Mismatch repair (MMR) is a near ubiquitous pathway, essential for the maintenance of genome stability. Members of the MutS and MutL protein families perform key steps in mismatch correction. Despite the major importance of this repair pathway, MutS–MutL are absent in almost all Actinobacteria and many Archaea. However, these organisms exhibit rates and spectra of spontaneous mutations similar to MMR-bearing species, suggesting the existence of an alternative to the canonical MutS–MutL-based MMR. Here we report that Mycobacterium smegmatis NucS/EndoMS, a putative endonuclease with no structural homology to known MMR factors, is required for mutation avoidance and anti-recombination, hallmarks of the canonical MMR. Furthermore, phenotypic analysis of naturally occurring polymorphic NucS in a M. smegmatis surrogate model, suggests the existence of M. tuberculosis mutator strains. The phylogenetic analysis of NucS indicates a complex evolutionary process leading to a disperse distribution pattern in prokaryotes. Together, these findings indicate that distinct pathways for MMR have evolved at least twice in nature.
Cells ensure the maintenance of genome stability and a low mutation rate using a plethora of DNA surveillance and correction processes. These include base selection, proofreading, mismatch repair (MMR), base/nucleotide excision repair, recombination repair and non-homologous end-joining1. The recognized MMR pathway is highly conserved among the three domains of life2. In all cases, members of the MutS and MutL protein families perform key steps in mismatch correction. This MutS–MutL-based MMR system (canonical MMR) is a sophisticated DNA repair pathway that detects and removes incorrect mismatched nucleobases. Mismatched base pairs in DNA arise mainly as a result of DNA replication errors due to the incorporation of wrong nucleobases by DNA polymerases. To correct them, the system detects incorrect although chemically normal bases that are mismatched with the complementary strand, discriminating between the parental template and the newly synthesized strand3.
Loss of this activity has very important consequences, such as high rates of mutation (hypermutability) and increased recombination between non perfectly identical (homeologous) DNA sequences4, both hallmarks of MMR inactivation. Nevertheless, despite the quasi-ubiquitous nature of this pathway, there are some important exceptions. The genomes of many Archaea, including Crenarchaeota and a few groups of Euryarchaeota, and almost all members of the bacterial phylum Actinobacteria, including Mycobacterium, have been shown to possess no identifiable MutS or MutL homologues5,6,7. However, these prokaryotes exhibit rates and spectra of spontaneous mutations similar to canonical MMR-bearing bacterial species8,9,10, suggesting the existence of unidentified mechanisms responsible for mismatch repair.
To identify novel mutation avoidance genes in mycobacteria, we performed a genetic screen and discovered that inactivation of the MSMEG_4923 gene in Mycobacterium smegmatis, encoding a homologue of an archaeal endonuclease dubbed NucS (for nuclease specific for ssDNA)11, produced a hypermutable phenotype. NucS from Pyrococcus abyssi was initially identified as a member of a new family of novel structure-specific DNA endonucleases in Archaea11. Notably, a recent report revealed that the protein NucS from the archaeal species Thermococcus kodakarensis (renamed as EndoMS) is a mismatch-specific endonuclease, acting specifically on double-stranded DNA (dsDNA) substrates containing mismatched bases12. The possibility that a non-canonical mismatch repair could be triggered by a specific double-strand break (DSB) endonuclease, able to act at the site of a mispair, followed by DSB repair was hypothesized 30 years ago13. The archaeal NucS binds and cleaves both strands at dsDNA mismatched substrates, with the mispaired bases in the central position, leaving 5-nucleotide long 5′-cohesive ends12. Consequently, it has been suggested that these specific DSBs may promote the repair of mismatches, acting in a novel MMR process12. Moreover, very recently, the structure of the T. kodakarensis NucS-mismatched dsDNA complex has been determined, strongly supporting the idea that NucS acts in a mismatch repair pathway14. Although these biochemical and structural studies have shed some light on the role of NucS at the molecular level, the cellular and biological function of NucS and its impact on genome stability remains unknown.
Hypermutable bacterial pathogens, very often associated with defects in MMR components, are frequently isolated and pose a serious risk in many clinical infections15,16,17,18,19,20,21. The major pathogen Mycobacterium tuberculosis appears to be genetically isolated, acquires antibiotic resistance exclusively through chromosomal mutations22 and presents variability in mutation rates between strains23. These factors should contribute to the selection of hypermutable M. tuberculosis strains under antibiotic pressure, as it occurs with other chronic pathogens18,23. However, hypermutable strains have not yet been detected in this pathogen. To investigate the possible existence of M. tuberculosis hypermutable strains affected in NucS activity, we analysed the effect of naturally occurring polymorphisms in nucS from M. tuberculosis clinical isolates on mutation rates, using M. smegmatis as a surrogate model.
In this study, we first establish that NucS is essential for maintaining DNA stability, by preventing the acquisition of DNA mutations in Mycobacterium and Streptomyces. Inactivation of nucS in M. smegmatis produces specific phenotypes that mimic those of canonical MMR-null mutants (increased mutation rate, biased mutational spectrum and increased homeologous recombination). Finally, we conduct here distribution and phylogenetic analyses of NucS across the prokaryotic domains to understand its evolutionary origins.
