Search tips
Search criteria 


Logo of gthreeG3 Genes | Genomoes | GeneticsInformation for AuthorsEditorial BoardSubmit a Manuscript
G3 (Bethesda). 2012 September; 2(9): 1003–1017.
Published online 2012 September 1. doi:  10.1534/g3.112.002808
PMCID: PMC3429914

Glucose, Nitrogen, and Phosphate Repletion in Saccharomyces cerevisiae: Common Transcriptional Responses to Different Nutrient Signals


Saccharomyces cerevisiae are able to control growth in response to changes in nutrient availability. The limitation for single macronutrients, including nitrogen (N) and phosphate (P), produces stable arrest in G1/G0. Restoration of the limiting nutrient quickly restores growth. It has been shown that glucose (G) depletion/repletion very rapidly alters the levels of more than 2000 transcripts by at least 2-fold, a large portion of which are involved with either protein production in growth or stress responses in starvation. Although the signals generated by G, N, and P are thought to be quite distinct, we tested the hypothesis that depletion and repletion of any of these three nutrients would affect a common core set of genes as part of a generalized response to conditions that promote growth and quiescence. We found that the response to depletion of G, N, or P produced similar quiescent states with largely similar transcriptomes. As we predicted, repletion of each of the nutrients G, N, or P induced a large (501) common core set of genes and repressed a large (616) common gene set. Each nutrient also produced nutrient-specific transcript changes. The transcriptional responses to each of the three nutrients depended on cAMP and, to a lesser extent, the TOR pathway. All three nutrients stimulated cAMP production within minutes of repletion, and artificially increasing cAMP levels was sufficient to replicate much of the core transcriptional response. The recently identified transceptors Gap1, Mep1, Mep2, and Mep3, as well as Pho84, all played some role in the core transcriptional responses to N or P. As expected, we found some evidence of cross talk between nutrient signals, yet each nutrient sends distinct signals.

Keywords: mitogenesis, glucose, yeast, transcription, RRPE, glucose, nitrogen, phosphate, protein kinase A, TOR, cAMP

Yeast starved for macronutrients, such as glucose (G), nitrogen (N), or phosphorous (P), arrest growth and cell division and become quiescent, with cell wall thickening, reduced transcription and translation, and increased stress tolerance (Gray et al. 2004; Rowley et al. 1993). Upon nutrient repletion, yeast immediately return to growth and division (Unger and Hartwell 1976).

Glucose addition to starved, quiescent yeast rapidly alters the expression of more than a third of the yeast genome by at least 2-fold (Martinez et al. 2004; Radonjic et al. 2005; Slattery and Heideman 2007; Wang et al. 2004). Genes needed for ribosome biogenesis (RiBi), ribosomal proteins (RP) translation, mass accumulation, and cell division are induced (Jorgensen et al. 2004). In contrast, environmental stress response (ESR) (Gasch et al. 2000), gluconeogenic, respirative, and alternative metabolism genes are repressed.

This large-scale change depends on the Gpa2 G-protein associated with the Gpr1 glucose receptor (Santangelo 2006; Wang et al. 2004). The response is also largely dependent on cAMP production, as well as a functional TOR pathway (Slattery et al. 2008). Glucose produces this massive rearrangement of the transcriptome, even in cells lacking the ability to take up and metabolize glucose (Slattery et al. 2008). These results point to a cell surface receptor-mediated response.

Most study of nutrient sensing in S. cerevisiae has focused on specific metabolic challenges, such as glucose repression or regulation of amino acid synthesis. Thus, we have limited knowledge of how these different nutrients cause cells to return to growth (Forsberg and Ljungdahl 2001; Magasanik and Kaiser 2002; Wykoff and O’Shea 2001; Zaman et al. 2008).

Work from Thevelein et al. (2005) has shown a role in trehalase activation for cell surface N and P sensors that is largely dependent on PKA. Because these proteins needed for trehalase stimulation also serve as nutrient transporters, they have been termed transceptors (Donaton et al. 2003; Popova et al. 2010; Van Zeebroeck et al. 2009). One such transceptor is the Gap1 amino acid transporter (Jauniaux and Grenson 1990; Magasanik and Kaiser 2002). Trehalase activation by amino acids is Gap1-dependent. A similar finding was made in studying the role of the Pho84 phosphate transporter. Phosphate activation of trehalase activation is Pho84-dependent (Popova et al. 2010). Finally, the Mep family of ammonium transporters are important for ammonium stimulation of trehalase activity (Van Nuland et al. 2006).

Because the states of quiescence and growth appear have requirements that are the same regardless of the missing nutrient, we hypothesized that N, P, and G depletion and repletion would control large common gene sets needed for growth and quiescence. In this article, we confirm this hypothesis and show that all three nutrients produce responses that are similar in appearance and share common mechanisms. While the initial signals appear to come from different receptors, including Gpr1, Gap1, Pho84, and Mep proteins, the nutrient signals produce a response that is largely cAMP-dependent. Furthermore, all three nutrients elevate cAMP levels when repleted. These results indicate that different nutrient signals converge to control common states of quiescence and growth.

Materials and Methods

Yeast strains and growth media

S288C (MATα SUC2gal2 mal mel flo1flo8-1 hap1hobio1bio6) was used for glucose, nitrogen, and phosphate experiments. TC41-1 (MATα leu2-3 leu2-112 trp1-1 his3-532 his4cyr1::URA3cam) and the isogenic CYR1+ wild-type HR125 were used for PKA and TOR nutrient repletion experiments (Heideman et al. 1990). BY4742 (MATα his3Δ1 leu2Δ0 lys2Δ0 ura3Δ0) was used for transceptor work as wild-type and gap1Δ and pho84Δ mutants made in BY4742 were from the yeast knockout collection obtained from Open Biosystems, with either gene deleted by KanMX. Deletions were confirmed by PCR.

Growth conditions

Cells were grown in YPD (1% yeast extract, 2% peptone, 2% glucose, Sunrise Chemicals) or synthetic medium (SD) with 2% glucose containing 6.7 g/l yeast nitrogen base (US Biological) supplemented with adenine, uracil, and amino acids. Cells were cultured at 30° with shaking. Nitrogen deprivation medium (SD-N) consisted of SD made up with nitrogen-free Yeast Nitrogen Base (Difco) and without amino acids or uracil. Phosphate deprivation medium (SD-P) consisted of SD made with yeast nitrogen base in which potassium chloride was substituted for potassium phosphate. Rapamycin (10 µg/ml stock in ethanol, LC Laboratories) and cAMP (1M stock in water, pH 7, Sigma) treatments were as described previously (Newcomb et al. 2003; Russell et al. 1993; Slattery et al. 2008). When added, cAMP was used at 1 mM and rapamycin at 200 nM.

Nutrient depletion

Glucose depletion was as previously described (Slattery and Heideman 2007). Cells were grown in SD medium for 48–72 hr until they had arrested as a quiescent G1 phase population. Nitrogen starvation was achieved by inoculating cells from an overnight SD culture into SD-N at a density of 0.4 OD660. When growth stopped (24 hr, approximately 1.5 OD660), cells were transferred to a fresh volume of SD-N to a density of 0.5 OD660. These cells were incubated an additional 24 hr and generally reached a density of OD660 0.75–1. Finally, this culture was resuspended in fresh SD-N at OD660 of 1.0 and incubated for 12–24 hr. Depletion was confirmed by determining that cells would not proliferate in fresh SD-N but would grow in SD. Phosphate depletion was carried out in the same manner, except that phosphate depletion medium was used. In both cases, nutrient repletion was accomplished by pelleting in a Beckman J6 centrifuge at 30° at 2500 rpm for 5 min and resuspension in an equivalent volume of fresh SD medium.

For dual nutrient depletion experiments, cultures were grown in N- or P-free medium until they ceased dividing and were then transferred to medium also lacking G and incubated for an additional 48 hr to deplete any glucose remaining in the medium. This produced GN- and GP-depleted cells; we confirmed that repletion of only a single nutrient did not produce growth (data not shown).

