INTRODUCTION

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In the budding yeast Saccharomyces cerevisiae, starvation for an amino acid triggers the transcription of more than 40 genes involved in amino acid biosynthesis. This "general amino acid control" requires the expression of the transcriptional activator Gcn4. Gcn4 expression is increased at the translational level by a regulatory mechanism involving phosphorylation of the  subunit of translation initiation factor eIF-2 (eIF-2) by the protein kinase Gcn2 (18, 30, 31). When amino acids are abundant, four short open reading frames (uORFs) in the GCN4 mRNA leader sequence act in cis to repress translation of the GCN4 ORF. According to a model proposed by Abastado et al. (1), ribosomes translate the first encountered uORF (uORF1) and then resume scanning. Under normal conditions, essentially all ribosomes reinitiate translation at one of the remaining uORFs (uORF2 to uORF4) and fail to reinitiate translation at the GCN4 start codon. In amino acid-starved cells, ribosomes translate the first uORF and reinitiate at the GCN4 start codon instead of translating uORF2 to -4 because reinitiation is less efficient due to the reduction of functional eIF-2 levels.

It has been proposed (31) that Gcn2 is activated in amino acid-starved cells by direct binding of uncharged tRNA to a regulatory region located C-terminal to the kinase domain. This region has homology to the entire sequence of histidyl-tRNA synthetase (HisRS) (68, 69, 77). Consistent with this model, the HisRS-related domain in Gcn2 binds tRNAs in vitro and mutations in motifs characteristic of class II aminoacyl-tRNA synthetases abolish the phosphorylation of eIF-2 upon amino acid starvation (70).

Gcn2 is a serine/threonine protein kinase which belongs to the family of eIF-2 kinases, together with the heme-regulated inhibitor (HRI) (11), double-stranded RNA-activated protein kinase (PKR) (52, 67), Drosophila Gcn2 (44, 53), and cpc-3 from Neurospora crassa (54). The eIF-2 kinases are activated by various specific stress conditions: HRI is activated by heme deficiency, heat-shock, or heavy metal; PKR is activated by viral infection; and Gcn2 is activated by amino acid or purine starvation (for a review, see reference 16). The vertebrate eIF-2 kinase HRI has been shown to interact with the heat shock protein 90 (Hsp90) in rabbit reticulocyte lysates, and the activity of this molecular chaperone is required for full kinase activity (65).

Hsp90, a protein of the heat shock protein family, is expressed at high levels even under nonstress conditions and is required for viability in eukaryotes (for reviews see references 12, 33, and 49). Two genes encode closely related isoforms in mammals as well as in budding yeast. Deletion experiments with yeast have shown that the expression of at least one of the two Hsp90 isoforms, either Hsp82 or Hsc82, is essential for viability (7). Hsp90 can act as a molecular chaperone in vitro to promote refolding of denatured proteins, to hold denatured proteins in a folding-competent state for other chaperones, and to prevent protein unfolding and aggregation (see, for example, references 27, 34, and 75). A remarkably large subset of known Hsp90 substrates are signaling molecules, notably kinases and ligand-regulated transcription factors (see, for example, references 2, 48, 57, 63, and 76).

In this study, we have investigated the potential role of Hsp90 in yeast with respect to the eIF-2 kinase Gcn2. We have taken advantage of yeast genetics by using different strains containing mutations in HSP90. We present here genetic and biochemical evidence that Gcn2 requires Hsp90 for proper regulation. Moreover, Hsp90 is the first characterized protein interacting with Gcn2.

	MATERIALS AND METHODS

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Plasmids. (i) Reporter plasmids. The GCN4-lacZ plasmids p180 and p227 have been described previously (29). In plasmid pLG/LUC, firefly luciferase coding sequences are under the control of a galactose-inducible promoter; the parent vector is plasmid pLGSD5-ATG (56) with the 2µ replicon and the URA3 marker.

(ii) Hsp90 plasmids. Wild-type (WT) Hsp82, Hsp82 with a G313N mutation (Hsp82 G313N) and Hsp82 T525I (6), and Hsp82 G170D were expressed from plasmids pTCA/Hsp82 (6) and pHCA/Hsp82, pHCA/Hsp82 G313N and pHCA/Hsp82 T525I, and pTGPD/G170D (41), respectively, or various derivatives thereof with other auxotrophic markers. Human Hsp90 was expressed from plasmid p2HG/hHsp90 (36) or from plasmid p2U/hHsp90, which was constructed as follows: the coding sequence of human Hsp90 was excised as a BamHI-SacI fragment from plasmid p2TG/hHsp90 (36) and cloned into the BamHI-SacI sites of p2U (45). Plasmids pHCA/Hsp82 G313N and pHCA/Hsp82 T525I are identical to plasmid pHCA/Hsp82 (36) except for the point mutations; they are the HIS3 versions of plasmids pTCA/Hsp82 G313N and pTCA/Hsp82 T525I (4) and were obtained by substituting the backbone of shuttle vector pRS313 for that of pRS314 (59). Plasmid p2TG/flag.Hsp82wt or G313N served to express WT Hsp82 or Hsp82 G313N with a FLAG epitope at the N terminus (36). Unless indicated, the strong constitutive promoter from the glyceraldehyde-3-phosphate dehydrogenase (GPD) gene TDH3 was used to drive expression. To obtain reduced levels of Hsp82 (about 10% of the level of Hsp82 plus Hsc82 in a wild-type strain), Hsp82 was expressed from a construct containing the leaky GAL1 promoter from strain GRS4 (47) fused to HSP82 coding sequences in plasmid pRS304 (59). On medium with 2% glucose, repression of this mutant GAL1 promoter construct is only partial and low levels of Hsp82 accumulate.