Identification and characterization of M. smegmatis nucS
To identify novel mutation avoidance genes in mycobacteria, a M. smegmatis mc2 155 library of ∼11,000 independent transposon insertion mutants was generated and screened for spontaneous mutations that confer rifampicin resistance (Rif-R), used as a hypermutator hallmark (Fig. 1a). One transposon insertion, which inactivated the MSMEG_4923 (nucS) gene, conferred a strong hypermutable phenotype. The NucS/EndoMS translated protein sequence is 27% identical to NucS from the hyperthermophilic archaeal P. abyssi and 87% to that of M. tuberculosis (Fig. 1b). P. abyssi NucS was defined as the first member of a new family of structure-specific endonucleases with a mismatch-specific endonuclease activity11,12 containing an N-terminal DNA-binding domain and a C-terminal RecB-like nuclease domain11. All the catalytic residues required for nuclease activity in P. abyssi are conserved in the mycobacterial NucS (Fig. 1b).
Recombinant M. smegmatis NucS was expressed and purified. The apparent molecular mass of the purified native protein fits with the expected size (25 kDa) (Supplementary Fig. 1A). The biochemical activity was analysed by DNA electrophoretic mobility shift assays (EMSAs) and nuclease enzymatic assays. M. smegmatis NucS was capable of binding to single-stranded DNA (ssDNA), as seen in the archaeal P. abyssi NucS11, but not to dsDNA (Fig. 1c). Regarding cleavage of mismatched substrates, no significant specific cleavage activity was observed on different substrates containing a single nucleotide mismatch in the central region of the strand (Supplementary Fig. 1B), in contrast with previous results obtained with the archaeal T. kodakarensis NucS12. The binding to ssDNA indicates that the protein is correctly folded, as it can bind to its substrate. This suggests that different requirements, such as the binding of additional partners, protein modifications or different DNA substrates, may be required to activate the mismatch-specific cleavage activity of the bacterial NucS.
NucS is essential to maintain low levels of spontaneous mutation
To verify that NucS has a key role in maintaining DNA fidelity, we constructed an in-frame deletion of nucS (ΔnucS, nucS-null derivative) in M. smegmatis and measured the rate at which drug resistance was acquired. Notably, the nucS-null strain displayed a hypermutable phenotype, increasing the rate of spontaneously emerging rifampicin and streptomycin (Str-R) resistances by a factor of 150-fold and 86-fold, respectively, above the wild-type strain (3.1 × 10−7 versus 2.1 × 10−9 and 4.8 × 10−8 versus 5.6 × 10−10, ΔnucS versus wild type, respectively). These results are equivalent to those observed for mutS- or mutL-deficient Escherichia coli (102–103-fold increases)24. Significantly, basal mutation rates were recovered when the nucS deletion was chromosomally complemented with the wild-type gene MSMEG_4923 (nucSSm) (Fig. 2a, Supplementary Table 1), confirming that inactivation of this gene was responsible for the high mutation rates observed.
Notably, M. smegmatis mc2 155 and its ΔnucS derivative produced a different mutational signature. While spontaneous Rif-R mutations detected in the wild-type strain comprise different base substitutions, including transitions, but also transversions and even an in-frame deletion, all mutations detected in the ΔnucS strain were specifically transitions (A:T→G:C or G:C→A:T) (Fig. 2b, Supplementary Tables 2A,B). Transitions occur much more frequently than transversions or indels in any cell, due to spontaneous or induced errors in the DNA, and are the preferred substrates for MMR mechanism. The ΔnucS strain accumulates a high number of uncorrected transitions, masking transversions and indels to undetectable levels under our experimental conditions. This transition-biased mutational spectrum is a hallmark signature of canonical MMR pathway25,26.
To demonstrate the generality of the mutation-avoidance activity in species encoding NucS, the nucS gene was deleted in Streptomyces coelicolor A3(2), a different actinobacterial species. The precise deletion of nucS in this species increased the rate of spontaneous mutations conferring Rif-R and Str-R by a factor of 108-fold and 197-fold, respectively. As with M. smegmatis, low mutation rates were recovered by complementation with the wild-type S. coelicolor nucS gene (Fig. 2c, Supplementary Table 3). Together, these results highlight the essential role of NucS in mutation avoidance.
NucS inhibits homeologous but not homologous recombination
These results prompted us to investigate whether NucS is involved in reduction of recombination between non-identical (homeologous) DNA sequences, but not between 100% identical, as described for the canonical MMR-null mutants in other bacterial species4,27. The rates of recombination between homologous and homeologous sequences were measured using specific engineered tools (Fig. 3a, Supplementary Fig. 2A,B). Recombination rates between 100% identical sequences were similar in the wild-type and its ΔnucS derivative (2.42 × 10−6 and 2.86 × 10−6, respectively). However, when the identity of DNA sequences decreased, the recombination rate was comparatively higher in the nucS-null derivative: 95%, 4.68 × 10−7 versus 1.41 × 10−6 (3-fold difference), 90%, 1.71 × 10−8 versus 1.82 × 10−7 (10-fold) and 85%, 6.47 × 10−9 versus 3.36 × 10−8 (5-fold) for wild type versus ΔnucS, respectively (Fig. 3b). We verified that recombinants detected were exclusively due to recombination events but not spontaneous mutation (see ‘Methods’ section). The inhibitory effect of NucS on homeologous but not homologous recombination again resembles an important tell-tale signature of a canonical MMR pathway28,29.
