INTRODUCTION

Top Abstract Introduction Materials and Methods Results Discussion References

The major heat shock proteins (HSPs) of Escherichia coli are molecular chaperones and proteases that constitute a cytosolic system for folding, repair and degradation of proteins (5, 6, 11). Their synthesis is induced as part of the cellular heat shock response after exposure to a large variety of stress conditions which appear to have in common the ability to cause protein misfolding (4, 7, 10, 16, 40). When induced by upshift of the cells to a nonlethal temperature (e.g., 42°C), the heat shock response is transient and consists of a rapid induction phase followed by a shutoff phase starting approximately 5 to 10 min. after upshift.

Expression of HSPs is positively controlled at the transcriptional level by the heat shock promoter-specific ³² subunit of RNA polymerase, encoded by rpoH (4, 11, 42). Stress-dependent changes in heat shock gene expression are mediated by the antagonistic action of ³² and negative modulators which act upon ³² (34-36). These modulators are the DnaK chaperone and its DnaJ and GrpE cochaperones, which inactivate ³² by direct association and mediate its degradation by proteases (8, 9, 20, 21, 34, 35, 38). Degradation of ³² is mediated mainly by FtsH (HflB), an ATP-dependent metalloprotease associated with the inner membrane (14, 37, 39, 40). FtsH degrades free ³² but not RNA polymerase-bound ³², indicating that protease and RNA polymerase compete for binding to ³² (40). The role of the chaperones in ³² degradation is poorly understood. Inactivation of ³² occurs by association of DnaK and DnaJ with the free form of ³², thereby preventing its binding to RNA polymerase (8, 9, 20, 22). There is increasing evidence that the sequestration of the DnaK chaperone system through binding to misfolded proteins is a direct determinant of the induction of the heat shock response (4, 7, 37, 40). Conversely, the shutoff of the heat shock response is assumed to result from HSP-mediated repair and degradation of misfolded proteins, which frees the DnaK chaperone system to inactivate ³² and to promote its degradation. Furthermore, a competition may exist in vivo between ³² and other sigma factors including ⁷⁰ for association with RNA polymerase. This competition is subject to stress-dependent changes and, consequently, leads to alterations in transcriptional activity of ³² (2).

A central open question is the identity of the binding sites within ³² for DnaK, DnaJ, FtsH, and the core of RNA polymerase and the functional interplay between these sites. Previous work showed that the in vivo half-life of fusions between N-terminal fragments of ³² and -galactosidase increased when a stretch of 23 residues (R122 to Q144), located between conserved regions 2 and 3 of ³² and termed region C (Fig. 1), is deleted or replaced by other residues (27). Within region C, a segment of 9 amino acids between residues 132 and 140 of ³² (QRKLFFNLR) is almost entirely conserved within ³² homologs but not other sigma factors; it was therefore termed the RpoH box (28). This specific conservation strongly suggests a regulatory role for the RpoH box. Consistent with this assumption were the results of a study in which a ³²-derived peptide library was screened for DnaK binding sites. A high-affinity DnaK binding site exists within the RpoH box in the center of region C, and a second binding site was found close to the RpoH box at the periphery of region C (between residues L118 and K125) (25). Based on this peptide analysis, the RpoH box, and possibly the peripheral DnaK binding motif, is a prime candidate for a regulatory site within the ³² protein which allows binding of DnaK and possibly also degradation by FtsH (25).

View larger version (21K): [in this window] [in a new window]   FIG. 1.   Mutational alterations of 32. 32 is shown schematically, with the locations of conserved regions 1 to 4 and details of region C including the RpoH box indicated. Sequences of two potential DnaK binding sites identified by peptide scanning are boxed, and mutational alterations of amino acid residues introduced into peptides and/or 32 proteins are indicated.

The aim of the present study is to experimentally investigate the regulatory role of region C, in particular of the two DnaK binding motifs. In contrast to our expectations, we did not find evidence for a role of region C in chaperone binding and degradation by FtsH. Instead, we found that region C was involved in high-affinity binding of ³² to RNA polymerase, thereby providing to ³² a competitive advantage over other sigma factors in association with RNA polymerase.