The pho84Δ cells were starved for P as described above and challenged with KH2PO4 or Gly3P (both 10 mM). The Gap1 cells were nitrogen depleted as described above and repleted with SD-N with 10 mM L-citrulline added. The MEP-deletion strains were N-depleted as described above and repleted by addition of SD-N plus 10 mM ammonium sulfate.

The cyr1Δ strain TC41 was nutrient depleted using the techniques previously described (Slattery and Heideman 2007), in which the nutrient depletion followed the schedule described above except that during nutrient the first 24 hr of depletion the cells were cultured with 1 mM cAMP and 0.5× auxotrophic supplements to be certain that the cells could remain growing enough to deplete the missing macronutrient. This was followed by 24 hr in depletion medium with 1 mM cAMP and by an additional 24 hr with no cAMP. This procedure was used to avoid halting growth and metabolism prematurely by cAMP withdrawal before true nutrient depletion had occurred.

cAMP measurements

Twenty-five optical density (OD) units of cells were harvested into ice-cold TCA to a final concentration of 5% and vortexed briefly to mix. The lysates were neutralized with NaHCO3 to pH ~6.5–7 and snap-frozen on liquid nitrogen. Immediately prior to assay, samples were thawed on ice and centrifuged at 4° for 1 min, and then 20 µL of supernatant was used in the R&D Systems cAMP Parameter Assay Kit (KGE002B) as indicated by the manufacturer.

RNA isolation and microarray hybridization

Samples of cells were collected in independent experiments to produce true biological replicates. For these experiments, cultures from independent colonies on the same plate were started and grown in separate flasks to nutrient limitation as described above. In some cases, duplicate cultures were grown on separate days, and in others, the cultures were grown in the same shaker started on the same day. Samples were kept separate, and the results from the duplicates are shown.

For each hybridization, 10 ODU cells were collected and pelleted at 5000 RPM in a Beckman J6 centrifuge for 2 min at 30°. Then the supernatant was removed and the pellets were frozen with liquid nitrogen.

RNA was isolated using MasterPure Yeast RNA Purification Kits (Epicentre Technologies), and the quality was assayed by gel electrophoresis. cRNA synthesis was carried out using the GeneChip Expression 3′ Amplification One-Cycle Target Labeling and Control Reagents kit from Affymetrix following the manufacturer’s instructions. cRNA samples were hybridized to GeneChip Yeast Genome 2.0 Arrays for 16 hr. Arrays were washed, stained, and scanned according to the manufacture’s recommendation. Affymetrix .CEL files were RMA normalized with R and the Bioconductor Suite (Gentleman et al. 2004). Data analysis was performed within TIGR Multiexperiment Viewer, v4.5.1 (Saeed et al. 2003; 2006), in-house Perl scripting, R, and Bioconductor.

Genes that were differentially expressed between the fed and starved states from each nutrient condition were selected using the following criteria: a P value less than 0.05; a false discovery rate less than 0.01 (q-value); and a 2-fold change in expression. The individual nutrient lists were compared to identify the genes in common, as well as those unique to each combination, resulting in the Venn diagrams shown in Figures 3 and and44 and supporting information, Table S1 and Table S2.

Figure 3
Genes induced by G, N, and P repletion. Microarray data from Figure 2 was used to identify genes induced at least 2-fold by G, N, or P repletion using cutoffs described in Materials and Methods. The Venn diagram shows the intersections between the sets ...
Figure 4
Genes repressed by G, N, and P repletion. Microarray data from Figure 2 was used to identify transcripts reduced by at least 2-fold by G, N or P repletion compared with quiescence levels as described in Materials and Methods. The Venn diagram shows the ...

GO enrichment analysis was performed through FUNSPEC tool (Robinson et al. 2002) at Under- and overrepresented DNA motifs were identified using the RSAT online motif discovery tool at (van Helden 2003), where oligomer length was scanned between 4 and 8 bases and the best-consensus sequence scores were collected. Transcription factor target and motif enrichment significance were calculated using a hypergeometric distribution test.


Different nutrient limitations produce a similar transcriptome

Starvation for glucose (G), nitrogen (N), or phosphate (P) each produces a morphologically similar G1 arrested population (Gasch et al. 2000; Giots et al. 2003; Gray et al. 2004; Johnston et al. 1977; Mazon 1978). This leads to the idea that while the signals from these nutrients are distinct, they converge in some way to control quiescence and growth.

We first compared transcripts in yeast starved for G, N, or P. Prototrophic S288C cells were transferred from complete medium to synthetic medium lacking G, N, or P and incubated until they had arrested growth as described in Materials and Methods. Total RNA was isolated and used to probe Affymetrix microarrays. The experiments were conducted using duplicate yeast cultures started from separate colonies. Paired biological replicate signal intensities for each mRNA for each starvation condition are shown as a heat map (Figure 1A). In this arrangement, genes at the top of the map with the brightest color have the highest hybridization signals, whereas those at the bottom had the lowest. Replicate experiments are shown side by side, but in most cases, the replicate values were so similar that they cannot be visually distinguished.

Figure 1
Comparing transcript levels in G-, N-, or P-depleted cells. Wild-type (S288C) cultures were transferred into S medium lacking G, N, or P and were cultured until growth was arrested, and then samples were collected for Affymetrix microarray analysis as ...

Qualitatively, the heat map in Figure 1A indicates that all three nutrient limitations produce regions of strong similarity in transcript abundance pattern; with the G-depleted samples somewhat distinct from the N- and P-depleted samples. We calculated Pearson correlation coefficients and produced linear regression plots to compare the patterns of transcript abundances produced by each type of depletion (Figure 1B). Each transcript is plotted as a dot positioned with its abundance in one nutrient condition plotted on the Y-axis, and abundance in the other nutrient condition on the X-axis. Overall, there was high correlation between the three starvation states (Chua et al. 2006; Grigull et al. 2004), but as noted, the responses to N and P limitation were more similar to each other than either was to the response produced by G limitation. Comparison of the N and P starvation responses produced a correlation of 0.93, whereas comparison of G limitation to N and P starvation yielded Pearson correlations of 0.79 and 0.77 respectively.

In general, these results indicate that the quiescent states produced by the separate nutrient limitations are quite similar in terms of global gene expression, a conclusion recently reported by Klosinska et al. (2011). Although we used an S288C strain and Broach and co-workers in that study used a W303 derivative, both experiments yielded similar results. Comparing our single time point values with the published results, we found the highest correlations to their 5760 (96 hr) time point samples, with Pearson correlations of 0.78, 0.75, and 0.64 between the G-, N-, and P-depletion results, respectively.

Nutrient repletion triggers massive changes in transcript abundance

The cellular pathways for sensing G, N, or P are thought to be quite distinct (Santangelo 2006; Schneper et al. 2004; Zaman et al. 2008). Yet, repletion of each of these nutrients causes growth, protein synthesis, and reversal of quiescence. We hypothesized that repletion of each nutrient would produce a set of transcriptional changes overlapping those produced by G (Radonjic et al. 2005; Slattery and Heideman 2007; Wang et al. 2004).

To test this, we added back the limiting nutrient to quiescent G-, N- or P-depleted S288C cells and collected samples for microarray analysis at 60 min. By 90 min, cells had begun to produce buds, indicating a return to growth (not shown). Figure 2A shows the changes in gene expression produced by each nutrient, expressed as fold change (log2) relative to quiescent samples. Red indicates increased expression, and green indicates repression caused by nutrient repletion.

Figure 2
Large-scale transcriptional responses to G, N, and P repletion. Wild-type (S288C) cells were starved for G, N, or P until growth was arrested as in Figure 1, and then the missing nutrient was repleted as described in Materials and Methods. Samples for ...

Large groups of genes were upregulated by all three nutrient repletions, as revealed by clusters toward the top of the figure, whereas other groups, shown toward the bottom, were downregulated by all three repletions. Other gene sets were nutrient-specific.

