INTRODUCTION

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The heat shock response is a universal, adaptive, and homeostatic cellular response against damage to protein folding under heat and other stresses. In Escherichia coli, the response results primarily from a transient increase in the level of ³², which is encoded by rpoH and which is specifically required for the transcription of the set of well-conserved heat shock genes (11, 35). The increase in the ³² level results from both the enhanced synthesis and the stabilization of normally unstable ³² (12, 30). Whereas the stabilization of ³² is thought to be triggered by the titration of free DnaK/DnaJ chaperones by stress-induced misfolded proteins (1, 4, 9, 16, 32), the increased synthesis occurs at the level of translation (15, 21, 30) and presumably is regulated via a separate pathway (22, 29, 35). The production of abnormal proteins under various conditions also induces the heat shock response through an increase in the ³² level (10), but such induction appears to involve only the stabilization and not the increased synthesis of ³² (16). Furthermore, exposure to extremely high temperatures (e.g., 50°C) can induce ³² synthesis by enhancing rpoH transcription by activating the second heat shock  factor, ^E (7, 33), in response to misfolded proteins accumulated in the periplasm (11, 19). Thus, E. coli cells strictly regulate ³² at various levels to cope with increasing demands for chaperones, ATP-dependent proteases, and other heat shock proteins under a variety of stress conditions (1, 9, 11, 25, 35).

As to the mechanism of translational induction of ³², extensive deletion analyses of an rpoH-lacZ gene fusion revealed the involvement of positive and negative regulatory regions (regions A and B, respectively) on the 5' portion of rpoH mRNA (15, 21). Region A (15 nucleotides [nt]), located close to the initiation codon, represents the "downstream box," (27) which is complementary to part of the 16S rRNA and which potentially enhances translation. Region B, an internal coding segment of ca. 100 nt, is a negative element involved in repressing translation under nonstress conditions. A computer prediction revealed a secondary structure for the 5' segment (nt 19 to +247) of rpoH mRNA which is fully consistent with the above findings; base pairings between region A and part of region B appeared to negatively modulate rpoH translation (21) (Fig. 1).

View larger version (23K): [in this window] [in a new window]   FIG. 1.   Schematic representation of the 5' portion (nt 19 to +247) of E. coli rpoH mRNA as predicted by use of Mulfold (14). (A) Secondary structure thought to be involved in modulating heat-induced synthesis of 32 (21). Region A (nt +6 to 20), the initiation codon, and the Shine-Dalgarno (SD) sequence are indicated. Region B (nt +112 to 208) is shaded. Numbers refer to the nucleotides of the coding sequence. (B) Putative base pairing between the downstream box (region A) of rpoH and the "anti-downstream box" of 16S rRNA (spanning nt 1469 to 1483). , G-U pairs.

Mutational analyses of rpoH mRNA deficient in the expression or regulation of a GF364 fusion carrying the initial 364 nt of the rpoH coding region (Fig. 2A) not only substantiated the importance of some of the critical base pairings but also suggested the possible involvement of specific nucleotide sequences in heat induction (36). It was surmised that the translation of rpoH mRNA is restricted by the formation of secondary structure(s) that would limit ribosome entry under nonstress conditions. Upon mild heat shock (e.g., a shift from 30 to 42°C), such mRNA structures were thought to be disrupted to enhance translation, although the mechanism remained unknown (21, 35, 36). In addition, the isolation and characterization of rpoH homologs from a number of gram-negative bacteria revealed evolutionary conservation of both region A and the mRNA secondary structure among the gamma proteobacteria (23). All members of the latter group of bacteria examined seemed to exhibit heat-induced synthesis of ³² homologs at the translational level, as in E. coli (24).