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results Discussion References

Bacterial strains, plasmids, and growth conditions. Cells of strains BB2019 [GW1000 recA441 sulA11 (argF-lac)U169 supC(Ts) rpoH165(Am) pDMI,1] (8) and BB7089 (C600 thr-1 leuB6 thi-1 lacY supE44 rfbD1 fhuA21 lacI^q P_A1/lacO-1dnaKJ) (40) were grown aerobically at 30 or 42°C in Luria broth or M9 minimal medium supplemented with 0.2% glucose (M9-Glu) or 0.2% maltose (M9-Mal) as the carbon source, thiamine (20 µg/ml), and appropriate amino acids (50 µg/ml). The growth media were also supplemented with 100 µM isopropyl--D-thiogalactopyranoside (IPTG) for BB7089 and kanamycin (40 µg/ml) and ampicillin (100 µg/ml) when required. The wild-type rpoH gene cloned into plasmid pUHE21-2fd12 (9) was used as template for mutagenesis by the method of Kunkel et al. (17). pBAD30 (rpoH) (wild type or mutant) was obtained by cloning the EcoRI-HindIII fragment from pUHE21-2fd12 (rpoH) into pBAD30 (12). For production of hexahistidine-tagged ³² variants, wild-type and mutant alleles of rpoH were subcloned by inserting the EcoRI-PstI fragment into pUHE211-1 (rpoH) (carboxy-terminal histidine fusion, used for all mutant ³²) or the MluI-HindIII fragment into pUHE212-1 (amino-terminal histidine fusion, used for ³²-F137E) (8, 9). For C-terminal fusion of ³² to the intein-chitin binding domain, we amplified by PCR a 0.3-kb fragment corresponding to the coding sequence of the C-terminal 80 residues of ³², using primers P1 (5'-GGAATTCTGCAGGATAAATCATCTAAC) and P2 (5'-GGGGTACCCTTGGCAAAGCACGCTTCAATGGCAGCACGC) and pUHE21-2fd12 (rpoH) as the template. The P1 sequence comprises internal coding sequences of rpoH containing an additional EcoRI site at the 5' end. The 3' end of P2 is complementary to the 3'-end coding sequence of rpoH (from the codon for amino acid 276 to the stop codon). The 5' end of P2 is complementary to the sequence coding for intein (the N-terminal 6 amino acids) and contains a KpnI site. The sequence complementary to the stop codon of rpoH (CAT) was changed to CAC, allowing us to genetically fuse ³² with the first cysteine of intein. The EcoRI-PstI fragment from pCYB1 (New England Biolabs) was cloned into pUHE21-2fd12 by using as the linker a small DNA fragment containing a multiple-cloning site (XhoI, BglII, and HindIII). The 0.3-kb fragment obtained by PCR was cloned in this pUHE21-2fd12 derivative (EcoRI-KpnI). Finally, the 5' end of the rpoH gene (EcoRI-PstI) (wild-type or mutant alleles) was cloned into the resulting plasmid.

Half-life determination. For determination of ³² stability in strain BB2019, the cells were grown at 30°C in M9-Glu without methionine or IPTG to an optical density at 600 nm of 0.4. A 1-ml volume of culture was labeled for 2 min with 70 µCi of [³⁵S]methionine, and this was followed by chase with unlabeled methionine (final concentration, 200 µg/ml). Aliquots of 100 µl were collected at the indicated times, mixed with 10% (vol/vol) trichloroacetic acid (TCA), and incubated for 15 min on ice. After centrifugation for 15 min at 16.000 × g, the pellets were washed with acetone and resuspended in 50 mM Tris-HCl (pH 8.0)-1% sodium dodecyl sulfate (SDS)-1 mM EDTA. Half of each sample was subjected to SDS-polyacrylamide gel electrophoresis (PAGE), and the other half was used for immunoprecipitation with ³²-specific rabbit antiserum as described previously (41). The immunoprecipitated material was separated by SDS-PAGE and quantified by phosphorimaging with MacBas software (Fuji Film Co.). For half-life determination of ³² in strain BB7089, the cells were grown in M9-Mal without methionine but with 100 µM IPTG to an optical density at 600 nm of 0.4. Expression of rpoH was induced by addition of arabinose (100 µM) for 5 min. Then [³⁵S]methionine to label the cells and glucose (0.4%) to stop further expression of rpoH were added, and the chase and immunoprecipitation steps were performed as described above.

