Schematic diagram of the main pathways of nitrogen metabolism. The entry routes of several nitrogen sources into the central core reactions are shown. The class A preferred and class B nonpreferred nitrogen sources are in green and red text, respectively. The nitrogen of preferred nitrogen sources is incorporated into glutamate, and the resulting carbon skeletons are shunted into pyruvate and α-ketoglutarate. Nitrogen from branched-chain amino acids, aromatic amino acids, and methionine (within box) is transferred to α-ketoglutarate by transaminases forming glutamate; the resulting deaminated carbon skeletons are converted to noncatabolizable and growth-inhibitory fusel oils (). Nitrogenous compounds are synthesized with nitrogen derived from glutamate or glutamine as indicated (blue arrows). Central anabolic reactions 1 and 2 are catalyzed by NADPH-dependent glutamate dehydrogenase (GDH1) and glutamine synthetase (GLN1). Central catabolic reactions 3 and 4 are catalyzed by NADH-dependent glutamate synthase (GLT1) and NAD⁺-linked glutamate dehydrogenase (GDH2). For detailed descriptions of the pathways, the reader is referred to the SGD (http://pathway.yeastgenome.org/) or KEGG (http://www.genome.jp/kegg/pathway.html) databases.

General scheme for the biosynthesis of amino acids from glucose and ammonia. Ammonia is incorporated during the formation of glutamate from α-ketoglutarate (reaction 1) by NADPH-dependent glutamate dehydrogenase (GDH1) and of glutamine from glutamate (reaction 2) by glutamine synthetase (GLN1). The transamination reactions transferring nitrogen from glutamate (yellow) or glutamine (green) are shown. For detailed descriptions of the pathways, the reader is referred to the SGD (http://pathway.yeastgenome.org/) or KEGG (http://www.genome.jp/kegg/pathway.html) databases.

Model of GATA factor and NCR-controlled gene expression. The promoters of GAT1, GZF3, and DAL80 contain multiple GATAAG sequences, and their expression is sensitive to NCR. These factors regulate each other’s expression (cross-regulation) and in certain instances exhibit partial autogenous regulation. GAT1 and DAL80 expression is primarily dependent on Gln3 and Dal80; the expression of these factors is the highest in cells grown under nonrepressive conditions. Inactivation of GZF3 results in the derepressed expression of several NCR-sensitive genes including GAT1, indicating that, in contrast to Dal80, Gzf3 is expressed at functionally significant levels and active in the presence of repressing nitrogen sources. Consistent with this latter finding, GZF3 expression is induced by Gat1 under conditions when Gln3 is apparently inactive (). Gzf3 maintains low levels of GAT1 expression by competing with Gat1 at GATAAG-binding sites; in essence, these two factors participate in an autoregulatory loop. Green lines and arrows indicate positive regulation; red lines and bars indicate negative regulation; and dashed lines reflect relatively weaker regulation. The model is modified from and ).

Schematic depiction of the GAAC pathway and the global affect of Gcn4-dependent transcription. (A) GAAC is activated when the levels of any amino acid become limiting, leading to alterations in the pools of charged tRNAs (, ). Uncharged tRNAs bind and activate the Gcn2 kinase, which phosphorylates Ser-51 of the α-subunit of the translation initiation factor eIF2 (; ; ). The phosphorylated eIF2α exhibits an enhanced affinity for the GTP-GDP exchange factor eIF2Β (GEF), competitively inhibiting the rate of nucleotide exchange, resulting in a reduction in the rate of TC eIF2-GTP-Met-tRNAi formation (gray dashed arrows). (B) The gene encoding the transcription factor Gcn4, the effector of GAAC, is transcribed as an mRNA with four small open reading frames in the 5′-untranslated region (uORF; boxes 1–4) (). As a scanning 40S ribosome with a TC (light green) encounters the first initiator codon of uORF1, the GTP bound to the TC is hydrolyzed to GDP, releasing the eIF2-GDP, and the 60S ribosome is recruited and translation initiates (80S ribosome, dark green). Translation terminates at the uORF1 stop codon, and the 60S ribosome dislocates; the 40S ribosome continues to scan but is unable (red) to initiate translation until it reacquires a TC. Under non-inducing conditions with a high level of TC, the 40S ribosome regains competence (light green) to initiate translation at uORF4. The translation of uORF4 interferes with initiation at GCN4. Under GAAC-inducing conditions, due to a low level of ternary complex, the 40S ribosome regains competence after passing uORF4 and initiates translation at GCN4. (C) Gcn4 binds to promoters of genes possessing the consensus UAS_GCRE sequence motif GAGTCA. Activation of GAAC leads to major reprograming of transcription (>500 genes are induced and >1000 are repressed) (). The number of induced genes (parentheses) in the categories of proteins relevant to amino acid and nucleotide metabolism is indicated. As indicated in A, a variety of stimuli have been shown to result in increased levels of Gcn4 (). Some of these responses impinge directly on Gcn2 (; , ) and some function independently, apparently in parallel. Notably, Gcn4 stability is increased under amino acid starvation (; ; ; ; ).