(iii) Gcn2 plasmids. For galactose-inducible expression of Gcn2, plasmid pYES/Gcn2 was constructed by inserting the Gcn2 coding sequence into the BamHI-SphI sites of pYES2 (Invitrogen) as two fragments: a PCR-generated BamHI-XhoI fragment (with the sequence GGATCCCCGGGGCG preceding the AUG of GCN2) and an XhoI-SphI fragment from plasmid c-102-2 coding for the remainder of Gcn2 (68). To construct plasmid pYes/Gcn2^K559V, the PCR fragment was generated with plasmid p530 (69) as the template. Plasmid pYES/Gcn2N was constructed like pYES/Gcn2 except that the BamHI-XhoI PCR fragment started at codon 438 (beginning of the kinase domain). Plasmid p2U/GSTGcn2 was constructed by inserting the sequences encoding glutathione S-transferase (GST) and Gcn2 between the SacI and NaeI sites of the yeast expression vector p2U (45). It contains the GST coding sequence as a SacI-BglII fragment (with the sequence GAGCTCAAAGC preceding the AUG of GST) fused to the same GCN2 sequences present in plasmid pYES/Gcn2. Note that this results in an in-frame fusion of the BglII and BamHI sites of the GST and GCN2 moieties, respectively. Plasmid YcpGCN2:TRP1 was constructed from plasmid c-102-2. A SnaBI-PvuII insert was removed from plasmid c-102-2 and exchanged with the SnaBI-NaeI fragment containing the TRP1 gene from plasmid pRS314 (59). Note that the clones used in this study encode the 1,590-amino-acid version of Gcn2, which can complement a gcn2 deletion strain as an overexpressed GST fusion protein (see below and Table 2); a potential N-terminal extension of 69 amino acids has recently been revealed by the yeast genome project (yeast ORF: YDR283C).

Strains. The parent strains and some of the derivatives are listed in Table 1. The yeast strain background HH1a (36) was used to replace the endogenous Hsp82/Hsc82 with Hsp90 mutants by plasmid shuffling. Plasmids were introduced into yeast by the LiAc/polyethylene glycol method and selected for on appropriate minimal media. The GCN2 deletion was introduced into strains HH1a-pHCA/Hsp82wt (36) and HH1a-pHCA/Hsp82 G313N with the ClaI-SphI insert of the plasmid YcpGCN2:TRP1 to yield strains OD1 and OD2, respectively. Following transformation, strains auxotrophic for tryptophan were selected and checked for GCN2 deletion by PCR and immunoblot analysis.

Immunoprecipitation experiments. (i) Yeast extracts. Coimmunoprecipitation experiments using the FLAG tag were done as follows: extracts from strain HH1a-pHCA/Hsp82wt transformed with plasmid p2TG/flag.Hsp82wt or p2TG/flag.HSP82 G313N and with plasmid p2U/GSTGcn2 were lysed in buffer A (10 mM Tris-HCl [pH 7.5], 50 mM NaCl, 1 mM dithiothreitol, 10 mM sodium molybdate, 1 mM EDTA, 10% glycerol, 1 mM phenylmethylsulfonyl fluoride, 3 µg of chymostatin/ml, 1.5 µg of pepstatin A/ml, 0.75 µg of leupeptin/ml, 3.8 µg of antipain/ml). After the extracts were adjusted to 0.1% Triton X-100, they were incubated at 4°C with the anti-FLAG monoclonal antibody M2 (Kodak) for 2 h, followed by 1 h with protein G-Sepharose (Pharmacia). Immunoprecipitates were washed four times for 10 min at 4°C with buffer A containing 0.1% Triton X-100, solubilized in sodium dodecyl sulfate (SDS) sample buffer, and loaded onto SDS-8% polyacrylamide gels. The same protocol was used for immunoprecipitation by a Gcn2-specific rabbit polyclonal antiserum (77) (a kind gift from Ronald Wek, Indiana University) of overexpressed Gcn2 from 0.5 mg of extracts from strain HH1a-p2HG/hHsp90 (36). Immunoprecipitation of human Hsp90 from strain HH1a-p2HG/hHsp90 was done with the monoclonal antibody H90-10 (a kind gift from David O. Toft, Mayo Clinic). For the coimmunoprecipitation of endogenous Gcn2, strains HH1a-pHCA/Hsp82wt and OD1 transformed with plasmid p2TG/flag.Hsp82 or strains HH1a-p2HG/hHsp90 and OD1 transformed with plasmid p2U/hHsp90 were grown in the presence of 30 mM 3-aminotriazole (3-AT) and lysed in buffer A with 100 mM NaCl. 3-AT increases the levels of Flag.Hsp82 and human Hsp90 in the extract thereby facilitating the analysis; this unexplained effect is unrelated to Gcn2 and does not affect the coprecipitation of Gcn2 with Hsp90 (data not shown). Immunoprecipitations were done as described above.