Protein and peptide purification. Histidine-tagged ³² proteins were purified essentially as described previously (8), except that cell lysis was performed with the French press (500 lb/in²) and buffer containing 100 mM NaCl, 20 mM Tris-HCl (pH 7.9), 0.05% sodium deoxycholate, and 1 mM phenylmethylsulfonyl fluoride. After elution from Ni²⁺-nitrilotriacetic acid columns, the pooled fractions containing ³² were subjected to gel filtration on a Superose 12 column (Pharmacia) with a mobile buffer containing 40 mM HEPES-KOH (pH 8.0), 100 mM KCl, 0.1 mM EDTA, 10% glycerol, and 1 mM -mercaptoethanol. A final purification step was performed by using a MonoQ column (HR5/5; Pharmacia) and elution of the bound protein by a linear 100 to 1,000 mM KCl gradient. Untagged ³² and ³²-F137E were purified as fusion proteins with self-cleavable intein-chitin binding domains on chitin affinity columns as specified by the supplier (New England Biolabs), except that a different running buffer was used (20 mM Hepes-KOH, 500 mM NaCl, 0.5% Triton X-100) and an additional washing step of the cell extract-loaded chitin column with 20 mM HEPES-KOH-500 mM NaCl-5 mM MgCl₂-5 mM ATP was performed to elute DnaK bound to ³². The chitin bound intein-³² was eluted from the intein moiety with running buffer containing 50 mM dithiothreitol (DTT), which induces self-splicing, and further purified using a MonoQ column. RNA polymerase (holoenzyme and core), ⁷⁰, DnaK, DnaJ, and FtsH were purified (purity of approximately 70% for ⁷⁰ and >90% for the other proteins) as described previously (3, 23, 32, 39). Protein concentrations were routinely determined by a Bradford assay (Bio-Rad) with bovine serum albumin (BSA) as the standard and, for ³², calibrated by the bicinchoninic acid protein assay (Pierce). The peptides used were synthesized by R. Franck (ZMBH, University of Heidelberg, Heidelberg, Germany) and (for ³²-E115-A131-C/I123D) by Jerini Bio Tools (Berlin, Germany). Peptide concentrations were determined by measurement of the absorption at 280 nm.

³H labeling of proteins and in vitro degradation assays. To assay the degradation of ³², the proteins were labeled with N-succinimidyl-[2,3-³H]propionate (Amersham) as described previously (9), except that free N-succinimidyl-[2,3-³H]propionate was removed by dialysis against transcription buffer (20 mM Tris-HCl [pH 8.0], 200 mM KCl, 5 mM MgCl₂, 1 mM DTT, 5% glycerol). Degradation of labeled ³² by FtsH was assayed in a purified system adapted from that of Tomoyasu et al. (39). Briefly, FtsH (1.2 µg) preincubated on ice for 30 min with 50 µM Zn²⁺-25 mM Tris-acetate (pH 8.0)-2.5 mM magnesium acetate (final concentration) was mixed with ³² (1 µM, final concentration) in a final volume of 20 µl of reaction buffer (50 mM Tris-acetate [pH 8.0], 5 mM magnesium acetate, 2 mM -mercaptoethanol, 50 mM KCl, 5 mM ATP) and incubated at 42°C. Aliquots of 2 µl were withdrawn at the indicated times, mixed with BSA (0.5 mg/ml) and EDTA (20 mM), and precipitated with TCA (10%, vol/vol). Radioactivity in the supernatant was determined in a scintillation cocktail (Roth) with a Perkin-Elmer counter. To assay the degradation of peptides, the final volume of the reaction mixture was 60 µl and the concentration of peptide was 50 µM. At the indicated time points, aliquots of 18 µl were mixed with 92 µl of 0.5% trifluoroacetic acid to stop the reaction. Products were analyzed by reverse-phase chromatography with a 5 to 80% acetonitrile gradient in 0.1% trifluoroacetic acid.

Analysis of protein interactions. Association of ³² with DnaK, DnaJ, and RNA polymerase core enzyme (RNAP core) was determined by gel filtration with a Superdex 200 column essentially as described previously (9). To determine the association of ³² with RNAP core, 0.5 µM (in competition experiments) or 1 µM ³² was incubated with 1.5 µM RNAP core for 10 min at 30°C in transcription buffer (20 µl, final volume). To determine the association of ³² with DnaK, 5 µM DnaK was incubated for 2 h at 30°C in transcription buffer (to discourage oligomerization), mixed with 1 µM ³² in a final volume of 20 µl, and further incubated for 30 min at 30°C. These mixtures were shifted to ice, adjusted to 100 µl by addition of transcription buffer which for competition experiments contained a 10- or 30-fold excess of unlabeled ⁷⁰ or ³², respectively, and loaded on a Superdex 200 column at 4°C. Labeled ³² was detected in the elution fractions by liquid scintillation counting.

