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PLoS Genet. Oct 2009; 5(10): e1000689.
Published online Oct 16, 2009. doi:  10.1371/journal.pgen.1000689
PMCID: PMC2753651

A Novel Mechanism of Transposon-Mediated Gene Activation

Josep Casadesús, Editor

Abstract

Transposable Insertion Sequences (IS elements) have been shown to provide various benefits to their hosts via gene activation or inactivation under stress conditions by appropriately inserting into specific chromosomal sites. Activation is usually due to derepression or introduction of a complete or partial promoter located within the element. Here we define a novel mechanism of gene activation by the transposon IS5 in Escherichia coli. The glycerol utilization operon, glpFK, that is silent in the absence of the cAMP-Crp complex, is activated by IS5 when inserted upstream of its promoter. High-level expression is nearly constitutive, only mildly dependent on glycerol, glucose, GlpR, and Crp, and allows growth at a rate similar to or more rapid than that of wild-type cells. Expression is from the glpFK promoter and dependent on (1) the DNA phase, (2) integration host factor (IHF), and (3) a short region at the 3′ end of IS5 harboring a permanent bend and an IHF binding site. The lacZYA operon is also subject to such activation in the absence of Crp. Thus, we have defined a novel mechanism of gene activation involving transposon insertion that may be generally applicable to many organisms.

Author Summary

Transposons are “jumping genes” that can move from one location within a genome to another. Insertion of a transponson changes the DNA sequence and therefore gives rise to mutations that can activate or inactivate gene expression. Here, we demonstrate for the first time that one such transposon, Insertion Sequence 5 (IS5), when positioned upstream of a metabolic operon (glpFK) of E. coli, can activate the otherwise cryptic expression of the operon. This effect is due solely to a short region at the 3′ end of IS5 that harbors a permanent bend and an overlapping nucleoid protein binding site, both of which are required for maximal gene expression. We demonstrate the importance of phasing and conclude that DNA looping probably plays a role. We also show that another operon, the E. coli lactose operon (lacZYA), can be similarly activated by IS5. Although this is the first study to show that unique sequences within a transposon are necessary and sufficient to activate a downstream silent promoter, similar mechanisms of gene activation may occur for other operons.

Introduction

Living organisms possess a variety of mutagenic means to generate genetic diversity, and these depend on environmental conditions and genomic composition [1],[2]. One frequently encountered type of mutation results from the insertion of transposable elements, transposons, which when inserted in appropriate locations of the genome, can activate or inactivate critical genes [3],[4]. One transposon-mediated mechanism of gene activation involves the formation of a “hybrid promoter” when a small transposon, an Insertion Sequence (IS) element, inserts into the promoter region. In this case, insertion of an IS element results in placing an outwardly directed −35 hexamer in one of the terminal inverted repeats (IRs) of the transposon at the correct distance from a resident −10 hexamer. Such −35 elements have been observed experimentally in several ISs [5]. Activation can also occur by initiating transcription within the transposon, traversing the terminal IR and reading the gene of interest. This second type of mechanism has been observed for IS3 [6] and IS10 [7].

A distinct type of gene regulation by ISs is illustrated by activation of the normally cryptic β-glucoside (bgl) catabolic operon in E. coli. Activation of this operon can be accomplished in several ways, one of which involves insertion of either IS5 or IS1 upstream or downstream of the promoter [8],[9]. For bgl operon activation, IS5 need not be in a specific position and orientation [9],[10], and the nucleoid structuring protein H-NS is required [11],[12].

The IS5 element has been found to activate the fucAO promoter [13], the flhDC promoter [14], and the ade promoter [15]. In wild type (wt) E. coli cells, expression of the fucAO operon is dependent on FucR, an activator of the fuc genes, and the cyclic AMP receptor protein (Crp). Prolonged incubation of wt cells with L-1,2-propanediol (which does not activate FucR) produced mutants that could grow on this carbon source. These mutants express fucAO independently of FucR and harbor IS5 inserted upstream of the fucAO promoter, always in the same orientation with its ins5A promoter distal to fucA [13]. In the case of flhDC, motility of wt cells on semisolid agar is substantially enhanced when IS5 is inserted at either of two locations (−99.5 and −169.5) upstream of the transcriptional start site. The IS5 orientations proved to be the same, with the ins5A promoter distal to the downstream flhDC promoter [14], as in the case of IS5 insertion in the fucAO promoter. In addition, IS5 has been shown to activate the cryptic ade gene encoding an adenine deaminase that catalyzes deamination of adenine to hypoxanthine in E. coli [15]. In the cases of flhDC and ade, activation is proposed to be due to the relief of HNS-mediated normal repression by IS5 insertion [14],[15] but the mechanism of IS5 activation of the fucAO promoter is unknown [13].