As with the data in the first figure, we used dot plots to compare the fold change induced by one nutrient with the changes induced by another (Figure 2B). As before, the similarities between the responses were reflected in the correlation coefficients, and the N- and P-repletion responses were more similar to each other than they were to the G response. N and P repletion produced responses with a correlation of 0.82, whereas the response to N repletion produced a correlation coefficient of 0.69 compared with the response to G. Comparison of the responses to G and P repletion produced a correlation of 0.67.

Growth genes are upregulated by all three nutrients

To identify a core set of genes induced in response to all three nutrients, we selected sets of genes that were induced by each of the nutrient repletions. These sets were made up of transcripts that met the following criteria: P < 0.05, a false discovery rate (q-value) less than 0.01, and at least a 2-fold induction by the nutrient repletion (log2 ratio greater than or equal to 1).

This arbitrary cutoff yielded the following gene sets: 1601 increased by glucose; 877 increased by nitrogen; and 1003 increased by phosphate. Of the genes upregulated by both nitrogen and phosphate, 83% (P < 2.139 × 10−257) were also upregulated by glucose, producing an overlapping set of 501 genes induced by each of the three nutrients (Figure 3).

This common set of 501 genes was greatly enriched for protein synthesis genes. GO functional classification showed significant enrichment for rRNA processing (<1e−14), tRNA processing (<1e−14), ribosome biogenesis (<1e−14), rRNA synthesis (<1.84e−12), and related growth functions (Table 1). This set was also significantly enriched for genes mapping to the nucleolus (<1e−14), a key site for ribosome development. Of the 236 recognized RiBi transcripts we measured, 160 (67%, P < 1.145e−117) were found in this common cluster (Jorgensen et al. 2004). G, N, and P repletions all induced ribosomal protein (RP) transcripts; however, the fold induction by G averaged well above the 2-fold cutoff, while for most RP genes, induction by N or P fell slightly below this cutoff (Table S1).

Table 1
Transcription factor target and binding motif enrichment, gene ontology enrichment, and overrepresented promoter motifs found in the induced Venn diagram genes

We also looked for short over-enriched motifs within promoter regions of each gene in each cluster using RSAT, an online motif discovery tool for de novo promoter enrichment analysis (Thomas-Chollier et al. 2008; van Helden 2003). In a related search, we examined transcription factor target enrichments and binding sequence enrichments based on previous genome-wide studies (Macisaac et al. 2006; Robert et al. 2004; Zhu et al. 2009). These enrichments are summarized in Table 1. We find the set of 501 genes induced in common by G, N, and P to be significantly enriched for RRPE (AAAWTTTT) and PAC (GATGAG) elements (Dequard-Chablat et al. 1991; Hughes et al. 2000; Slattery and Heideman 2007). Of the 501 G-, N-, and P-induced genes, 64% (P < 2.3e−85) contain at least one RRPE, 53% (P < 6.17e−44) at least one PAC, and approximately 42% (P < 3.67e−90) contain both an RRPE and a PAC. This is not surprising in that a connection between genes induced by G repletion and the presence of PAC and RRPE elements has previously been made (Fingerman et al. 2003; Hughes et al. 2000; Slattery and Heideman 2007; Wade et al. 2001).

Nutrient-specific differences: genes not upregulated in common

In addition to genes displaying a common response, we anticipated nutrient-specific expression patterns. A set of 780 genes met our criteria for G induction, but not for N or P. These transcripts induced 2-fold specifically by G repletion showed a connection to growth metabolism, perhaps distinct from the N and P sets because of the dual energy and carbon source potential provided by G. This set was significantly enriched for RP genes (P < 1.42e−14), containing 97 of the 137 RP genes (P < 3.83e−52). As mentioned above, the RP genes were also significantly induced by N or P repletion, but they failed to pass the 2-fold cut off. On closer examination, we found that the RP transcripts had the greater fold induction in G largely because of a greater repression during G starvation (See Discussion and Figure S1). In this G-induced set, we found enrichment for gene targets for Rap1, Fhl1, and Sfp1, regulators of RP transcription, and we also found enrichment for their corresponding binding motifs (Fingerman et al. 2003; Lieb et al. 2001; Marion et al. 2004; Pina et al. 2003; Schawalder et al. 2004). GO enrichments were also observed for translation-related, protein-trafficking, and ER-localization functions (Table 1).

As might be expected, the subset of 115 N-induced genes was enriched for genes involved with amino acid biosynthesis and nitrogen metabolism. This set was enriched for targets bound by Gcn4, Bas1, Met32, Met4, and Cbf1, and it was also enriched for their binding sequence motifs (Table 1).

The 183 genes specifically induced by P were less obviously connected with P metabolism by GO enrichment analysis, appearing enriched for transcriptional control and DNA binding (Table 1). Ino4 and Ino2 targets are enriched, suggesting a need for phospholipid synthesis after P deprivation, an observation noted previously (Greenberg and Lopes 1996).

Stress genes are downregulated by all three nutrients

We used the cutoff screen described above to identify a set of 616 genes downregulated in common by G, N, or P (Figure 4). Each nutrient decreased the expression of a large group of stress-related genes. Functional classifications showed significant enrichment in the following groups: oxidative stress response (P < 6.32e−9), heat shock response (P < 3.16e−7), autoproteolytic processing (P < 1.07e−06), metabolism of energy reserves (P < 3.1e−5), and autophagy (P < 1e−14) (Table 2). We also found this set enriched for peroxisome (P < 6.65e−9) and vacuolar lumen concentration (P < 9.5e−4). Perhaps most noteworthy, this set also contains 197 of the approximately 272 (P < 1.07e−134) environmental stress response (ESR) genes originally identified by Gasch et al. (2000). Consistent with this, the group is enriched for STRE elements (Martinez-Pastor et al. 1996) in the 5′ intragenic regions (Table 2). This group is also enriched for Hsf1, Msn2, and Msn4 targets important for stress gene regulation (Gasch et al. 2000).

Table 2
Transcription factor target and binding motif enrichment, gene ontology 25 enrichment, and overrepresented promoter motifs found in the repressed Venn diagram genes

Nutrient-specific differences: nutrient-specific downregulation

We found 537 genes downregulated by G repletion but not N or P. This group was enriched for sugar transport (P < 3.15e−8), aerobic respiration (P < 3.5e−4), transcriptional control (P < 1.92e−8), and homeostasis of metal ions (P < 2.6e−4). This cluster was enriched for gene products localizing to the mitochondrial inner membrane, consistent with GO enrichment for aerobic respiration. Gal4, Hap1, Sok2, and Sut1 targets were also enriched in this set, and motifs for Mig1 and Rtg3 were enriched in the 5′ intragenic regions (Table 2).

The 136 genes specifically downregulated by N alone were enriched for catabolism of nitrogenous compounds (P < 8.29e−5) and amino acid/amino acid derivative transport. While this set was enriched for nitrogen catabolite repression (NCR) genes (P < 1.9e−9), the majority of NCR genes were found in the set repressed in common by G, N, and P, an observation in concordance with the fact that many NCR genes are elevated in starvation (Wu et al. 2004). Finally, the 5′ intragenic regions of this cluster were enriched for Stp1, Gln3, Bas1, Gat1 binding targets, and their corresponding sequence motifs.

Interestingly, the set specifically repressed by P was enriched for genes associated with glycolysis and gluconeogenesis (P < 7.084e−11), as well as sugar, glucoside, polyol, and carboxylate catabolism (P < 9.988e−7). The 5′ intragenic regions of this set were enriched with Gcr1, Gcr2, and Hap4 targets. As expected, the set was also enriched for Pho4 targets; however, Pho4 target genes were spread between several repressed clusters, especially the common G, N, P cluster.