Cross-linking experiments. To couple the cysteine-specific cross-linker N-(4-azido-2,3,5,6-tetrafluorobenzyl)-3-maleimidylpropionamide (TFPAM-3) to cysteine-containing ³² mutant proteins, 50 µl of a 20 µM protein solution was dialyzed against buffer A (20 mM HEPES-KCl [pH 8.0], 200 mM KCl, 5 mM EDTA), incubated for 1 h at 30°C in the dark with a 10-fold molar excess of TFPAM-3, and then dialyzed against buffer B (20 mM HEPES-KOH [pH 8.0], 200 mM KCl, 5 mM MgCl₂) to remove free TFPAM-3. All other proteins were dialyzed against buffer B before use. For cross-linking, the proteins were mixed as indicated (150 pmol each) in 20 µl of buffer B and incubated at 30°C for 2 h in the dark. DnaJ (150 pmol) and ATP (5 mM) were added when indicated, and the mixtures were incubated for a further 10 min on ice. Cross-linking was induced on ice by illumination under UV light (360 nm) for 5 min. After addition of sample buffer (18) and boiling for 5 min, the samples were subjected to electrophoresis on SDS-10% polyacrylamide gels. The gels were silver stained or electroblotted onto polyvinylidene difluoride membranes (Amersham) for immunodetection. Immunoblots were developed with a Vistra ECF fluorescence Western blotting kit (Amersham, Inc.), using Fluoroimager and MacBas software (Fuji Film Co.).

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

In vitro analysis of region C-derived peptides. To investigate whether region C comprises binding sites for DnaK and FtsH that are responsible for the control of ³² activity and stability, we designed amino acid alterations predicted to perturb these sites (Fig. 1). For DnaK, this approach is straightforward since two potential binding sites central and peripheral to region C had been identified (25). Furthermore, the consensus sequence motif recognized by DnaK and the sequence features which prevent DnaK binding have been elucidated. The binding motif consists of a hydrophobic core of up to five consecutive hydrophobic residues flanked by segments enriched in basic residues (30), features which are compatible with the architecture of the substrate binding cavity of DnaK (29, 44). Introduction of negatively charged residues into the hydrophobic core prevent DnaK binding (30). These findings provide a rational basis for introducing alterations into the two potential DnaK binding sites central and peripheral to region C. Recent results concerning the substrate specificity of FtsH (40a) led us to speculate that this protease also recognizes hydrophobic stretches within protein sequences. We therefore changed hydrophobic residues within the hydrophobic stretches located in region C to negatively charged residues in order to perturb DnaK binding and degradation by FtsH.

View larger version (27K): [in this window] [in a new window]   FIG. 2.   DnaK binding and FtsH-mediated degradation of peptides derived from region C. (A) Amino acid sequences of the peptides used. Mutated residues are boxed. (B) Dissociation constants (Kd) of the peptide-DnaK complexes. The Kd values were determined by peptide titration with fluorescently labeled peptide 32-Q132-Q144-C-IAANS as competitor as described previously (25). (C) In vitro degradation of peptides by FtsH. Degradation is shown as a percentage of the amount of peptide remaining.

In vivo activity of ³² mutant proteins with altered region C. The above results formed the basis for a rational design of mutational alterations of region C within the ³² protein (Fig. 1). rpoH was mutated to introduce the F137E (rpoH-F137E) or I123D mutation (rpoH-I123D), or the rpoH-WRI121,122,123ART mutation. This mutation generates a mutant protein with increased similarity to ⁷⁰. The mutant rpoH genes were cloned into plasmid pUHE21-2fd12 (9) such that their expression is controlled by the IPTG-regulatable P_A1/lacO-1 promoter. When produced to the levels used in the experiments described below, the three mutant ³² proteins were recovered in the soluble fractions of cells growing at 30 and 42°C (data not shown). The mutational alterations therefore did not cause structural changes in ³² leading to aggregation, allowing further analysis of the in vivo activities of the mutant proteins.

View larger version (76K): [in this window] [in a new window]   FIG. 3.   Ability of rpoH mutant alleles to restore the heat shock response in rpoH165(Am) cells. Cells of strain BB2019 [rpoH165(Am)] which carry plasmids (pUHE21-2fd12) expressing wild-type or mutant rpoH were grown in M9-Glu without methionine. At midexponential growth phase, expression of plasmid-borne rpoH alleles was induced by IPTG (500 µM) for 10 min. The cultures were split and further grown at 30 and 42°C. At the indicated times, aliquots (160 µl) were pulse-labeled with [35S]methionine (7.5 µCi) for 1 min and 40 µl of fivefold-concentrated sample buffer was added. Aliquots were subjected to SDS-PAGE (12% polyacrylamide) followed by development with a phosphorimager. The positions of GroEL, DnaK, and 32 are indicated.

