Atypical Role for PhoU in Mutagenic Break Repair under Stress in Escherichia coli.

Mechanisms of mutagenesis activated by stress responses drive pathogen/host adaptation, antibiotic and anti-fungal-drug resistance, and perhaps much of evolution generally. In Escherichia coli, repair of double-strand breaks (DSBs) by homologous recombination is high fidelity in unstressed cells, but switches to a mutagenic mode using error-prone DNA polymerases when the both the SOS and general (σS) stress responses are activated. Additionally, the σE response promotes spontaneous DNA breakage that leads to mutagenic break repair (MBR). We identified the regulatory protein PhoU in a genetic screen for functions required for MBR. PhoU negatively regulates the phosphate-transport and utilization (Pho) regulon when phosphate is in excess, including the PstB and PstC subunits of the phosphate-specific ABC transporter PstSCAB. Here, we characterize the PhoU mutation-promoting role. First, some mutations that affect phosphate transport and Pho transcriptional regulation decrease mutagenesis. Second, the mutagenesis and regulon-expression phenotypes do not correspond, revealing an apparent new function(s) for PhoU. Third, the PhoU mutagenic role is not via activation of the σS, SOS or σE responses, because mutations (or DSBs) that restore mutagenesis to cells defective in these stress responses do not restore mutagenesis to phoU cells. Fourth, the mutagenesis defect in phoU-mutant cells is partially restored by deletion of arcA, a gene normally repressed by PhoU, implying that a gene(s) repressed by ArcA promotes mutagenic break repair. The data show a new role for PhoU in regulation, and a new regulatory branch of the stress-response signaling web that activates mutagenic break repair in E. coli.

Introduction

Bacterial, yeast and human cells generate mutations under growth-limiting stress by mutation mechanisms activated by stress responses [1-3]. These mechanisms increase genetic diversity, potentially accelerating adaptation, specifically when cells are maladapted to their environment. Although mutations can be deleterious, the adaptive value of mutagenesis under stress to bacterial populations is supported by mathematical modeling [4,5]. Various stress-induced mutagenesis mechanisms have been described in bacteria [1,2,6-8], yeast [9], and human cancer cells [3], the latter induced by hypoxic stress responses. Stress-induced mutagenesis mechanisms are induced in response to antibiotics [10,11] and anti-fungal drugs [12]. These various mechanisms produce base substitutions, and small insertions and deletions (indels), transpositions, gross chromosomal rearrangements, copy-number alterations and aneuploidy (above and [13]). Mechanisms of stress-induced mutagenesis are important to evolution of microbial pathogens (to drug resistance, increased virulence, escape of immune surveillance, for example) and also because of the mechanistic parallels to mutation in human cells, which pertain to oncogenesis, cancer progression, and resistance to chemotherapeutic agents [14].

In Escherichia coli, repair of DNA double-strand breaks by homologous recombination is non-mutagenic in unstressed cells, but under stress, switches to a mutagenic mode activated by stress responses [2,15,16]. Mutagenic break repair (MBR) is therefore a mechanism of stress-induced mutagenesis. MBR requires proteins that repair double-strand breaks (DSBs) via homologous recombination: RecA, RecBC and RuvABC, as well as error-prone DNA polymerase (Pol) IV (DinB), and to lesser extents Pols II and V, and activation of the SOS DNA-damage response, the σS-controlled general/starvation stress-response, and the σE membrane-protein-stress response [2]. The membrane-protein-stress response promotes spontaneous DNA breakage in some DNA regions [17]. The SOS response is activated by DSBs and promotes mutagenesis by upregulation of DNA polymerases (Pols) IV and V. Break repair nevertheless remains non-mutagenic unless the σS response is also activated either by starvation (and presumably other inducers such as antibiotics [11]) or artificially. The general/σS stress response licenses the use of Pols IV, II and V in DSB repair by an as yet unknown mechanism, and thus executes the switch to mutagenic repair under stress in plasmids [15] and chromosomes of plasmid-free cells [16]. The MBR mechanism is supported by a 93-gene network, more than half of which functions in sensing stress and signal transduction that ultimately activates the σS, σE, and SOS responses, which allow mutagenesis [18].

We developed a genetic screen for MBR-deficient mutants, screened transposon insertion libraries, and identified a network of 93 genes that contribute to MBR [18]. We focus here on mutations that affect PhoU, a regulator of the PhoBR phosphate utilization regulon. The PhoBR (hereafter termed Pho) regulon is induced in response to phosphate limitation, but also functions in transport of inorganic phosphate (Pi) when Pi is in excess [19] and includes a large number of genes involved in transporting and catabolizing phosphate-containing compounds (reviewed by [20]) (Fig 1). PhoB, a response regulator, and PhoR, the membrane-bound sensor-kinase, comprise a two-component regulatory system that activates the Pho regulon, whereas PhoU is a poorly understood negative regulator of the Pho regulon. Genetic studies indicate that PhoB activity is repressed by the combined action of PhoR, PhoU, and the PstSCAB phosphate transport system in the presence of high extracellular phosphate concentrations [20] (Fig 1). Mutations in phoU, phoR, or pstSCAB result in de-repression of the regulon. These and other data have led to the proposal that the PstSCAB Pi transporter, PhoR, and PhoU, may form a chaperone-like signaling complex [19] at the membrane that inhibits PhoB-dependent transcription [20,21] (Fig 1).

Fig 1

Model of regulation of the Pho regulon.

Figure based on conclusions, models and interpretations of Hsieh and Wanner [19].

Transposon insertions in phoU isolated in our screen cause a dramatic decrease in stress-induced MBR, and transposon insertions in pstB and pstC cause less severe but significant decreases in mutation, leading us to examine the role of the Pho regulon in stress-induced mutagenesis. We report that defects in phosphate transport and regulation can have both mild and dramatic effects on MBR uncorrelated with their known phosphate-regulatory roles.

Materials and Methods

Bacterial strains and growth conditions

Strains and plasmids used are listed in Table 1. Standard genetic techniques were used in strain construction [22]. All M9 minimal media [22] had carbon sources added at 0.1% and thiamine (vitamin B1) at 10 μg/ml. Antibiotic and other additives were used at the following final concentrations: chloramphenicol (Cam), 25 μg/ml; kanamycin (Kan), 50 μg/ml; tetracycline, 10 μg/ml; rifampicin, 100 μg/ml; 5-bromo-4-chloro-3-indolyl-phosphate-p-toluidine (XP), 4 μg/ml; 5-bromo-4-chloro-3-indolyl-β-D-galactoside (X-gal), 40 μg/ml; sodium citrate, 20 mM. The presence of pst and pho alleles that affect Pho-regulon expression were confirmed using Pho indicator plates [22] which contain the dye XP, a chromogenic substrate for alkaline phosphatase. Pho-de-repressed strains are dark blue on high-phosphate XP plates, whereas Pho-repressed strains are light blue to white [23].