Arginine metabolic network. Arginine is primarily transported into cells by the arginine permease Can1 (), and once internalized, the bulk of arginine is transported into the vacuole by the Vba2 transporter (). Cytoplasmic arginine exerts positive (green) and negative (red) effects on gene expression encoding enzymes required for arginine utilization and catabolism, respectively. Both positive and negative regulation relies on the ArgM/Mcm1 complex, which in an arginine-dependent manner participates in activating the expression of the genes in green and repressing the genes in red. (Arginine utilization; bottom) Arginine is degraded to form glutamate. Arginine is initially degraded in the cytoplasm to form proline; this requires the concerted action of arginase (CAR1) and ornithine aminotransferase (CAR2) to form glutamate γ-semialdehyde, which spontaneously converts to Δ¹-pyrroline-5-carboxylate (P5C). P5C is converted to proline by the PRO3 gene product. Cytoplasmic proline is transported into the mitochondria where it is converted back to P5C by proline oxidase (PUT1). Finally, the mitochondrial P5C is converted to glutamate by the PUT2 gene product. Whereas CAR1 and CAR2 are positively regulated by the presence of arginine (discussed below), the expression of PUT1 and PUT2 is induced by proline (; ). Proline binds directly to the transcription factor Put3, a member of the well-studied Zn(II)₂Cys₆ binuclear cluster family of transcriptional regulators (). The activation of Put3 requires no additional components and can be induced by certain proline analogs with an unmodified pyrrolidine ring (). Detailed structural analysis indicates that proline directly controls the regulatory properties of transcriptional activator, providing a clear demonstration of how metabolite recognition and transcriptional control can be directly coupled (). (Arginine biosynthesis; top) The first five steps of biosynthesis take place in the mitochondria (ARG2, ARG5,-6, ARG8, ARG7) and result in the synthesis of ornithine. ARG5,-6 encode the enzymes that catalyze the second and third steps and are translated into a pre-protein that is imported into mitochondria, where it is cleaved, resulting in separate proteins, i.e., N-acetylglutamate kinase (Arg6) and N-acetylglutamyl-phosphate reductase (Arg5) (). The first two enzymes in the pathway, N-acetylglutamate synthase (Arg2) and N-acetylglutamate kinase (Arg6), bind each other, forming a complex that is necessary for their stability and for feedback inhibition by arginine (, ; ). The ornithine synthesized in mitochondria is transported to the cytoplasm via the mitochondrial carrier protein Ort1 (), and the remaining steps are carried out in the cytoplasm. Carbomoyl phosphate reacts with ornithine to form arginine in three steps (ARG3, ARG1, ARG4). Carbomoyl phosphate is synthesized from CO₂, ATP, and the amide nitrogen of glutamine in a reaction catalyzed by the arginine-specific carbomoyl phosphate synthetase, a heterodimeric enzyme composed of a small regulatory subunit (CPA1) and a catalytic subunit (CPA2).

Schematic diagram of the arginine-sensitive promoters P_CAR1, P_CAR2, P_ARG1, and P_ARG3. P_CAR1 and P_CAR2 are induced, whereas P_ARG1 and P_ARG3 are repressed by arginine in an ArgR/Mcm1-dependent manner. The promoter elements, i.e., the sites for specific DNA-binding proteins, are color coded as follows: red, URS1 (Ume6 binding); blue, UAS_i and UAS_r (ArgR/MCM1 binding); black, GC rich; light yellow, Rap1; purple, Abf1; green, UAS_NTR (P_CAR1; GATA factor Gln3 and Gat1 binding), UIS_ALL (P_CAR2; Dal82/Dal81 binding), or UAS_GCRE (P_AGR1 and P_ARG3; Gcn4 binding). Coordinates are relative to the translation start sites.

