Eukaryotic DNA Mismatch Repair (MMR) involves redundant exonuclease 1 (Exo1)-dependent and Exo1-independent pathways, of which the Exo1-independent pathway(s) is not well understood. The exo1Δ440-702 mutation, which deletes the MutS Homolog 2 (Msh2) and MutL Homolog 1 (Mlh1) interacting peptides (SHIP and MIP boxes, respectively), eliminates the Exo1 MMR functions but is not lethal in combination with rad27Δ mutations. Analyzing the effect of different combinations of the exo1Δ440-702 mutation, a rad27Δ mutation and the pms1-A99V mutation, which inactivates an Exo1-independent MMR pathway, demonstrated that each of these mutations inactivates a different MMR pathway. Furthermore, it was possible to reconstitute a Rad27- and Msh2-Msh6-dependent MMR reaction in vitro using a mispaired DNA substrate and other MMR proteins. Our results demonstrate Rad27 defines an Exo1-independent eukaryotic MMR pathway that is redundant with at least two other MMR pathways.
Eukaryotic MMR plays a critical role in suppressing spontaneous mutations caused by DNA replication errors and consequently plays an important role in suppressing the development of cancer1,2,3,4,5,6,7,8. The core eukaryotic MMR machinery required for all MMR pathways consists of a mispair recognition complex and an endonuclease active site-containing accessory factor. The mispair recognition complex can be either Msh2-Msh6 or Msh2-Msh3, which have partially overlapping mispair recognition specificities2,3,7,9,10,11. The primary accessory factor in MMR is the Mlh1-Pms1 endonuclease (called MLH1-PMS2 in humans), although a second endonuclease, Mlh1-Mlh3, can substitute for Mlh1-Pms1 to a small extent2,3,7,12,13,14,15,16. These proteins promote MMR in combination with appropriate combinations of Exo1, DNA polymerase δ, DNA polymerase ε, PCNA, RFC, and RPA15,17,18,19,20,21,22. The best understood MMR reaction involves recruitment of Exo1 by mispair-bound Msh2-Msh6 (or Msh2-Msh3) to degrade one DNA strand from a preexisting 5’ nick or a 5’ nick introduced by Mlh1-Pms1 to excise the mispair followed by a gap-filling reaction15,17,18,19,20,21,22. Deletion of EXO1 only causes a small increase in mutation rate and hence only causes a small MMR defect compared to the deletion of genes that are absolutely required for MMR (e.g., MSH2, MLH1), implying that Exo1-independent MMR pathways exist23,24,25. Genetic studies have defined MMR excision-resynthesis pathways that depend on or are independent of Exo11,23,26,27. These pathways appear to differ in their requirement for the level of activation of the Mlh1-Pms1 endonuclease, as well as in their requirement for Exo1 recruitment1,21,26,28. However, comparatively little is known about the mechanism of Exo1-independent MMR due to the limited state of genetic analysis of potential Exo1-independent MMR mechanisms1,23,26,29. Furthermore, since no combination of exo1Δ and known mutations that inactivate Exo1-independent MMR pathways completely eliminates MMR23,26,28,30, it is not clear how many Exo1-independent MMR mechanisms exist.
One candidate for an enzyme that, like Exo1, catalyzes excision during MMR is the flap endonuclease Rad27 (called Rth1 in some studies and FEN1 in humans). Rad27 processes the 5’ ends of Okazaki fragments and also acts in base-excision repair31,32. A role for Rad27 in MMR was initially suggested because rad27Δ strains have a strong mutator phenotype with increased rates of dinucleotide repeat instability and accumulation of mutations in the CAN1 gene33. However, several lines of evidence initially argued against a primary role for Rad27 in MMR. First, defects in RAD27 primarily increased the rate of insertions in dinucleotide repeats, whereas defects in MSH2, MLH1, or PMS1 primarily increased the rate of deletions33. Second, combining a deletion of RAD27 with deletions in MSH2, MLH1 or PMS1 often resulted in a greater-than-additive increase in the rate of accumulating inactivating mutations in the CAN1 gene compared to the respective single mutants33,34, which could reflect defects in more than one DNA repair pathway. Third, defects in RAD27 caused the accumulation of distinctive large insertion/deletion mutations in CAN1 that were flanked by short direct repeats that were not caused by a deletion of MSH2 that causes a complete defect in MMR35; increased rates of similar complex mutations, as well as increased rates of genome rearrangements including translocations, were also seen in subsequent studies of rad27 mutants34,36,37. The initial study documenting the occurrence of complex mutations in rad27 mutants also observed that deletion of RAD27 caused a small increase in mutation rate in the hom3-10 frameshift reversion assay35, which detects frameshift mutations in a mononucleotide repeat sequence and is highly specific for detecting MMR defects9; note that MMR defects caused by deletion of genes like MSH2 cause very large increases in mononucleotide repeat frameshift reversion assays like the hom3-10 assay9,35,38,39,40. This latter result was interpreted as suggesting Rad27 could play a minor role in MMR35. Biochemical studies have shown that Rad27 can cleave 5’ flaps produced by strand-displacement synthesis by DNA polymerase δ on nicked, mispair-containing DNA substrates resulting in mispair excision29 and Rad27 along with MMR proteins can excise mispairs at the 5’ end of Okazaki fragments by DNA polymerase α segment error editing41; however, it has not demonstrated that these reactions are related to bona fide general MMR. In addition, MMR can act as a complementary pathway to Rad27 in the removal of short 5’ flaps that can occur during the processing of the 5’ ends of Okazaki fragments34.