NucS polymorphisms in M. tuberculosis clinical strains
Once the possibility of hypermutability was demonstrated in M. smegmatis, we searched for the existence of M. tuberculosis hypermutable clinical isolates by nucS inactivation. Analysis of the nucSTB sequences from ∼1,600 clinical M. tuberculosis strains available in the databases revealed a total of nine missense single nucleotide polymorphisms (SNPs) (Supplementary Table 4, Supplementary Fig. 3). The effects of these polymorphisms on NucS activity were experimentally analysed by checking their impact on mutation rates, using a M. smegmatis heterologous system, as previously reported for other mutagenesis studies30. Ten nucSTB alleles (nine polymorphic plus the wild type) were integrated into the chromosome of M. smegmatis ΔnucS. Complementation with wild-type nucSTB restored low mutation rates to M. smegmatis ΔnucS. However, five alleles increased mutation rate significantly (Fig. 4, Supplementary Table 5), with allele S39R presenting the strongest observed mutator phenotype (83-fold increase). Alleles A135S, R144S, T168A and K184E produced increases in mutation rates close to one order of magnitude, whereas alleles S54I, A67S, V69A and D162H produced low increases (∼2) or no changes. These results suggest the existence of hypermutable M. tuberculosis clinical strains affected by modulation of NucS activity.
NucS taxonomic distribution
Taken together, our results compellingly suggest a functional connection between NucS and known MMR pathways. We analysed the species distribution of NucS taking also into account the canonical MMR proteins, MutS and MutL (for MutS and MutL analyses see Supplementary Methods). A total of 3,942 reference proteomes were scanned for presence/absence of NucS (Supplementary Data 1, Supplementary Fig. 4). Bacteria are represented by 2,709 proteomes (68%) and Archaea by 132 (4%), the remaining 1,101 (28%) belonging to Eukaryota and Virus. NucS is present in 370 organisms, from the domains Archaea (60 species) and Bacteria (310 species) (Supplementary Data 1). It is totally absent from eukaryotes and virus.
To highlight the distribution of NucS in all organisms, we built a phylogenetic profile of NucS. Figure 5 shows this profile mapped onto the NCBI taxonomy tree, containing 2,186 bacterial and archaeal species (Supplementary Data 2). The NucS distribution pattern indicates that this protein exhibits a disperse distribution (Fig. 5, Supplementary Data 1).
In Bacteria, the phylum Actinobacteria is the one containing the majority of NucS with 300 species in the class Actinobacteria (only two exceptions) and three species in other classes of the phylum (Supplementary Data 1), Conexibacter woesei (class Thermoleophilia), Patulibacter medicamentivorans (class Thermoleophilia) and Ilumatobacter coccineus (class Acidimicrobiia). All the analysed members of the class Coriobacteriia, from the Actinobacteria phylum, lack NucS and MutS–MutL proteins, while the two species from the class Rubrobacteria lack NucS, but present MutS–MutL. The pattern is even more disperse in Archaea. From 132 species, 60 have NucS (21 also contain MutS–MutL). NucS, but not MutS–MutL, is present in 17 out of 24 species of the phylum Crenarchaeota and in 18 out of 88 of the phylum Euryarchaeota. By contrast, MutS–MutL (but not NucS) is completely absent in crenarchaeotal species while it is restricted to 29 euryarchaeotal species (Supplementary Data 1).
Interestingly, only 28 organisms, 21 halobacterial species (domain Archaea) and 7 species of the phylum Deinococcus-Thermus (domain Bacteria), have both NucS and MutS–MutL sequences. Notably, when we focused our analysis in the two main NucS-containing groups (Actinobacteria and Archaea), some species still lack both NucS and MutS–MutL (confirmed by protein translated searches -tblastn- in Actinobacteria and Archaea, Supplementary Data 1).
A model for the origin and evolution of NucS
Our results support a complex evolutionary ancestry for NucS. Comprehensive protein sequence analyses of NucS indicate that the protein contains two distinct regions, a DNA-binding N-terminal domain (NucS-NT) and an endonuclease C-terminal domain (NucS-CT) (Supplementary Figs 3 and 4), in agreement with previous structural studies11. At the sequence level, using profile hidden Markov models (HMMs), we also detected these regions in alternative proteins outside the context of NucS, supporting the original independence of these domains, which have been subsequently fused during evolution.
To understand the particular distribution observed in the phylogenetic profile, we conducted sequence and phylogenetic independent analyses of full NucS and also the N-terminal and C-terminal regions (Supplementary Figs 5–7). The actinobacterial NucS representatives are well separated from those of Archaea. On the other hand, the NucS from Deinococcus-Thermus species group together with the archaeal proteins, instead of the actinobacterial orthologues, suggesting that NucS has recently been transferred from Archaea to these Deinococcus-Thermus species (Supplementary Figs 5–7).