Requirement for cAMP and TOR

The large transcriptional response to G is dependent on sensory pathways requiring Gpa2, cAMP/PKA, and to a lesser extent, TOR signaling (Slattery et al. 2008; Wang et al. 2004). Addition of G to post-log cells has long been linked to activation of PKA via cAMP (Matsumoto et al. 1985). However, the receptors that link G signals to cAMP production are quite distinct from those that sense N and P (Zaman et al. 2008). Nonetheless, the similarities between the transcriptional responses to G, N, and P suggested that PKA and TOR might be involved in the responses to all three nutrients.

To test this, we selectively blocked PKA, TOR, or both, and we measured the effect on the transcriptional response to repletion of G, N, or P. We blocked cAMP production using a cyr1Δ strain (TC41) and blocked TOR with rapamycin (Mitts et al. 1990; Russell et al. 1993; Slattery et al. 2008). For each of the three nutrients, both gene induction and repression were highly dependent on cAMP/PKA and TOR. The heat map in Figure 5A focuses on the core 501 upregulated and 616 downregulated genes responding to G, N, or P. Loss of both PKA and TOR signaling essentially blocked the large-scale transcriptional response to nutrient repletion. We found that most transcript changes showed a greater dependence on cAMP/PKA than on Tor.

Figure 5
The effect of PKA and TOR signaling in the transcriptional response to G, N, and P. Cells carrying a cyr1Δ mutation (TC41) were starved for G, N, or P until growth arrested, and cAMP was removed as described in Materials and Methods. Samples for ...

The plots in Figure 5B compare the responses to nutrient repletion between cells with normal cAMP/PKA and TOR with the responses in cells when different pathways are blocked. Each transcript on the array is plotted as a dot, with the X-axis position indicating the fold change caused by nutrient repletion with both TOR and cAMP/PKA intact; the position on the Y-axis indicates the response when the indicated pathways are blocked. The different pathway manipulations are represented by different colors, and each nutrient repletion, G, N, or P, is presented as a separate graph.

As a control, we plotted the response to each nutrient in a wild-type CYR1+ strain against our cyr1Δ strain supplied with cAMP. This produced an almost perfect diagonal line, shown as dark blue; the line obscures the dots. This indicates that our cyr1Δ mutant can respond normally when cAMP is provided.

TOR blockade (red dots) caused some loss of response, while loss of cAMP (dark green) had a striking impact on the response to each nutrient. With both TOR and PKA knocked out (turquoise), the responses to nutrient addition were substantially reduced: the G and N responses were almost completely blocked, and a small amount of the response to P repletion remained.

Nutrient signaling through cAMP

Although the connection between glucose and cAMP production is well known (Boy-Marcotte et al. 1987; Camonis et al. 1986; Matsumoto et al. 1982; 1985; Thevelein and Beullens 1985), we were surprised to find that the response to N and P repletion was cAMP-dependent. If N and P produce the transcriptional response through cAMP/PKA, then directly stimulating this pathway by adding cAMP should bypass the nutrients and replicate the response. On the other hand, cAMP might be necessary without playing a direct role in transmitting the signal. In this permissive role, cAMP alone should be inactive without N or P.

To test this, cyr1Δ cells were N or P depleted with cAMP present to ensure growth into quiescence, and then moved to starvation minus cAMP for 24 hr. The cultures were then divided, and the missing nutrient plus cAMP was added to one aliquot, while cAMP alone was added to the other, and then the samples were prepared for microarray analysis. Changes in gene expression produced by cAMP alone are plotted on the Y-axes, and the responses to the nutrient with cAMP on the X-axes (Figure 6). The response to cAMP produced transcriptional changes that were largely similar to those produced by the nutrient itself with cAMP present. The correlation between cAMP alone and cAMP and N was 0.79, while the correlation with cAMP and P was 0.87.

Figure 6
Response of N- or P-starved cells to cAMP addition. Cells carrying a CYR1 deletion (TC41) were grown until limited for N or P as described in Materials and Methods, and then challenged with either cAMP alone or cAMP with the limiting nutrient. Samples ...

Of note is the fact that when cAMP alone was added, these cells did not grow and under the microscope maintained a quiescent appearance. The transcriptional response is not sufficient to produce growth in the absence of the missing nutrient.

Thus, the responses to N and P were largely cAMP-dependent. Furthermore, cAMP was able to produce similar transcriptional responses to those produced by N or P repletion. We have previously observed very similar results with G repletion (Slattery et al. 2008).

The obvious next step was to examine the effect of G, N, and P repletion on cAMP levels. While glucose tended to produce a more robust response, in repeated experiments, we consistently found that all three nutrients increased cAMP levels when added back to quiescent cells (Figure 7). The sustained cAMP levels following G repletion are consistent with our previous results (Russell et al. 1993).

Figure 7
G, N, and P repletions increase cAMP. Prototrophic yeast (S288C) were starved for G, N, or P and then repleted with the missing nutrient as described in Materials and Methods. Levels of cAMP were measured at the indicated time after repletion using an ...

Cross talk between nutrient signals

The fact that cAMP is required for the transcriptional responses to G, N, and P, that the nutrients produce increases in cAMP, and that cAMP alone can simulate the repletion response indicates that nutrients regulate these large changes in part through cAMP/PKA. However, this model poses problems: How can a cell halt growth when just one nutrient is depleted? How does the cell know which nutrient is sending the signal? Indeed, we wondered whether there were cases where adding one nutrient could substitute for the lack of another.

To examine this, we simultaneously depleted cells for two nutrients, and then repleted only one of the pair. We measured changes in transcripts when we added each nutrient alone or with its missing partner. For comparison, we also repeated the depletion experiments in which a single nutrient was depleted and repleted (Figure 8A).

Figure 8
Cross talk between nutrient signals. S288C cells were starved for the indicated nutrients and repleted with either a single nutrient or both of the limiting nutrients as described in Materials and Methods. (A) As a point of reference, the results for ...

As expected, The GP- and GN-depleted cells showed robust responses to repletion of both limiting nutrients together (Figure 8, B and C). These responses were largely similar to those studied earlier when a single nutrient was depleted and repleted (Figure 8A). However, addition of N alone to a GN-depleted culture produced almost no response; nor did addition of P to a GP-depleted culture. In contrast, addition of G alone, while not producing growth, produced a large transcriptional response in the doubly depleted cultures, despite the fact that the cells were still growth limited by N or P.

Origin of nutrient signals

Gap1 activates trehalase in response to amino acid stimulation (Donaton et al. 2003). To determine whether Gap1 carries signals regulating the large-scale response to nitrogen repletion, we challenged wild-type and gap1Δ cells with citrulline and then collected RNA for microarray analysis. We used citrulline because it is a relatively specific Gap1 agonist (Donaton et al. 2003; Grenson et al. 1970). We found that addition of citrulline to N-depleted wild-type cells produced a marked change in transcript levels relative to the starved state as shown in the heat map in Figure 9. However, this response was almost entirely silenced by loss of GAP1, indicating that the signal induced by citrulline repletion requires Gap1.

Figure 9
Effect of GAP1 deletion on the transcriptional response to N. Wild-type (BY4742) or the isogenic gap1Δ cells were starved for N as in Figure 1 and then challenged with 10 mM L-citrulline. Samples for microarray analysis were collected at the starved ...

The dot plot in Figure 9B shows for each transcript the fold change produced by L-citrulline plotted on the X-axis for wild-type cells and on the Y-axis for the gap1Δ mutant samples. For most transcripts that responded to citrulline, loss of Gap1 had a profound effect.

The box and whisker plots in Figure 9C show the effect of citrulline on the sets of 501 and 616 core genes induced or repressed at least 2-fold by G, N, or P in Figures 3 and and4.4. It can be seen that the responses produced by L-citrulline average less than 2-fold, so L-citrulline produces a less robust response than the original N repletion, which included both ammonium and amino acids. However, more than 75% of the 501 genes in this set were induced by citrulline, and this was almost completely dependent on Gap1. Repression was also Gap1-dependent.

The ammonium permeases Mep1, Mep2, and Mep3 are all involved in ammonium activation of trehalase, although Mep2 produces the most prominent signal (Van Nuland et al. 2006). Mep2 has also been implicated in regulating the ammonium control of pseudohyphal growth (Lorenz and Heitman 1998).