E. coli can use glycerol, glycerol-3-phosphate, or glycerophosphodiesters as sole carbon and energy sources. The loss of Crp abolishes its growth on glycerol. This is due to the fact that expression of one operon in the glp regulon, glpFK, encoding proteins essential for glycerol utilization [16],[17], is strongly dependent on the Crp-cAMP complex (Figure 1) [18],[19]. In addition, glpFK expression is repressed by the binding of GlpR, the glp regulon repressor, to the four operators in the glpFK promoter region (Figure 1) [20]. Repression is relieved in the presence of glycerol-3-phosphate, the inducer of the glp regulon.

Figure 1
Schematic diagram of IS5 and its various regions upstream of the glpFK promoter (PglpFK) region used in this study (A), the 177-bp region (IB) at the 3′ end of IS5 and the glpFK promoter region (B).

Our previous research [21] demonstrated that crp deletion mutants can mutate specifically to utilize glycerol (Glp+). The frequencies of such mutations are enhanced by the presence of glycerol and decreased by GlpR. Of the four GlpR operators (O1-O4) upstream of glpFK, O1 primarily controls mutation rate while O4 specifically controls glpFK expression. All Glp+ mutants contain an IS5 upstream of the glpFK promoter, always in the same position and orientation [21].

Here, we describe a novel mechanism of gene activation due to IS5 insertion upstream of the promoter of the glpFK operon. Activation is so strong that it overcomes the repression resulting from the absence of Crp. A 177-bp fragment at the 3′ end of IS5, proximal to the downstream promoter, is both necessary and sufficient for full activation. Although for activation, IS5 always inserts into the same position upstream of the glpFK promoter, the activating effect is still observed when a 10 bp fragment, but not a 5 bp fragment, is inserted between IS5 and the glpFK promoter. Thus, the active element, encompassing a permanent bend and an IHF binding site, must be present at the correct phase angle relative to the promoter to be effective. Finally, it is shown that in the absence of Crp, the E. coli lactose operon can also be activated by upstream IS5 insertion. These results reveal a novel mechanism of gene activation by insertion sequences.

Results

Effects of IS5 Insertion on Expression of glp Genes in Various Genetic Backgrounds

Using real-time PCR, we determined mRNA levels of the five glp operons comparing crp Glp+ cells (with an IS5 insertion upstream of the glpFK promoter) [21] with parental crp cells. No differences were observed in expression levels of four of the five operons, but the glpFK operon showed a dramatic difference. Figure 2A shows expression of glpFK in wt, crp and crp Glp+ cells. In the absence of glycerol, glpFK expression was >50 fold higher in crp Glp+ cells than in crp cells (see columns 3 and 5 from the left side), showing that the IS5 insertion led to high level expression of this operon. In the presence of glycerol, glpFK expression increased in all cell types examined, but expression was the highest in crp Glp+ cells, about 15-fold higher than in the crp cells incubated under the same conditions. However, the degree of induction by glycerol in crp Glp+ cells was greatly decreased, suggesting that in these cells, repression by GlpR is weak (~2.5 fold, see columns 5 and 6) compared to that in wt cells (>10 fold, see columns 1 and 2).

Figure 2
Real time PCR analysis of glpFK expression (A,B) and determination of glycerol kinase (GlpK) activity (C).

When the glpR gene was deleted from each of these three backgrounds, glycerol induction of glpFK expression was abolished (Figure 2B), indicating that increased glpFK expression in wt, crp and crp Glp+ cells in response to glycerol is solely due to the release of GlpR from the control region of the operon.

We measured in vitro glycerol kinase activity in wt, crp and crp Glp+ cells using [14C]glycerol as substrate. The highest levels of glycerol phosphorylation activity were observed in extracts of crp Glp+ cells cultured in LB medium either with or without glycerol (Figure 2C). Glycerol induction was observed in all three genetic backgrounds, with induction levels similar to those of the mRNA revealed by real-time PCR (see Figure 2A).

To test if IS5 activation of the glpFK promoter (PglpFK) is due to relief of repression by H-NS as observed for the bgl operon [11],[12] and the ade operon [15], we mutated the hns gene in wt, crp and crp Glp+ backgrounds. Using real-time PCR, we found that the hns mutation had only a slight (<0.2 fold) effect on glpFK expression in all three genetic backgrounds compared to the same cells without the hns mutation (Figure S1), indicating that IS5 activation of PglpFK in the absence of Crp is not due to relief of H-NS mediated repression.