(ii) Reticulocyte lysate. Coimmunoprecipitation of rabbit Hsp90 and Gcn2 from rabbit reticulocyte lysate was performed with the monoclonal antibody H90-10. After synthesis of Gcn2 from plasmid pYES/Gcn2 with the TNT RRL kit (Promega), Hsp90 was immunoprecipitated in buffer A with Triton X-100. After addition of protein G-Sepharose, the beads containing the immune complex were washed three times with buffer A with Triton X-100, followed by a wash with buffer A without Triton X-100. The proteins were analyzed by gel electrophoresis on an SDS-8% polyacrylamide gel.

In vitro kinase assay. Gcn2 protein was synthesized from plasmid pYES/Gcn2 in rabbit reticulocyte lysate (TNT RRL kit; Promega) containing [³⁵S]methionine according to the manufacturer's recommendations with or without geldanamycin (GA) or macbecin I (provided by J. Johnson, Drug Synthesis and Chemistry Branch, National Cancer Institute). Gcn2 was immunoprecipitated by adding a rabbit polyclonal anti-Gcn2 serum to the reticulocyte lysate plus buffer A and 0.5% Triton X-100. After addition of protein A-Sepharose to harvest the antibody complex, immune pellets were washed with buffer A with Triton X-100 three times, followed by two washes with kinase buffer (20 mM Tris-HCl [pH 7.9], 50 mM NaCl, 10 mM MgCl₂, 1 mM dithiothreitol). A 30-µl slurry of Sepharose-bound Gcn2 was incubated with 10 µl of [-³²P]ATP (10 mCi/mmol) at a final concentration of 10 µM ATP for 20 min at 30°C. Beads were washed twice with kinase buffer, and SDS sample buffer was added to each sample to terminate the reaction. Samples were boiled for 2 min and analyzed on an SDS-8% polyacrylamide gel.

Western blot experiments. After transfer of proteins from SDS-polyacrylamide gels to nitrocellulose membranes, the membranes were blocked with Tris-buffered saline-0.2% Tween-20 (TBST) containing 5% (wt/vol) milk powder and probed with appropriate antibodies (HS90-10, rabbit antisera against Gcn2, and firefly luciferase) in TBST-milk powder at room temperature for 1 h. Membranes were washed three times for 10 min with TBST. The secondary antibodies were alkaline phosphatase-conjugated goat anti-rabbit (Bio-Rad) or anti-chicken (Promega) antibodies and horseradish peroxidase-conjugated anti-mouse antibodies (Cappel). They were used in TBST-milk powder at room temperature for 1 h. After three washes with TBST, the blots were developed either with the nitroblue tetrazolium-5-bromo-4-chloro-3-indolylphosphate (NBT/BCIP) reagent for alkaline phosphatase or with the enhanced chemiluminescence reagent (Amersham) for horseradish peroxidase.

Assay of GCN4-lacZ reporter plasmid. -Galactosidase assays were conducted with cultures grown in minimal SD medium containing only the required supplements (66). For repressing conditions, saturated cultures were diluted 1:50 and harvested in mid-logarithmic phase after 6 h of growth at 30°C. For derepressing conditions, cultures were grown for 2 h under repressing conditions and then for 6 h after the addition of 3-AT to 40 mM. -Galactosidase assays were corrected for cell density.

Luciferase assay. Strain HH1a-pHCA/Hsp82wt was transformed with the plasmid pLG/LUC. Cells were grown with 2% glucose or galactose in the presence or absence of macbecin I (50 µM) for 24 h. Luciferase activity was measured according to the manufacturer's recommendations (Promega).

Growth tests. Strains containing mutations in HSP90 or deletions in different cochaperone genes were tested for their ability to grow on 3% agar plates containing histidine dropout medium supplemented with 30 mM 3-AT and excess (40 mM) leucine at 30°C (69). Note that all strains have the HIS3 marker.