Proteolysis of ³² mutant proteins in vivo. We investigated the effects of the mutational alterations in region C on ³² stability by performing pulse-chase experiments followed by immunoprecipitation of ³². The ³²-F137E mutant protein produced from a plasmid was stabilized in rpoH165(Am) mutant cells at 30°C (t_1/2, 30 min) (Fig. 4) and at 42°C (t_1/2, 17 min [data not shown]). In comparison, wild-type ³² produced from plasmids was rapidly degraded after prolonged growth at both temperatures (t_1/2, ca. 1 min) (Fig. 4).

View larger version (37K): [in this window] [in a new window]   FIG. 4.   In vivo stability of the 32-F137E mutant protein at 30°C. Wild-type 32 and the 32-F137E mutant protein were produced from plasmids containing rpoH and tested for their stabilities in both BB2019 cells expressing the dnaK and dnaJ genes from authentic 32-dependent heat shock promoters (left panel) and BB7089 cells expressing the dnaK and dnaJ genes from the IPTG-regulated PA1/lacO-1 promoter. After pulse-labeling with [35S]methionine and a chase step, aliquots were taken at the indicated time points followed by immunoprecipitation of 32 (top). The bottom panels show quantification of the precipitated proteins relative to time zero. Mean values of the results of at least two experiments are given.

Proteolysis of ³² mutant proteins in vitro. To further substantiate these in vivo results, we investigated the half-life of each mutated ³² proteins in vitro by using purified histidine-tagged ³² and FtsH. The three ³² mutant proteins had wild-type-like elution profiles during gel filtration and ion-exchange chromatography. Furthermore, they were indistinguishable from the wild type with respect to the proteolysis pattern obtained by partial proteinase K and trypsin digestion (data not shown). We thus have no indication for changes in their overall tertiary structures.

View larger version (23K): [in this window] [in a new window]   FIG. 5.   In vitro degradation of 32 mutant proteins by FtsH. 3H-labeled 32 proteins and 3H-labeled 70 (as control) were incubated with FtsH in the absence or presence of 5 mM ATP, followed by TCA precipitation at the indicated time points. The curves represent the percentage of the radioactivity in the supernatants which contain the proteolytic fragments. 32 and 32-I123D have C-terminal histidine tags, and 32-F137E has an N-terminal histidine tag. N-terminally and C-terminally histidine tagged 32 did not differ in the kinetics of degradation (data not shown). Open squares, 32-F137E; solid circles, wild-type 32; solid triangles, 32-I123D; open circles, 70; open triangles, wild-type 32 without ATP.

DnaK and DnaJ binding to ³² mutant proteins in vitro. Several in vitro approaches were used to test whether DnaK and DnaJ binding to ³² is impaired by the mutational alterations in region C. In one approach, we used gel filtration to detect complexes between ³² and the chaperones. ³H-labeled wild-type and mutant ³² proteins, all histidine tag fusions, were incubated with DnaK and subjected to gel filtration to separate DnaK-³² complexes from free ³² (Fig. 6). Under the conditions used, approximately 75% of wild-type ³H-labeled ³² was recovered in complex with DnaK (eluting in fractions 12 to 17). The ³H-labeled ³² mutant proteins (³²-F137E, ³²-I123D, ³²-WRI121,122,123ART) showed similar efficiencies of complex formation, even under chase conditions in which the complexes were separated after the addition of a 30-fold molar excess of unlabeled wild-type ³². Thus, the mutations introduced into region C of ³² had no defect in binding of DnaK. For the ³²-F137E mutant protein and wild-type ³², we verified that these results are also valid for authentic proteins lacking histidine tags (data not shown). Furthermore, no defect in chaperone binding was observed when the ³² mutant proteins were incubated with DnaK together with DnaJ in the presence of ATP (data not shown).

View larger version (20K): [in this window] [in a new window]   FIG. 6.   Binding of 32 mutant proteins to DnaK. 3H-labeled 32, 32-F137E, and 32-I123D proteins were incubated with DnaK and the reaction mixtures were subjected to gel filtration either immediately ( competitor) or after further incubation with a 30-fold excess of unlabeled wild-type 32 (+ competitor). Labeled protein was quantified in the elution fractions and is expressed as a percentage of total radioactivity. The peaks corresponding to the DnaK-32 complex and free 32 are indicated. Solid circles, wild-type 32; open circles, 32-I123D; solid triangles, 32-F137E.