Determination of the Start Site of glpFK Transcription in crp Glp+ Mutants

To determine if the presence of the IS5 element provides a new promoter driving glpFK transcription, we measured the transcriptional initiation site of the operon using RNA ligase mediated RT-PCR. The total RNA was treated with tobacco acid pyrophosphatase (TAP) prior to cDNA synthesis. The 5′-end region of the glpFK cDNA was amplified using a pair of primers (Table S2), one (PglpFK-extn-F) binding to the adaptor sequence and the other (PglpFK-extn-R) binding to a region between 115th and 137th nucleotides downstream of the glpF start codon. Two PCR products were obtained for both the wild type and the crp Glp+ strain (Figure 3A). Using PglpFK-extn-R as primer, DNA sequencing showed that the larger product was non-specific; the smaller one was the 5′-end region of the glpFK cDNA product (Figure 3B). The junction was found to correspond precisely to the 5′ end mapped by primer extension (see Figure 1B) [18]. When the total RNA was not treated with TAP, only the nonspecific PCR product was obtained (see Figure 3A) for both the wild type and the crp Glp+ strains. Activation of transcription by IS5 in crp Glp+ cells is therefore driven by the native glpFK promoter. The start site was the same with or without glycerol (1%) in the growth medium.

Figure 3
Analysis of the 5′ end of the glpFK message.

Effects of Different Regions within IS5 on glpFK Promoter Activity

Using chromosomal lacZ fusions, we examined the effect of IS5 and different regions within IS5 on PglpFK activity (Figure 1A and Figure 4A). Consistent with the RT-PCR results, the presence of IS5 upstream of PglpFK (IS5:PglpFK) in crp cells dramatically increased the activity of the promoter regardless of the medium used. Both promoter-less IS5 (P-less IS5, in which the 98 bp 5′ end region containing the promoter of the transposase gene was deleted), and the 177 bp 3′ end region (called “Internal Bend”, IB) of IS5 activated PglpFK in crp cells to an extent comparable to that observed with the intact IS5. However, the 130 bp 3′ end region of IS5 (i.e., IB with 47 nucleotides removed from the 5′ end) activated the promoter about 40% less efficiently than the 177 bp IB region (data not shown, see below for explanation).

Figure 4
Control of glpFK operon promoter activity.

Addition of glycerol to LB medium further increased the promoter activity, in agreement with the conclusion that GlpR weakly decreased IS5:PglpFK activity. The increased level (~1.5 fold) of PglpFK activity caused by the presence of glycerol in a crp genetic background, measured by β-galactosidase activity in a glpF-lacZ fusion strain, was lower than that observed (~2.5 fold) for glpFK mRNA in a crp Glp+ background (Figure 2A). Such a difference may be due to the fact that crp Glp+ cells transport and subsequently phosphorylate glycerol more rapidly than crp cells. Addition of glucose to the medium slightly reduced the activities of the promoters tested, showing that the strong catabolite repression observed in the wild type strain was largely abolished. Further experiments reported below confirmed and extended this conclusion.

IB:PglpFK-lacZ activity was subsequently characterized in other genetic backgrounds. High levels of β-galactosidase activity were observed for wt, crp, glpR and crp glpR genetic backgrounds with cells grown in LB ± glycerol or ± glucose (Figure 4B). Similar levels of promoter activity were observed in wt and crp cells in the absence of glycerol, suggesting that the Crp protein does not appreciably influence IB:PglpFK activity. Addition of glycerol increased the overall IB:PglpFK activity by ~2 fold in wt cells (column 1 and column 5 in Figure 4B) and ~1.3 fold in crp cells (columns 2 and 6 in Figure 4B), while addition of glucose slightly decreased it. Higher promoter activities were detected in glpR and crp glpR cells than in wt and crp cells, respectively, in the absence of glycerol. Addition of glycerol did not further increase these activities in cells containing the glpR mutation (columns 4 and 8). However, in the absence of GlpR, deletion of the crp gene reduced the activating effect of IB by about 20% (Figure 4B). It is possible that Crp positively influences the expression of a gene encoding a protein such as IHF, which is required for full activation of PglpFK by IB. The role of Crp in IB activation of PglpFK thus appears to be minimal, but it could be indirect and complex.