The sequence analyses provide different distributions for the two regions of NucS. While the N-terminal region is limited exclusively to Archaea and some Bacteria (Supplementary Fig. 7), the C-terminal region was found in many archaeal species, some Bacteria, and in a few eukaryotes (Supplementary Fig. 6) and, importantly, also in different domain architectures. These observations, in the context of our phylogenetic analyses, suggest that both regions may have emerged in Archaea. Subsequently, the C-terminal region may have been transferred to some bacterial species and to a few eukaryotes, and got fixed in different protein contexts. The full protein and the individual domains likely got lost in certain groups during the evolution of Archaea. However, the reconstruction of the precise evolution of these individual domains requires deeper analyses in the context of related protein domains.
Phylogenetic analysis of the full protein suggests that NucS emerged after the archaeal divergence by a rearrangement of these domains and then it was transferred from Archaea to certain Deinococcus-Thermus species in at least one event. For Actinobacteria, the most parsimonious explanation suggests a horizontal transfer event of NucS from Archaea coupled with a likely MutS–MutL loss event in the last common ancestor of Actinobacteria (as most of the contemporary NucS-encoding species lack MutS and MutL). This is consistent with the fact that we did not find any species from the entire Bacteria group, except those from Actinobacteria and the Deinococcus-Thermus group, having NucS or NucS-like proteins. Our model (Fig. 6) favours the simplest scenario to explain the complex pattern distribution of the full NucS protein and its absence in all eukaryotes, the vast majority of bacteria, and some archaeal organisms without invoking unlikely massive losses. This is in agreement with our phylogenetic observations.
This study provides genetic and biological evidence that establish the existence of a DNA repair system that mimics the canonical MutS–MutL-based MMR pathway.
To date, the correction of mismatched nucleobases has been defined as a highly conserved mechanism whose key steps are performed, in all cases, by members of the MutS and MutL protein families. Despite the genomes of Crenarchaeota, a few groups of Euryarchaeota and almost all members of the phylum Actinobacteria lacking identifiable MutS or MutL homologues5,6,7, they exhibit rates and spectra of spontaneous mutations similar to canonical MMR-bearing bacterial species8,9,10, suggesting the existence of still undetected pathway responsible for this type of correction. Although recent biochemical and structural reports suggested the existence of a novel mismatch-specific endonuclease, NucS, in the archaeal species T. kodakarensis12,14 that is able to recognize and cleave mismatched bases in dsDNA in vitro, no genetic and/or biological evidence had been reported to date on the activity of a novel mismatch repair pathway.
The screening of a large library of M. smegmatis mutants revealed that NucS is a key mutation avoidance component in Actinobacteria. Through genetic and biological analysis, we demonstrate that the nucS-null phenotypes in M. smegmatis are almost identical to those produced by the MMR deficiency in other bacteria (very high mutation rates, transition-biased mutational spectrum and increased homeologous recombination rates). The anti-mutator nature of NucS is also demonstrated in Streptomyces coelicolor, a different species of the class Actinobacteria. Therefore, NucS appears to be an important DNA repair factor which, together with the high-fidelity DNA-polymerase DnaE1 and its PHP domain-proofreader30, maintain low mutation rates (∼10−10 mutations per base per generation9,10), ensuring genome stability and DNA fidelity in mycobacteria and in other Actinobacteria.
Although SNPs in DNA repair/replication genes have been suggested as a source of hypermutation in M. tuberculosis31,32, only small increases in mutation rates have been observed due to these polymorphic genes (for example, polymorphisms in PHP exonuclease domain of the DNA-polymerase DnaE1 (ref. 30)). Our results suggest the existence of naturally occurring hypermutable M. tuberculosis variants with diminished NucS activity. Whether or not this is relevant for the virulence and adaptation to antibiotic treatments remains to be deciphered.
Although we observed that purified mycobacterial NucS binds to ssDNA but not to dsDNA, as described for archaeal NucS proteins11,12, no significant specific cleavage activity was observed on mismatched substrates, suggesting that activation by other partners and/or modifications (for example, post-translational modifications) is required in M. smegmatis. Also, the possibility of a functional difference between bacterial and archaeal NucS cannot be ruled out. Therefore, additional studies are needed to assess whether mycobacterial and archaeal NucS proteins have the same functional requirements.
Our computational studies support an archaeal origin for NucS, as previously suggested12, built upon two distinct domains that suffered a complex evolutionary history of transfers and/or losses, including at least two HGT events to Actinobacteria and Deinococcus-Thermus. Indeed, the contribution of horizontal gene transfer in bacterial and archaeal evolution is well-established33,34. Interestingly, NucS and MutS–MutL systems seem to be present alternatively in different species, with only a few exceptions. In Actinobacteria, it is possible that the acquisition of NucS may have facilitated the subsequent loss of MutS–MutL, as these canonical proteins are so widely conserved across Bacteria.
On the other hand, there are two groups (Halobacteria and some Deinococcus-Thermus) where NucS and MutS–MutL coexist. Notably, in a Halobacteria, Halobacterium salinarum, inactivation of mutS or mutL produced no hypermutability35, suggesting that MutS and MutL are redundant to an alternative system that controls spontaneous mutation. This indicates that evolution of these particular species may have opted to keep both systems. The possible interplay between both pathways remains to be elucidated. Surprisingly, NucS and MutS–MutL are apparently absent in some species. Therefore, the possible existence of additional alternative MMR repair pathways, yet to be identified, cannot be discarded.