Exo1 and Rad27 catalyze similar reactions. On a 5’ nicked substrate, 5’ to 3’ excision by Exo1 promotes gap filling by DNA polymerase δ, leading to repair of a mispair 3’ to the nick17,18,19,20,22. Similarly, Rad27 will cleave 5’ flaps generated during strand-displacement synthesis by DNA polymerase δ on a nicked substrate, resulting in nick translation leading to the same type of reaction products42,43. This biochemical similarity suggested it would be useful to investigate the effect of exo1Δ rad27Δ double mutations on MMR; however, this combination of mutations is lethal25,44. Recently, we observed that the role of Exo1 in MMR is mediated by two Msh2-interacting sequences28 (SHIP boxes) and one Mlh1-interacting sequence28,45,46,47 (MIP box) in the unstructured C-terminus of Exo128. Deleting these sequences results in a mutant Exo1 that is fully defective for MMR but retains its other functions, including those required in the absence of Rad2728. Using an exo1 truncation mutation that eliminates the SHIP and MIP boxes, we have now been able to perform genetic studies that demonstrate that Exo1 and Rad27 play redundant roles in MMR. In addition, we have reconstituted a Rad27-dependent and Msh2-Msh6-dependent MMR reaction in vitro, providing biochemical insight into the mechanism of Rad27-dependent MMR.
Genetic evidence that Rad27 and Exo1 function in redundant MMR pathways
To study genetic interactions between a rad27Δ mutation and an MMR-defective exo1 mutation, we created the exo1Δ440-702 mutation, which truncates Exo1 after codon 439 and removes the MIP and SHIP boxes that mediate interactions with Mlh1 and Msh228. The exo1Δ440-702 and rad27Δ single and double mutations were tested for their effects on MMR using the hom3-10 and lys2-10A frameshift reversion mutation rate assays, which are highly specific for detecting MMR defects as MMR defects cause high rates of reversion of a single nucleotide insertion in a mononucleotide repeat9,35,38,39,40 (Table 1). Consistent with previous studies, the exo1Δ440-702 mutation caused a small 3-fold increase in mutation rate in both assays, and the rad27Δ mutation caused 97-fold and 308-fold increases in mutation rates in the hom3-10 and lys2-10A frameshift reversion assays, respectively. The exo1Δ440-702 rad27Δ double mutant had a synergistic increase in mutation rate in both assays compared to both single mutants that were highly significant (Mann−Whitney U-test; Supplementary Table 1). Importantly, the resulting double mutant mutation rate was not as high as that of an msh2Δ single mutant, which is completely defective for MMR9,38,40,48.
To determine the spectrum of mutations that reverted the hom3-10 mutation, 24 to 36 independent hom3-10 revertants were sequenced from the exo1Δ440-702 and rad27Δ single and double mutants, as well as from the wild-type and msh2Δ strains. The hom3-10 mutation is caused by a single T insertion in a run of six Ts in the HOM3 gene9, and >89% of the reverting mutations from each strain were caused by deletion of a single T in this seven-T run (Supplementary Fig. 1). The remaining reverting mutations were single nucleotide deletions within 10 nucleotides of the seven-T run, often in shorter mononucleotide repeats, which also restored the HOM3 reading frame (Supplementary Fig. 1). The accumulation of single base deletions and not direct-repeat mediated insertions and deletions is consistent with mutations arising due to MMR defects35. Note that previous studies have also shown that the exo1Δ msh2Δ and rad27Δ msh2Δ double mutation combinations caused the same mutation rate in the hom3-10 reversion assay as an msh2Δ single mutation and, where tested, resulted in the same spectrum of hom3-10 reverting mutations24,25,35. In aggregate, these results and previous results support the hypothesis that Rad27 and Exo1 function in redundant MMR pathways that together only partially account for MMR, which is absolutely dependent on Msh2.