As a control, a 178 bp internal fragment of IS5 (nucleotides 226 to 403 from its 5′ end), similar in length to that of IB (177 bps), was substituted for IB in IB:PglpFK, and the activity of the construct (178bp:PglpFK) was determined in crp cells. β-Galactosidase activity was not increased compared to PglpFK alone (Figure 4A). Another control showed that IB alone in front of lacZ (IB-lacZ) had no promoter activity regardless of the medium used (Figure 4A). The results presented in Figure 4A and 4B together show that the stimulation of PglpFK activity mediated by IS5 insertion is due to the IB segment (i.e., the 177 bases located at the 3′-end of IS5). Such activation is so strong that (1) Crp is not required and (2) GlpR only weakly represses.

To further show that the transposase, encoded by ins5A (981 bp) [22],[23], is not involved in IS5 activation, IS5:PglpFK-lacZ, promoter-less IS5:PglpFK-lacZ, IB:PglpFK-lacZ, PglpFK-lacZ and 178 bp:PglpFK-lacZ fusions were individually moved to a crp mutant background of E. coli strain B which lacks IS5 [24]. Similar to BW25113 crp cells, IS5 and IB equally elevated promoter activity in strain B crp cells compared to PglpFK alone (Figure S2). The 178-bp IS5 internal fragment was unable to activate PglpFK in these IS5-free crp cells. This experiment clearly demonstrates that the transposase does not contribute to IS5 activation of PglpFK. It is IB, the 3′ end region of IS5 that activates PglpFK in the absence of Crp.

Effect of IB Positioning on the Activity of IB:PglpFK

To determine if IB activation of PglpFK is DNA phase dependent, two oligonucleotide sequences (5 bp and 10 bp) were individually inserted at −117.5 (relative to +1 of PglpFK) between IB and PglpFK (Figure 1). As shown in Figure 4C, insertion of a 5 bp nucleotide sequence almost completely abolished promoter activity in both crp and crp glpR cells although insertion of a 10 bp oligonucleotide sequence only slightly reduced promoter activity. These results indicate that the proper positioning of the upstream IB relative to PglpFK is essential for full promoter activation in crp cells. They are consistent with a requirement for a 10 bp periodicity in the position of the insert for strong stimulation as expected for B-DNA. The latter implies the involvement of DNA structure (e.g., bending or looping) in PglpFK activation by IB. These results were obtained for both IB and IS5 (data not shown).

Requirement of IHF and the IHF Binding Site in IB for Full Activation of PglpFK

As demonstrated above, the IB segment has the same ability as the intact IS5 to activate PglpFK in the crp genetic background. A putative IHF binding site is present in the middle of IB [25]. To determine if the host IHF protein plays a role in activation of PglpFK, we generated a null ihfA mutant in wt and crp Glp+ backgrounds. These mutant strains were compared for growth in M9 minimal medium with glycerol as the sole carbon source (Figure 5A). No obvious difference in growth was found between wt and ihfA mutant cells. However, growth of crp Glp+ cells was substantially reduced by the ihfA mutation.

Figure 5
Dependency of glpFK promoter activation on IHF binding to IB (A–C) as well as the A-tract-promoting permanent bend in IB (D).

To determine the effect of the loss of IHF on transcription of IB:PglpFK, an IB:PglpFK-lacZ fusion was transferred into a crp ihfA double mutant genetic background by P1 transduction. β-Galactosidase assays were performed after growing cells in LB media with or without glycerol or glucose. As shown in Figure 5B, the activity of IB:PglpFK was reduced ~60% by the loss of IHF. Similar results were obtained when M9 + casamino acids + glucose medium was used (data not shown). These results are consistent with the growth data described above and indicate that IHF is required for maximal activation of PglpFK by the IB segment.

To determine if the putative IHF binding site in IB is responsible for IHF-mediated activation, we mutated the site as follows (see Figure 1A): (1) TCAA (−218 to −221, relative to +1 of PglpFK) to GTCT (single mutation) and (2) TCAA to GTCT together with TT (−212 to −213) to GC (double mutations). The activities of the IB:PglpFK constructs with any one of these mutated IHF binding sites were determined using transcriptional lacZ fusions (Figure 5C). When cells were grown in minimal or LB medium, these alterations resulted in 50–60% reductions in the activity of IB:PglpFK compared to the parental construct. These results clearly indicate that the IHF binding site in the middle of IB is required for activation of PglpFK by the host IHF protein.