In conclusion, we propose that MMR is a mechanism that can be either accomplished by either the MutS-L or the NucS pathway. Understanding the mechanisms and pathways that influence genome stability may unveil new strategies to predict and combat the development of drug resistance. In addition, engineered Mycobacterium strains lacking this mutation-avoidance pathway, may be valuable tools for evaluating anti-tuberculosis treatments, including new drugs, drug combinations and non-antibiotic based regimes.
Bacterial strains and growth conditions
M. smegmatis wild-type strain mc2 155 and its mutant derivatives were grown at 37 °C in Middlebrook 7H9 broth or Middlebrook 7H10 agar (Difco) with 0.5% glycerol and 0.05% Tween 80, and enriched with 10% albumin-dextrose-catalase (Difco). E. coli strains were cultured at 37 °C in LB medium. Streptomyces coelicolor A3(2) M145 and its derivatives were grown at 30 °C on mannitol–soya (MS) agar.
All primers used in this work are listed in Supplementary Table 6.
Generation and screening of a M. smegmatis insertion library
Transposon ΦMycoMarT7 (ref. 36) was used to obtain a M. smegmatis mutant library of 11,000 independent clones. For transduction, M. smegmatis mc2 155 cultures were washed, mixed with the phage stock at a multiplicity of infection of 1:10 (37 °C, 3 h) and plated on kanamycin (25 μg ml−1). The insertion mutants were isolated and inoculated into 96-well microtiter plates containing Middlebrook 7H9 medium. To identify hypermutators, each mutant was inoculated onto 7H10 agar plates with rifampicin (20 μg ml−1). One transposon mutant, producing a high number of rifampicin resistant (Rif-R) colonies, was selected for further characterization. The transposon insertion site in the chromosome was determined by sequencing.
Generation of a ΔnucS knockout mutant in M. smegmatis
M. smegmatis ΔnucS (MSMEG_4923, nucSSm) in-frame deletion mutant was generated by allelic replacement37. Briefly, p2NIL-ΔnucSSm, harbouring an in-frame deletion of the target gene, was electroporated into M. smegmatis mc2 155. Single-crossover merodiploid clones were isolated and after that, counter-selected to generate the unmarked deletion by a second crossover event. Finally, putative M. smegmatis ΔnucS colonies were checked by PCR and sequencing. For additional details see Supplementary Methods.
Complementation of the M. smegmatis ΔnucS mutant
For complementation, a wild type of the MSMEG_4923 gene (nucSSm) and the wild-type full-length MT_1321 gene from CDC1551 control strain (nucSTB), including their own promoter regions, were cloned into the vector pMV361 (ref. 38) and introduced into M. smegmatis ΔnucS by electroporation. pMV361 is an integrative vector that carries a site-specific integration system derived from the mycobacteriophage L5. It integrates at a single site in the M. smegmatis chromosome, the attB, which overlaps the 3′ end of the tRNA-glycine gene39. Integration at the appropriate site was verified for all constructs by PCR. For additional details see Supplementary Methods.
ΔnucS S. coelicolor knockout mutant and complementation
S. coelicolor ΔnucS (gene SCO5388, nucSSco) in-frame deletion mutant was constructed by double crossover recombination using the plasmid pIJ6650 (ref. 40). pIJ-ΔnucSSco (containing the in-frame deletion of the nucSSco gene) was introduced in S. coelicolor A3(2) M145 to generate the unmarked deletion of the nucSSco gene. Finally, S. coelicolor ΔnucS was complemented with a wild-type copy of nucSSco inserted in the attB site of the S. coelicolor ΔnucS via the integrative vector pSET152 (Supplementary Methods).
Estimation of mutation rates
Fluctuation analyses were used to experimentally address mutation rates. For each experiment, 20 independent cultures of M. smegmatis mc2 155 and its derivatives were grown and diluted to inoculate 1,000–10,000 cells per ml into fresh medium. All the cultures were incubated until they reached stationary phase (about 109 cells per ml). Appropriate dilutions were plated on Middlebrook 7H10 medium with or without rifampicin (100 μg ml−1) or streptomycin (50 μg ml−1). For S. coelicolor, 20 independent concentrated spore suspensions (containing ∼109 spores per ml) from each analysed strain were generated on MS agar, and after that, plated on MS agar with or without rifampicin (100 μg ml−1) or streptomycin (50 μg ml−1). At least three different experiments were performed for each fluctuation analysis in both cases.
The expected number of mutations per culture (m) and 95% confidence intervals were calculated using the maximum likelihood estimator applying the newton.LD.plating and confint.LD.plating functions that account for differences in plating efficiency implemented in the package rSalvador (http://eeeeeric.com/rSalvador/) (Qi Zheng. Rsalvador: an assay. R package version 1.3) for R (www.R-project.org/). Mutation rates (mutations per cell per generation) were then calculated by dividing m by the total number of generations, assumed to be roughly equal to the average final number of cells. Statistical comparisons were carried out by the use of the LRT.LD.plating function of the same package, which accounts for the differences in final number of cells and plating efficiency. Finally, in case of multiple comparisons P values were corrected by the Bonferroni method.