Genetic evidence for at least two Exo1-independent MMR pathways
Previous genetic studies have identified mutations inactivating at least one Exo1-independent MMR pathway1,23,26,27. The best-characterized mutations affect PCNA (e.g., pol30-K217E) and Mlh1-Pms1 (e.g., pms1-A99V) and reduce, but do not eliminate, PCNA-activated Mlh1-Pms1 endonuclease activity. This result suggests that at least one Exo1-independent MMR pathway requires higher levels of Mlh1-Pms1 endonuclease activity than Exo1-dependent MMR1,26,27. Combining an exo1Δ mutation with the pms1-A99V or pol30-K217E mutations resulted in highly synergistic mutation rates; however, these mutation combinations did not inactivate MMR to the extent caused by an msh2Δ mutation23,26,27. To determine if Rad27 accounts for the residual Exo1-independent MMR, we combined the exo1Δ440-702 and rad27Δ single and double mutations with the pms1-A99V mutation and tested their effects in the hom3-10 and lys2-10A frameshift reversion assays (Table 1). Both the exo1Δ440-702 and rad27Δ single mutations had significant synergistic interactions with the pms1-A99V mutation in both assays (Mann Whitney U-test, Supplementary Table 1). In addition, the exo1Δ440-702 rad27Δ pms1-A99V triple mutant had a synergistic increase in the mutation rate in the two frameshift mutation rate assays compared to the respective double mutants that were statistically significant (Mann Whitney U-test, Supplementary Table 2). The mutation rates of the exo1Δ440-702 rad27Δ pms1-A99V triple mutant were modestly lower than that of an msh2Δ single mutant, based on 95% confidence intervals. We then determined the mutation rates of the msh2Δ exo1Δ440-702 rad27Δ and pms1Δ exo1Δ440-702 rad27Δ triple mutants and found that the mutation rates were slightly higher than the mutation rates of the msh2Δ and pms1Δ single mutants by 1.5 to 4 fold, although based on 95% confidence intervals, the differences seen in the lys2-10A frameshift reversion assay were not significant (Table 1). These results support the hypothesis that the exo1Δ440-702, rad27Δ, and pms1-A99V mutations inactivate three different redundant MMR pathways that account for most of Msh2-dependent MMR.
To further characterize the role of Rad27 in MMR, we examined the genetic interaction between rad27Δ and pol30-K217E, which was identified in a screen for PCNA mutations that synergize with an exo1Δ mutation in mutator assays; pol30-K217E also causes a partial defect in activation of the Mlh1-Pms1 endonuclease26. The lys2-10A frameshift reversion rates of the rad27Δ and pol30-K217E single mutants and the rad27Δ pol30-K217E double mutant were 1.83 × 10−6 (308 × wild-type), 3.26 × 10−7 (55 × wild-type), and 1.02 × 10−5 (1717 × wild-type), respectively. Thus, combining the rad27Δ and pol30-K217E mutations resulted in a significant synergistic increase in mutation rates compared to the respective single mutations (p = 5.3 × 10−9 and p = 8.6 × 10−10, respectively; Mann−Whitney U-test), similar to the genetic interaction between exo1Δ and pol30-K217E26, exo1Δ and pms1-A99V23, and rad27Δ and pms1-A99V (Table 1).
Deletion of RAD27 results in the accumulation of Mlh1-Pms1 foci MMR intermediates
Previous studies have shown that Mlh1-Pms1, detected using a functional Pms1-GFP fusion protein, forms foci during S-phase and that the formation of these foci requires the presence of mispaired bases and MSH2, and are promoted by the Msh2-Msh6 and Msh2-Msh3 complexes, leading to the conclusion that Mlh1-Pms1 foci are key MMR intermediates26,27,30,49. These Mlh1-Pms1 foci accumulate at increased levels in exo1Δ mutants, suggesting that Exo1-dependent MMR may be more rapid than Exo1-independent MMR or may require less Mlh1-Pms130. We, therefore, investigated the effect of exo1Δ440-702 and rad27Δ mutations on the levels of Pms1 foci (Fig. 1). The exo1Δ440-702 and rad27Δ single mutants had increased levels of Pms1 foci that were essentially the same as and slightly higher than those observed in an exo1Δ mutant. The exo1Δ440-702 rad27Δ double mutant had a modest but significantly higher increase in the level of Pms1 foci than the respective single mutants. Importantly, an msh2Δ mutation eliminated the Pms1 foci in all of the mutants tested. These results suggest that Rad27-dependent MMR and Exo1-dependent MMR have similar mispair excision kinetics and/or require similar levels of Mlh1-Pms130.
Reconstitution of Rad27-dependent MMR using purified proteins
Previously we reconstituted an MMR reaction on circular DNA substrates containing different mispairs and a 5’ nick17,50. These reactions used S. cerevisiae Msh2-Msh6, Exo1, DNA polymerase δ, PCNA, RPA, and RFC-Δ1N, which is a version of Replication Factor C in which the ligase homology domain of Rfc1 was deleted to allow for overexpression51. Repair of the CC mispair-containing substrate tested here allows PstI to cleave at a site that is cleavage-resistant due to the mispair (Fig. 2a). PstI cleavage of the repaired substrate combined with cleavage at a distal ScaI site resulted in characteristic 1.8 and 1.1 kb products (Fig. 2b, lane 1). Omitting Exo1 in these reactions almost completely abolished repair; however, in the small amount of apparent repair products observed, the larger product species appeared to migrate more slowly than the normal 1.8 kb product (Fig. 2b, lane 2). It seemed likely that this apparent repair was due to strand-displacement synthesis by DNA polymerase δ and that the slowly migrating product contained a branch due to the displaced strand (Fig. 2a); in previous studies, these products were not seen when Exo1 was omitted because we used lower amounts of DNA polymerase δ17. To investigate this possibility, different amounts of Rad27 were added to the reactions (Fig. 2b). Increasing amounts of Rad27 markedly stimulated the repair reaction and reduced the aberrant migration of the large product species; the highest levels of Rad27 caused the large product species to co-migrate with the mature 1.8 kb repair product. Stimulation of DNA polymerase δ by Rad27 has been previously observed using different assays42. In repair reactions with levels of DNA polymerase ε that promote repair in the presence of Exo118, no apparent repair was seen at any amount of Rad27 tested (Fig. 2c); this is consistent with the fact that DNA polymerase ε does not catalyze strand-displacement DNA synthesis52.