To determine if an IHF binding site alone is capable of stimulating the activity of the glpFK promoter, an IHF binding site was introduced upstream of PglpFK by changing gccttgcagatta (−222 to −210 relative to +1 of PglpFK) to aatcaagcagtta (Figure S3A). The newly created site was at the same distance as that of the IHF site in IB:PglpFK relative to the promoter (Figure 1B and Figure S3A). Using a chromosomal lacZ fusion, the activity of PglpFK containing this upstream IHF binding site was examined in wt and crp cells grown in LB medium. The promoter activity was increased by ~40% in wt cells but was not changed in crp cells (Figure S3B). These results show that (1) IHF can bind to the created binding site; (2) the binding of IHF is capable of partially stimulating PglpFK activity but only in the presence of Crp; and (3) IHF stimulation of IB:PglpFK in the absence of Crp is dependent not only on the IHF binding site present in IB but also on the adjacent sequences (e.g., the A-tracts) surrounding the site.

Dependency of glpFK Operon Activation on the Permanent Bend in IS5

A characteristic of a permanent DNA bend is the presence of in-phase A-tracts of 3–6 tandem As. The permanent bend in the IB region of IS5 has been shown to be one of the largest bend angles in the E. coli chromosome [25].

To examine the dependency of glpFK expression in a crp Glp+ genetic background on the A-tracts in the IB region of IS5, three different sets of mutated A-tracts were constructed by changing specific As in these tracts to Cs or Gs (see Figure 1A). The mutated strains were then examined for expression using a PglpFK-lacZ reporter gene fusion. All three sets of A-tract mutations lowered the expression level. However, mutating the five upstream A-tracts (A-tracts 4–8, see Figure 1A) had a minimal effect on expression (Figure 5D). Mutation of A-tract 3 only (A-tract 3) also had a minimal effect. However, mutational alteration of three consecutive A-tracts in the downstream region (A-tracts 1–3) had a dramatic effect on gene expression. From these observations and those reported in the previous section, we conclude that (i) the downstream permanent bend is important for gene activation, (ii) the upstream A-tract region is of minimal importance for gene expression, and (iii) IHF binding and the three downstream A-tracts are roughly of equal importance. We can therefore account for IS5 activation of glpFK operon expression by IHF binding and the downstream A-tracts which apparently activate gene expression in an additive fashion, probably by bending the DNA.

To confirm the importance of both the A-tracts and the IHF binding site in IB to IS5 activation of PglpFK, the IB:PglpFK-lacZ fusion containing mutations in A-tracts 1–3 in IB was transferred into the ihfA genetic background. As shown in Figure S4, promoter activity was completely abolished. This experiment therefore shows that the activating effects of IHF and the downstream permanent bend are responsible for promoter activation, and that these two effects are additive.

As shown above, when the upstream 47 bps in the 177 bp fragment (IB) were deleted, 60% of the activation was retained. When the upstream A-tracts were disrupted by point mutations, 85% of the activation was retained (Figure 5D). There may therefore be a mild dependency of activation on these upstream sequences, but we do not know exactly why this difference was observed. Possibly, deletion of this upstream region has an indirect contextual effect on the downstream region that plays a dominant role in glpFK promoter activation.

Effects of IS5 and IB on the Activity of the lacZYA Promoter (Plac)

To determine if IB can activate a different Crp-dependent promoter in a crp genetic background, IB was placed at positions −126.5 (the same relative position as in IB:PglpFK) and −178.5 (relative to +1 of Plac) upstream of Plac, yielding IB:Plac and IB:Plac', respectively. These two sites differ by 22 bps, are therefore should be in phase. The difference in activation of Plac would presumably reflect the distance from the activated promoter.

Using chromosomal lacZ fusions, the activities of these constructs were examined in both crp and crp lacI cells grown in M9 medium + 0.66% casamino acids +1% glucose (Figure 6A). In the absence of IPTG, no appreciable activity was observed for Plac with or without the upstream IB sequence in crp cells (columns 1–3 of Figure 6A). However, in the presence of IPTG, IB increased the Plac activity 8 fold when it was located at −126.5, and 2 fold when it was located at −178.5 compared to Plac alone (columns 7–9 of Figure 6A). These two positions are in phase assuming 10.5 bp per turn in DNA. We also measured the activities of IB:Plac and IB:Plac' in crp lacI double mutant cells. As expected, regardless of the presence of IPTG, they behaved similarly as in crp cells with IPTG (i.e., 8 and 2 fold increased activation for IB:Plac and IB:Plac', respectively). The entire IS5 element showed the same ability as the IB element to activate Plac (data not shown). These results indicate that (i) IS5 or IB can at least partially replace the function of Crp in activating Plac; (ii) a proper location of these fragments is important for activation of gene expression in the absence of Crp; and (iii) in contrast to the glpFK system, activation is fully blocked by operator-bound LacI.