View larger version (25K): [in this window] [in a new window]   FIG. 2.   Structure and expression of an rpoH-lacZ gene fusion (TLF247). (A) Schematic diagrams of the TLF247 fusion construct and GF364, studied previously (21). The locations of regions A and B are indicated. (B) SDS-PAGE patterns of fusion proteins expressed from the wild-type and mutant forms of TLF247. Cells were grown at 30°C and shifted to 42°C. Pulse-labeling with [35S]methionine was done for 2 min before or 3 min after the temperature shift. The labeled cells were disrupted, and immunoprecipitates obtained with anti--galactosidase serum were analyzed by SDS-PAGE as described in Materials and Methods. Closed and open arrows indicate fusion proteins and -galactosidase  protein (internal reference), respectively.

The translational induction of ³² is transient and is followed by a shutoff phase mediated by the DnaK-DnaJ-GrpE chaperones (9, 12, 29). The translational repression and destabilization of ³² during adaptation periods are part of the feedback regulatory mechanisms (29, 31, 32) mediated by a segment of ³² protein (18, 22, 35) which contains a highly and uniquely conserved sequence among the rpoH homologs (23, 34). Several lines of evidence suggest that this region plays important roles in the chaperone-mediated negative control of the synthesis and/or stability of ³² (8, 17, 18). However, the exact regulatory mechanisms of the transient heat induction of ³² synthesis, including the nature of the sensor(s) and signaling pathway(s), remain largely unresolved.

We now report a structural and functional analysis of the 5' segment of rpoH mRNA responsible for thermoregulation. We first probed the structures of rpoH RNAs from the wild type and several mutants in vitro and then analyzed their expression in vivo after transcription from a single-copy rpoH-lacZ gene fusion. The data supported some salient features of the predicted mRNA secondary structure and provided the basis for further analysis of each of the component stem-loop structures. The results led us to propose that an mRNA secondary structure with appropriate stability and formed between the translation initiation region (the AUG initiation codon and region A) and the internal coding region is a prerequisite for the thermoregulation of ³² synthesis.

	MATERIALS AND METHODS

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Strains, phages, and media. E. coli K-12 strain MC4100 [araD (argF-lac)U169 rpsL relA flbB deoC ptsF rbsR] (2) was used for all experiments in vivo. The TLF97-3 vector (28) was used to construct rpoH-lacZ gene fusions. Minimal medium M9 (20) with 0.2% glucose, thiamine (2 µg/ml), and all amino acids except for methionine (20 µg/ml each) was used for pulse-labeling experiments. MacConkey lactose agar (Difco) and L agar containing 5-bromo-4-chloro-3-indolyl--D-galactopyranoside (X-Gal) (30 µg/ml) were used for isolating  lysogens containing rpoH-lacZ gene fusions. Recombinant DNA and other general techniques were as described by Sambrook et al. (26) and by Miller (20).

Chemicals, enzymes, and buffers. 1-Cyclohexyl-3-(2-morpholinoethyl)-carbodiimide metho-p-toluene sulfonate (CMCT) and diethyl pyrocarbonate (DEP) were purchased from Sigma. RNase V₁ was obtained from Pharmacia, and avian myeloblastosis virus reverse transcriptase was obtained from Life Science. Buffer H was 70 mM HEPES-KOH (pH 7.8) containing 10 mM MgCl₂, 270 mM KCl, and 1 mM dithiothreitol, and buffer V1 was 30 mM Tris-HCl (pH 7.8) containing 20 mM MgCl₂, 300 mM KCl, and 1 mM dithiothreitol.