Lysine biosynthetic pathway. LYS gene expression is controlled in response to the levels of α-AAS. This pathway intermediate binds and activates the pathway-specific transcription factor Lys14. As a consequence of a pathway intermediate controlling Lys14, conditions that increase or decrease the flux through the pathway, positively or negatively, affect LYS gene expression, respectively. The pathway is stimulated by the precursor α-ketoglutarate and consistently activated in cells lacking MKS1. Conversely, due to feedback inhibition of the first step of the pathway (catalyzed by either Lys20 or Lys21), excess lysine reduces the production of α-AAS and causes apparent repression of the LYS genes. LYS14 is subject to GAAC regulation, which suggests that derepression of all eight LYS genes under amino acid starvation conditions is mediated through Gcn4-induced LYS14 expression ().

Transcriptional regulation of biosynthetic pathways by metabolic intermediates. The expression of genes encoding catalytic components in the lysine (green), leucine (red), pyrimidine (blue), and purine (black) is controlled by pathway-specific transcription factors that induce transcription upon binding a metabolic intermediate of the pathway. In these pathways, feedback inhibition by the end product of the first and committing step of the pathway provides the means to decrease the production of the inducer and cause the apparent repression of the pathway. This dual-sensing mechanism permits fine-tuning of biosynthetic pathways by integrating both the final end-product concentration, whether synthesized or transported into cells via salvage mechanisms, and the flux in the pathway (as sensed via the concentration of strategic metabolic intermediates).

Sulfur metabolic network. Three major branches of the sulfur metabolic network have been defined. First, sulfate is transported into cells via the sulfate permeases (SUL1 and SUL2) and is reduced to sulfide (MET3, MET14, MET16, MET5, and MET10). Second, sulfide is incorporated in the formation of homocysteine (MET17) from O-acetylhomoserine that is derived from homoserine (MET2). Third, homocysteine is converted to methionine and SAM in the methyl cycle (MET6, SAM1, SAM2, SAH1) or converted to cysteine in the two steps of the trans-sulfuration pathway (CYS4 and CYS3). Glutathione is synthesized from cysteine (GSH1, GSH2). The sulfur-containing compounds are written in black. The levels of cysteine negatively control the activity of Met4-dependent transcription. The genes under positive control by Met4 are indicated in green.

Model for the repression of SER3 by SRG1 intergenic transcription. In the absence of serine, the Cha4 activator is bound to the SRG1 promoter but is unable to initiate transcription. The SER3 promoter is depleted of nucleosomes allowing proteins, either an as-yet-unknown sequence-specific activator or general transcription factors, to bind and activate SER3 transcription. In response to serine, Cha4 recruits SAGA and Swi/Snf to reposition the nucleosomes at the 5′ end of SRG1 toward the SER3 promoter, permitting initiation of SRG1 transcription. These repositioned nucleosomes are then disassembled ahead of the transcribing RNA Pol II and reassembled after passage of RNA Pol II by the Spt6 and Spt16 histone chaperones. The nucleosomes being maintained by SRG1 transcription occlude the SER3 promoter, preventing the binding of transcription factors and SER3 transcription. This figure and legend, orginally published in , are reproduced in accordance with Landes Bioscience policy, the publishers of Cell Cycle, with permission of the authors.