As in the previous experiment, we used N-starved wild-type or mep1Δ, mep2Δ, or mep3Δ, mutant cells and challenged them with 10 mM ammonium. The heat map shows that each mutation has some impact on the overall response to ammonium, with the mep3Δ mutant producing the most blunted response (Figure 10). The relative impacts that the mutations had are shown in the dot plot in Figure 10B, and the effects on the 501 induced and 616 repressed genes described above are shown in the box and whisker plots of Figure 10C. Overall, it appears that, as with trehalase, all three MEP genes contribute to the transcriptional response to ammonium repletion.

Figure 10
Role of Mep transceptors in the response to N. Wild-type (BY4742) and the isogenic mep1Δ, mep2Δ, and mep3Δ cells were starved for N, and then challenged with 10 mM ammonium sulfate. Samples for microarray analysis were taken at ...

The Pho84 phosphate transporter has been reported to act as a phosphorous sensor (Popova et al. 2010). We challenged wild-type and pho84Δ cells with two P sources: KH2PO4, the a Pho84-transportedP source used in the previous repletions, and glycerol-3-phosphate (Gly3P) as a specific agonist for Pho84 (Popova et al. 2010). We found that loss of PHO84 produced different effects depending on the P source. As shown by the heat maps and dot plots in Figure 11, the response to Gly3P was considerably attenuated by loss of PHO84, while the KH2PO4 response was not.

Figure 11
Role of PHO84 in the transcriptional response to P. Wild-type (BY4742) or isogenic pho84Δ cells were starved for P, and then challenged with KH2PO4 or Gly3P as described in Materials and Methods. Samples for microarray analysis were taken from ...

Figure 11C shows a box and whisker plot focused on the sets of 501 and 616 transcripts upregulated and downregulated, respectively, by all three nutrients. The effect of PHO84 deletion on the KH2PO4 response was quite subtle: the response to Gly3P repletion was more distinct. Overall, these data suggest that PHO84 plays a role in, but is not solely responsible for, signaling the transcriptional response to P.


Growth and quiescence

The ability of yeast cells to cease division and attain a stress-resistant state in response to different nutrient limitations was recognized some time ago (Lillie and Pringle 1980; Paris and Pringle 1983). This somewhat commonplace occurrence has several implications. First, it appears that quiescence and growth, while influenced by different conditions, are two fundamental states for yeast cells. This conclusion was recently strengthened by Klosinska et al. (2011). Another implication is that cells must use different nutrient signals to control entry into growth and quiescence.

A simple idea would be that as any nutrient becomes limiting, metabolic activity subsides and that drop is sensed. While this plan relieves the cell of having to sense many different important nutrients, two arguments can be made against it. First, allowing critical resources to reach such low levels so as to limit metabolism would be expected to substantially reduce fitness; in fact, nutrients are stored prior to quiescence. Perhaps more compelling are the numerous nutrient-sensing mechanisms that are now being discovered. Indeed, many of the responses described in this article can be observed under conditions in which the cell cannot, or does not, metabolize the nutrient producing the signal.

One important difference that we noted between nutrient-limited states was that cells deprived of glucose respond more conservatively than those limited for N or P. This is best observed in the group of 137 RP genes, which are considerably more repressed when cells are limited for G than by N or P. In fact, it was because of this failure to repress the RP genes during N or P starvation that the N induction of this set by N or P failed to make the ≥ 2× cut off (Figure 3 and Figure S1). A similar effect was observed with the 230 RiBi transcripts, being on average about 2-fold more repressed in G-depleted cells than in N- or P-depleted cells (Figure S1). This effect contributes to the observation that the fold changes produced by N and P resembled each other more closely than they resembled the response to G.

While N and P are needed primarily as elemental building blocks, limitation for G affects both the availability of carbon and cellular energy. We speculate that because cells are adept at recycling nutrients as long as energy is plentiful, they can afford to maintain higher levels of RP and RiBi gene expression if G is present than they do if starved for G and the energy G provides. The RP and RiBi transcripts represent a large fraction of the total mRNA.

A common response triggered by different chemical signals

Glucose has been studied in relation to growth, metabolic regulation, respiration, and glucose repression (Carlson 1999; Hedbacker and Carlson 2008). Many studies of N signalng have focused on the role of N as a regulator of metabolic processes requiring nitrogen as an element. Many studies have focused on nitrogen metabolism and the TOR pathway (Cardenas et al. 1999; Cooper 2002; Crespo et al. 2002; Hardwick et al. 1999; Hinnebusch 2005). A similar approach has been used in studying P signals, focusing on phosphate in metabolism (Wykoff and O’Shea 2001). This has produced models in which G, N, and P initiate signals in yeast through very distinct pathways (Forsberg and Ljungdahl 2001; Magasanik and Kaiser 2002; Schneper et al. 2004). With this in mind, it was possible that the transcriptional responses might converge in a minor way but be largely distinct and non-overlapping.

A set of experiments by Thevelein et al. (2005) indicated that all three nutrients were tied together in a PKA-dependent process (Giots et al. 2003; Popova et al. 2010; Van Zeebroeck et al. 2009). However, this work left two points in question. First, trehalase activation, while providing an indirect measurement of PKA activity, does not shed light on the scope of the response. Second, only G, and not N or P, was thought to increase cAMP.

We found that the response to G, N, and P involves a core set of at least 1117 genes: approximately 18% of the yeast genome. We conclude that the need to induce genes for growth and to repress unneeded stress genes is compelling and generalized. The gene set induced was enriched for ribosome biogenesis and translation genes; these would be required for growth regardless of the initiating nutrient signal. By the same token, the set of 616 repressed genes was enriched with stress response genes (Gasch et al. 2000). Cells initiating growth in newly repleted medium under favorable conditions are best off putting their energy into other processes and reducing stress-response transcripts, again regardless of the repleted nutrient.

Role of cAMP and PKA

Glucose induces cAMP production (Boy-Marcotte et al. 1987; François et al. 1987; Russell et al. 1993). However, while N and P have been shown to produce responses indicative of PKA activation, there has been little if any positive link between the repletion of these nutrients and cAMP production (Donaton et al. 2003; Popova et al. 2010; Van Nuland et al. 2006; Van Zeebroeck et al. 2009). In our hands, all three repletions consistently produced increases in cAMP levels that were sustained over an hour. This is consistent with the trehalase activation as well as the cAMP requirement for the large-scale transcriptional response to all three nutrients and the ability of cAMP itself to mimic nutrient repletion in the absence of the missing nutrient.

Clearly, induction and repression of mRNAs is not enough to make cells grow: metabolism, protein synthesis, and many other processes are required in parallel. Thus, simply creating a large transcriptional response by itself without also providing the missing nutrient did not produce growth.

While the TOR pathway is clearly important in nutrient signaling (Cardenas et al. 1999; Cooper 2002; Wullschleger et al. 2006), we found TOR inhibition produced a smaller overall effect than loss of cAMP production. In fact the largest effect was observed when both pathways were blocked, suggesting overlapping and partially redundant roles for the two kinase pathways (Martin et al. 2004; Roosen et al. 2005; Santangelo 2006; Zurita-Martinez and Cardenas 2005).


The response to G repletion can be explained by stimulation of the glucose receptor Gpr1, coupled to the Gpa2 G-protein to stimulate cAMP production by adenylyl cyclase, encoded by CYR1. While not fully understood, this mechanism of cAMP generation has long been studied (Santangelo 2006; Zaman et al. 2008, 2009). The connections between N, P, and cAMP/PKA are less well understood.

Gap1 has recently been discovered to produce signals in response to amino acid substrates to control Gap1 processing as well as trehalase activation (Cain and Kaiser 2011; Kriel et al. 2011; Merhi et al. 2011; Van Zeebroeck et al. 2009). Citrulline has been identified as a specific Gap1 agonist that can generate a signal inducing trehalase without being metabolized as a nitrogen source (Donaton et al. 2003). We found the response to L-citrulline was Gap1-dependent. Therefore, in addition to regulating the PKA-dependent posttranslational increase in trehalase, we found that Gap1 plays a role in our cAMP-dependent transcriptome response to N repletion.