Construction of rpoH-lacZ gene fusions. The gene fusion (translational fusion) designated TLF247 was constructed by in-frame fusion between the XhoI-BamHI fragment of pGF247 (21) containing the rpoH promoters and the 5' portion of the coding region (nt 677 to +247) and codon 9 of lacZ on the TLF97-3 vector. The same fragment of pGF247 was also inserted into pBluescript SK(+), yielding pBSK247. Derivatives of TLF247 carrying base substitutions were constructed by PCR with plasmid pFRP103 containing each of the mutations (36) as a template and synthetic oligonucleotide primers that corresponded to the 5' (nt 46 to 27) and 3' (nt +227 to 247) portions of the coding region. Seven extra bases containing the BamHI site were added to the latter primer to make in-frame fusions to lacZ (21). A set of 3' deletions of GFR153 was constructed by PCR with the same 5' primer as that used above and 3' primers that corresponded to the end of each deletion (with the same seven extra bases) and with GFR153 (21) as a template. DNA fragments with the desired sequences containing PCR-amplified products were inserted into pBSK247, and nucleotide sequences were confirmed by dideoxy sequencing. The XhoI-BamHI fragments of the resulting plasmids were then transferred to the TLF97-3 vector by in vitro packaging. TLF229(stemIII) was constructed from TLF247 by deleting the apical portion of stem II (nt +30 to 110) and all of stem III (nt +128 to 178). Four synthetic oligonucleotides (ca. 60 nt long) were annealed and ligated to create a DNA fragment with 5' protruding ends for joining with the ClaI or BamHI site at the 5' or 3' end, respectively. The resulting fragment was cloned into pBSK247 by replacing the ClaI-BamHI fragment to obtain pBSK229(stemIII).

Determination of rates of synthesis of fusion proteins. The procedure used for the determination of fusion protein synthesis rates was essentially that described previously (21). Portions (0.1 ml) of log-phase cultures were pulse-labeled with L-[³⁵S]methionine (1,200 Ci/mmol). Extracts were prepared, and portions with equal radioactivity were mixed with a fixed amount of JM103 cell extract (labeled with [³⁵S]methionine) containing -galactosidase  protein and treated with antibody against -galactosidase (Organon Teknika Cappel). The immunoprecipitates were subjected to sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (PAGE) (7.5% gel), and the intensities of radioactive bands were quantified with a Fujix BAS2000 imaging analyzer to determine the rates of synthesis of fusion proteins after correction for recovery with  protein as a reference.

RNA preparation. RNA containing the upstream region and part of the rpoH coding region (nt 60 to +247) was prepared in vitro with T7 RNA polymerase by use of an RNA transcription kit (Stratagene). The AflII-BamHI fragments of pBSK247 were placed under the control of the T7 promoter of vector pSP72, and the resulting plasmids were digested with BamHI and used as templates for RNA synthesis. The RNA obtained was treated at 65°C for 3 min, followed by slow cooling to room temperature prior to use.

Structure probing of RNA. The procedures used for RNA structure probing were essentially those described by Christiansen et al. (3). Prior to treatment with CMCT, DEP, or RNase V₁, RNA (4 µg) was renatured (heating and slow cooling) in 20 µl of buffer H, 200 µl of buffer H, or 20 µl of buffer V1, respectively. RNA was treated with CMCT (50 mM) or DEP (96 µM), and the reaction was terminated by the addition of ethanol on dry ice. For RNase V₁ treatment, 6 µl of RNA was mixed with an equal volume of buffer V1 containing enzyme on ice for 30 min, treated with phenol, and precipitated with ethanol. RNA incubated without probes served as a control in all experiments. The identification of modified bases was carried out by primer extension analysis: 0.3 pmol of modified RNA and 3 pmol of 5'-fluorescence-labeled primer complementary to the 5' (nt +79 to 101) or 3' (nt +227 to 247) region were incubated with avian myeloblastosis virus reverse transcriptase. Portions of primer extention products were loaded on a 5% polyacrylamide-8 M urea sequencing gel and electrophoresed at 1,400 V for 2.5 h. The bands were detected with Fluorescence BioImage Analyzer FMBIO II Multi-View (Hitachi), and the modified bases were identified by comparison with sequence ladders simultaneously run with the same end-labeled primers.