Characterization of the mutational spectrum
The mutational spectra conferred by M. smegmatis mc2 155 and its ΔnucS derivative were characterized by selecting for resistance to rifampicin and sequencing the rifampicin resistance-determining region in the rpoB gene, from independent Rif-R isolates.
The recombination assay vectors (pRhomyco series) were generated by cloning two overlapping fragments of the hygromycin-resistance gene (hyg), from pRAM41, flanking a functional kanamycin-resistance (kan) gene in the pMV361 plasmid (Supplementary Fig. 2). Neither of the fragments of hyg conferred resistance to hygromycin on their own. Fragments share a duplicated 517 bp overlapping region, with different degrees of sequence identity (100, 95, 90 or 85%). M. smegmatis mc2 155 and its ΔnucS derivative were transformed by electroporation with the integrative plasmids pRhomyco 100%, 95%, 90% and 85% designed for the recombination assays and plated on Middlebrook 7H10 containing kanamycin (25 μg μl−1). Integration of pRhomyco vectors in the appropriate site (attB) of the M. smegmatis mc2 155 (wild type and ΔnucS) chromosome was verified by PCR.
To measure recombination rates, we analysed the restoration of a functional hyg gene that confers Hyg-R by a recombination event between the two overlapping fragments of the hyg gene. Sixteen independent overnight cultures from each strain were grown in Middlebrook 7H9 broth plus kanamycin (to prevent the selection of Hyg-R bacteria coming from the early recombination of pRhomyco). Approximately, 104 bacteria were inoculated in plain 7H9 broth (without kanamycin) to allow the recombination events and cultured 24 h at 37 °C with shaking. Cultures were plated on 7H10 plus 50 μg ml−1 hygromycin (for recombinant cells count) and in addition, appropriate dilutions were plated on plain 7H10 (for viable cell counts) and incubated for 3–5 days. Total number of Hyg-R colonies was considered to calculate recombination rates. Recombination rates were calculated and analysed as described in estimation of mutation rates.
To validate the recombination assay, we first verified that no Hyg-R colonies were generated by spontaneous mutation, even in the ΔnucS derivative. The mutation rate was ≤1 × 10−10 for the hypermutable derivative, far below the lowest recombination value (6 × 10−9 for WT, 15% non-identical sequences). These results indicate that the Hyg-R colonies from our recombination assay were not generated by spontaneous mutations. Moreover, we verified that recombinant clones express hygromycin resistance and kanamycin susceptibility by picking 20–30 Hyg-R colonies from each strain onto kanamycin plates. In all cases they were Hyg-R and Kan-S. Finally, we randomly isolated 10 independent Hyg-R presumptive recombinant colonies from each construct (80 colonies total) and verified by PCR that a single fragment of the size of the reconstituted hyg gene was amplified in all cases.
NucS purification and biochemical activity
M. smegmatis nucS was cloned as a SUMO fusion and expressed in E. coli BL21 cells overnight at 16 °C. NucS protein was purified by affinity chromatography using Ni2+–NTA agarose column followed by an additional step of anion exchange purification in HiTrap Q HP column. NucS-SUMO fusion was cleaved by Ulp protease to release a native protein. Purified protein was collected and concentrated to perform the activity assays (Supplementary Fig. 1A). In addition, His-tagged M. smegmatis nucS was also cloned in pET28b (for E. coli expression) and pYUB28b (for M. smegmatis expression). His-tagged NucS was also purified by affinity chromatography and anion exchange purification as described before.
For DNA EMSA assays, NucS purified protein (1–16 μM) was incubated with fluorescein-labelled ssDNA (45-mer DNA, 50 nM) or dsDNA (45 bp DNA, 50 nM), in 50 mM Tris–HCl (pH 7.5), 1 mM EDTA, 10% glycerol and 10 μg ml−1 BSA for 30 min at 37 °C. Protein–DNA complexes were resolved on 5% polyacrylamide gel in × 0.25 TBE plus 1% glycerol and run under refrigerated conditions (5–10 °C).
For nuclease activity, fluorescein-labelled 36-mer DNA was annealed to a fully complementary opposite strand (control) or carrying a single nucleotide mismatch in the central region of the strand (mismatch substrates). In total, 30 nM dsDNA substrates were incubated with 300 nM of recombinant, tag free NucS in 20 mM Tris–HCl pH 7.5, 6 mM ammonium sulfate, 2 mM MgCl2 and 100 mM NaCl, 0.1 mg ml−1 BSA and 0.1% TritonX-100. The reactions were carried out at 37 °C for 30 min when 0.5 U Proteinase K was added to each reaction to digest NucS nuclease. Digestion was continued for 30 min at 50 °C. Stop solution was added (95% formamide, 0.09% xylene cyanol), samples were boiled at 95 °C for 10 min and resolved on 7 M urea, 15% polyacrylamide gel in 1 × TBE for 2 h. Mg, Mn and Zn ions, and combinations of these three metals, were tested as cofactors with no cleavage observed.