Mep2 is involved in controlling pseudohyphal growth and trehalase activation (Rutherford et al. 2008; Van Nuland et al. 2006). Therefore, Mep protein involvement in the transcriptional response to ammonium is not surprising. We found that each of the Mep1–3 proteins played a role in the response to ammonium.

There has also been growing evidence that Pho84 can serve as a transceptor regulating both aspects of phosphate metabolism and PKA-dependent trehalase activation (Giots et al. 2003; Lagerstedt et al. 2004; Lundh et al. 2009; Thevelein et al. 2005). Gly3P has been found to be a transceptor agonist that can activate Pho84 without transport by Pho84 (Popova et al. 2010). Loss of Pho84 had little impact on the response to orthophosphate repletion, but it did inhibit the response to Gly3P. Because Gly3P signaling is largely Pho84-dependent, this suggests that the receptors for orthophosphate are redundant: other receptors maintain the response in the absence of Pho84. We speculate that Gly3P is not a good agonist for the redundant receptors.

Prior to the advent of microarrays, a prevalent idea was that yeast growth fueled transcription in general. We show that large changes in mRNA abundance precede growth rather than result from growth and that they are readily decoupled from growth. For example, both citrulline and Gly3P are known agonists for their respective transceptors, yet they are poor nutrients. However, both of these agents produced a large-scale response. A strain unable to take in and grow on glucose still produces a normal large-scale transcriptional response to G repletion (Slattery et al. 2008). In dually starved cells, addition of G alone produced a transcriptional response that was not sufficient to induce growth. Finally, the addition of cAMP mimicked the nutrient repletion responses in cells that remained nutrient depleted. These results are evidence for a sensing system that can directly determine when a missing nutrient is restored.

Cross talk

Because G, N, and P each appear to signal through PKA in a cAMP-dependent manner, it is not clear how the cell can differentiate between the nutrients. In fact, one would predict that cross talk would occur. We found some evidence for cross talk in which G alone induced transcriptional responses in dually GN- or GP-limited cells. N or P alone did not produce a response when G was absent. We have found that G upshifts can produce some transcriptional responses in N- or P-limited cultures (data not shown). Griffioen et al. (1996) observed that G upshift produced RP gene induction that was initially independent of growth. With the information available at present, we conclude that the three nutrients examined produce a common response through mechanisms that have common elements, yet in at least some circumstances, they can maintain specificity. We speculate that the response to G, which provides energy as well as material, has features that are qualitatively different from the other responses. How the cell actually distinguishes between nutrients remains a mystery.

Supplementary Material

Supporting Information:


We thank B. Jansch for help in developing the manuscript. Funding for this research was provided by the DOE Great Lakes Bioenergy Research Center supported by the US Department of Energy.