	RESULTS

Top Abstract Introduction Materials and methods Results Discussion References

Thermoregulation of a TLF247 gene fusion mediated by an mRNA secondary structure. To further understand the rpoH translational control mechanisms, it was important to analyze structural features of the "minimal" mRNA segment(s) essential for thermoregulation. Based on our previous work (21), we constructed a new rpoH-lacZ gene fusion carrying only the first 247 nt of rpoH (TLF247) (Fig. 2A) and reexamined the effects of mutations previously characterized with GF364 carrying the first 364 nt (36). Cells of MC4100 carrying TLF247 or its mutant derivatives were grown at 30°C, shifted to 42°C, and pulse-labeled with [³⁵S]methionine to determine fusion protein synthesis rates (Fig. 2B). Wild-type TLF247 exhibited five- to sixfold induction upon the temperature upshift. In contrast, the mutant fusions (15A, 15C, or 124T) carrying a base substitution predicted to disrupt the 15G-124C base pairing showed enhanced expression at 30°C and reduced induction upon the shift to 42°C (Fig. 3B), consistent with our previous results obtained with GF364 (we discuss below the relatively small effect observed with 15C).

View larger version (44K): [in this window] [in a new window]   View larger version (20K): [in this window] [in a new window]   FIG. 3.   Structure probing of rpoH mRNA. (A) Urea-PAGE patterns of primer extension products. A 5' segment (nt 60 to +247) of wild-type (WT) or mutant RNAs prepared in vitro was treated with CMCT, DEP, or RNase V1, and modified bases were identified by reverse transcription analysis as described in Materials and Methods. Treatment with CMCT was carried out at 30°C for 0 min (lanes c), 10 min (lanes 1), or 30 min (lanes 2), whereas treatment with DEP was done at 30°C for 0 min (lanes c), 5 min (lanes 1), or 10 min (lanes 2). Digestion with RNase V1 was done at 0°C for 30 min with 0 U (lanes c), 0.0005 U (lanes 1), or 0.001 U (lanes 2) of enzyme. Only some of the bases that were clearly modified by each treatment are indicated by nucleotide numbers. Relevant sequence ladders (wild type) are shown to the side as a reference. When comparing the observed bands with the sequence ladders, one should note that cDNA synthesis stops one residue before the modified base. Arrowheads indicate some of the modifications uniquely found in mutant RNA(s), whereas arrows indicate positions at which reverse transcriptase was arrested. Only the data for wild-type RNA are shown for experiments with RNase V1. (B) Modified bases identified with wild-type RNA in panel A are indicated on the mRNA secondary structure. The bases modified by CMCT or DEP are represented by squares or circles, respectively. The relative extents of modification are indicated by outlined stippled, outlined open, and nonoutlined shaded symbols for strong, modest, and weak reactivities, respectively. Arrowheads indicate sites cleaved by RNase V1. C-53 was fortuitously modified by DEP. Stems I, II, III, and IV are indicated, as are the initiation codon, region A, and the Shine-Dalgarno (SD) sequence. Region B (nt +112 to 208) is shown in boldface letters.

Structure probing of the rpoH mRNA secondary structure. The structure of the 5' segment of rpoH mRNA (nt 60 to +247) used for construction of the TLF247 fusion was examined with two chemical probes (CMCT and DEP) and an enzymatic probe (RNase V₁) (Fig. 3A). RNA prepared by in vitro transcription with T7 RNA polymerase was heated at 65°C for 3 min, slowly cooled to room temperature, and treated with CMCT or DEP, which specifically modifies single-stranded U/G or A, respectively, or with RNase V₁, which cleaves double-stranded RNA with no apparent sequence specificity. The modified bases were identified by reverse transcription analysis, and the relative reactivities of individual bases to each of the probes used are illustrated semiquantitatively on the predicted RNA secondary structure (Fig. 3B). The region upstream of nt 19 is not shown here, since it is known not to be involved in thermoregulation (21).

Altered secondary structure of some mutant rpoH RNAs. To determine the effects of base changes on the mRNA secondary structure, RNAs prepared from five mutants examined above (Fig. 2B) were subjected to similar structural analyses (Fig. 3A). The results obtained, combined with those for the wild-type RNA, revealed certain interesting differences as well as similarities (Table 1). Evidently, stems II and III in the 15A and 15C mutant RNAs were modified to greater extents than those in the wild-type RNA. A-15 was clearly modified by DEP in 15A RNA; in contrast, G-15 in wild-type RNA was not modified by CMCT as expected. More importantly, U-14 was also modified strongly in 15A RNA but not in wild-type RNA, indicating that the neighboring structure was affected by the G-to-A mutation at +15. Since C should not be modified by either probe, the change at +15 could not be seen in 15C RNA. However, U-14 was not modified in 15C RNA, indicating that the change in the neighboring structure was more pronounced in 15A RNA than in 15C RNA. Such differential base modifications, which presumably reflected differences in local secondary structures between the two RNAs, were well correlated with differential fusion protein expression levels at 30°C, namely, higher expression of the 15A mutant than of the 15C mutant (Fig. 2B).