Analysis of nucS SNPs in M. tuberculosis clinical strains
Sequences from the MT_1321 gene product were downloaded from the Ensembl database (http://bacteria.ensembl.org/index.html), M. tuberculosis variome resource42 and Comas et al. data43. A total of 1,600 proteins were aligned using MAFFT and the polymorphisms were visualized with Jalview.
Construction of nucS alleles by site-directed mutagenesis
To construct nucS alleles, wild-type nucSTB gene was PCR amplified and cloned into pUC19 to be used as template for mutagenic PCRs. Single specific mutations were introduced into nucSTB by PCR with the suitable mutagenic pairs of primers. Following the PCR reaction, a DpnI digestion was carried out for 4 h at 37 °C. Mutagenized plasmids obtained after transformation into E. coli DH5α were verified by DNA sequencing. All the nucS alleles were re-cloned into the integrative vector pMV361 to generate a set of complementation plasmids and introduced by transformation into M. smegmatis mc2 155 ΔnucS. These plasmids integrate at a single site, attB, in the M. smegmatis chromosome.
To test the efficiency of each nucS allele to restore normal mutation rates, the plasmids pMV361 carrying the mutated alleles were integrated in M. smegmatis ΔnucS chromosome. Integration of each nucSTB allele in the appropriate site (attB) of the chromosome was verified by PCR.
Computational analyses of the NucS protein
A summary of all the computational approaches conducted is depicted in Supplementary Fig. 4.
To establish how general the presence of NucS is in the domains on life, we conducted sequence analyses to initially identify NucS proteins (Supplementary Fig. 4). NUCS_MYCTU (M. tuberculosis NucS) and NUCS_PYRAB (P. abyssi NucS) sequences were used to find homologues. Each full sequence was used as an independent query in pHMMER searches (HMMER3; http://hmmer.org/) against the large database of the concatenated reference proteomes (2016_02 release of 17th February 2016). We next collected sequences excluding the original sequences used to conduct the queries. The remaining sequences were filtered by e-value (removed >0.0001), bit score >50, and length (only those >75% length were kept), and further aligned by MAFFT [ http://mafft.cbrc.jp/alignment/software/]44. The alignments were visualized with Belvu [ http://sonnhammer.sbc.su.se/Belvu.html]45 to check for quality. We removed the redundancy of the alignment discarding sequences with more than 63% of sequence identity. We next generated Markov profiles trained with the non-redundant multiple sequence alignment (using HHMER3). For each protein, we obtained about the same 400 sequences that would give also partial hits to different species, which suggested a potential existence of different domains in the protein. Further checking of the sequences retrieved the final 370 sequences. As NucS was not identified in eukaryotes or viruses, they were discarded for further analyses.
We constructed a phylogenetic profile of NucS (Supplementary Data 1) and mapped it into the NCBI taxonomic tree (Fig. 5, the newick tree format is available in Supplementary Data 2). The tree was annotated using ggtree (http://www.bioconductor.org/packages/ggtree).
Characterization of the two NucS regions
To identify potential domains in NucS, we focused on the archaeal P. abyssi NucS, whose 3D structure was previously resolved (PDB 2VLD chain B)11. This structure is composed by two distinct regions: the N-terminal DNA-binding region (1–114 amino acids) and the C-terminal catalytic region (126–233 amino acids)11. Given the absence of structural data for the bacterial NucS protein, the M. tuberculosis NucS structure was modelled using the archaeal P. abyssi NucS as a template using I-TASSER16 and generated a reliable model (Supplementary Fig. 3). Template and model were structurally aligned using the Combinatorial Extension (CE) algorithm17, built-in with PyMOL, to identify relevant residues. We used the structure-based alignment between this template and M. tuberculosis NucS (NucS_MYCTU) (Supplementary Fig. 3) to determine the different regions for further sequence analyses (N-terminal and C-terminal regions). These analyses were conducted using profile searches as above and confirmed by independent analyses of the PF01939 domain trained with NucS (for details see Supplementary Methods and Supplementary Fig. 4).
We conducted sequence searches of NucS_MYCTU in the PFAM database, where the PF01939 domain (DUF91, automatic) was identified. From the PF01939 domain (539 sequences in 464 species), only 368 entries in 363 species (archaeal and bacterial) gave a match with the full protein (Supplementary Data File 1). The results obtained from the PFAM database searches for the PF01939 domain, are in agreement with the structure-based profiles analyses (see above) confirming the existence of two distinct regions.
Taking into account the domain boundaries established above, we next aligned the 368 full NucS proteins (from PFAM PF01939) to profiles built from the structural alignment corresponding to (i) the whole protein, (ii) the N-terminal region (NT) and (iii) the C-terminal region (CT).
Sequence analysis of NucS domains
Using the different defined regions by structural bioinformatics, we first conducted sequence searches against the large database. We made non-redundant alignments of the N-terminal region (containing 63 sequences) and the C-terminal region (containing 39 sequences) and built profile HMMs. These profiles were searched using pHMMER46 against the large References Proteomes file.