Table 1

Escherichia coli strains and plasmids used.

Strain or plasmid	Relevant genotype	Reference or source
ANCH1	Δ(phoB-phoR)kmR	[58]
BW3904	phoU35	[40]
BW7150	ilvY864::Tn10	B. Wanner
BW13713	phoR68(Oc)	[59]
BW13989	proC::Tn5-132	[23]
BW17335	Δ(pstSCAB-phoU)560::Kan	[23]
CAG18599	ilvD3164::Tn10Kan	E. coli Genetic Stock Center
FC29	Δ(lac-proB)XIII ara thi [F´ proAB + Δ(lacI-lacZ)]	[32]
FC40	Δ(lac-proB) XIII ara thi RifR [F´ proAB + lacI33-lacZ]	[32]
SMR828	Δ(lac-proB) XIII ara thi zaj-3053::Tn10	[28]
SMR3770 a	FC40 [F’ zah-281::Tn10 lacI33-lacZ] a	[60]
SMR3855-3856 b , SMR3858-3859 b	FC40 Lac+ (day 5)	Independent isolates [41]
SMR4045	ilvY864::Tn10 phoU35	P1(BW7150) x BW3904
SMR4047	FC40 Δ(pstSCAB-phoU)560::Kan	P1(BW17335) x FC40
SMR4056	FC40 ilvY864::Tn10 phoU35	P1(SMR4045) x FC40
SMR4058	proC::Tn5-132 phoR68	P1(BW13989) x BW13713
SMR4059	FC40 phoU35	P1(FC40) x SMR4056
SMR4060	FC40 proC::Tn5-132 phoR68	P1(SMR4058) x FC40
SMR4061	FC40 phoR68	P1(FC40) x SMR4060
SMR4562	Δ(lac-proB) XIII ara thi RifR [F´ proAB + lacI33-lacZ]	Independent construction of FC40 [44]
SMR4604	SMR4562 Δ(phoB-phoR)kmR	P1(ANCH1) x SMR4562
SMR4623	SMR4562 ilvD3164::Tn10Kan	P1(CAG18599) x SMR4562
SMR4953	FC40 phoU83::Tn10dCam	This work, Results
SMR4954	FC40 phoU84::Tn10dCam	This work, Results
SMR5235	SMR4562 phoU83::Tn10dCam Δ(phoB-phoR)kmR	P1(SMR4953) x SMR4604
SMR5443	SMR4562 Δ(phoB-phoR)kmR proC::Tn5-132	P1(BW13989) x SMR4604
SMR5846	SMR4562 Δ(pstSCAB-phoU)560::Kan Δ(phoB-phoR)kmR proC::Tn5-132	P1(SMR4047) x SMR5443
SMR5860	SMR4562 Δ(pstSCAB-phoU)560::Kan Δ(phoB-phoR)kmR	P1(FC40) xSMR5846
SMR6280	FC40 ΔaraBAD567 Δattλ::PBADI-SceI [F' mhpA32::miniTn7Kan(I-SceI site)]	[15]
SMR6281	FC40 ΔaraBAD567 Δattλ::PBAD [F' mhpA32::miniTn7Kan(I-SceI site)]	[15]
SMR6758	SMR4562 ΔpstS40::Kan	SMR4562[pKD46] x short homology from pKD13 using primers ΔpstS1 and ΔpstS2
SMR6759	SMR4562 ΔpstS41	SMR6758 with KanR flipped out using pCP20
SMR6760	SMR4562 ΔpstS41 Δ(phoB-phoR)kmR	P1(ANCH1) x SMR6759
SMR6761	SMR4562 phoU83::Tn10dCam ΔpstS40::Kan	P1(SMR4953) x SMR6758
SMR6762	SMR4562 phoU83::Tn10dCam ΔpstS41	SMR6761 with KanR flipped out using pCP20
SMR7351	SMR4562 phoU83::Tn10dCam ΔpstS41 Δ(phoB-phoR)kmR	P1(ANCH1) x SMR6762
SMR10308	SMR4562 [F′ lafU2∷FRTcatFRT dinBo-21(oc)]	[45]
SMR10865	FC36 ΔaraBAD567 Δzie3913.1::tetRtetA+1FRT Δzie3920.5::3ChiKanISceIsite	[16]
SMR10866	FC36 ΔaraBAD567 Δattλ::PBADI-SceI Δzie3913.1::tetRtetA+1FRT Δzie3920.5::3ChiKanISceIsite	[16]
SMR12566	SMR4562 rssB::Tet	[18]
SMR12672	SMR4562 ΔarcA726::FRT	[18]
SMR12673	SMR4562 ΔarcB738::FRT	[18]
SMR13353	SMR4562 ΔphoU::FRTKan	(17)
SMR17049	SMR4562 [F′ lafU2∷FRT dinBo-21 (oc)]	SMR10308 x pCP20
SMR19235	FC40 ΔaraBAD567 Δattλ::PBADI-SceI phoU83::Tn10dCam [F' mhpA32::miniTn7Kan(I-SceI site)]	P1(SMR4953) x SMR6280
SMR19236	FC40 ΔaraBAD567 Δattλ::PBAD phoU83::Tn10dCam [F'mhpA32::miniTn7Kan(I-SceI site)]	P1(SMR4953) x SMR6281
SMR19248	SMR4562 rssB:: tet phoU83::Tn10dCam	P1(SMR4953) x SMR12566
SMR19249	SMR4562 arcA726::FRTKan phoU83::Tn10dCam	P1(SMR4953) x SMR12672
SMR19250	SMR4562 arcB738::FRTKan phoU83::Tn10dCam	P1(SMR4953) x SMR12673
SMR20214	SMR4562 phoU83::Tn10dCam [F′ lafU2∷FRT dinBo-21(oc)]	P1(SMR4953) x SMR17049
SMR20344	FC36 ΔaraBAD567 Δattλ::PBADI-SceI Δzie3913.1::tetRtetA+1FRT Δzie3920.5::3ChiKanISceIsite phoU83::Tn10dCam	P1(SMR4953) x SMR10866
SMR21643	FC40 ΔaraBAD567 Δattλ::PBADI-SceI [F' mhpA32::miniTn7Kan(I-SceI site)] phoU83::Tn10dCam pstB	P1(SMR4953) x SMR6281
SMR21644	FC36 ΔaraBAD567 Δattλ::PBADI-SceI Δzie3913.1::tetRtetA+1FRT Δzie3920.5::3ChiKanISceIsite phoU83::Tn10dCam pstB	P1(SMR4953) x SMR10866
pKD46	ori101 repA101ts PBAD-gam-bet-exo AmpR	[24]
pKD13	Source of FRTcatFRT	[24]
pCP20	Yeast Flp recombinase on a temperature-sensitive replicon λpr-FLP, λcIts857, RepTS, AmpR, CamR	[25]