Further deletion analysis of critical regulatory regions. To further define the rpoH regions critical for thermoregulation, we constructed and examined a set of 5' and 3' deletions of the rpoH-lacZ fusion on TLF247. It had been shown that the internal segment of 127 nt that contains the 5' half of region B (nt +27 to 153) (Fig. 2) could be deleted from GF364 without affecting regulation, despite the drastic alteration of the predicted mRNA secondary structure; part of stem III formed base pairings with region A (nt +12 to 17) and with seven artificial nucleotides inserted during construction (21) (see Fig. 5). Similarly, the newly constructed fusion TLF247(27-153), which lacked the same segment, exhibited essentially normal expression at 30°C and induction at 42°C, indicating that the altered secondary structure due to the (27-153) deletion fortuitously gained the capacity for thermoregulation (Fig. 4A, line 2). In spite of this anomaly, however, when some of the above mutations (15A, 15A-124T, and 17C-122G) were introduced into the latter construct, they had similar effects on thermoregulation, although less striking than those obtained with the TLF247 derivatives (data not shown). Thus, the thermoregulation observed with TLF247(27-153) appeared to involve mechanisms similar to that found with the parental TLF247 fusion. These results also suggested that the apical portion of stem II and the intact form of stem III were not essential for regulation.

View larger version (25K): [in this window] [in a new window]   FIG. 4.   Structure and expression of fusion proteins from deletion derivatives of TLF247. (A) A series of 3' deletions derived from the internal deletion TLF247(27-153). Segments of mRNA that correspond to each of the stem structures (I to IV) are shown above the diagram, and nucleotide numbers are shown below. Regions A and B are indicated by stippled and hatched boxes, respectively. (B) A pair of deletions lacking stem III. Arrowheads indicate the positions of two G's derived from the (27-153) deletion. Cells were grown at 30°C and shifted to 42°C. Samples taken at time 0 (30°C) and 3 min after the shift were pulse-labeled with [35S]methionine for 1 min, followed by a 3-min chase. The labeled proteins were analyzed by immunoprecipitation, followed by SDS-PAGE as described in the legend to Fig. 2. Synthesis rates were normalized to that for the wild type (TLF247) labeled at 30°C. The apparently lower extents of induction observed here compared to those shown in Fig. 2B were due to slightly different procedures and not to instability of the fusion proteins examined (data not shown).

View larger version (23K): [in this window] [in a new window]   FIG. 5.   Predicted mRNA secondary structures for some of the deletion derivatives used. Structures predicted for RNA of 150 nt (starting from nt 19 for each; the sequences may include a BamHI junction and part of lacZ) and that have minimum free energy are shown for some representative constructs examined in Fig. 4. Only relevant portions are presented. The initiation codon, region A, and region B are indicated as described in the legend to Fig. 3B. The Shine-Dalgarno sequence is shown by shaded letters. Arrowheads indicate the positions where two G's were replaced in constructing TLF229(stemIII)GG (Fig. 4B). The broken line indicates extra bases inserted during construction (21).