Our analyses identified the C-terminal region in all the original 368 NucS sequences (for details see Supplementary Methods and Supplementary Fig. 4). In addition, the C-terminal was also found in proteins containing a variety of additional protein domains in other prokaryotic species and in few additional eukaryotic sequences. We checked the alignments to confirm that the catalytic residues were conserved, as described in the structure of P. abyssi11. When a profile with the eukaryotic sequences (excluding any bacterial or archaeal sequences) was generated, we retrieved again the C-terminal regions of NucS above threshold at significant values, but we did not retrieve any other eukaryotic sequences at reliable values. On the other hand, the N-terminal region was found mainly in bacterial and archaeal NucS, but also in two archaeal proteins annotated as topoisomerases. A pHMMER search of the regions of these sequences yielded the N-terminal of NucS.
To run phylogenetic analyses, NucS sequences from the PF01939 domain were used, but aligned to their corresponding structure-based regions. Sequences found in our searches with independent regions were also included. Out of 539, 368 unique sequences aligned with the full NucS structure-based profile (Supplementary Fig. 5, Supplementary Data 3), 422 sequences containing the C-terminal region (NucS-CT) (Supplementary Fig. 6), 370 sequences containing the N-terminal region (NucS-NT) (Supplementary Fig. 7) were run.
Sequences were aligned to the structure-based profiles, and the alignments were subjected to ML search and 1,500 bootstrap replicates using RAXML47. All free model parameters were estimated by RAxML where we used a GAMMA model of rate heterogeneity and ML estimate of alpha-parameter. The most likely selected model was LG48. For accuracy and focus on our alignment, we run the sequential version of RAxML creating various sets of starting trees (10 by manual inferring different starting trees and 10 as automatically inferred by the programme). The best setting (the closest likelihood to zero) was used for further calculations.
To run phylogenetic analyses, sequences from the PFAM PF01939 domain were used, but aligned to their corresponding region. For details of the particular regions for each domain see Supplementary Data 4. Sequences found in our searches with NT or CT regions outside NucS were also included. Phylogenetic trees were visualized with iTOL (http://itol.embl.de)49. The raw trees corresponding to both CT and NT regions (Supplementary Figs 6 and 7) are available as Supplementary Data 5 and 6 respectively.
The authors declare that all data supporting the findings of this study are available within the paper and its Supplementary Information files or from the authors upon reasonable request.
How to cite this article: Castañeda-García, A. et al. A non-canonical mismatch repair pathway in prokaryotes. Nat. Commun. 8, 14246 doi: 10.1038/ncomms14246 (2017).
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J.B. was supported by Plan Nacional de I+D+i and Instituto de Salud Carlos III, Subdirección General de Redes y Centros de Investigación Cooperativa, Ministerio de Economía y Competitividad, Spanish Network for Research in Infectious Diseases (REIPI RD12/0015) – co-financed by European Development Regional Fund ‘A way to achieve Europe’ ERDF and SAF2015-72793-EXP and BFU2016-78250-P from Spanish Ministry of Science and Competitiveness (MINECO)-FEDER). A.J.D. was supported by a grant from the Biotechnology and Biological Sciences Research Council (BB/J018643/1). A.C.-G. and J.R.-B. were supported by contracts from REIPI RD15/0012 and A.C.-G. also by a Ramon Areces fellowship for Life Sciences. A.I.P. was supported by a ‘Sara Borrell’ contract, Instituto de Salud Carlos III. T.T. was supported by the Research Council of Norway, GLOBVAC project 234506. We are grateful to I. Cases for his help customizing the R libraries for tree visualization, Federico Abascal for critical input regarding models of evolution, I. Comas for critical reading of the manuscript and J. Glynn and S. Hoffner for providing additional data of M. tuberculosis strains.
The authors declare no competing financial interests.
Supplementary Figures, Supplementary Tables, Supplementary Methods, and Supplementary References (PDF 8096 kb)
Taxonomic distribution of NucS and MutS-MutL in reference proteomes (Big excel data file). (XLS 902 kb)
Taxonomic tree for phylogenetic profiling in newick format. Raw NCBI profiling tree from archaeal and bacterial species extracted from NCBI in newick format, corresponding to Figure 5. (TXT 54 kb)
Phylogenetic tree of full NucS in newick format. Raw Maximum Likelihood and bootstrap phylogenetic tree corresponding to Supplementary Figure 5 (full NucS) in newick format. (TXT 30 kb)
Detailed information for phylogenetic trees of NucS regions. Sequence details of NucS-CT and NucS-NT labels on Supplementary Figures 6-7 trees (Excel file). (XLSX 94 kb)
Phylogenetic tree of C-terminal NucS in newick format. Raw Maximum Likelihood and bootstrap phylogenetic tree corresponding to Supplementary Figure 6 (NucS-CT region) in newick format. (TXT 36 kb)
Phylogenetic tree of N-terminal NucS in newick format. Raw Maximum Likelihood and bootstrap phylogenetic tree corresponding to Supplementary figure 7 (NucS-NT region) in newick format. (TXT 31 kb)
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Castañeda-García, A., Prieto, A., Rodríguez-Beltrán, J. et al. A non-canonical mismatch repair pathway in prokaryotes. Nat Commun 8, 14246 (2017). https://doi.org/10.1038/ncomms14246
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