To investigate the requirements for Rad27 and Msh2-Msh6 in these reactions, a series of reactions were performed containing 5 pmoles of Rad27, Msh2-Msh6, DNA polymerase δ, PCNA, RFC-Δ1N, and RPA in which different proteins were omitted as indicated (Fig. 3). In the presence of both Rad27 and Msh2-Msh6, both the mature 1.1 and 1.8 kb species were observed, similar to the Exo1-dependent reaction. In the absence of both Rad27 and Msh2-Msh6, the mature 1.1 kb species and the slowly migrating branched species resulting from strand-displacement synthesis were observed. In the absence of Msh2-Msh6 but in the presence of Rad27, a mixture of the strand-displacement synthesis product and 1.8 kb mature repair species were observed, consistent with the cleavage of a fraction of the strand displacement products by Rad27. Remarkably, in the absence of Rad27 but in the presence of Msh2-Msh6, essentially no products were observed, indicating that Msh2-Msh6 suppresses strand-displacement synthesis by DNA polymerase δ in the absence of Rad27. Thus, the formation of only mature repair products was dependent on both Rad27 and Msh2-Msh6 under these reaction conditions, indicative of a bona fide MMR reaction.
Mispair and PCNA binding by Msh2-Msh6 function in Rad27-dependent MMR
We then tested the effect of substituting wild-type Msh2-Msh6 with Msh2-Msh6-F337A, which is defective for mispairing binding53, or Msh2-Msh6-F33AF34A, which is defective for binding PCNA54 (Fig. 4). Msh2-Msh6-F337A completely eliminated repair, consistent with a requirement for mispair binding by Msh2-Msh6 for the ability of Rad27 to overcome Msh2-Msh6-mediated suppression of strand-displacement synthesis. Msh2-Msh6-F33AF34A resulted in an increased level of apparent repair compared to that seen in the presence of wild-type Msh2-Msh6, and the same distribution of branched and mature repair product bands as that seen when Msh2-Msh6 was omitted from the reactions. This latter result suggests that the interaction between Msh2-Msh6 and PCNA is required to stimulate the formation of mature repair products.
Given the dramatic changes caused by mutant Msh2-Msh6 complexes in the Rad27-dependent MMR reactions, we investigated the effects of these mutant complexes in the absence of Rad27 (Fig. 5). Only strand displacement products were formed in reactions containing DNA polymerase δ but no Rad27 or Msh2-Msh6, as previously observed (Fig. 4). The addition of Msh2-Msh6 suppressed the formation of strand displacement products, as was also previously observed (Fig. 3). The mispair-binding defective Msh2-Msh6-F337A mutant eliminated the formation of strand displacement products, similar to its effect in the presence of Rad27 (Fig. 4), and indicates that mispair binding is not required to suppress strand displacement synthesis. The PCNA-binding defective Msh2-Msh6-F33AF34A mutant resulted in only strand displacement products, although the overall level of these products was lower than seen with DNA polymerase δ alone (Fig. 5). This mirrors the effect of the Msh2-Msh6-F33AF34A mutant in the presence of Rad27 (Fig. 4) and demonstrates that the Msh2-Msh6-PCNA interaction is required for Msh2-Msh6 to suppress the strand displacement reaction catalyzed by DNA polymerase δ.
To gain further insight into the inhibition of DNA synthesis by Msh2-Msh6, experiments were performed in which either the amount of Msh2-Msh6 was decreased or the amount of PCNA was increased in reactions containing DNA polymerase δ, RFC-Δ1N and RPA (Supplementary Fig. 2). Decreasing the amount of Msh2-Msh6 resulted in the restoration of DNA synthesis-mediated repair products, although ratios of 0.77 and 0.38 molecules of Msh2-Msh6 per PCNA trimer still resulted in some inhibition of DNA synthesis-mediated repair products. Similarly, increasing PCNA to amounts that were greater than the amount of Msh2-Msh6 restored the formation of DNA synthesis-mediated repair products. These results are consistent with the previous observation (see above) that the interaction between the Msh6 subunit of Msh2-Msh6 and PCNA is critical to coordinate Rad27-dependent MMR in vitro and suppress the strand displacement reaction catalyzed by DNA polymerase δ.
