BL21(DE3) Gold strain (Stratagene, La Jolla, California) as previously described (Kuznetsova et al, 2010). The recombinant proteins were purified using metal ion affinity chromatography on nickel affinity resin (Qiagen, Hilden, Germany) to high homogeneity and stored at −80°C. Purified Phm8 and Sdt1 were screened for the presence of phosphatase activity against the general phosphatase substrate p‐nitrophenyl phosphate (pNPP) and 90 phosphorylated metabolites as described previously (Kuznetsova et al, 2006). For the determination of kinetic parameters (Km and kcat), phosphatase activity was determined in the presence of 5 mM MgCl2 over the range of substrate concentrations (0.001–9.5 mM), and the kinetic parameters were calculated by nonlinear regression analysis of raw data to fit to the Michaelis–Menten function using the GraphPad Prism Software (GraphPad Software, San Diego, CA).
We thank Pat Gibney, Sanford Silverman, Sean Hackett and David Botstein for helpful discussions. This research was funded by NSF CAREER award MCB‐0643859, Joint DOE‐AFOSR Award DOE DE‐SC0002077—AFOSR FA9550‐09‐1‐0580, NSF grant CBET‐0941143, and NIH grants R01 grant CA163591 (to JDR) and RO1 GM076562 (to JRB), with additional support from the Princeton University Center for Quantitative Biology (P50 GM071508) and from the Government of Canada through Genome Canada, Ontario Genomics Institute (2009‐OGI‐ABC‐1405) and Ontario Research Fund (ORF‐GL2‐01‐004).
Author contributions: Y‐F X and JDR designed experiments, analyzed data and wrote the paper. FA, AAC and JRB contributed to strain constructions. WL, EK, GB and AFY contributed to biochemistry. FL contributed to preliminary experiments. FL, AAC, AFY and JRB supported the work and helped with the manuscript.
Conflict of Interest
The authors declare that they have no conflict of interest.
Supplementary Figures S1–4, Supplementary Tables S1–3 [msb201321-sup-0001.pdf]
Supplementary Dataset [msb201321-sup-0002.xlsx]
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