Figure 6
Effects of IB and its location on the activity of the lacZYA promoter (Plac).

We further measured IB effects on Plac activity in wild type (crp+) cells grown in the same M9 minimal medium as above. In the absence of IPTG, the activities of Plac with or without the upstream IB were extremely low (20 Miller units or less) (Columns 1, 3 and 4 of Figure 6B). In the presence of IPTG, IB increased the lac promoter activity ~2.5 fold when it was located at −126.5 compared to the lac promoter alone. No increased Plac activity was observed when IB was located at −178.5 upstream of the promoter. These results indicate that (i) LacI still blocks the activation of Plac by both Crp and IB, and (ii) when present at an appropriate position, IB is still capable of enhancing the activity of Plac in the presence of Crp. In other words, IB and Crp activate Plac in an additive fashion. This is different from IB activation of PglpFK, in which case, the presence of Crp did not further elevate the activity of IB:PglpFK (see Figure 4B).

Discussion

We have demonstrated that a transposon, IS5, is capable of activation of the glpFK operon, rendering E. coli cells capable of utilizing glycerol in the absence of Crp. Transposable elements have been found to activate transcription of adjacent genes by introducing complete or partial promoters located within the element or by disrupting or displacing a negative element that normally blocks transcription [3],[4]. The mechanism of glpFK activation by IS5 is distinct from these reported mechanisms. In this case, a part of IS5, which is proximal to the adjacent gene and harbors unique sequences (A-tracts and an IHF binding site), can functionally replace Crp and directly activate the native downstream promoter.

Prior to the work reported here, the best-characterized example of transposon-mediated gene activation was of the β-glucoside (bgl) operon in E. coli (see Introduction) [8][12]. This system shows the following characteristics: 1) The bgl operon is not active in wild-type E. coli. 2) Either IS1 or IS5 can activate bgl operon expression. 3) When it is activated, bgl expression is subject to catabolite control by Crp as well as inducer sensitivity by an anti-termination mechanism. 4) Activation by the IS element occurs by an enhancer-type mechanism. 5) The IS element can activate when either upstream or downstream of the promoter, and in either orientation. 6) Activation is at least partially dependent on the IS-encoded transposase. 7) Activation is dependent on relief of repression by H-NS. 8) Although the most frequent mechanism for activation involves insertion sequence elements, activation can also be caused by mutations in gyrA or gyrB [26], hns [27], bglJ [28],[29], leuO [30] or the Crp binding site of the bgl promoter [31],[32].

In all of these respects, activation of glpFK appears to differ from that of the bgl operon: 1) The glpFK operon is active in wild-type E. coli. 2) Only IS5 has been observed to activate glpFK operon expression in a crp genetic background. 3) Once activated, the operon is expressed independently of Crp and largely independently of the glp regulon repressor, GlpR. 4) There is no evidence that IS5 acts on PglpFK by an enhancer-type mechanism. 5) Only a single site of insertion and only one orientation were demonstrated, and this site proved to be the IS5 tetranucleotide target sequence, CTAA, located at a specific position upstream of the promoter. 6) Activation is independent of the IS5-encoded transposase. 7) IHF, but not H-NS, is required for maximal gene activation. 8) Except for IS5 insertion, no other mutations have been identified to account for activation of glpFK expression.

We identified a short sequence in IS5 (IB) that is fully responsible for PglpFK activation. This sequence includes a permanent bend and an IHF binding site. An IHF binding site has been found to be present in the ends of the IS1 element, but several lines of evidence have shown that this IHF site does not play a role in gene activation although it bends the DNA [33]. In the present study, we showed that the IHF binding site in IS5 plays an important role since an ihfA null mutation or alteration of the IHF binding site partially abolished activation to the same degree. No function for the IB region had been recognized prior to our studies. It may have evolved specifically for the purpose of gene activation, for another unrecognized purpose, or for both.

We further showed that DNA phasing is important since the insertion of 5 bps (but not 10 bps) between the activating element and PglpFK abolished activation. Preliminary evidence suggested that the C-terminal domain of the α-subunit of RNA polymerase is not required for activation (unpublished results), but a DNA looping mechanism is nevertheless proposed.