RNAP binding of ³² mutant proteins in vitro. Our findings that the mutational alterations introduced into region C of ³² failed to show defects in the interaction with FtsH and DnaK-DnaJ led us to search for other roles for this region. Since several ³² mutant proteins analyzed in this study had defects in activity, we investigated whether the mutated segments of region C are involved in the interaction of ³² with the RNAP core enzyme. We determined the efficiency of association of ³H-labeled ³² with RNAP by using gel filtration. We focused on the ³²-F137E and ³²-I123D mutant proteins, since they showed functional defects in vivo. The relative amounts of the ³²-I123D mutant protein recovered in association with RNAP (eluting in fractions 8 to 15) were similar to those of wild-type ³². In contrast, the amounts of ³²-F137E recovered in association with RNAP were reduced two- to threefold compared to those of wild-type ³² (data not shown). We then determined the half-lives of the RNAP holoenzymes in chase experiments as outlined in Fig. 7A. The amounts of holoenzymes containing ³H-labeled wild-type or mutant ³² were determined by gel filtration at various time points after the addition of excess unlabeled wild-type ³². Differences in the stability of the mutant ³²-core complexes were evident immediately after addition of the competitor, and 5 min after addition almost no holoenzymes containing the ³²-F137E and ³²-I123D mutant proteins were recovered (Fig. 7B). We therefore chose shorter chase times to determine the half-lives of the holoenzymes (Fig. 7C, left panel). The half-lives of the holoenzymes containing ³H-labeled ³²-F137E (0.7 ± 0.07 min) and ³H-labeled ³²-I123D (0.8 ± 0.2 min) were five- and fourfold reduced, respectively, compared to the half-life of the holoenzyme containing the wild-type ³H-labeled ³² (3.5 ± 0.2 min). For the ³H-labeled ³²-F137E mutant protein, we performed additional experiments with a 10-fold excess of ⁷⁰ as competitor and found a 6-fold decrease in the half-life (6.4 ± 0.6 min for the holoenzyme containing ³H-labeled ³² and 1 ± 0.1 min for the holoenzyme containing ³H-labeled ³²-F137E) (Fig. 7C, right panel). These results show that the mutational alterations in region C decrease the affinity of ³² for RNAP by four- to sixfold.

View larger version (26K): [in this window] [in a new window]   FIG. 7.   Binding of 32 mutant proteins to RNAP. 3H-labeled 32 proteins (wild type [WT], 32-F137E, and 32-I123D) (A) were incubated with RNAP, and a 30-fold excess of wild-type unlabeled 32 (B and C, left) or a 10-fold excess of unlabeled 70 (C, right) was added. At the indicated times, samples were subjected to gel filtration, and the amount of labeled protein was quantified and is expressed as the percentage of the total labeled protein (B) or as a relative amount of RNAP-bound 32 recovered at time zero after the addition of competitor (C). (B) Open circles, 0-min chase with competitor; solid squares, 5-min chase; solid triangles, 60-min chase. (C) Open squares, 32-F137E; solid circles, wild-type 32; solid triangles, 32-I123D.

Transcriptional activity of ³² mutant proteins in vitro. The reduced affinity of the ³² mutant proteins for RNAP may have consequences for their activity in the transcription of heat shock genes, in particular in a situation of competition with other sigma factors. This possibility was tested by runoff transcription assays with the ³²-dependent P2 heat shock promoter of the dnaK dnaJ operon as a template. The reactions were performed in the presence or absence of ⁷⁰ as competitor, with the ³²-F137E and ³²-I123D mutant proteins, since they had reduced activities in vivo and reduced ability to compete with ⁷⁰ for RNAP binding in vitro. In the absence of competitor, both ³² mutant proteins had strongly reduced activities compared to wild-type ³² (Fig. 8). Moreover, the addition of equimolar concentrations of ⁷⁰ was sufficient to strongly reduce the activities of both ³² mutant proteins, whereas the activity of wild-type ³² was affected only in the presence of a fivefold excess of ⁷⁰ (Fig. 8). The ³²-F137E and ³²-I123D mutant proteins thus had reduced activities in heat shock gene transcription, which were further reduced in the presence of ⁷⁰ as competitor.