aThis strain is derived from a Lac+ colony isolated from a stress-induced mutagenic break-repair experiment and so may carry additional mutations.

bThese are independent Lac+ stress-induced point mutants. See [61], for the sequence to which the nt positions correspond.

A pstS nonpolar deletion allele, ΔpstS41 was constructed using short homology recombineering [24] using primers ΔpstS1 (5’GCTTTATGAATCCTCCCAGGAGACATTATGAAAGTTATG) and ΔpstS2 (5’ACACCGTACCCGGCCTGGAGTTTTATTAGTACAGCGGCTT) and pKD13 as template to create ΔpstS40::Kan. ΔpstS41 (created by removal of Kan from ΔpstS40::Kan per [25]) caused de-repression of the Pho regulon, observed on XP medium, as expected. Bases 12–1035 of pst are deleted in ΔpstS40 and ΔpstS41.

Stress-induced mutagenic break-repair assays

Stress-induced Lac-reversion assays were performed as described [26] at 37°C. phoU83::Tn10dCam strains were concentrated 10-fold before plating to obtain sufficient Lac+ colony counts. All experiments presented showed less than two-fold net population change during the first 1–3 days after plating per [26]. Stress-induced mutation assays with I-SceI-produced DSBs were performed exactly as described [15]. The chromosomal tet +1bp frameshift assay was carried out as described [16] using the tet2 allele and I-site A [16].

Reconstruction experiments

Reconstruction experiments to determine the speed of colony formation of Lac+ derivatives of various mutants under exact selective experimental conditions, in the presence of neighbor (scavenger) cells, which consume any non-lactose carbon sources present, were performed as described [27].

Generation-dependent mutation-rate determinations

Fluctuation tests were used to determine frequencies of generation-dependent Lac+ revertants formed in rapidly growing cells as described previously [28,29]. Mutation rates were estimated from these mutant frequencies based on a modified method of the median [30,31]. To determine Lac+ mutant frequencies, rather than scoring only at 48 hr, we plated several independent Lac+ derivatives of each strain in parallel and scored all strains for Lac+ colonies several times over a 4–6 hr period (see Results for rationale for this approach, and reviewed by [29]). Lac+ derivatives were confirmed to be stably Lac+ rather than unstably Lac+, due to amplification of the leaky lac allele, by scoring Lac+ phenotypes on rich medium containing X-gal [27]. For each genotype, a t50 to colony formation (time at which 50% of the Lac+ control colonies were visible) was calculated and the median Lac+ mutant frequency at the t50 was used to calculate the mutation rate to Lac+. A final cell count was taken after 4 to 5 days when no further Lac+ control colonies were appearing (t100) and used to calculate the t50. The mutation rates were then multiplied by two to give the rate at t100.

Whole-genome sequencing

Genomic DNA was extracted from each strain and purified for sequencing using DNeasy Blood & tissue kits (Qiagen). Sequencing was performed in a Mi-Seq using Nextera XT kits for library preparation, producing paired-end reads of ~150 nt. The data were processed using CASAVA 1.8a5 software; the reference genome was MG1655 (NCBI accession number: NC_000913.3) corrected for the 81 SNVs present in SMR4562 (the Lac-assay strain) discovered by our laboratory, and the sequence of plasmid F’128 retrieved from http://rothlab.ucdavis.edu/refseqs/fc40.fasta. Apparent variants (mutations, or SNVs) were filtered such that those present in ≥70% of reads of any segment containing the variant were called as variants. A subsequent alignment of the reads using BLASTn was made to detect reads that contained noncontiguous sequences in the reference genome, and so confirm indels and detect boundaries of possible genome rearrangements. In the genome sequences reported, there were no indels or genome-rearrangement junctions detected.

Results

The Lac MBR assay

Mutagenic break repair (MBR) can be observed using the E. coli Lac assay [32], and several other assay systems (e.g., [16,18]), some used here. In the Lac assay cells with a lac +1bp frameshift mutation in an F’ conjugative plasmid are starved on solid minimal medium with lactose as the sole carbon source. Lac+ revertant colonies accumulate from the second day after plating onward for more than seven days (e.g., Fig 2A). The majority of Lac+ colonies that appear before day 6 carry a compensatory frameshift “point” mutation [33,34]; a minority carry an amplified array of tandem copies of the leaky lac allele which confers enough β-galactosidase activity to allow growth [27]. Here we use this (and other) assays, and score the Lac+ colonies before day 6, and so focus principally on the point-mutagenesis MBR mechanism which generates base substitutions and indels [2].

Fig 2

Mutations affecting the Pho regulon can decrease stress-induced Lac+ reversion.

(A) Representative experiment. Strains (top to bottom in legend): SMR4562, SMR4061, SMR4604, SMR4059, SMR4047, SMR4953, and SMR5235. Values are means ± one SEM for eight independent cultures per strain in one representative experiment (where not visible, error bars are smaller than the symbol). (B) Mean of multiple experiments. Complex effects of double and triple mutations affecting the Pho regulon on MBR in the Lac assay. Strains (top to bottom in legend): SMR5235, SMR4953, SMR4059, SMR7351, SMR6762, SMR6760, SMR6759, SMR4061, SMR5860, SMR4047, and SMR4604. Fold decrease in the change in Lac+ from day 4 to day 5 relative to the pho + strain SMR4562 was calculated for each genotype in several experiments of multiple cultures (like that shown in A). The values (shown next to the bars) are the mean fold decreases in mutagenesis from multiple experiments ± SEM (error bars, n ≥ 3). (C) A different phoU::Tn10 transposon insertion (SMR4954) also depresses MBR, indicating that the phoU mutagenesis-deficiency is not the result of a specific truncation/fusion protein. Representative experiment.