Schematic diagram of the SPS-sensing pathway of extracellular amino acids. (A) In cells grown in the absence of inducing amino acids (left), the SPS sensor of extracellular amino acids is present in the plasma membrane (PM) in its preactivation conformation (), and the transcription of SPS-sensor-regulated genes, i.e., amino acid permeases (AAP), occurs at basal levels, and cells exhibit low rates of amino acid uptake. The transcription factors Stp1 and Stp2 (DNA-binding motifs, green boxes) are synthesized as inactive precursors that localize to the cytosol due to the presence of their N-terminal regulatory domain (anchor) that prevents them from efficiently entering the nucleus. Low levels of full-length Stp1 and Stp2 that escape cytoplasmic retention (dashed arrow, left panel) are prevented from derepressing AAP gene expression due to activity of the Asi complex (Asi1–Asi2–Asi3) (; ). In the presence of extracellular amino acids (right panel), the SPS (Ssy1-Ptr3-Ssy5) sensor activates the intrinsic proteolytic activity of the Ssy5 protease, resulting in the endoproteolytic processing of Stp1 and Stp2 (scissors). The shorter activated forms of Stp1 and Stp2 lacking regulatory domains are targeted to the nucleus where, together with Dal81, they bind SPS-sensor-regulated promoters (UAS_aa) and induce transcription (; ). The increased transcription of AAP genes results in increased rates of amino uptake. AAPs are cotranslationally inserted into the ER membrane, which is contiguous with the outer nuclear membrane. Movement of AAPs to the PM (represented by the dashed arrow, right panel) requires the ER membrane-localized chaperone Shr3 ( ; ). (B) Transporter-based model for Ssy1 amino acid receptor function (). Similar to canonical transporters, Ssy1 can attain four conformational states. However, in contrast to transporters, interconversion between the outward-facing ligand bound state and the inward-facing ligand bound state (reaction 3) is prevented by a ligand-induced reaction barrier. The outward-facing conformations of the Ssy1 sensor are thought to be signaling (green), and the inward-facing conformations are nonsignaling (red). (C) Multistep regulation of the Ssy5 endoprotease. Ssy5 is expressed as an inactive zymogen (left) composed of a prodomain that assists the folding of the Cat domain. Ssy5 is auto-processed when the Cat domain attains an active conformation. The noncovalently attached prodomain remains bound to the Cat domain, forming an inactive but catalytically competent “primed” protease complex. Primed Ssy5 is incorporated as a subcomplex of the SPS sensor via protein–protein interactions involving Ptr3, where it binds, but does not cleave, its substrates Stp1 and Stp2. In the absence of extracellular amino acids, i.e., under non-inducing conditions (left), the basal level of phosphorylation of a phosphodegron in the prodomain is likely to be determined by counteracting activities of casein kinase I (Yck1 and Yck2) and the phosphatase PP2A with its regulatory subunit Rts1 (Eckert-Boulet et al. 2006). In the presence of extracellular amino acids (right), the primary amino acid sensor Ssy1 is stabilized in a conformation that triggers intracellular signaling. This conformation increases the level of phosphorylation of the prodomain phosphodegron (), presumably by increasing the accessibility of Yck1 or Yck2. An increased level of phosphorylation within the degron provides the requisite surface recognized by the SCF^Grr1 complex and subsequent polyubiquitylation of lysine residues of the degron. Concomitant with being ubiquitylated, the prodomain is directly targeted for degradation by the 26S proteasome, unfettering the Stp1 and Stp2 processing activity of the Cat domain.

Membrane transport systems of nitrogenous compounds relevant to amino acid metabolism. Plasma membrane-localized permeases/transporters are shown with their corresponding substrates. The expression of transport proteins in green text is under nitrogen regulation (NCR). The expression of transport proteins in blue text is transcriptionally controlled by the SPS sensor of extracellular amino acids. Transporters thought to be involved in the excretion of amino acids, either functioning in the late secretory pathway or at the plasma membrane, are shown with red outwardly pointing arrows. Transporters localized to intracellular organelle membranes, i.e., mitochondria (M), peroxisome (P), and vacuole (V), are depicted; the arrows indicate the direction of the transport catalyzed.

Pyrimidine synthesis and salvage pathways. DHO, dihydro-orotate; OA, orotic acid; USA, ureidosuccinic acid. Gene names are italicized. Regulatory molecules are shown in red.

Organization of the URA2 and IMD2 promoter regions. The transcription start sites are shown, and their respective distances from the mRNA start site are indicated. Unstable transcripts are shown in gray.

Purine and histidine pathways in yeast. Ado, adenosine; AICAR, 5′-phosphoribosyl-5-amino-4-imidazole carboxamide; Ino, inosine; guo, guanosine; IMP, inosine 5′-monophosphate; PRPP, 5-phosphoribosyl-1-pyrophosphate; SAICAR, 5′-phosphoribosyl-4-(N-succinocarboxamide)-5-amino-imidazole. Gene names are italicized. Regulatory molecules are shown in red.

Regulation of phosphate utilization. The phosphate regulatory cascade is shown. New genes recently identified as important for regulation of phosphate utilization are shown in red. Question marks designate the steps for which no molecular mechanism has been documented yet.