A minimal gene fusion that can respond to heat shock. To construct a minimal fusion with maximum structural similarity to TLF247, the apical portion of the major stem, including seven extra bases of TLF229(27-153), was replaced with part of region B (nt +111 to 127). The resulting fusion, called TLF229(stemIII) (Fig. 5D), lacked the apical half of stem II and all of stem III, in comparison with the parental TLF247 fusion (Fig. 3B). Despite the structural similarity, this construct exhibited extremely low expression at 30°C and was induced little at 42°C (Fig. 4B, line 1). These results were not unexpected, because GF364 lacking all of stem III was unable to be induced upon heat shock, presumably due to the hyperstabilization of stems I and II (36). Thus, to keep the appropriate instability of the RNA secondary structure, the A-13/G-126 mismatch and the U-14·G-125 pairing derived from A-13/G-177 and U-14·G-176, respectively, of TLF247(27-153) (Fig. 5A) were introduced into TLF229(stemIII). The resulting construct, TLF229(stemIII)GG, showed essentially normal thermoregulation, although expression at 30°C was significantly reduced (Fig. 4B, line 2).

	DISCUSSION

Top Abstract Introduction Materials and methods Results Discussion References

The efficiency of translation in E. coli is determined primarily at the stage of initiation, which includes binding of the 30S ribosome to 5' segments (from approximately nt 20 to +15) of mRNA spanning the Shine-Dalgarno sequence and the initiation codon (6). Thus, the secondary structure of such mRNA segments can play an important role in modulating translation efficiency (5). In the case of rpoH, part of the ribosome binding site (nt +1 to 20) including the AUG codon and region A (downstream box) was thought to be masked through the formation of base pairs with the internal region (region B). This idea was initially suggested by computer prediction (21) and subsequently supported by mutational analyses (21, 36) and structural conservation among the rpoH homologs (23). Such a structure seemed most likely to restrict translation by preventing ribosome entry under nonstress conditions. The present results of structure probing of rpoH mRNA directly supported this model (Fig. 3). Based on the structural information, possible roles of each of the major stems that constitute the whole structure were assessed by further deletion analyses.

The structure probing analyses revealed that mutations within stem II affecting translational repression (15A and 15C) affect not only the neighboring structures of stem II but also the structures of stem III (Table 1). The simultaneous recovery of both of these effects of compensatory mutations (15A-124T and 15C-124G) was well correlated with the expression and regulation of fusion proteins in vivo (Fig. 2B). This finding was not unexpected, because some of the partially constitutive mutations previously isolated from GF346 (133A, 136A, and 142A) (36) were actually localized within stem III. All of these results indicated that the stabilities of stems II and III are interdependent and that changes in stem II stability, at least those involving the mutations analyzed in this study, have particularly striking effects on thermoregulation.

The results of deletion analyses indicated that most of stem II (nt +27 to 111) and stem III were not indispensable for thermoregulation (36) (Fig. 4). However, as discussed below, appropriate stability or instability of the mRNA secondary structure was an essential requirement for normal regulation. In the fusion construct TLF247(27-153), which lacked an appreciable portion of the internal segment, part of stem III (nt +165 to 178) was predicted to form several fortuitous base pairings (as well as some mismatches) with part of stem II (nt +12 to 26) (Fig. 5A). Remarkably, the minimal fusion construct TLF229(stemIII)GG, with much greater similarity to the parental TLF247 fusion, had to retain two mismatches (two G's) derived from TLF247(27-153) to be heat inducible (Fig. 4B); a similar construct with the parental sequence but lacking the mismatches [TLF229(stemIII)] failed to show heat induction. In this connection, the inability to respond to heat shock was previously observed when stem III was totally deleted from the GF364 fusion (36). Although stem III was not essential, when it was absent, certain mismatches had to be introduced to the remaining segment of RNA to substitute for its function. In other words, stem III appeared to serve as a "wedge" between stems I and II, conferring appropriate instability to the mRNA secondary structure.

3' Deletions extending into stem IV reduced basal expression significantly and slightly affected heat induction (Fig. 4A, lines 5 and 6). TLF211(27-153) retained intact stem IV, but the sequence immediately downstream at the lacZ junction (BamHI site) was predicted to form base pairings with the Shine-Dalgarno sequence and reduce basal-level expression, as was actually observed (Fig. 4A, line 4), although not as strikingly as in TLF190(27-153) (line 7). These combined results suggested that stem IV was not essential for thermoregulation but would serve to keep the upstream Shine-Dalgarno and adjacent regions "open" for ribosome entry.