The circular products of Rad27-dependent MMR contain nicks that can be sealed with DNA ligase
To determine if the circular products of Rad27-dependent MMR were nick-containing plasmids that could be sealed by DNA ligase, we studied the repair of a DNA substrate containing a CC mispair in which the 5’ phosphate present at the NaeI site was removed so that ligatable products could be distinguished from the non-ligatable starting substrate (Supplementary Fig. 3). Dephosphorylation of the substrate was not expected to affect MMR in vitro because it retains the normal 3’ hydroxyl terminus extended by DNA polymerase δ during the repair. In control reactions, treatment of the dephosphorylated substrate with either T4 DNA ligase or T4 DNA ligase followed by treatment with DNA gyrase did not convert any of the DNA to covalently closed circular supercoiled (CCC SC) DNA (Supplementary Fig. 3a). In contrast, treatment of substrate that had not been dephosphorylated with T4 DNA ligase converted a large proportion of the DNA to forms that migrated more rapidly on agarose gels than the nicked circular substrate, and treatment with T4 DNA ligase and DNA gyrase converted most of the substrate to a single, more rapidly migrating CCC SC DNA species (Supplementary Fig. 3b); thus we used treatment with T4 DNA ligase followed by treatment with DNA gyrase as an assay for circular DNAs that contained nicks that could be sealed with DNA ligase.
DNA repair reactions were performed under our established conditions except that they contained the CC mispaired substrate with the dephosphorylated 5’ nick at the NaeI site and high amounts of Rad27 minus and plus Msh2-Msh6 (Supplementary Fig. 3c). Under these conditions, a large proportion of the substrate was converted to repair products in reactions lacking Msh2-Msh6, and a somewhat reduced proportion of the substrate was converted to repair products in reactions containing Msh2-Msh6; in both cases, the repair products lacked a 5’ displaced strand. Treatment of the repair products with T4 DNA ligase and DNA gyrase converted a large proportion of the repair products to the CCC SC DNA species indicating that mature repair products were formed that contained nicks that could be sealed with DNA ligase (Supplementary Fig. 3d). The repair was then examined at a reduced amount of Rad27 resulting in lower repair where in the absence of Msh2-Msh6 the repair products were a mixture of mature and strand displaced products and in the presence of Msh2-Msh6 the repair products were almost exclusively mature repair products (Supplementary Fig. 3e) as previously seen. In both cases, treatment with T4 DNA ligase and DNA gyrase converted a proportion of the products to the CCC SC DNA species (Supplementary Fig. 3f). These results indicate that at a minimum, a large proportion of the products of Rad27-dependent MMR in vitro are circular DNA molecules containing a nick that is a substrate for DNA ligase; this is similar to that seen in Exo1-dependent MMR reactions reconstituted with human MMR proteins22.
Genetic and biochemical studies have demonstrated the existence of both Exo1-dependent and Exo1-independent MMR pathways1,23,26,27. Here we constructed an exo1 separation-of-function mutation, exo1Δ440-702, that inactivates the ability of Exo1 to function in MMR but not the ability of Exo1 to maintain cell viability in the absence of Rad2728. This exo1 mutation allowed us to demonstrate that Rad27 can support MMR in the absence of Exo1-dependent and other known Exo1-independent MMR pathways in vivo21,28. Defects in RAD27 resulted in the accumulation of Mlh1-Pms1 MMR foci intermediates similar to defects in EXO127,30, suggesting that the Exo1-dependent MMR and Rad27-dependent MMR have similar kinetic properties30. Finally, we reconstituted MMR reactions in vitro with a combination of Msh2-Msh6, Rad27, DNA polymerase δ, PCNA, RFC-Δ1N, and RPA. The formation of mature MMR products was dependent on Msh2-Msh6, Rad27, and DNA polymerase δ, as well as the ability of Msh2-Msh6 to both bind mispairs and interact with PCNA through the PCNA interaction site in the N-terminus of Msh6. These studies establish the existence of a general Rad27-dependent MMR pathway.
Most of the mutations that arise in rad27Δ mutants are due to mutagenesis mechanisms other than loss of MMR35,36,37,55; however, a minor role for Rad27 in MMR was postulated due to the observation that rad27Δ mutations caused modest increases in the rate of mutations detected using MMR-specific frameshift mutation reversion assays35. Here, we found that combining a rad27Δ mutation with the exo1Δ440-702 mutation caused synergistic increases in mutation rates in frameshift reversion assays that are highly specific for MMR defects9,35,38. In addition, the exo1Δ440-702 rad27Δ double mutant had increased levels of Pms1 foci relative to the respective single mutants. These data are consistent with redundant roles for Rad27 and Exo1 in MMR. The mutation rates caused by the exo1Δ440-702 and rad27Δ single and double mutations were further increased by the addition of the pms1-A99V mutation, and the mutation rates caused by the rad27Δ mutation was also further increased by the addition of the pol30-K217E mutation. Both pms1-A99V and pol30-K217E were previously shown to enhance the weak MMR defect caused by an exo1Δ mutation23,26. The mutation rate of the rad27Δ exo1Δ440-702 pms1-A99V triple mutant was close to but slightly lower than that of msh2Δ and pms1Δ single mutants. In addition, the mutation rates of the msh2Δ exo1Δ440-702 rad27Δ and pms1Δ exo1Δ440-702 rad27Δ triple mutants were similar to the mutation rates of the msh2Δ and pms1Δ single mutants, respectively. In aggregate, these results suggest the presence of at least three MMR excision pathways (Fig. 6): (1) Exo1-dependent excision, (2) Rad27-dependent excision, and (3) a pathway that is independent of Exo1 and Rad27 but is promoted by elevated levels of Mlh1-Pms1 endonuclease activity, which we have previously called the Exo1-independent pathway1,21,23,26,27. Together, these three pathways account for most of Msh2-dependent MMR.