Communicating editor: C. S. Hoffman

Literature Cited

  • Boy-Marcotte E., Garreau H., Jacquet M., 1987.  Cyclic AMP controls the switch between division cycle and resting state programs in response to ammonium availability in Saccharomyces cerevisiae. Yeast 3: 85–93 [PubMed]
  • Cain N. E., Kaiser C. A., 2011.  Transport activity-dependent intracellular sorting of the yeast general amino acid permease. Mol. Biol. Cell 22: 1919–1929 [PMC free article] [PubMed]
  • Camonis J. H., Kalekine M., Bernard G., Garreau H., Boy-Marcotte E., et al. , 1986.  Characterization, cloning and sequence analysis of the CDC25 gene which controls the cAMP level of Saccharomyces cerevisiae. EMBO 5: 375–380 [PubMed]
  • Cardenas M. E., Cutler N. S., Lorenz M. C., Di Como C. J., Heitman J., 1999.  The TOR signaling cascade regulates gene expression in response to nutrients. Genes Dev. 13: 3271–3279 [PubMed]
  • Carlson M., 1999.  Glucose repression in yeast. Curr. Opin. Microbiol. 2: 202–207 [PubMed]
  • Chua G., Morris Q. D., Sopko R., Robinson M. D., Ryan O., et al. , 2006.  Identifying transcription factor functions and targets by phenotypic activation. Proc. Natl. Acad. Sci. USA 103: 12045–12050 [PubMed]
  • Cooper T. G., 2002.  Transmitting the signal of excess nitrogen in Saccharomyces cerevisiae from the Tor proteins to the GATA factors: connecting the dots. FEMS Microbiol. Rev. 26: 223–238 [PubMed]
  • Crespo J. L., Powers T., Fowler B., Hall M. N., 2002.  The TOR-controlled transcription activators GLN3, RTG1, and RTG3 are regulated in response to intracellular levels of glutamine. Proc. Natl. Acad. Sci. USA 99: 6784–6789 [PubMed]
  • Dequard-Chablat M., Riva M., Carles C., Sentenac A., 1991.  RPC19, the gene for a subunit common to yeast RNA polymerases A (I) and C (III). J. Biol. Chem. 266: 15300–15307 [PubMed]
  • Donaton M. C., Holsbeeks I., Lagatie O., Van Zeebroeck G., Crauwels M., et al. , 2003.  The Gap1 general amino acid permease acts as an amino acid sensor for activation of protein kinase A targets in the yeast Saccharomyces cerevisiae. Mol. Microbiol. 50: 911–929 [PubMed]
  • Fingerman I., Nagaraj V., Norris D., Vershon A. K., 2003.  Sfp1 plays a key role in yeast ribosome biogenesis. Eukaryot. Cell 2: 1061–1068 [PMC free article] [PubMed]
  • Forsberg H., Ljungdahl P. O., 2001.  Sensors of extracellular nutrients in Saccharomyces cerevisiae. Curr. Genet. 40: 91–109 [PubMed]
  • François J., Eraso P., Gancedo C., 1987.  Changes in the concentration of cAMP, fructose 2,6-biphosphate and related metabolites and enzymes in Saccharomyces cerevisiae during growth on glucose. Eur. J. Biochem. 164: 369–373 [PubMed]
  • Gasch A. P., Spellman P. T., Kao C. M., Carmel-Harel O., Eisen M. B., et al. , 2000.  Genomic expression programs in the response of yeast cells to environmental changes. Mol. Biol. Cell 11: 4241–4257 [PMC free article] [PubMed]
  • Gentleman R. C., Carey V. J., Bates D. M., Bolstad B., Dettling M., et al. , 2004.  Bioconductor: open software development for computational biology and bioinformatics. Genome Biol. 5: R80. [PMC free article] [PubMed]
  • Giots F., Donaton M. C., Thevelein J. M., 2003.  Inorganic phosphate is sensed by specific phosphate carriers and acts in concert with glucose as a nutrient signal for activation of the protein kinase A pathway in the yeast Saccharomyces cerevisiae. Mol. Microbiol. 47: 1163–1181 [PubMed]
  • Gray J. V., Petsko G. A., Johnston G. C., Ringe D., Singer R. A., et al. , 2004.  “Sleeping beauty”: quiescence in Saccharomyces cerevisiae. Microbiol. Mol. Biol. Rev. 68: 187–206 [PMC free article] [PubMed]
  • Greenberg M. L., Lopes J. M., 1996.  Genetic regulation of phospholipid biosynthesis in Saccharomyces cerevisiae. Microbiol. Rev. 60: 1–20 [PMC free article] [PubMed]
  • Grenson M., Hou C., Crabeel M., 1970.  Multiplicity of the amino acid permeases in Saccharomyces cerevisiae. IV. Evidence for a general amino acid permease. J. Bacteriol. 103: 770–777 [PMC free article] [PubMed]
  • Griffioen G., Laan R. J., Mager W. H., Planta R. J., 1996.  Ribosomal protein gene transcription in Saccharomyces cerevisiae shows a biphasic response to nutritional changes. Microbiology 142: 2279–2287 [PubMed]
  • Grigull J., Mnaimneh S., Pootoolal J., Robinson M. D., Hughes T. R., 2004.  Genome-wide analysis of mRNA stability using transcription inhibitors and microarrays reveals posttranscriptional control of ribosome biogenesis factors. Mol. Cell. Biol. 24: 5534–5547 [PMC free article] [PubMed]
  • Hahn J. S., Hu Z., Thiele D. J., Iyer V. R., 2004.  Genome-wide analysis of the biology of stress responses through heat shock transcription factor. Mol. Cell. Biol. 24: 5249–5256 [PMC free article] [PubMed]
  • Harbison C. T., Gordon D. B., Lee T. I., Rinaldi N. J., Macisaac K. D., et al. , 2004.  Transcriptional regulatory code of a eukaryotic genome. Nature 431: 99–104 [PMC free article] [PubMed]
  • Hardwick J. S., Kuruvilla F. G., Tong J. K., Shamji A. F., Schreiber S. L., 1999.  Rapamycin-modulated transcription defines the subset of nutrient-sensitive signaling pathways directly controlled by the Tor proteins. Proc. Natl. Acad. Sci. USA 96: 14866–14870 [PubMed]
  • Hedbacker K., Carlson M., 2008.  SNF1/AMPK pathways in yeast. Front. Biosci. 13: 2408–2420 [PMC free article] [PubMed]
  • Heideman W., Casperson G. F., Bourne H. R., 1990.  Adenylyl cyclase in yeast: antibodies and mutations identify a regulatory domain. J. Cell. Biochem. 42: 229–242 [PubMed]
  • Hinnebusch A. G., 2005.  Translational regulation of GCN4 and the general amino acid control of yeast. Annu. Rev. Microbiol. 59: 407–450 [PubMed]
  • Hughes J. D., Estep P. W., Tavazoie S., Church G. M., 2000.  Computational identification of cis-regulatory elements associated with groups of functionally related genes in Saccharomyces cerevisiae. J. Mol. Biol. 296: 1205–1214 [PubMed]
  • Jauniaux J. C., Grenson M., 1990.  GAP1, the general amino acid permease gene of Saccharomyces cerevisiae. Nucleotide sequence, protein similarity with the other bakers yeast amino acid permeases, and nitrogen catabolite repression. Eur. J. Biochem. 190: 39–44 [PubMed]
  • Johnston G. C., Singer R. A., McFarlane S., 1977.  Growth and cell division during nitrogen starvation of the yeast Saccharomyces cerevisiae. J. Bacteriol. 132: 723–730 [PMC free article] [PubMed]
  • Jorgensen P., Rupes I., Sharom J. R., Schneper L., Broach J. R., et al. , 2004.  A dynamic transcriptional network communicates growth potential to ribosome synthesis and critical cell size. Genes Dev. 18: 2491–2505 [PubMed]
  • Klosinska M. M., Crutchfield C. A., Bradley P. H., Rabinowitz J. D., Broach J. R., 2011.  Yeast cells can access distinct quiescent states. Genes Dev. 25: 336–349 [PubMed]
  • Kriel J., Haesendonckx S., Rubio-Texeira M., Van Zeebroeck G., Thevelein J. M., 2011.  From transporter to transceptor: signaling from transporters provokes re-evaluation of complex trafficking and regulatory controls: endocytic internalization and intracellular trafficking of nutrient transceptors may, at least in part, be governed by their signaling function. Bioessays 33: 870–879 [PMC free article] [PubMed]
  • Lagerstedt J. O., Voss J. C., Wieslander A., Persson B. L., 2004.  Structural modeling of dual-affinity purified Pho84 phosphate transporter. FEBS Lett. 578: 262–268 [PubMed]
  • Lieb J. D., Liu X., Botstein D., Brown P. O., 2001.  Promoter-specific binding of Rap1 revealed by genome-wide maps of protein-DNA association. Nat. Genet. 28: 327–334 [PubMed]
  • Lillie S. H., Pringle J. R., 1980.  Reserve carbohydrate metabolism in Saccharomyces cerevisiae: responses to nutrient limitation. J. Bacteriol. 143: 1384–1394 [PMC free article] [PubMed]
  • Lorenz M. C., Heitman J., 1998.  The MEP2 ammonium permease regulates pseudohyphal differentiation in Saccharomyces cerevisiae. EMBO J. 17: 1236–1247 [PubMed]
  • Lundh F., Mouillon J. M., Samyn D., Stadler K., Popova Y., et al. , 2009.  Molecular mechanisms controlling phosphate-induced downregulation of the yeast Pho84 phosphate transporter. Biochemistry 48: 4497–4505 [PubMed]
  • Macisaac K. D., Gordon D. B., Nekludova L., Odom D. T., Schreiber J., et al. , 2006.  A hypothesis-based approach for identifying the binding specificity of regulatory proteins from chromatin immunoprecipitation data. Bioinformatics 22: 423–429 [PubMed]
  • Magasanik B., Kaiser C. A., 2002.  Nitrogen regulation in Saccharomyces cerevisiae. Gene 290: 1–18 [PubMed]
  • Marion R. M., Regev A., Segal E., Barash Y., Koller D., et al. , 2004.  Sfp1 is a stress- and nutrient-sensitive regulator of ribosomal protein gene expression. Proc. Natl. Acad. Sci. USA 101: 14315–14322 [PubMed]