The internal deletion TLF247(27-153), like GFR153 studied previously (21), exhibited essentially normal heat induction despite the drastic alteration from the parental TLF247 fusion in the apical (but not the basal) portion of the predicted RNA secondary structure (Fig. 5A). This result indicated that the basal portion containing the translation initiation region (stem I) was most critical for thermoregulation. However, stem I by itself was not sufficient, since TLF190(27-153) containing stem I failed to be heat induced (Fig. 4A, line 7). Also, TLF229(stemIII), which retained intact stem I and part of stem II, was not heat induced (Fig. 4B, line 1). The facts that a drastic alteration in stems II and III did not affect thermoregulation and that the two-G substitution could restore the regulation of TLF229(stemIII) (Fig. 4B, line 2) strongly suggested that the stability of the translation initiation region of rpoH mRNA rather than other structural features was primarily important for thermoregulation. We conclude that there are two major requirements for normal rpoH thermoregulation. First, the translation initiation region (initiation codon plus region A) must be masked through formation of base pairs with part of the internal coding sequence (region B); this factor is crucial for translational repression at a low temperature (30°C). Second, the secondary structure involving the initiation region that includes the Shine-Dalgarno sequence must retain appropriate instability; this factor is essential for heat induction to be observed upon the temperature upshift (42°C).

Besides the mRNA secondary structure, previous results suggested the possible involvement of a specific sequence which may provide a site for protein binding in modulating the heat induction of rpoH translation. This suggestion was based mainly on the noninducible and barely inducible phenotypes of the 15C-124G and 16G-123C mutants, respectively, each containing two compensatory mutations (36). Although we confirmed the results for the latter mutant (16G-123C; data not shown), the 15C-124G mutant actually exhibited slightly reduced but appreciable heat induction (Fig. 2B), eliminating the major basis for suggesting the above possibility. It seemed possible that the subnormal heat induction observed with both of these mutants carrying an alteration in region A (G to C at +15 or C to G at +16) came from the differential effects of decreased complementarity for the anti-downstream box of 16S rRNA (G-15·U to C-15/U or C-16-G to G-16/G) on the translational efficiency at the two temperatures used (30 and 42°C). At present, the involvement of a trans-acting factor(s) in thermoregulation appears unlikely, although it cannot be excluded.

The fact that some of the nucleotides expected to form a stem I structure were modified by chemical probes, albeit weakly (Fig. 3B), suggested that this region was relatively unstable, presumably permitting the limited entry of ribosomes at a low temperature. Moreover, transcription-translation coupling may facilitate a productive interaction between rpoH mRNA and ribosomes because of a delay in forming the stem I structure due to the distance (ca. 180 nt) between the AUG codon and the internal region presumably required for base pairings. In any event, such a dynamic mRNA secondary structure should ensure the production of low but essential basal levels of ³² at physiological temperatures under nonstress conditions. Mutations such as 15A or 15C may decelerate the formation of an inhibitory RNA structure, thereby permitting ribosome entry and constitutively high expression even at low temperatures.

Finally, ^S encoded by the rpoS gene is another global regulator for a set of genes induced at the stationary phase or upon hyperosmotic stress. Interestingly, ^S itself is regulated primarily at the posttranscriptional level, and recent work indicated the involvement of some specific gene products in the translational control of ^S synthesis (13). In addition, the rpoS mRNA secondary structure was suggested to play a regulatory role, although the mechanism remains unknown. Thus, translational control of global transcription factors such as ³² and ^S appears to be mediated by an mRNA secondary structure and confers an efficient means for a rapid response to heat or other stress. The results reported here also raise the intriguing possibility that a 5' portion of the rpoH mRNA secondary structure is involved in direct sensing and responding to high temperatures by enhancing ribosome entry and translation initiation, leading to a rapid increase in the ³² level and the induction of heat shock proteins. Further work is in progress to examine such possibilities.