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

HSP82 mutations affect translation regulated by the 5'-untranslated region of the GCN4 mRNA. To determine whether yeast Hsp90 is involved in Gcn2 regulation, a GCN4-lacZ reporter plasmid containing the GCN4 translational control elements (uORFs) in the mRNA leader region (plasmid p180) (39) was introduced into yeast strains carrying different Hsp90 mutants. Some of the HSP90 mutations used here are known to produce defects in steroid receptor regulation (6, 47). Reporter gene activity was measured in the presence of amino acids (repressed conditions) or upon histidine starvation (derepressed), which was induced by 3-AT, a chemical inhibitor of the histidine biosynthetic enzyme His3 (70). As shown in Fig. 1A, GCN4-lacZ activity in the parent WT strain was stimulated fivefold by addition of 3-AT (derepressed). In cells expressing human Hsp90 instead of the yeast complement, regulation was similar to that for the parental strain, indicating that human Hsp90 can substitute for the yeast homologs in this assay. Surprisingly, compared with the activity in isogenic WT cells, -galactosidase activity was higher in the Hsp90 mutant strains under repressed conditions (Fig. 1A). In a strain with Hsp82 levels reduced to 10% those of the WT (strain 10% Hsp82wt) (47), the activity observed in the repressed state was fivefold higher. In both strains with Hsp82 point mutations (Gly-313 to Asn [G313N] and Thr-525 to Ile [T525I]) (6), the activity of the GCN4-lacZ reporter was upregulated in the repressed state as observed for strain 10% Hsp82wt. In all mutant strains, the expression of -galactosidase was further enhanced under conditions of amino acid limitations (Fig. 1A), reaching a level of activity slightly above that for the WT.

View larger version (31K): [in this window] [in a new window]   FIG. 1.   Hsp90 mutants stimulate GCN4-lacZ expression under repressed conditions. (A) -Galactosidase activity assayed in extracts prepared from the different yeast strains expressing Hsp90 mutants transformed with the GCN4-lacZ reporter plasmid p180 (schematically represented). Enzyme activities are given in units. (B) -Galactosidase activity assayed for the panel A strains transformed with the control reporter plasmid p227 containing point mutations (×) in the ATGs of the four uORFs in the 5'-untranslated region of the GCN4 mRNA. The values are the means of three to four independent experiments. + a.a., with amino acids;  a.a., without amino acids; hHsp90, human Hsp90; 10%, strain 10% Hsp82wt; G313N, HH1a-pHCA/Hsp82 G313N; T525I, HH1a-pHCA/Hsp82 T525I.

The increased expression of GCN4-lacZ in Hsp82 mutant strains requires the kinase Gcn2. It has been reported that GCN4 translational regulation requires the protein kinase Gcn2 (30). To determine whether the derepression of -galactosidase expression observed in the different Hsp82 mutant strains requires Gcn2, the GCN2 gene was deleted from the parental strain and the strain with the G313N mutation (WTgcn2 and G313Ngcn2). Expression from the reporter plasmid p180 was checked under repressed conditions in both strains. As shown in Fig. 2, strain G313Ngcn2 fails to display increased GCN4-lacZ expression under repressed conditions, indicating that Gcn2 is involved in this process. Conversely, the increased basal activity in the different Hsp90 mutants is not due to higher levels of Gcn2. Levels of endogenous Gcn2 in the mutant strains were observed to be similar to the levels in the WT strain (data not shown).

View larger version (31K): [in this window] [in a new window]   FIG. 2.   Gcn2 is required for the increased expression of the GCN4-lacZ reporter. -Galactosidase activities of WT and G313N strains with a deletion of the gcn2 gene (strains OD1 and OD2) transformed with plasmid p180 are shown. Cells were grown only under repressed conditions (with amino acids). The experiments were carried out twice with less than 20% difference.

HSP90 mutations are directly responsible for the increased expression of GCN4-lacZ. The increased expression of GCN4-lacZ was observed in different independent mutants of Hsp82, which led us to conclude that the observed phenotype was indeed due to an alteration of Hsp90. To exclude the formal possibility that the altered phenotype could be due to another genomic mutation, we reintroduced the WT allele of HSP82 into the cells carrying the G313N mutation (Fig. 3). This restores a WT pattern, indicating that hsp82^G313N is responsible for the enhancement of translation through the GCN4 leader and that the G313N mutation is recessive relative to the WT HSP82.

View larger version (35K): [in this window] [in a new window]   FIG. 3.   The G313N mutation is responsible for increased GCN4-lacZ expression under repressed conditions. -Galactosidase activity from reporter plasmid p180 was assayed in extracts prepared from the different yeast strains (WT or Hsp82 G313N or Hsp82 G313N transformed with the plasmid pTCA/Hsp82 which codes for the WT allele of Hsp82). The experiments were carried out twice. + a.a., with amino acids;  a.a., without amino acids.