Mutagenesis in this assay is known to result from mutagenic repair of spontaneous DNA double-strand breaks (DSBs) near lac as follows. The specific mutagenic pathway acting, which requires the DSB-repair proteins, error-prone DNA Pols and stress-response proteins reviewed above—acts only in DNA molecules that have DSBs [15,16]; forms mutations near the DSB site [35]; is inhibited by a phage DSB-end trapping protein that blocks repair [36]; and requires RecBC, a specific DSB-binding repair protein [37].

phoU mutations inhibit mutagenic break repair

In a general screen for MBR-deficiency using the E. coli Lac assay and transposon mutagenesis, two unpublished transposon insertions in phoU were isolated in an earlier version of the screen of [18]. Both of the insertions are near the C-terminal end of the phoU coding region. The phoU C-terminal insertions including phoU83::Tn10dCam have severe mutagenesis defects [18] (Fig 2A–2C). Two additional mutations isolated in genes pstA and pstC, which encode part of the phosphate-specific ABC transporter, PstSCAB, exhibit relatively modest mutagenesis defects [18]. A second assay for MBR measures indel mutation via reversion of a chromosomal tet frameshift reporter gene in plasmid-free cells to which a DSB has been delivered near the reporter gene using a regulatable I-SceI endonuclease [16]. We show below that phoU83::Tn10dCam cells are defective in MBR in this chromosomal assay as well.

The insertion in SMR4953 (phoU83::Tn10dCam, used throughout this work) has Tn10dCam inserted such that the last 23 amino acids of the predicted 241-amino-acid PhoU protein are replaced with 12 amino acids encoded by the transposon (ADESPNDFGKNH). This insertion reduced MBR in the Lac assay dramatically (Fig 2A, closed diamonds). Similarly reduced mutagenesis was seen with a different insertion (Fig 2C) in which the last 21 amino acids of PhoU are replaced. A third phoU transposon insertion in the ribosome-binding site also showed reduced MBR [18]. Thus, the reduction in mutagenesis is not the result of a specific fusion protein. The data below indicate that a function of wild-type PhoU is required for MBR.

phoU83::Tn10dCam is a separation-of-function allele that retains the PhoU essential function

We show that the phoU83::Tn10dCam allele is a partial-loss-of-function allele in that it is deficient in Pho regulon repression but retains the PhoU essential function as follows. First, cells carrying phoU83::Tn10dCam are unable to repress the Pho regulon, as seen by their blue-colony phenotype on XP phosphate-indicator medium (Table 2) indicating de-repression of the Pho regulon (Materials and Methods) [23]. Second, further indicating reduced PhoU function, phoU83::Tn10dCam causes a slow-growth (small-colony) phenotype (Table 2). However, third, phoU83::Tn10dCam is demonstrably not a null allele as follows. PhoU is an essential gene, though the nature of its essential function is unknown [23]. Null mutants are viable only with an additional suppressor mutation in any of the pstSCAB or phoBR genes [23]. These suppressor mutations cause rapid growth and large colonies [23]. We find that phoU83::Tn10dCam strains show a stable small-colony phenotype (Table 2), and do not carry suppressor mutations as shown by whole-genome sequencing (unless grown rapidly on glucose medium, discussed below), and so are not phoU null mutants. Two phoU83::Tn10dCam (small-colony) strains were sequenced, SMR20344 and SMR4953, and neither contained mutations in the pstSCAB or phoBR genes indicative of suppression [23]. The first contained no mutation in its genome (relative to its isogenic parent) other than phoU83::Tn10dCam. SMR4953 carries an apparently incidental silent bioA mutation encoding a W186L substitution that does not cause auxotrophy. As a positive control, when grown rapidly on glucose medium, phoU83::Tn10dCam strains derived from SMR6280 and SMR10866 acquired large-colony phenotype and carried suppressor mutations in pstB (Table 2). We conclude that phoU83::Tn10dCam is a separation-of-function allele that retains the PhoU essential function but is defective in Pho-regulon repression.

Table 2

Pho-regulon-repression defect without pst/phoBR suppressor mutations in phoU83::Tn10dCam strains.

Strain	Pho genotype	Colony size	Colony color on phosphate indicator	pst or phoBR mutations
SMR4562	phoU +	Large	White	none
SMR4953	phoU83::Tn10dCam	Small	Blue	none
SMR13353	ΔphoU::FRTKan	Large	Blue	pstB 7bp deletion after Y256
SMR20344	phoU83::Tn10dCam	Small	Blue	none
SMR21643	phoU83::Tn10dCam	Large	Blue	pstB 2bp deletion after aa153
SMR21644	phoU83::Tn10dCam	Large	Blue	pstB P14S

Colony size was observed on M9 B1 glycerol medium. pstSCAB suppressor mutations or their absence were identified either by whole-genome sequencing (strains SMR4562, SMR4953, SMR20344, SMR21643, SMR21644) or by targeted sequencing of those genes (SMR13353).

Neither poor growth nor de-repression of the Pho regulon account for whole mutagenesis deficiency