The activating IB region contains as many as 10 A-tracts, which in general can induce permanent bends in DNA (see Figure 5D) [25],[34] and can increase promoter activity [35],[36]. In one case, transcriptional activation involves binding of the DNA to the C-terminal domain of the RNA polymerase α-subunit (35). In view of our results, it seems likely that the permanent bend in the downstream region of IS5 together with bound IHF activates glpFK promoter activity at least in part by bending the upstream DNA. A direct interaction of IHF with the transcriptional initiation complex is possible [37].

Although this is the first study to show that unique sequences inside a transposon are necessary and sufficient to activate a downstream silent promoter, similar mechanisms of gene activation may occur for other operons (see Figure 6 and unpublished results). These include the lacZYA, fucAO and flhDC operons [13],[14 and observations reported here]. On the other hand, the isolation and analysis of mutations that allow E. coli crp mutants to grow on several other Crp-dependent carbon sources [38] indicate that IS-mediated gene activation is not the only mechanism available to E. coli. We propose that IS5 insertion under the control of a host regulatory protein represents just one of many mechanisms of operon adaptive activation that will prove to occur under stressful conditions.

Materials and Methods

Bacterial Strains and Growth Conditions

Strains and oligonucleotides used in this study are described in Table S1 and Table S2, respectively. The crp, glpR, crp Glp+ and crp glpR Glp+ mutants, derived from E. coli K-12 strain BW25113, were constructed previously [21]. The crp lacI double mutant was made by transferring the lacI insertion mutation from MG1655 [39] to a BW25115 crp deletion background using P1 transduction. The hns and ihfA isogenic deletion mutant was derived from the same wt strain BW25113 using the method of Datsenko and Wanner [40]. Double and triple mutants, crp hns, crp Glp+ hns, crp ihfA and crp Glp+ ihfA, were made by P1 transduction. The detailed procedures for generating single or double mutants are described in the reference 21. Strain BW25113 is deleted for the lacZ gene and the araBAD operon encoding proteins required for L-arabinose metabolism [40]. All mutants were verified by PCR. The strains were cultured in LB or minimal M9 media with various carbon sources at 37°C or 30°C. When appropriate, kanamycin (Km; 25 µg/ml), or ampicillin (Ap; 100 µg/ml) was added to the media.

Glycerol Kinase Activity Assay

The activity of glycerol kinase encoded by glpK was determined using [1,3-14C]glycerol as substrate. Cells were cultured in LB with or without 1% glycerol, and cellular extracts were prepared using a French press and the subsequent ultracentrifugation. Glycerol phosphorylation by GlpK in the extracts was quantitated as described previously [41].

Site-Directed Mutagenesis

Using the quick-change site-directed mutagenesis kit (Stratagene), the following modifications were made in IS5, its IB region or the glpFK promoter region: (i) removal of the EcoRI site in IS5 by changing A (135 bp from the 5′ end) to G; (ii) insertion of a 5-bp (tacct) or a 10-bp (taccttacct) oligonucleotide at −117.5 (relative to +1 of PglpFK) in the IB:PglpFK junctional region (see Figure 1B); (iii) mutation of the IHF binding site in IB by changing TCAA to GTCT (−221 to −218, relative to +1 of PglpFK) and TT (−213 to −212, relative to +1 of PglpFK) to GC (see Figure 1B); iv) mutations of individual or multiple A-tracts in IB by changing one or two As to Cs or Gs (see Figure 1B). All the mutation primers are listed in Table S2. Sequence alterations were confirmed by DNA sequencing.

Real Time (RT) PCR

RT-PCR was performed as described previously [42]. Cells were grown in LB with or without 1% glycerol. Total RNA was prepared using an EZgene™ RNA purification kit (Biomiga). The contaminated chromosomal DNA in RNA samples was removed by DNase I treatment. cDNAs were synthesized using an Invitrogen superscript first-strand synthesis kit. polA, encoding DNA polymerase I, was included as an internal control [43]. Primers used for RT-PCR are listed in Table S2. RT-PCR was carried out with a LightCycler instrument (Roche).

Chromosomal lacZ Fusions and β-Galactosidase Assays

The glpFK promoter region (−203 to +67 relative to the transcriptional start site), with or without the upstream IS5 element or part of the IS5 element, was PCR amplified from the chromosome of crp or crp Glp+ cells. The PCR products were digested with BamHI and EcoRI, gel purified using an EZgene™ gel purification kit (Biomiga), and then ligated into the same sites of pRS551 [44]. Transcriptional lacZ fusions present in the pRS551 plasmids were integrated into the lambda attachment site (attB) in the E. coli chromosome using the method of Simons et al. [44]. P1 transduction was used to transfer a chromosomal promoter:lacZ fusion from one strain to another strain.