Gcn2 binds to Hsp90 in vivo. The genetic data suggested that Gcn2 is regulated by Hsp90. This could occur by the formation of a complex between Hsp90 and the kinase. We therefore examined whether overexpressed Gcn2 could be coimmunoprecipitated from yeast whole-cell extracts with an anti-Hsp90 antibody. As reported above, Gcn2 regulation is normal in a strain with human Hsp90 antibody. As reported above, Gcn2 regulation is normal in a strain with human Hsp90. Since a good monoclonal antibody to immunoprecipitate the human Hsp90 (monoclonal antibody H90-10) is available, we examined this interaction first. We overexpressed it as a GST fusion protein (GSTGcn2). We ascertained that GSTGcn2 is functional by showing that it can complement a gcn2 deletion strain (see Table 2). Extracts expressing GSTGcn2 were immunoprecipitated with the anti-Hsp90 antibody, and the immune complexes were probed by immunoblot analysis with an antiserum against Gcn2. Figure 4A shows that GSTGcn2 was coimmunoprecipitated with Hsp90 and not by control antibodies. GST alone does not coprecipitate with Hsp90 (data not shown), indicating that the Gcn2 moiety is responsible for this interaction. As an additional negative control, the immunoprecipitation was performed with the anti-human Hsp90 antibody with extracts from the parental strain (containing yeast and not human Hsp90); no GSTGcn2 could be coimmunoprecipitated in this experiment (data not shown). The inverse experiment was also performed: GSTGcn2 was immunoprecipitated with a rabbit polyclonal antibody directed against Gcn2, and human Hsp90 was revealed by immunoblot analysis. As shown in Fig. 4B, Hsp90 is coimmunoprecipitated with GSTGcn2. The experiments were done with extracts from cells grown under repressed or derepressed conditions with identical results (data not shown; see also Discussion).

View larger version (21K): [in this window] [in a new window]   FIG. 4.   Gcn2 binds Hsp90 in vivo. (A) Antibodies to human Hsp90 coprecipitate Gcn2. Equal amounts of yeast extracts (0.5 mg) from cells expressing human Hsp90 transformed with the plasmid p2U/GSTGcn2 were used with different antibodies as indicated below the panel. GSTGcn2 was revealed by immunoblotting with an anti-Gcn2 antiserum. -Hsp90, antibody against human Hsp90; -lacZ, antibody against -galactosidase (Promega); -flu, antibody against flu-tag (Aves Laboratory); -Gcn2, polyclonal antibody against Gcn2 (77). IP, immunoprecipitation. (B) Antibodies to Gcn2 coprecipitate human Hsp90. Equal amounts of yeast extracts (0.5 mg) from cells expressing the human Hsp90 transformed with the plasmid p2U/GSTGcn2 were used with different antibodies as indicated below the panel. Hsp90 was revealed by immunoblotting with the monoclonal antibody against Hsp90 (H90-10). (C) FLAG-tagged Hsp82 associates with GSTGcn2. Equal amounts of yeast extracts (0.5 mg) from isogenic strains expressing Hsp82wt or G313N with or without the FLAG tag were used with the FLAG antibody. All strains also expressed GSTGcn2 from plasmid p2U/GSTGcn2. Gcn2 was revealed by immunoblotting with an anti-Gcn2 antiserum. (D) Endogenous Gcn2 interacts with human Hsp90. Equal amounts of yeast extracts from cells expressing the human Hsp90 were used with the monoclonal anti-human Hsp90 antibody. Gcn2 was revealed as described for panel A. Lane 1, strain expressing human Hsp90; lane 2, strain expressing human Hsp90 with a gcn2 deletion; lane 3, strain expressing the yeast Hsp82. (E) Endogenous Gcn2 interacts with FLAG-tagged Hsp82. Equal amounts of yeast extracts from cells expressing the FLAG-tagged yeast Hsp82 were used with the FLAG antibody. Lane 1, strain with GCN2; lane 2, strain carrying a gcn2 deletion.