We tested whether the phoU mutagenesis deficiency might relate to the growth defect known to be associated with increased PstSCAB protein function in phoU strains (in which PhoU cannot inhibit the PstSCAB growth-inhibitory activity [38,39]), which presumably accounts for the small-colony morphology of phoU83::Tn10dCam cells. We did this by examining phoU strains that carry mutations that decrease PstSCAB function, and so should have no growth defect. We did this by reducing PstSCAB function in several different ways. We created ΔpstS, a nonpolar in-frame deletion (Materials and Methods). In a Δ(pstSCAB-phoU) strain and a phoU::Tn10dCam ΔpstS strain, PstSCAB function is eliminated, and in a phoU::Tn10dCam ΔphoBR strain, lacking its transcriptional activator, PstS-dependent PstSCAB function is low, remaining at uninduced levels [23]. These reductions in PstSCAB activity allow large-colony formation (not shown) but do not restore mutagenesis proficiency. The Δ(pstSCAB-phoU), phoU::Tn10dCam ΔpstS and phoU::Tn10dCam ΔphoBR strains form normal-size colonies, yet still have somewhat reduced MBR (Fig 2A and 2B) indicating that increased PstSCAB and consequent growth defect is not the sole cause of the mutagenesis defect in phoU83::Tn10dCam cells. The Δ(pstSCAB-phoU) and phoU83::Tn10dCam ΔpstS strains (with no PstSCAB activity) manifest three- and two-fold decreases in mutant-colony production, respectively (Fig 2A and 2B). This is significantly less mutagenesis than in pho + (P = 0.027 and 3.2 × 10-5, respectively, t-test) but significantly more mutagenesis than in phoU83::Tn10dCam (Fig 2A and 2B), and implies that the strong mutagenesis defect of phoU83::Tn10dCam may relate partially but not solely to increased PstSCAB activity. Suggesting that blocking induction of the Pho regulon, including pstSCAB, only partially alleviates the phoU83::Tn10dCam phenotype, we see that mutagenesis in the phoU83::Tn10dCam ΔphoBR (pstSCAB-uninducible) strain is reduced about five-fold relative to pho + (Fig 2A and 2B, P = 1.2 × 10-5, t-test). All of these results imply that in wild-type PhoU+ cells, repression of PstSCAB promotes MBR. However, the less severe mutation-down phenotype in phoU83::Tn10dCam strains that lack PstSCAB implies that an additional function of PhoU may exist outside of repression of the Pho operon and promotes MBR.

De-repression of the Pho regulon does not correlate with MBR deficiency

De-repression of the Pho regulon is not required for mutagenesis because the ΔphoBR strain, in which the gene encoding the transcriptional activator PhoB is deleted, has mutation levels similar to pho + (Fig 2A and 2B). This is not surprising because the Pho regulon is repressed on the high phosphate M9 medium on which the mutagenesis experiments are performed. However, perhaps the inappropriate de-repression of the regulon associated with pstSCAB or phoU mutations [20] is mildly detrimental to mutagenesis. We tested this in several ways.

First, indicating that Pho regulon de-repression per se does not inhibit mutagenesis, we find that phoU35, a mutant with de-repressed Pho regulon but rapid growth (large colonies without suppressor mutations) has normal mutagenesis. phoU35 is an altered-function allele [40], which causes de-repression of the Pho regulon in high phosphate conditions, but does not cause the slow-growth phenotype associated with a phoU deletion. These phenotypes suggest that the PhoU35 protein retains the ability to block the PstSCAB growth-inhibitory function, but cannot mediate repression of the Pho regulon (reviewed, [20]). We find that phoU35 does not affect mutagenesis (Fig 2A and 2B), suggesting that the mutagenesis defect of phoU83::Tn10dCam is not caused by simple de-repression of the Pho regulon.

Second, we find that the phoR68 null allele, which also leads to regulon de-repression [20], also had no effect on MBR (Fig 2A and 2B).

Third, loss of PstSCAB function achieved via the null alleles ΔpstS or Δ(pstSCAB-phoU), both of which also cause de-repression (reviewed, [20], Materials and Methods), decrease mutagenesis roughly two- and three-fold, respectively (Fig 2A and 2B, P = 1.4 × 10-8 and -2.0 × 10-8, t-test), not the >20-fold of phoU::Tn10dCam (Fig 2A and 2B) or phoU::Tn-2 (Fig 2C). We show that de-repression does not account for the MBR reduction in Δ(pstSCAB-phoU) by showing that combining Δ(pstSCAB-phoU) with the ΔphoBR allele, which makes the Pho regulon uninducible, does not alter the mutagenesis defect: Δ(pstSCAB-phoU) ΔphoBR is as MBR-deficient as Δ(pstSCAB-phoU) cells (Fig 2B, P = 0.5018, t test).

Unexpectedly, introducing the ΔphoBR allele into ΔpstS cells to create the ΔpstS ΔphoBR strain (phoU +) strain reduced mutagenesis >40-fold, a stronger phenotype than that of phoU83::Tn10dCam (Fig 2B). Again, because the Pho regulon is uninducible in this strain because of the ΔphoBR mutation, this MBR-deficiency is not caused by Pho-regulon de-repression. The ΔpstS ΔphoBR strain does not have the small-colony phenotype of the phoU83::Tn10dCam, implying a different block to mutagenesis—not growth inhibition. The strong ΔpstS ΔphoBR mutagenesis defect contrasts with that of two ΔphoBR strains that lack phoU +: the Δ(pstSCAB-phoU) ΔphoBR strain, in which mutagenesis is decreased only 2-fold, and phoU83::Tn10dCam ΔphoBR, in which mutagenesis is reduced 6-fold (Fig 2B). These data imply that phoU + may be responsible for the strong reduction in mutagenesis in the absence of pstS and phoBR. To explore this further we constructed the triple mutant strain phoU83::Tn10dCam ΔpstS ΔphoBR, and found that it has wild-type levels of mutagenesis (Fig 2B). Thus, it appears that either pstS + or phoBR + is required for mutagenesis in a phoU + background and that either pstS or phoBR must be absent for mutation to occur in a phoU-mutant background. The lack of correlation between de-repression of the Pho regulon and MBR phenotypes in the experiments above rules out a role for simple Pho regulon de-repression and suggests some other role of PhoU in mutagenesis. The unexpected phenotypes in PhoU+ strains suggest multiple routes for Pho regulation and regulators to impact MBR and roles for PhoU other than simple modulation of repression and constraining PstSCAB function.

Slow Lac+ colony formation in pho strains does not account for MBR defects

We used reconstruction experiments to show that poor colony formation under selective conditions is not the major cause of MBR-deficiency of pho strains. In reconstruction experiments, a known number of Lac+ cells are plated under the conditions of a stress-induced-mutation experiment: on lactose minimal medium with neighbor cells present (Δlac cells that scavenge any non-lactose carbon sources, reviewed [41,42]). Most day-5-Lac+ mutant colonies are visible as colonies two days after plating [41]. We find that the two strains with the strongest mutagenesis defects (phoU83::Tn10dCam and ΔpstS ΔphoBR), and none of the other strains, show altered growth in these reconstruction experiments. The phoU83::Tn10dCam strain forms colonies slightly more slowly than its pho + parental strain (three days versus two, Table 3), but with poor efficiency; only about 15–20% of the phoU83::Tn10dCam Lac+ cells ultimately form colonies (Table 3). This poor efficiency of colony formation is not seen when phoU83::Tn10dCam Lac+ cells are plated on selective medium without scavenging neighbor cells, suggesting poor competition with the faster growing pho + scavenger cells (data not shown). The ΔpstS ΔphoBR strain formed colonies efficiently but slightly more slowly than its isogenic parents (about three days) and variably from culture to culture (Table 3). This suggests, first, that the few late Lac+ mutants generated in the mutation-deficient ΔpstS ΔphoBR strain (Fig 2B) might include slow-growing generation-dependent mutants such that the strain might be more deficient in MBR than is evident. Second, this average one-day lag in colony growth cannot account for the strong mutagenesis defect of this strain. We conclude that at least some of the effects of phoU83::Tn10dCam on Lac reversion may be via poor colony formation under selective conditions. The MBR defect of phoU83::Tn10dCam is confirmed in a separate chromosomal assay not subject to these concerns, below, further demonstrating roles of in mutagenesis independent of colony growth rates.