View larger version (29K): [in this window] [in a new window]   FIG. 8.   In vitro transcriptional activity of 32 mutant proteins. Runoff transcription assays were performed in transcription buffer (20 mM Tris-HCl [pH 8.0], 200 mM KCl, 5 mM MgCl2, 1 mM DTT, 5% glycerol) as described previously (9), with a template consisting of a linear 360-bp DNA fragment (blunt ends) containing the P2 promoter of dnaK. The transcription assay mixtures contained 120 nM RNAP, 70, wild-type 32, 32-F137E, or 32-I123D as indicated. ++, fivefold molar excess (600 nM) of the corresponding protein over the other proteins in the assay. Transcripts were analyzed by polyacrylamide-urea gel electrophoresis (9) followed by autoradiography. The relative amounts of transcripts were quantified and are expressed as a percentage of the transcript obtained with wild-type 32 in the absence of 70 (defined as 100%).

Cross-linking of region C of ³² to RNAP. To obtain physical evidence for a role of region C in the association of ³² with RNAP, we determined by cysteine-specific cross-linking whether region C is surface exposed within ³² and in proximity to the RNAP in the holoenzyme. This approach was facilitated by the fact that ³² lacks cysteine, which allowed us to specifically engineer cysteines into region C. Plasmid-borne rpoH was mutagenized to encode a ³² mutant protein (³²-TN128,138CC) which has two residues within region C replaced by cysteines (Fig. 1). The ³²-TN128,138CC protein retained full activity in vivo, was a soluble monomer when purified as His tag fusion, and showed similar efficiencies in complex formation with DnaK and RNAP to those of wild-type ³² (data not shown).

View larger version (64K): [in this window] [in a new window]   FIG. 9.   Cysteine-specific cross-linking of 32-TN128,138CC with RNAP. RNAP, DnaK, wild-type 32, or 32-TN128,138CC proteins were mixed as indicated (+, 150 pmol; ++, 450 pmol). After exposure to UV light, the samples were separated by SDS-PAGE followed by silver staining or immunostaining with 32- or RNAP-specific antiserum. Cross-linking products (CL1, CL2, and CL3), DnaK, DnaJ, 32, and subunits of RNAP (, , ') are indicated.

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

The aim of this study was to establish whether region C plays a role in the regulation of ³². Such a role had been suggested by (i) the high conservation of region C, in particular of the nonameric RpoH box, specifically among ³² homologs (28); (ii) demonstration that the in vivo stability of protein fusions between ³² segments and -galactosidase strongly increases when region C is deleted or replaced by other residues (27); and (iii) identification at the peptide level of two high-affinity binding sites for DnaK within the RpoH box and peripheral to region C (25).

In view of the above evidence, it seemed plausible to postulate that region C provides recognition sites for DnaK and FtsH which allow the regulation of ³² activity and stability. To analyze this possibility, we mutationally altered region C by rational design. Using peptides, McCarty et al. found that a 31-mer peptide comprising the wild-type sequence of region C is a high-affinity substrate for DnaK (K_d, ca. 80 nM) (25). This qualifies region C as recognition site for DnaK. We found that the 21-mer peptide comprising only the RpoH box is an excellent substrate for DnaK (K_d, 40 nM), in accordance with our earlier findings (25), but also for FtsH (t_1/2, 7 min). Replacement of a single hydrophobic residue in this 21-mer peptide, positioned in the hydrophobic core segment of the DnaK binding motif, by a negatively charged residue (F137E) strongly decreased the affinity for DnaK (K_d, 2 µM) and the efficiency of degradation by FtsH (t_1/2, 28 min). To our knowledge, this is the first evidence that a protease and a chaperone recognize the same sequence stretch within a substrate, possibly establishing a competitive relationship allowing kinetic partitioning of the substrate between the chaperone and the protease.

The identification of amino acid substitutions within region C peptides that affect the recognition of DnaK and FtsH provided a rational basis for specific mutagenesis of ³². It was surprising that ³² mutant proteins carrying the I123D and F137E substitutions, as well as a third mutant protein carrying the WRI121,122,123ART substitution which renders the ³² sequence more similar to ⁷⁰, showed no defects in affinity for DnaK or in degradation by FtsH. With respect to DnaK, wild-type-like interactions with the ³² mutant proteins were found in vitro by gel filtration, surface plasmon resonance spectroscopy, and a functional assay for substrate binding to DnaK. Furthermore, in cells producing ³²-F137E, ³²-I123D, or ³²-WRI121,122,123ART, a DnaK-mediated shutoff of the heat shock response was still observed. However, in these cells the amplitude of the heat shock response was reduced, and in cells producing the ³²-F137E and ³²-I123D mutant proteins the induction kinetics were slower than in cells expressing wild-type ³². These differences are assumed to result from reduced affinities of the ³² mutant proteins for RNAP (see below). With respect to proteolytic susceptibility, the half-life of each ³² mutant protein was almost normal in vivo at 30°C, provided that the DnaK and DnaJ levels were adjusted, and in vitro in FtsH- and ATP-dependent degradation assays. It is important to note that the amino acid substitutions in the three ³² mutant proteins do not appear to cause overall structural changes, as evidenced by the unaltered partial proteolysis pattern and solubility of the proteins. It is therefore unlikely that the ability of DnaK and FtsH to recognize the ³² mutant proteins is caused by exposure of novel recognition sites induced by unfolding. Together, our data indicate that region C is not a regulatory site in ³² that is essential for binding of DnaK and degradation by FtsH. Recently, it was proposed that the C termini of protein substrates including cI and ³² are determinants for degradation by FtsH (1, 13), although recent experiments from our laboratory question the importance of the C terminus of ³² for degradation (unpublished results).