Hsp90 inhibitors prevent the maturation of the kinase Gcn2 in vitro. Hsp90 can be specifically inhibited by the benzoquinone ansamycins geldanamycin (GA) (64, 72) and macbecin I (3, 24), the latter being more effective in yeast. We postulated that if Gcn2 activity depends on Hsp90, then addition of these compounds might block its kinase activity. To test this hypothesis, we synthesized Gcn2 de novo in rabbit reticulocyte lysate and performed immunoprecipitation experiments with an antiserum against Gcn2. The immunoprecipitates were subsequently subjected to an in vitro kinase assay (77), which is based on the ability of Gcn2 to autophosphorylate (69). As presented in Fig. 5 (top), Gcn2 is translated to a similar extent in the presence or absence of GA, macbecin I, or vehicle (dimethyl sulfoxide). Increasing the concentration of GA further to 50 µM decreased Gcn2 levels but not those of an unrelated protein (data not shown). Following immunoprecipitation, [-³²P]ATP was added for an in vitro kinase reaction and the products were separated on an SDS-8% polyacrylamide gel (Fig. 5, bottom). Incorporation of phosphates into Gcn2 was seen only in the absence of drug (Fig. 5, bottom, left lane). Addition of 20 µM GA or macbecin I completely inhibited the kinase reaction. The same results were observed in the presence of 10 µM GA (data not shown). Addition of GA after completion of Gcn2 translation (during the immunoprecipitation reaction or kinase assay) did not inhibit the kinase reaction, indicating that Hsp90 function is only required during synthesis of Gcn2. GA does not act unspecifically in rabbit reticulocyte lysate, since luciferase synthesized de novo in the presence or absence of 20 µM GA showed the same activity (data not shown) (55). These results demonstrate that Hsp90 activity is required during synthesis of Gcn2 and for it to become an active kinase.

View larger version (47K): [in this window] [in a new window]   FIG. 5.   Ansamycin benzoquinones block kinase activity of Gcn2 in vitro. Gcn2 was translated at 30°C in rabbit reticulocyte lysate. Macbecin I (Mc) and GA were added during synthesis, where indicated. After immunoprecipitation with an anti-Gcn2 antiserum, the samples were used for in vitro kinase assays and electrophoresed on an SDS-polyacrylamide gel electrophoresis gel. The two panels represent the same gel with differential detection of incorporated 35S (upper panel) and 32P (lower panel) by using two sheets of X-ray film. The numbers above the panels represent the concentrations of compounds used (in micromolar). Note that the slightly reduced levels of immunoprecipitated Gcn2 in the presence of Mc were specific to this particular experiment and are not generally observed. , no drug added.

The association of Hsp90 with Gcn2 is stabilized in vitro in the presence of GA or macbecin I. We next investigated the in vitro association of Gcn2 with Hsp90. Since Hsp90 binds to GSTGcn2 in vivo and since benzoquinone ansamycins have an effect on Gcn2 activity (see above), we assessed the coimmunoprecipitation of rabbit reticulocyte Hsp90 with in vitro-synthesized Gcn2 by using the anti-Hsp90 monoclonal antibody in the presence or absence of the Hsp90-specific inhibitors, GA and macbecin I. As shown in Fig. 6A, the amount of Gcn2 that is coimmunoprecipitated is much larger in the presence of GA than with the vehicle dimethyl sulfoxide alone. The amount of immunoprecipitated Hsp90 was the same in the presence or absence of Hsp90 inhibitors (data not shown). The same results were also observed with macbecin I. The interaction was specific for Gcn2 since unrelated control proteins did not interact with Hsp90 in the presence or absence of GA (data not shown). The effect was similar with three different constructs coding for Gcn2, GSTGcn2, Gcn2, and Gcn2 N. The result with the last construct indicates that the N-terminal domain (amino acids [aa] 1 to 437) of Gcn2, which is dispensable for in vitro autophosphorylation (69), is not required for the association with Hsp90. A deletion of the C-terminal domain (aa 1024 to 1590) also did not affect Hsp90 binding (data not shown), suggesting that the kinase domain alone is sufficient to bind Hsp90.

View larger version (44K): [in this window] [in a new window]   FIG. 6.   GA increases the association of Hsp90 with Gcn2 in vitro. Gcn2 was translated at 30°C in rabbit reticulocyte lysate. GA was added during synthesis at a concentration of 20 µM. The top sections represent the input, and the bottom sections represent the immune pellets after coimmunoprecipitation (IP) with the anti-Hsp90 monoclonal antibody. (A) Plasmids pYes/GSTGcn2, pYes/Gcn2, and pYes/Gcn2N were used for in vitro translation; (B) plasmids pYes/Gcn2 and pYes/Gcn2K559V were used. The migration positions of the different Gcn2 variants are indicated with arrows.