Table 3

pho mutation effects on speed and efficiency of Lac+-colony formation do not account for MBR-deficiency.

Strain	Relevant genotype	Average days to Lac+ colony formation a		% viable cells forming Lac+ colonies a
		Exp. 1	Exp. 2	Exp. 1	Exp. 2
SMR4562	pho +	2.1 ± 0.03	2.0 ± 0.02	100 ± 7	110 ± 10
SMR4059	phoU35	2.2 ± 0.2	2.0 ± 0.3	81 ± 11	96 ± 10
SMR4061	phoR	2.7 ± 1	2.5 ± 0.8	100 ± 20	91 ± 20
SMR4953	phoU::Tn10dCam	3.4 ± 0.74	2.5 ± 1.2 b	18 ± 12	13 ± 7
SMR4047	Δ(pstSCAB-phoU)	2.2 ± 0.35	2.1 ± 0.15	92 ± 9	87 ± 36
SMR6759	ΔpstS	2.2 ± 0.32	2.1 ± 0.15	93 ± 10	97 ± 22
SMR4604	ΔphoBR	2.1 ± 0.03	2.0 ± 0.02	100 ± 8	100 ± 15
SMR6762	phoU::Tn10dCam ΔpstS	2.6 ± 0.5	2.3 ± 0.39	96 ± 9	95 ± 40
SMR5860	Δ(pstSCAB-phoU) ΔphoBR	2.5 ± 0.53	2.2 ± 0.25	98 ± 13	105 ± 30
SMR6760 c	ΔpstS ΔphoBR	3.2 ± 1.0	3.1 ± 0.93	91 ± 8	92 ± 13

aValues are means ± one standard deviation (SD). In each case, four-six independent day-5 or day-6 Lac+ mutants were used as controls for the time of colony formation (see Materials and Methods), with the exception of SMR4562 for which day-2 mutants were used (they behave similarly [41]). Exp. 1 was carried out to day 5, and Exp. 2 to day 6.

b Only two Lac+ control strains were used in this case and so a range, rather than SD is given.

c We note that the time to Lac+ colony formation for different isolates of ΔpstS ΔphoBR strain SMR6760 varies from two to five days. They all form normal-size colonies and are not detectably amplified (amplified Lac+ take 3–5 days to form, [27]).

Weak effects of pho mutations on generation-dependent Lac+ reversion in rapidly growing cells are uncorrelated with MBR defects

Generation-dependent Lac+ reversion in rapidly growing cells occurs by multiple molecular mechanisms other than, and in addition to, MBR [1,2,16]. We examined the generation-dependent mutation rates to Lac+ to determine whether pho mutations also affect mutagenesis mechanisms other than MBR, which is confined to stationary-phase and other times of σS-response induction [2,15,16]. An equalizing method was used that minimizes the possible inclusion of stress-induced mutants and accounts for possibly different times-to-Lac+-colony formation for different genotypes [29,43] (see Materials and Methods). For example, because the ΔpstS ΔphoBR strain forms Lac+ colonies more slowly than the wild-type (Table 3), we score generation-dependent Lac+ revertant colonies of this strain proportionately later than for the wild-type. We were unable to determine a generation-dependent Lac+ reversion rate for the phoU83::Tn10dCam strain due to poor efficiency of colony formation by Lac+ cells under the selective conditions (see above, Table 3), but all other pho mutants (Table 4) have only modest 2-4-fold effects on generation-dependent Lac+ reversion in growing cells. Due to the nature of mutation rate determinations, more experiments would be required to conclude that these small differences were significant. The lack of correlation between these rates and the phenotypes in stress-induced Lac+ reversion implies that the effects are specific to stress-induced MBR. Certainly the ΔpstS ΔphoBR combination affects stress-induced Lac+ reversion more strongly (40-fold) than generation-dependent reversion (4-fold, Table 4).

Table 4

pho mutations do not strongly affect generation-dependent Lac+ reversion rates.

Strain	Relevant genotype	Mutation rate x 10-9 (mutations/cell/generation) a
		Exp. 1	Exp. 2	Avg.
SMR4562	pho +	3.6	3.7	3.7
SMR4047	Δ(pstSCAB-phoU)	4.2	12	8.1
SMR6759	ΔpstS	4.8	4.7	4.8
SMR4604	ΔphoBR	4.0	1.4	2.7
SMR6760	ΔpstS ΔphoBR	1.0	0.99	1.0
SMR5235	phoU::Tn10dCam ΔphoBR	1.4	0.79	1.1

aMutation rates were calculated as described in Materials and Methods. Exp. 1 and 2 consisted of 19 and 14–15 independent cultures of each strain respectively. Four to six Lac+ derivatives of each strain were plated in parallel as controls as described in Materials and Methods.

Neither I-SceI-induced DSBs nor SOS-induced levels of DinB substitute for PhoU+ in mutagenesis

We tested whether PhoU promotes mutagenesis via activation of the SOS DNA-damage response, the σE, or σS responses, stress-sensing for and activation of which accounts for more than half of the functions in the 93-gene MBR network [18]. SOS is required for MBR [32,44], and though ~40 genes are induced in the SOS response, the induction of dinB alone is sufficient for stress-induced Lac reversion [45]. A dinB operator constitutive (oc) mutant that provides SOS-induced levels of DinB constitutively restores wild-type-like mutation rates to an SOS-non-inducible strain [45], bypassing the need for SOS induction. By contrast, we found that the dinB(oc) mutation did not restore mutagenesis in phoU83::Tn10 dinB(oc) cells (Fig 3A–3C). We conclude that PhoU functions in mutagenesis other than, or in addition to, by activation of the SOS response.