In retrospect, the identification of DnaK and FtsH recognition sites at the peptide level did not lead to elucidation of essential DnaK and FtsH recognition sites within the ³² protein. Several reasons may account for this failure. It is possible that region C plays a nonessential role in the DnaK- and FtsH-dependent regulation. Alternatively, and perhaps more probably, the segments within region C that act as recognition sites for DnaK and FtsH at the peptide level may not be accessible to interactions with these ligands in the context of the folded ³². For DnaK, this may be caused by helix formation by the respective segments in the folded state of ³², a conformation that is incompatible with the architecture of the substrate binding cavity (29, 44). It should be emphasized that the approach of using peptides as first indicators for potential chaperone and protease binding sites in protein substrates is not devalued by our findings. However, as expected for folded protein substrates, peptides do not provide information on the accessibility of such sites in the context of a folded protein. Validation of peptide data by transfer of corresponding mutations into the protein substrate is therefore an essential step of this approach. Here we investigated two of approximately seven major DnaK binding regions within the ³² sequence. Further experiments will be performed to investigate the regulatory potential of the other regions.

Our experimental results provide evidence for a role of region C in the interaction of ³² with the core enzyme of RNAP. This is consistent with a similar conclusion obtained from an independent study of mutational alterations within the entire ³² protein (15). By glycerol gradient sedimentation analysis, Joo et al. showed that a ³² mutant protein altered in region C (F136L) has decreased affinity for RNAP and only partial transcriptional activity in vitro. However, this study did not provide quantitative data on the dissociation rate of the RNAP holoenzyme and did not investigate the in vivo activity of the ³² mutant protein and the interaction with FtsH and DnaK. Our present work thus considerably extends the findings of Joo et al. We quantified the RNAP binding defects of the ³²-F137E or ³²-I123D mutant proteins by measuring the half-lives of the RNAP holoenzymes in the presence of competitor. For both proteins, a sixfold-decreased half-life was obtained compared to that of the holoenzyme containing wild-type ³². These defects in core binding are sufficient to account for the reduced activities of the mutant proteins in vivo at 30 and 42°C and in runoff transcription in vitro at 30°C. However, the in vivo activity of the ³²-F137E mutant protein is more dramatically affected than that of the ³²-I123D mutant protein. The reason for this difference is unclear. We speculate that the ³²-F137E mutant protein has additional defects in promoter recognition.

The ability of region C to increase the affinity of ³² for RNAP has physiological consequences. Region C may provide competitive advantages of both ³² over other sigma factors for RNAP binding and RNAP over DnaK, DnaJ, and FtsH for ³² binding. Region C thereby may increase the efficiency and speed by which the heat shock response is induced upon temperature upshift and the efficiency of heat shock gene transcription under steady-state conditions. In fact, only 10 to 30 molecules of ³² that exist in a cell growing at 30°C (35) are sufficient to produce HSPs that account for at least 5% of the total cytosolic protein (11). The observed delay in the induction of the heat shock response in cells producing the ³²-F137E and ³²-I123D mutant proteins is consistent with this proposed role of region C.

Our cross-linking experiments provide the first indication that region C is in close proximity to the RNAP. It is possible that region C provides directly the physical contacts which increase the affinity of ³² for RNAP core. However, since the sequence of region C is absent in other sigma factors not belonging to the ³² branch, it is clear that this region cannot be involved in essential contacts to RNAP but that it seems to be required to enhance affinity. Several regions within the polypeptide chains of ³² and ⁷⁰, including the conserved regions 2.1., 2.2., 3, and 4, have been implicated in core interaction (15, 19, 24, 26, 33, 43). This multitude of potential interacting sites suggests a high structural complexity of the sigma factor-RNAP interaction which may be fully understood only upon elucidation of the atomic structures of the involved proteins.