To add an IHF binding site upstream of the glpFK promoter at the same relative distance as in IB:PglpFK, a separate PglpFK (−220 to +67) was amplified from the wt chromosome using primers PglpFK_IHF-F and PglpFK-R1 (Table S2). An IHF binding site (aatcaagcagtta) was present at the 5′ end of primer PglpFK_IHF-F. The PCR products that contained the IHF binding site were fused to a promoter-less lacZ gene, and the resultant transcriptional promoter:lacZ fusion was moved to the chromosome as described above (see Figure S3).

To make chromosomal Plac-lacZ, PlacZYA (−126 to +38 or −178 to +38) was first cloned into the BamHI and EcoRI sites of pRS551. The entire IS5 or IB was inserted into the BamHI site of the plasmid so that IS5 or IB was located at −126.5 or −178.5, relative to +1 of PlacZYA. The fusions of Plac with or without IS5 or IB to lacZ were integrated to the chromosome of crp cells. Primers used for RT-PCR and lacZ fusion construction are listed in Table S2.

β-Galactosidase assays, conducted after growth in either LB or M9 minimal media ± 1% glycerol, 1% glucose or 0.66% casamino acids (CAA), were as described by Miller [45]. CAA was added to improve growth of crp cells in minimal media.

RNA Ligase Mediated PCR

RNA ligase mediated PCR was used to determine the transcriptional start site of the glpFK operon as described by Bensing et al. [46]. Cells were grown in LB with or without 1% glycerol. The total RNA was prepared using a Biomiga RNA purification kit and treated with or without tobacco acid pyrophosphatase (TAP). The RNA oligonucleotide adaptor (Table S2) was ligated to all RNAs, and the 5′-end of the glpFK cDNA was synthesized using an oligonucleotide (PglpFK-extn-R) complementary to nucleotides 118–139 (Table S2) downstream of the ATG start codon. cDNA was amplified using primers PglpFK-extn-F and PglpFK-extn-R, and the PCR product was sequenced using the same primer (PglpFK-extn-R) as for cDNA synthesis. The transcriptional start site, i.e., the junction between the cDNA and the RNA oligonucleotide, was determined by sequencing.

Supporting Information

Figure S1

Real-time PCR analysis of effects of the hns mutation on glpFK expression in wt, crp and crp Glp+ backgrounds. Cells were grown in LB liquid medium.

(0.10 MB TIF)

Figure S2

Effects of IS5 and various regions within IS5 on expression of the downstream glpFK promoter in crp cells lacking IS5. ‘IS’, ‘Pless’, ‘IB’, ‘none’, and ‘178’, refer to transcriptional lacZ fusions for IS5:PglpFK, promoter-less IS5:PglpFK, IB:PglpFK, native PglpFK, and 178bp:PglpFK, respectively (see Figure 1A). E. coli strain B has been reported to lack IS5 in its genome [24]. The crp mutation was transferred to strain B by P1 transduction. The promoter:lacZ fusions described above were individually transferred to strain B crp cells from BW25113 by P1 transduction. For β-galactosidase assays, E. coli strain B crp cells containing these lacZ fusion constructs were grown in LB with shaking.

(0.12 MB TIF)

Figure S3

Effect of addition of an IHF binding site upstream of PglpFK on promoter activity. (A) The glpFK promoter region showing that an IHF binding site is added upstream of PglpFK by changing gccttgcagatta (−222 to −210) to aatcaagcagtta. The newly added IHF binding site is located at the same relative distance as in IB:PglpFK. (B) Effect of the added IHF site on PglpFK activity in wt and crp cells grown in LB medium. PglpFK and PglpFK_IHF refer to the transcriptional lacZ fusions for native PglpFK and the same promoter with an upstream IHF binding site, respectively.

(0.37 MB TIF)

Figure S4

Effect of A-tract mutations in IB on glpFK promoter activity in the ihfA genetic background. The IB:PglpFK-lacZ fusion with or without mutations in A-tracts 1–3 in IB was transferred into the crp ihfA double genetic background. The cells were cultured in LB medium.

(0.12 MB TIF)

Table S1

Strains used in this study.

(0.06 MB DOC)

Table S2

Oligonucleotides used in this study.

(0.08 MB DOC)

Acknowledgments

We thank Drs. Barbara Wright and Karin Schnetz for critically reviewing this manuscript and Drs. Terry Hwa and David Meyer for helpful discussions.

Footnotes

The authors have declared that no competing interests exist.

This work was supported by NIH grants GM 64368 and GM 077402. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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