Fig 3

PhoU is not substituted by SOS-induced levels of DinB (the SOS response) or by DSBs, the role of the σ, indicating that PhoU promotes MBR other than or in addition to by formation of DSBs, activation of the σE or SOS responses.

(A, B) Representative experiments. (C, D) Multiple experiments. Lac+ mutation rates are Lac+ colonies/108 cells /day from days 3–5 [46] (mean of 2–3 experiments ± range or SEM, respectively). The first set of isogenic strains carry a dinB operator-constitutive allele dinB(oc) [45], which produces SOS-induced levels of DinB protein at all times, and completely substitutes for a functional SOS response in MBR [45]. dinB(oc) does not substitute for functional PhoU, indicating that PhoU promotes mutagenesis other than or in addition to by promoting the SOS response. The isogenic strains in the right panel (and right side of the left panel) carry either inducible I-SceI endonuclease and a cutsite near lac (DSB), or the cutsite-only (“No-DSB”), which has spontaneous DSBs but not additional DSBs induced by I-SceI. I-SceI-induced DSBs substitute for all components that contribute to spontaneous DSBs in the lac region: σE [17], TraI [15]; Mfd and RNA-DNA hybrids [36], but do not substitute for PhoU. Strains: WT, SMR4562; phoU, SMR4953; DSB, SMR6280; “No-DSB”, SMR6281; phoU DSB, SMR19235; dinB(oc), SMR17049; phoU dinB(oc), SMR20214. Rates were calculated from 3 separate experiments for phoU, wild-type and DSB strains, and error bars represent one SEM. For dinB(oc), error bars represent range calculated from two independent experiments.

The σE response promotes MBR in the Lac assay mainly via its contribution to spontaneous DNA breakage, as evidenced by the finding that DSBs created by I-SceI endonuclease near lac substitute for σE in mutagenesis [17]. I-SceI cuts also substitute for requirements for DSB-promoting TraI single-strand endonuclease [15], RNA/DNA hybrids and Mfd RNA-polymerase translocase [36], but not for DSB-repair, SOS- or σS-response functions, or error-prone DNA polymerases [2,15,16] (also [18]). We find that I-SceI-generated DSBs did not restore mutagenesis-proficiency to phoU83::Tn10dCam cells in two assays. First, though I-SceI cuts near lac increase overall Lac reversion ([15] and Fig 3B–3D), they did not relieve the strong phoU83::Tn10dCam mutagenesis defect (Fig 3B–3D). Second, we used the chromosomal Tet assay [16] in which I-SceI cuts delivered near a chromosomal revertible tet +1bp frameshift allele in plasmid-free cells (Fig 4A) promote Tet reversion via σS-, DinB-dependent MBR [16]. In the Tet assay as well, I-SceI cuts did not substitute for PhoU+ (Fig 4B). We conclude that PhoU promotes mutagenesis by some mechanism other than, or in addition to, via promotion of spontaneous DSBs, and thus also other than, or in addition to, via activation of σE.

Fig 4

PhoU is required for MBR in the E. coli chromosome.

(A) Diagram of relevant genetic elements in the E. coli chromosome. Experimental design of [16]. Cells expressing a chromosomal regulatable I-SceI endonuclease gene and carrying a chromosomal cutsite near a tet +1bp frameshift allele are starved in liquid for 84 hours (with no tetracycline), rescued to rich medium then plated on rich tetracycline and no-drug plates to score tetracycline-resistant (TetR) mutant colonies. (B) PhoU is required for I-SceI-induced MBR under stress, and DSBs do not substitute for PhoU in mutagenesis. DSB strains have I-SceI enzyme and cutsite and control “No-DSB” strains have I-SceI cutsite only. Strains: “No-DSB”, SMR10865; DSB, SMR10866; phoU DSB, SMR20344. The DSB mutant frequency is 14.5 TetR mutants /108 cells (1.5 x 10-7 TetR mutants per cell). Mean ± range of two independent experiments.

Post-translational σS-activating mutations do not substitute for PhoU in mutagenesis

MBR requires the σS response [15,16,46] and 30% of the genes in the MBR network promote mutagenesis via sensing stress and signal transduction that activates the σS response [18]. Two ways to artificially up-regulate σS (and induce the σS response) are knock-out of RssB, which promotes σS proteolytic degradation, or ArcB, the histidine-kinase component of the Arc two-component signal-transduction system which negatively regulates σS post-translationally [47-49]. ΔrssB and ΔarcB mutations suppress many MBR defects resulting from insufficient σS [18]. By contrast, we find that neither ΔarcB nor ΔrssB restore mutagenesis to phoU83::Tn10dCam cells (Fig 5). The mutation rate was decreased dramatically by phoU83::Tn10 in the rssB background (phoU83::Tn10 rssB compared with rssB, Fig 5) and the arcB background (phoU83::Tn10 arcB compared with arcB, Fig 5) suggesting that decreased mutagenesis may result from some mechanism other than, or in addition to, failure to induce the σS response. We cannot eliminate the possibility of a transcriptional upregulation of rpoS somehow caused by PhoU+, which might not be suppressed by mutations in rssB and arcB, which affect σS production post-translationally. However, many probable transcription-related defects in σS production were suppressed by rssB and arcB mutations [18], suggesting that PhoU does not promote mutagenesis via σS activation.

Fig 5

PhoU is not substituted by artificial upregulation of σS via arcB or rssB deletions, but is suppressed by deletion of arcA.

(A) Representative data. (B) Data for three-four separate experiments (means ± SEM) showing ratios of the mutation rates (Lac+ colonies / 108 cells plated / day between days 3–5 of experiments such as those in Fig 1A). The wild-type rate is 18.8 Lac+ colonies /108 cells plated / day. Strains: WT, SMR4562; rssB, SMR12566; arcA, SMR12672; arcB, SMR12673; phoU. SMR4953; phoU rssB, SMR19248; phoU arcA, SMR19249; phoU arcB, SMR19250.

Suppression of phoU::Tn10dCam mutation by arcA

Previously, a C-terminal transposon insertion in phoU was isolated in a screen for persister mutants, and conferred hyper-sensitivity to ampicillin [50]. Microarray analysis in the mutant showed overexpression of several energy-metabolism genes including arcA, the response regulator of the two-component Arc system [51]. In contrast with ArcB and RssB which negatively regulate σS post-translationally, ArcA represses transcription of σS [52]. Although mutations in each of the three cause net accumulation of σS in cells, arcA mutants are still slightly defective [2-fold reduced, [18] and Fig 5] in MBR, suggesting that the arcA role in mutagenesis is more complex than simple relief of σS repression [18]; that is, ArcA also promotes mutagenesis.