Inhibition of Hsp90 activity reduces Gcn2 levels in vivo. To investigate the effect of macbecin I in vivo, we transformed a WT strain with plasmid pYES/Gcn2, which allows the expression of Gcn2 to be induced by addition of galactose in the presence or absence of 50 µM macbecin I. After a 24-h induction, Gcn2 levels were monitored by Western blot analysis using an antiserum against Gcn2. As shown in Fig. 7A (lanes 1 and 2), Gcn2 is only expressed upon galactose induction; no protein is seen when cells are grown in glucose (lane 3). Addition of an inhibitor of Hsp90 macbecin I reduced the levels of Gcn2. As presented in Fig. 7B, in the presence of macbecin I, levels of Gcn2N (lacking the N-terminal region flanking the kinase domain) were also strongly reduced. An in vitro kinase assay was performed with Gcn2N after immunoprecipitation with an anti-Gcn2 antiserum. In Fig. 7B (bottom), we show that autophosphorylation is reduced in the presence of macbecin I to the same extent as are the levels of Gcn2 (Fig. 7B, top). As a control to confirm that macbecin I does not affect the galactose induction per se, we tested the induction and the activity of firefly luciferase induced by galactose in the presence or absence of macbecin I (Fig. 7C). No effect of macbecin I on luciferase activity was observed, indicating that the ansamycin does not affect galactose induction and that the effect is specific for Gcn2. Thus, in yeast, macbecin I at our experimental concentrations leads to a drop of Gcn2 levels, but the remaining Gcn2 molecules are still functional (see below). Therefore we conclude that Hsp90 is required for Gcn2 accumulation in vivo, confirming our in vitro results that Gcn2 maturation depends on Hsp90. Moreover the N-terminal region of Gcn2 is not necessary for regulation by Hsp90 both in vitro and in vivo.

View larger version (30K): [in this window] [in a new window]   FIG. 7.   Macbecin I reduces Gcn2 levels in vivo. Strain HH1a-pHCA/Hsp82 was transformed with plasmids pYes/Gcn2 (A) and pYes/Gcn2N (B). Gcn2 variants were induced for 24 h by 2% galactose in the presence or absence of macbecin I (50 µM) and immunoprecipitated with an anti-Gcn2 antiserum. (A) Gcn2 was revealed by immunoblotting with an antiserum against Gcn2. Lanes 1 and 2, induction in the presence of galactose (10-fold less material was loaded in lane 2 than in lane 1; lane 3, cells grown with 2% glucose; lane 4, induction with galactose in the presence of 50 µM macbecin I. (B) Gcn2N was either visualized by immunoblot analysis with an antibody against Gcn2 or used for an in vitro kinase assay. Lanes 1 and 2, parent strain; lanes 3 and 4, strain transformed with the plasmid pYes/Gcn2N. (C) The WT strain was transformed with the plasmid pLG/LUC and grown with glucose or galactose in the presence or absence of macbecin I for 24 h. The plotted luciferase activity represents the mean values from two independent experiments.

View larger version (31K): [in this window] [in a new window]   FIG. 8.   Inactivation of Hsp90 abolishes Gcn2 accumulation and activity in vivo. Strain HH1a-G170D was transformed with plasmids pYes/Gcn2N (A) and pLG/LUC (B). Cells grown to mid-logarithmic phase at 30°C in glucose were shifted to galactose and 37°C simultaneously for 6 h to induce the expression of Gcn2N (A) or luciferase (B). (A) Cell extracts from the different treatments were immunoprecipitated with an anti-Gcn2 antiserum, and an immunoblotting experiment with the same antibody (top) and a kinase assay (bottom) were performed. Lanes 1 and 2, shift to galactose. Cells were grown at 30°C (lanes 1 and 3) or at 37°C (lane 2). (B) Cells were grown with galactose (lanes 1, 2, and 3) or glucose (lane 4) at 30°C (lanes 1, 3, and 4) or at 37°C (lane 2) for 6 h. Lane 3, cells treated also with macbecin I (50 µM) for 24 h. Following immunoprecipitation with an anti-luciferase antiserum, luciferase was revealed with the same antibody. IgH, immunoglobulin heavy chain.

The cochaperones Cdc37, Sba1, and Sti1 are required for an intact general amino acid control. Hsp90 acts in collaboration with a series of other proteins, some of which have intrinsic chaperone activity themselves (49). The function of these factors, notably p50 (Cdc37 in yeast), p23 (Sba1), and p60/Hop (Sti1) remains unclear (48). It has been proposed that p50/Cdc37 and Hsp90 could act as a specific chaperone complex for protein kinases (13, 15, 19, 28, 35, 46). Sba1 has been shown to be associated with several proteins, including transcription factors, protein kinases, and a viral reverse transcriptase (32, 40, 74). Deletion of the SBA1 gene in yeast results in no striking phenotype (5, 24). Sti1 (the S. cerevisiae homolog of p60) is required for the assembly of the Hsp90-glucocorticoid receptor (GR) complex in vitro and contributes to the maturation of both GR and the tyrosine kinase pp60^v-src in budding yeast (8, 61). To investigate whether Cdc37, Sba1, and Sti1 are involved in regulating Gcn2 activity, we tested the general amino acid control in different Cdc37 mutant strains, in a strain lacking the SBA1 gene, and in cells lacking the STI1 gene (Table 2). We used a simple growth assay to monitor general control of amino acid biosynthesis, which involves growing the different strains on plates containing 3-AT, the inhibitor of histidine biosynthesis (17). Cells with an intact general control response will grow on medium containing the drug; however, the growth of yeast strains lacking any one of the factors required to mediate the induction of GCN4 expression will be defective under these starvation conditions. The different strains harboring Hsp90 mutants grow as well as the WT (Table 2), confirming that the Gcn2/Gcn4 pathway is not impaired under derepressed conditions (see above). Unlike the Hsp90 mutant cells, the two strains harboring cdc37 mutations, the sba1 cells, and the sti1 cells, have a slow-growth phenotype on plates containing 3-AT. These results show that three proteins known to interact with Hsp90, Cdc37, Sba1, and Sti1, are involved in the regulation of the general amino acid control, possibly by affecting the regulation of Gcn2.