To understand the mechanism of Rad27-dependent MMR, we reconstituted a Rad27-dependent MMR reaction in vitro using Msh2-Msh6, Rad27, DNA polymerase δ, PCNA, RFC-Δ1N and RPA and a mispaired DNA substrate containing a 5’ nick at a NaeI site. In the absence of Msh2-Msh6, DNA polymerase δ catalyzes strand displacement synthesis past the mispair, and Rad27 stimulates this synthesis, as well as cleaving off a portion of the branches produced by strand displacement synthesis by DNA polymerase δ. When Msh2-Msh6 was added, the strand displacement activity of DNA polymerase δ was eliminated unless Rad27 was present. In the presence of all three proteins, a coupled strand-displacement and flap-excision reaction were mediated such that only mature MMR products lacking DNA flaps and containing ligatable nicks were formed, consistent with a bona fide MMR reaction. The Msh2-Msh6-F337A mutant protein, which cannot bind mispairs53, retained the ability to eliminate strand-displacement synthesis but failed to coordinate the coupled reaction involving Rad27. In contrast, reactions containing the Msh2-Msh6-F33AF34A mutant protein, which lacks PCNA binding54, behaved as if Msh2-Msh6 was absent from the reactions, suggesting that the coupled reaction and inhibition of the strand displacement activity of DNA polymerase δ is coordinated by Msh2-Msh6 through PCNA42,56; the results of titration experiments in which the amounts of PCNA and Msh2-Msh6 were varied support this model. In aggregate, these results are consistent with a model (Fig. 6) in which mispair-bound Msh2-Msh6 targets DNA polymerase δ-PCNA, Rad27-PCNA, or DNA polymerase δ-Rad27-PCNA complexes to the repair reaction through the Msh6 interaction with PCNA42,56. This model is consistent with previous co-precipitation experiments showing that human Msh2-Msh6 interacts directly or indirectly with FEN141 (the homolog of Rad27). We have not yet established whether the Rad27 excision pathway can be coupled to mispair-dependent strand nicking by the Mlh1-Pms1 endonuclease, but this seems likely because 5’ nicks produced by Mlh1-Pms1 appear to act in a matter that is indistinguishable from pre-existing 5’ nicks15,21,29.
In summary, our results provide support for the hypothesis that Rad27 functions in a nick-directed Msh2-Msh6-dependent mispair excision pathway. In contrast to the Exo1-dependent pathway where a gap is generated and can then be filled by either DNA polymerase δ or DNA polymerase ε, Rad27 appears to act on the 5’ flap resulting from strand displacement synthesis by DNA polymerase δ and hence cannot promote repair by DNA polymerase ε, which does not perform strand-displacement synthesis52. Our results also support the hypothesis that at least three redundant MMR excision pathways account for all of or the majority of Msh2-dependent MMR (Fig. 6). Recent studies have suggested that strand displacement synthesis by DNA polymerase δ can potentially contribute to Exo1-independent MMR29 and have shown that FEN1 along with MMR proteins can excise mispairs at the 5’ end of Okazaki fragments by DNA polymerase α segment error editing that acts at the 5’ ends of Okazaki fragments41. Our results extend the results of these prior studies and also demonstrate that Rad27-mediated excision is a general mispair excision pathway like Exo1-mediated excision and is a bona fide MMR pathway that functions in vivo.
Strains and plasmids
S. cerevisiae strains were grown in YPD (1% yeast extract, 2% bacto peptone, and 2% dextrose) or in the appropriate synthetic dropout media (0.67% yeast nitrogen base without amino acids, 2% dextrose, and amino acid dropout mix at the concentration recommended by the manufacturer (US Biological) at 30 °C. All transformations with plasmids or PCR-based deletion cassettes were performed using standard lithium acetate transformation protocols.