We find that deletion of arcA in a phoU83::Tn10dCam cell restores mutagenesis to levels similar to that of the arcA mutant (Fig 5A). That is, ArcA is epistatic to phoU83::Tn10dCam. phoU83::Tn10dCam decreases mutagenesis 13-times less in an arcA strain that in a wild-type strain. The phoU83::Tn10dCam arcA: arcA mutagenesis ratio is 13-fold higher than phoU83::Tn10dCam: WT (meaning there is 13-fold less depression of mutagenesis by phoU83::Tn10dCam in an arcA strain than in WT) indicating that arcA partially suppresses the phoU mutagenesis defect (Fig 5B).

Discussion

The data presented show that PhoU and several proteins in phosphate regulation promote MBR in E. coli (Figs 2 and 4), in ways that do not correlate with their roles in phosphate regulation (Fig 2) indicating additional roles. PhoU+ does not promote mutagenesis mainly via activation of the SOS or σE responses (Figs 3 and 4) or via promotion of spontaneous DSBs that underlie MBR (Figs 3 and 4). The data suggest a possible PhoU mutagenic role partly via repression/antagonism of ArcA (Fig 5). The data also indicate that phoU83::Tn10dCam is a partial loss-of-function mutation that retains the (unknown) PhoU essential function, such that suppressor mutations are not required for viability, but lacks Pho-regulon repression (Table 2), and so may be a useful allele for studying PhoU functions in other pathways in which phoU mutations have phenotypes.

Although the roles of PhoU and the PhoBR regulon in MBR are complex, several points are clear. First, the ability to induce the Pho regulon is not required for MBR (a ΔphoBR strain, which lacks the PhoB transcriptional activator, is mutagenesis-proficient, Fig 2). This is not surprising given the high phosphate (repressing) conditions of the M9 minimal medium used in the mutation assay. Second, although some of the mutations examined lead to Pho regulon de-repression, inappropriate de-repression is not correlated with mutagenesis deficiency. For example, although phoU83::Tn10dCam is both mutagenesis-defective and de-repressed, other mutations that de-repress the regulon have no defect (phoU35, phoR68) or smaller defects [ΔpstS, Δ(pstSCAB-phoU)] (Fig 2A and 2B). Moreover, if the mild mutagenesis deficiencies of the ΔpstS, Δ(pstSCAB-phoU), and phoU83::Tn10dCam ΔpstS strains were caused by de-repression of the regulon, then introduction of the ΔphoBR deletion, which makes the regulon uninducible, should restore full mutagenesis proficiency, and this was not observed for the first two strains (though it was for third, Fig 2B).

The role of PhoU in MBR is difficult to model because our data do not correlate perfectly with the two functions, one known and one hypothesized, of PhoU. PhoU is required for repression of the Pho regulon in high phosphate, and also to prevent a PstSCAB-dependent inhibition of growth [20,23,39]. As just discussed, de-repression of the regulon associated with phoU and pstSCAB mutations does not inhibit mutagenesis per se. phoU83::Tn10dCam confers a growth defect (Tables 2 and 3), and mutagenesis-deficiency. Normal growth is restored (as expected [20]) by introducing mutations that block PstSCAB activity [ΔpstS, Δ(pstSCAB-phoU)] or prevent its induction (ΔphoBR), but mutagenesis-proficiency is only partially restored (Fig 2B and Results). Thus, we suggest that the strong phenotype of phoU83::Tn10dCam results from two deficiencies: a failure to block PstSCAB-mediated growth-inhibition, and lack of another, unknown, function of PhoU (not its regulon-repressing function). That the other phoU mutant strains all form colonies efficiently under selective conditions (Table 3) is consistent with the other PhoU function being necessary for MBR. A possible reason for the mutagenesis deficiency might be the level of polyphosphate within the cell. MBR is depressed by polyphosphate levels that are either too high or too low [53], and PhoU mutants have high levels of polyphosphate, whereas mutations in the PstSCAB transport genes lead to low polyphosphate levels [54,55]. Thus, mis-regulated polyphosphate levels are a plausible possible cause of part of the phoU mutagenesis-deficiency. Further experiments are required to test this hypothesis.

Our results suggest additional complexities to PhoU function. In addition to its separate functions in repressing the Pho regulon, preventing a pstSCAB-dependent growth defect (separable genetically by the phoU35 mutation, [20,23]), and its positive role in mutagenesis (here), PhoU can also inhibit mutagenesis. Inhibition is manifested as a strong PhoU-dependent mutagenesis deficiency in pstS phoBR cells, in which pstS-dependent effects are not a factor and the Pho regulon is uninducible (Fig 2B). The presence of either pstS + or phoBR +, or mutation of phoU can alleviate this defect. Thus, it appears that the PhoU+ function in mutagenesis must be constrained by either pstS + or phoBR + to achieve wild-type levels of MBR. This could reflect direct interactions with PstS(CAB) or PhoB or PhoR, all of which interact genetically to regulate the regulon, and are proposed to form a repressing complex at the membrane [20,21] (Fig 1), regulation of polyphosphate levels, or other. How PhoU both promotes and hinders mutagenesis, and what the relationship is between those two functions, remains to be determined.

The Pho regulon is required for survival in adverse conditions and so, not surprisingly, up-regulates expression of σS [56,57]. pstS mutation increases σS levels phoBR-dependently in exponentially growing cells, but not in stationary-phase cells, apparently mediated via a small regulatory RNA [56]. However, the effects of Pho mutations on σS expression, manifested only in exponentially growing cells, are not congruent with their effects on MBR, suggesting that Pho does not affect mutagenesis via σS up-regulation. Supporting a PhoU role other than in σS-response activation, neither rssB nor arcB deletion, both of which increase σS levels, restored mutagenesis to phoU83::Tn10dCam cells (Fig 5), whereas restoration of mutagenesis by ΔrssB and ΔarcB was seen for several σS-activator mutations [18]. Suppression of the phoU phenotype by ΔarcA (Fig 5) coupled with known arcA repression by PhoU [50] suggests that a gene repressed by ArcA may be required for MBR, and that the PhoU repression of arcA might underlie its role in mutagenesis.