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

We report that in the yeast S. cerevisiae the eIF-2 kinase Gcn2 requires the molecular chaperone Hsp90 for proper regulation. Hsp90 forms a complex with Gcn2 in vitro as well as in vivo. Using different Hsp90 mutants, we observed an enhancement of the translation of the Gcn2 target GCN4-lacZ under repressing conditions for GCN4 expression, suggesting that Hsp90 inhibits Gcn2 activity. The specific inhibitors of Hsp90, the benzoquinone ansamycins GA and macbecin I, block Gcn2 activity in vitro and lower Gcn2 levels in vivo. Gcn2 is thus one of the few known targets of Hsp90 in budding yeast, along with Hap1 (76) and Ste11 (36), and Hsp90 is the first characterized protein interacting with Gcn2.

Gcn2 activity and levels are dependent on Hsp90. In vitro, Gcn2 synthesized in the presence of the inhibitors of Hsp90 (GA or macbecin I), or at the restrictive temperature in a strain expressing a temperature-sensitive Hsp90 mutant (G170D mutant), is nonfunctional, showing that the chaperone activity of Hsp90 is required for Gcn2 maturation and/or activation. The binding of Gcn2 to Hsp90 is increased when Gcn2 is synthesized in the presence of the Hsp90 inhibitors, indicating that immature Gcn2 binds more tightly to Hsp90 and that Gcn2 forms a complex with Hsp90 during Gcn2 synthesis. Similarly, one of the vertebrate members of the Gcn2 family, HRI, also binds to Hsp90 in vitro in its inactive form (in the presence of hemin) (37, 65, 74). However, although both kinases belong to the same family (eIF-2 kinases) and both bind to Hsp90, the effects of Hsp90 inhibitors are different (65): (i) GA disrupts the interaction of Hsp90 with HRI, while it enhances the interaction with Gcn2 and (ii) release of Hsp90 from HRI depends on autophosphorylation (an inactive mutant of HRI binds Hsp90 in the presence or absence of the activating molecule hemin), while Gcn2 does not need autophosphorylation to dissociate from Hsp90 (an inactive kinase mutant of Gcn2 can still release Hsp90). The effects of GA are specific for Gcn2 since GA does not influence folding and the activity of unrelated proteins such as luciferase and does not force the binding of Hsp90 to these proteins. Thus, the stronger binding of Hsp90 to Gcn2 in the presence of the Hsp90 inhibitors suggests that the release of Hsp90 is blocked.

Certain mutations in HSP90 can derepress Gcn2. Gcn4 regulation is influenced by mutations in HSP90. In several Hsp90 mutant strains (10% Hsp82wt, Hsp82 G313N, Hsp82 T525I) that, unlike the temperature-sensitive mutant strain HH1a-G170D, have Hsp90 defects even at low temperature, GCN4-lacZ is constitutively expressed even under repressed conditions. This regulation requires the kinase Gcn2. The phenotypes of the derepressed HSP90 mutations might appear contradictory to the biochemical results obtained with the Hsp90 mutant HH1a-G170D and with macbecin I, and to the growth phenotypes of the cochaperone mutant strains. However, these differences are probably due to the nature of the mutations themselves. The activities of the three viable Hsp90 mutants (as listed above) are only partially defective and still support proper folding, but not repression, of the kinase domain of Gcn2. In contrast, a more severe block of Hsp90 functions as with HH1a-G170D and macbecin I or with defective cochaperones might even affect the maturation of the kinase activity.

Model for the regulation of Gcn2 by Hsp90. The mechanism of inhibition of Gcn2 during repressed conditions (in the presence of amino acids) is still unclear. Qiu and collaborators have proposed a model (50) which postulates that Gcn2 is kept in an inactive conformation by intramolecular interactions between the kinase domain and its flanking regions. Binding of uncharged tRNA to the HisRS region would trigger a conformational change that relieves these inhibitory interdomain interactions. Following this step, autophosphorylation, binding, and phosphorylation of the substrate eIF-2 is thought to occur.

View larger version (16K): [in this window] [in a new window]   FIG. 9.   Model for the role of Hsp90 in the maturation and inhibition of Gcn2. GA may block the transition from step II to III.