All S. cerevisiae strains used for mutation rate analysis were derived from the S288C strain RDKY5964 MATa ura3-52 leu2Δ1 trp1Δ63 his3Δ200 hom3-10 lys2::InsE-A10 and all strains used for microscopy studies were derived from RDKY7588, which is RDKY5964 containing the PMS1-4GFP::kanMX6 allele30. Mutations were introduced into these strains using standard gene disruption methods (Supplementary Table 3). The PCR primers used in gene disruption experiments are listed in Supplementary Table 4. The exo1Δ440-702 mutation was introduced into strains using a gene disruption cassette made by amplifying selectable genes from the pFA6a series of plasmids using the PCR primers (uppercase bases correspond to EXO1 sequence and lowercase sequences correspond to pFA6a plasmid sequence) Primer 1 upstream 5’-CAA TTA AGC GTA GGA AAT TAA GTA ATG CCA ATG TAG TCC AAG AAA CG tag atg aat aac gta cgc tgc agg tcg ac, where the first three bases in lower case are the stop codon that replaces EXO1 codon 440, and Primer 2 downstream 5’-TTT ACT GGG CAT TGA TTT TTT AAT TCT TGT CTT GAG GCA TTT CGA CGA GAT atc gat gaa ttc gag ctc g. The PCR primers used for generating the exo1Δ cassette were Primer 3 upstream 5’-GGT CTA GTA CAA TGG CTT TTT CCC AAA GTA GAA GGC TTC TTA CTC CAA CCG TAC CCT Gcg tac gct gca ggt cga c and Primer 4 downstream 5’-GAC AAT GGC AAT TAA GCG TAG GAA ATT AAG TAA TGC CAA TGT AGT CCA AGA AAC Gta gat gaa taa atc gat gaa ttc gag ctc g. The PCR primers used for generating the rad27Δ cassette were Primer 5 upstream 5’-TAT GCC AAG GTG AAG GAC CAA AAG AAG AAA GTG GAA AAA GAA CCC CCt cat cct gat gcg gta ttt tct cc and Primer 6 downstream 5’-CAG CAT ACA TTG GAA AGA AAT AGG AAA CGG ACA CCG GAA GAA AAA ATa tgc gtt tcg gtg atg acg gtg. Disruption mutations were verified by PCR amplification with appropriate upstream, downstream, and internal PCR primers.
Mutation rate analysis
Mutator phenotypes were evaluated using the hom3-10 and lys2-10A frameshift reversion assays essentially as previously described23,30. Qualitative analysis was done by patching colonies onto YPD plates and replica plating onto -Thr synthetic dropout media for analysis of papillae growth9,23. Mutation rates were determined by fluctuation analysis using a minimum of 2 independently derived strains and 14 or more independent cultures per experiment in each of at least 2 independent experiments and calculated using Microsoft Excel software; comparisons of mutation rates were evaluated using 95% confidence intervals or by Mann-Whitney two-tailed tests23,30.
Mutation spectra analysis
One independent Thr+ revertant was isolated per culture from fluctuation tests or per patch from qualitative tests9. Chromosomal DNA was isolated from each revertant using a Qiagen Puregene Yeast/Bact. Kit B and the hom3-10 region were amplified by PCR using the Primer 7 5’-AGTTGTTTGTTGATGACTGC and Primer 8 5’-TTCAGAAGCTTCTTCTGGAG and sequenced with the Primer 9 5’-CTTTCCTGGTTCAAGCATTG (Supplementary Table 4) using a commercial sequencing facility9.
MMR proteins were purified according to standard protocols as previously described for Exo117,18, Msh2-Msh654,57, PCNA17,58, DNA polymerase δ59, RFC-Δ1N51, and RPA60 and were greater than 95% pure as determined by SDS-PAGE. Multiple protein preparations were used during the course of the experiments presented and many of these preparations were validated in our previously published studies17,18,21,26,28.
Rad27 was purified as follows. The S. cerevisiae RAD27 gene was codon-optimized for expression in E. coli (Integrated DNA Technologies) and inserted into the pET28a vector. E. coli OneShot BL21 (DE3) pLysS cells (Invitrogen) were freshly transformed with the resulting expression vector pET28a/Rad27 (pRDK1913) before use. Two liters of culture were grown in LB (1% bacto peptone, 0.5% yeast extract, and 0.5% NaCl), 100 μg/mL kanamycin and 34 μg/mL chloramphenicol at 30 °C until the cell density reached 0.6, and then the expression of Rad27 was induced by addition of isopropyl β-D-thiogalactopyranoside (IPTG) at a final concentration of 0.5 mM for 5 h. The cells were harvested by centrifugation, resuspended in Buffer A100 consisting of Buffer A [20 mM Tris, pH 8.0, 0.5 mM ethylenediaminetetraacetic acid (EDTA), 10% (v/v) glycerol, 1 mM dithiothreitol (DTT), protease inhibitor mixture PIC D, (final concentrations of 1 mM phenylmethylsulfonyl fluoride (PMSF), 1 μg/L chymostatin, and 1 μg/L pepstatin A), protease inhibitor mixture PIC W (final concentrations of 1 mM benzamadine, 0.5 μg/L bestatin, 1 μg/L aprotinin, and 1 μg/L leupeptin)] containing 100 mM NaCl and lysed by sonication. The lysate was then clarified by centrifugation at 39,190 × g in a Beckman JA-25.50 Rotor at 4 °C for 1 h. The supernatant was then mixed for 1 hr with 72 mL (4 portions in 50 mL centrifuge tubes) of DEAE Sepharose that had been previously equilibrated with Buffer A100 and then the resin slurry was centrifuged and the supernatant was saved. The supernatant was centrifuged a second time to remove any residual resin and then loaded onto a 1 mL HiTrap Heparin column that had been previously equilibrated with Buffer A100 after which the column was washed with Buffer A100 and the bound proteins were eluted with a 20 mL gradient from Buffer A100 to Buffer A containing 1 M NaCl (Buffer A1000). The protein-containing fractions were loaded onto a 110 mL (1.6 × 55.5 cm) Superdex 75 column that had been previously equilibrated with Buffer A100 and then the column was washed with Buffer A100. The Rad27-containing fractions from the Superdex 75 column were subsequently loaded onto a 1 mL MonoS column, washed with Buffer A100, and the bound proteins were eluted with a 30 mL linear gradient from Buffer A100 to Buffer A1000. The resulting purified Rad27 was pooled and stored in small aliquots at −80 °C.