  • Martin D. E., Soulard A., Hall M. N., 2004.  TOR regulates ribosomal protein gene expression via PKA and the Forkhead transcription factor FHL1. Cell 119: 969–979 [PubMed]
  • Martinez M. J., Roy S., Archuletta A. B., Wentzell P. D., Anna-Arriola S. S., et al. , 2004.  Genomic analysis of stationary-phase and exit in Saccharomyces cerevisiae: gene expression and identification of novel essential genes. Mol. Biol. Cell 15: 5295–5305 [PMC free article] [PubMed]
  • Martinez-Pastor M. T., Marchler G., Schuller C., Marchler-Bauer A., Ruis H., et al. , 1996.  The Saccharomyces cerevisiae zinc finger proteins Msn2p and Msn4p are required for transcriptional induction through the stress response element (STRE). EMBO J. 15: 2227–2235 [PubMed]
  • Matsumoto K., Uno I., Oshima Y., Ishikawa T., 1982.  Isolation and characterization of yeast mutants defective in adenylate cyclase and cAMP-depenent protein kinase. Proc. Natl. Acad. Sci. USA 79: 2355–2359 [PubMed]
  • Matsumoto K., Uno I., Ishikawa T., 1985.  Genetic analysis of the role of cAMP in yeast. Yeast 1: 15–24 [PubMed]
  • Mazon M. J., 1978.  Effect of glucose starvation on the nicotinamide adenine dinucleotide phosphate-dependent glutamate dehydrogenase of yeast. J. Bacteriol. 133: 780–785 [PMC free article] [PubMed]
  • Merhi A., Gerard N., Lauwers E., Prevost M., Andre B., 2011.  Systematic mutational analysis of the intracellular regions of yeast Gap1 permease. PLoS ONE 6: e18457. [PMC free article] [PubMed]
  • Mitts M. R., Grant D. B., Heideman W., 1990.  Adenylate cyclase in Saccharomyces cerevisisae is a peripheral membrane protein. Mol. Cell. Biol. 10: 3873–3883 [PMC free article] [PubMed]
  • Newcomb L. L., Diderich J. A., Slattery M. G., Heideman W., 2003.  Glucose regulation of Saccharomyces cerevisiae cell cycle genes. Eukaryot. Cell 2: 143–149 [PMC free article] [PubMed]
  • Paris S., Pringle J. R., 1983.  Saccharomyces cerevisiae: heat and gluculase sensitivities of starved cells. Ann. Microbiol. (Paris) 134B: 379–385 [PubMed]
  • Pina B., Fernandez-Larrea J., Garcia-Reyero N., Idrissi F. Z., 2003.  The different (sur)faces of Rap1p. Mol. Genet. Genomics 268: 791–798 [PubMed]
  • Popova Y., Thayumanavan P., Lonati E., Agrochao M., Thevelein J. M., 2010.  Transport and signaling through the phosphate-binding site of the yeast Pho84 phosphate transceptor. Proc. Natl. Acad. Sci. USA 107: 2890–2895 [PubMed]
  • Radonjic M., Andrau J. C., Lijnzaad P., Kemmeren P., Kockelkorn T. T., et al. , 2005.  Genome-wide analyses reveal RNA polymerase II located upstream of genes poised for rapid response upon S. cerevisiae stationary phase exit. Mol. Cell 18: 171–183 [PubMed]
  • Robert F., Pokholok D. K., Hannett N. M., Rinaldi N. J., Chandy M., et al. , 2004.  Global position and recruitment of HATs and HDACs in the yeast genome. Mol. Cell 16: 199–209 [PMC free article] [PubMed]
  • Robinson M. D., Grigull J., Mohammad N., Hughes T. R., 2002.  FunSpec: a web-based cluster interpreter for yeast. BMC Bioinformatics 3: 35. [PMC free article] [PubMed]
  • Roosen J., Engelen K., Marchal K., Mathys J., Griffioen G., et al. , 2005.  PKA and Sch9 control a molecular switch important for the proper adaptation to nutrient availability. Mol. Microbiol. 55: 862–880 [PubMed]
  • Rowley A., Johnston G., Butler B., Werner-Washburne M., Singer R., 1993.  Heat shock-mediated cell cycle blockage and G1 cyclin expression in the yeast Saccharomyces cerevisiae. Mol. Cell. Biol. 13: 1034–1041 [PMC free article] [PubMed]
  • Russell M., Bradshaw-Rouse J., Markwardt D., Heideman W., 1993.  Changes in gene expression in the Ras/adenylate cyclase system of Saccharomyces cerevisiae: correlation with cAMP levels and growth arrest. Mol. Biol. Cell 4: 757–765 [PMC free article] [PubMed]
  • Rutherford J. C., Chua G., Hughes T., Cardenas M. E., Heitman J., 2008.  A Mep2-dependent transcriptional profile links permease function to gene expression during pseudohyphal growth in Saccharomyces cerevisiae. Mol. Biol. Cell 19: 3028–3039 [PMC free article] [PubMed]
  • Saeed A. I., Sharov V., White J., Li J., Liang W., et al. , 2003.  TM4: a free, open-source system for microarray data management and analysis. Biotechniques 34: 374–378 [PubMed]
  • Saeed A. I., Bhagabati N. K., Braisted J. C., Liang W., Sharov V., et al. , 2006.  TM4 microarray software suite. Methods Enzymol. 411: 134–193 [PubMed]
  • Santangelo G. M., 2006.  Glucose signaling in Saccharomyces cerevisiae. Microbiol. Mol. Biol. Rev. 70: 253–282 [PMC free article] [PubMed]
  • Schawalder S. B., Kabani M., Howald I., Choudhury U., Werner M., et al. , 2004.  Growth-regulated recruitment of the essential yeast ribosomal protein gene activator Ifh1. Nature 432: 1058–1061 [PubMed]
  • Scherens B., Feller A., Vierendeels F., Messenguy F., Dubois E., 2006.  Identification of direct and indirect targets of the Gln3 and Gat1 activators by transcriptional profiling in response to nitrogen availability in the short and long term. FEMS Yeast Res. 6: 777–791 [PubMed]
  • Schneper L., Duvel K., Broach J. R., 2004.  Sense and sensibility: nutritional response and signal integration in yeast. Curr. Opin. Microbiol. 7: 624–630 [PubMed]
  • Slattery M. G., Heideman W., 2007.  Coordinated regulation of growth genes in Saccharomyces cerevisiae. Cell Cycle 6: 1210–1219 [PubMed]
  • Slattery M. G., Liko D., Heideman W., 2008.  Protein kinase A, TOR, and glucose transport control the response to nutrient repletion in Saccharomyces cerevisiae. Eukaryot. Cell 7: 358–367 [PMC free article] [PubMed]
  • Thevelein J. M., Beullens M., 1985.  Cyclic AMP and the stimulation of trehalase activity in the yeast Saccharomyces cerevisiae by carbon sources, nitrogen sources and inhibitors of protein synthesis. J. Gen. Microbiol. 131: 3199–3209 [PubMed]
  • Thevelein J. M., Gelade R., Holsbeeks I., Lagatie O., Popova Y., et al. , 2005.  Nutrient sensing systems for rapid activation of the protein kinase A pathway in yeast. Biochem. Soc. Trans. 33: 253–256 [PubMed]
  • Thomas-Chollier M., Sand O., Turatsinze J. V., Janky R., Defrance M., et al. , 2008.  RSAT: regulatory sequence analysis tools. Nucleic Acids Res. 36: W119–W127 [PMC free article] [PubMed]
  • Unger M. W., Hartwell L. H., 1976.  Control of cell division in Saccharomyces cerevisiae by methionyl-tRNA. Proc. Natl. Acad. Sci. USA 73: 1664–1668 [PubMed]
  • van Helden J., 2003.  Regulatory sequence analysis tools. Nucleic Acids Res. 31: 3593–3596 [PMC free article] [PubMed]
  • Van Nuland A., Vandormael P., Donaton M., Alenquer M., Lourenco A., et al. , 2006.  Ammonium permease-based sensing mechanism for rapid ammonium activation of the protein kinase A pathway in yeast. Mol. Microbiol. 59: 1485–1505 [PubMed]
  • Van Zeebroeck G., Bonini B. M., Versele M., Thevelein J. M., 2009.  Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor. Nat. Chem. Biol. 5: 45–52 [PubMed]
  • Wade C., Shea K. A., Jensen R. V., McAlear M. A., 2001.  EBP2 is a member of the yeast RRB regulon, a transcriptionally coregulated set of genes that are required for ribosome and rRNA biosynthesis. Mol. Cell. Biol. 21: 8638–8650 [PMC free article] [PubMed]
  • Wang Y., Pierce M., Schneper L., Guldal C. G., Zhang X., et al. , 2004.  Ras and Gpa2 mediate one branch of a redundant glucose signaling pathway in yeast. PLoS Biol. 2: E128. [PMC free article] [PubMed]
  • Wu J., Zhang N., Hayes A., Panoutsopoulou K., Oliver S. G., 2004.  Global analysis of nutrient control of gene expression in Saccharomyces cerevisiae during growth and starvation. Proc. Natl. Acad. Sci. USA 101: 3148–3153 [PubMed]
  • Wullschleger S., Loewith R., Hall M. N., 2006.  TOR signaling in growth and metabolism. Cell 124: 471–484 [PubMed]
  • Wykoff D. D., O’Shea E. K., 2001.  Phosphate transport and sensing in Saccharomyces cerevisiae. Genetics 159: 1491–1499 [PubMed]
  • Zaman S., Lippman S. I., Zhao X., Broach J. R., 2008.  How Saccharomyces responds to nutrients. Annu. Rev. Genet. 42: 27–81 [PubMed]
  • Zaman S., Lippman S. I., Schneper L., Slonim N., Broach J. R., 2009.  Glucose regulates transcription in yeast through a network of signaling pathways. Mol. Syst. Biol. 5: 245. [PMC free article] [PubMed]
  • Zhu C., Byers K. J., McCord R. P., Shi Z., Berger M. F., et al. , 2009.  High-resolution DNA-binding specificity analysis of yeast transcription factors. Genome Res. 19: 556–566 [PubMed]
  • Zurita-Martinez S. A., Cardenas M. E., 2005.  Tor and cyclic AMP-protein kinase A: two parallel pathways regulating expression of genes required for cell growth. Eukaryot. Cell 4: 63–71 [PMC free article] [PubMed]

Articles from G3: Genes|Genomes|Genetics are provided here courtesy of Genetics Society of America