In vitro MMR assays
The in vitro MMR repair assay was performed essentially as described17,18. One hundred nanograms of circular DNA substrate containing a CC mispair disrupting a PstI site and a nick located 5’ of the mispair at the NaeI site was used as a substrate, and the final reaction contained 33 mM Tris pH 7.6, 75 mM KCl, 2.5 mM ATP, 1.66 mM glutathione, 8.3 mM MgCl2, 80 µg/mL BSA, and 200 µM of each dNTP, 290 fmole PCNA, 220 fmole RFC-Δ1N, 390 fmole Msh2-Msh6 or mutant Msh2-Msh6, as indicated, 20 fmole DNA polymerase δ, 1.05 fmole Exo1, as indicated, and 1800 fmole RPA in a 10 µL volume. As indicated in individual experiments, the reactions also contained different amounts of Rad27 that were added at the same time as the other proteins were added, although most reactions contained 5 pmole of Rad27. Where necessary, proteins were diluted in a buffer consisting of 7.5 mM HEPES pH 7.5, 200 mM KCl, 1 mM DTT, 10% (v/v) glycerol, and 0.5 mg/mL BSA prior to addition to the reactions. The reactions were then stopped by the addition of EDTA, Proteinase K (Sigma Aldrich), and glycogen (Thermo Scientific) to final concentrations of 21 mM, 24 µg/mL, and 13.4 µg/mL, respectively, followed by incubation for 30 min at 55 °C. Reactions were extracted with phenol, and the DNA substrate was precipitated with ethanol, followed by digestion with PstI and ScaI. Digested DNA substrate was subjected to electrophoresis on a 0.8% agarose gel run in a buffer containing 40 mM Tris, 20 mM acetic acid, 1 mM EDTA at pH 8.3 (TAE; Biorad) with 0.5 μg/mL ethidium bromide for 45 min at 100 V. Quantitation of the relative amounts of the different DNA species in each individual lane was performed with Alpha Imager HP software (ProteinSimple). Except as indicated in the legend to Supplementary Fig. 2b, all experiments were performed a minimum of 3 times and representative examples of each experiment are presented. When necessary, bar graphs were constructed in GraphPad Prism software.
One hundred nanograms of circular DNA substrate containing a CC mispair disrupting a PstI site and a nick located 5’ of the mispair at the NaeI site17,18 or a dephosphorylated version were used as substrate. Dephosphorylation was performed by incubating the substrate with rSAP (New England Biolabs) at 37 °C for 1 h, followed by incubation for 5 min at 65 °C, phenol extraction, and ethanol precipitation. In vitro MMR assays were then performed as described above. Two different amounts of Rad27, 5 and 2.5 poles, were used. After the DNAs were purified from the repair reactions, the DNA from each repair reaction was split into two equal parts and treated as follows: (1) The repair products were digested with PstI and ScaI for 1 h at 37 °C and then analyzed by electrophoresis on a 0.8% agarose gel run in TAE containing 0.5 μg/mL ethidium bromide for 45 min at 100 V17,18. (2) The repair products were incubated with T4 DNA ligase (New England Biolabs) for 2.5 h at room temperature and then incubated with E. coli DNA gyrase (Sigma Aldrich) for 1 h at 37 °C. The DNAs were then analyzed by electrophoresis on a 1.0% agarose gel run in TAE for 45 min at 100 V, which was stained with 0.5 μg/mL ethidium bromide for 30 min and destained in water for 30 min. Quantitation was performed with Alpha Imager HP software (ProteinSimple).
Cells were grown in synthetic complete medium to log phase and examined by live imaging essentially as previously described30,49 except using an ECHO Revolve epifluorescence microscope with an Olympus PlanApo N 60 × /1.42 Oil Ph3 immersion objective. GFP fluorescence was detected using a Revolve GFP Cube and ECHO Pro software. Images were saved as TIFF files and visualized using Adobe Photoshop to manually score cells for the presence of GFP foci. Figures were prepared in Adobe Photoshop, keeping processing parameters constant within each experiment. The reported experiments were done twice and a minimum of 8 independent fields were captured and quantified per strain analyzed.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
The data generated by this study are provided in the main text and figures and the accompanying Supplementary Information and are available from the corresponding author upon reasonable request. Source data are provided with this paper.
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This study was supported by NIH grant R01 GM50006. We would like to thank Matthew DuPrie for measuring the mutation rates of the msh2Δ and pms1Δ single mutants.
The authors declare no competing interests.
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Calil, F.A., Li, BZ., Torres, K.A. et al. Rad27 and Exo1 function in different excision pathways for mismatch repair in Saccharomyces cerevisiae. Nat Commun 12, 5568 (2021). https://doi.org/10.1038/s41467-021-25866-z
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