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• W3171107472 abstract "In a previous study, we showed that replication through the N1-methyl-deoxyadenosine (1-MeA) adduct in human cells is mediated via three different Polι/Polθ, Polη, and Polζ-dependent pathways. Based on biochemical studies with these Pols, in the Polι/Polθ pathway, we inferred a role for Polι in the insertion of a nucleotide (nt) opposite 1-MeA and of Polθ in extension of synthesis from the inserted nt; in the Polη pathway, we inferred that this Pol alone would replicate through 1-MeA; in the Polζ pathway, however, the Pol required for inserting an nt opposite 1-MeA had remained unidentified. In this study, we provide biochemical and genetic evidence for a role for Polλ in inserting the correct nt T opposite 1-MeA, from which Polζ would extend synthesis. The high proficiency of purified Polλ for inserting a T opposite 1-MeA implicates a role for Polλ—which normally uses W-C base pairing for DNA synthesis—in accommodating 1-MeA in a syn confirmation and forming a Hoogsteen base pair with T. The potential of Polλ to replicate through DNA lesions by Hoogsteen base pairing adds another novel aspect to Polλ’s role in translesion synthesis in addition to its role as a scaffolding component of Polζ. We discuss how the action mechanisms of Polλ and Polζ could be restrained to inserting a T opposite 1-MeA and extending synthesis thereafter, respectively. In a previous study, we showed that replication through the N1-methyl-deoxyadenosine (1-MeA) adduct in human cells is mediated via three different Polι/Polθ, Polη, and Polζ-dependent pathways. Based on biochemical studies with these Pols, in the Polι/Polθ pathway, we inferred a role for Polι in the insertion of a nucleotide (nt) opposite 1-MeA and of Polθ in extension of synthesis from the inserted nt; in the Polη pathway, we inferred that this Pol alone would replicate through 1-MeA; in the Polζ pathway, however, the Pol required for inserting an nt opposite 1-MeA had remained unidentified. In this study, we provide biochemical and genetic evidence for a role for Polλ in inserting the correct nt T opposite 1-MeA, from which Polζ would extend synthesis. The high proficiency of purified Polλ for inserting a T opposite 1-MeA implicates a role for Polλ—which normally uses W-C base pairing for DNA synthesis—in accommodating 1-MeA in a syn confirmation and forming a Hoogsteen base pair with T. The potential of Polλ to replicate through DNA lesions by Hoogsteen base pairing adds another novel aspect to Polλ’s role in translesion synthesis in addition to its role as a scaffolding component of Polζ. We discuss how the action mechanisms of Polλ and Polζ could be restrained to inserting a T opposite 1-MeA and extending synthesis thereafter, respectively. Translesion synthesis (TLS) DNA polymerases (Pols) exhibit a high specificity for replicating through different types of DNA lesions. Whereas replication through certain DNA lesions can be performed by just one Pol, such as by Polη opposite cyclobutane pyrimidine dimers (CPDs) (1Johnson R.E. Kondratick C.M. Prakash S. Prakash L. hRAD30 mutations in the variant form of xeroderma pigmentosum.Science. 1999; 285: 263-265Crossref PubMed Scopus (658) Google Scholar, 2Johnson R.E. Prakash S. Prakash L. Efficient bypass of a thymine-thymine dimer by yeast DNA polymerase, Polη.Science. 1999; 283: 1001-1004Crossref PubMed Scopus (677) Google Scholar, 3Johnson R.E. Washington M.T. Prakash S. Prakash L. Fidelity of human DNA polymerase η.J. Biol. Chem. 2000; 275: 7447-7450Abstract Full Text Full Text PDF PubMed Scopus (357) Google Scholar, 4Masutani C. Kusumoto R. Yamada A. Dohmae N. Yokoi M. Yuasa M. Araki M. Iwai S. Takio K. Hanaoka F. The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase η.Nature. 1999; 399: 700-704Crossref PubMed Scopus (1117) Google Scholar, 5Yoon J.H. McArthur M.J. Park J. Basu D. Wakamiya M. Prakash L. Prakash S. Error-prone replication through UV lesions by DNA polymerase theta protects against skin cancers.Cell. 2019; 176: 1295-1309Abstract Full Text Full Text PDF PubMed Scopus (47) Google Scholar, 6Yoon J.-H. Prakash L. Prakash S. Highly error-free role of DNA polymerase η in the replicative bypass of UV induced pyrimidine dimers in mouse and human cells.Proc. Natl. Acad. Sci. U. S. A. 2009; 106: 18219-18224Crossref PubMed Scopus (115) Google Scholar), replication through a vast array of DNA lesions requires the sequential action of two Pols, wherein one Pol inserts a nucleotide (nt) opposite the DNA lesion and another Pol extends synthesis from the inserted nt. Biochemical and structural studies with yeast Polζ have provided strong evidence for its role in extending synthesis from nts inserted opposite DNA lesions by other TLS Pols (7Johnson R.E. Haracska L. Prakash S. Prakash L. Role of DNA polymerase η in the bypass of a (6-4) TT photoproduct.Mol. Cell. Biol. 2001; 21: 3558-3563Crossref PubMed Scopus (173) Google Scholar, 8Johnson R.E. Washington M.T. Haracska L. Prakash S. Prakash L. Eukaryotic polymerases ι and ζ act sequentially to bypass DNA lesions.Nature. 2000; 406: 1015-1019Crossref PubMed Scopus (565) Google Scholar, 9Nair D.T. Johnson R.E. Prakash L. Prakash S. Aggarwal A.K. Hoogsteen base pair formation promotes synthesis opposite the 1,N6-ethenodeoxyadenosine lesion by human DNA polymerase iota.Nat. Struct. Mol. Biol. 2006; 13: 619-625Crossref PubMed Scopus (94) Google Scholar, 10Malik R. Kopylov M. Gomez-Liorente Y. Jain R. Johnson R.E. Prakash L. Prakash S. Ubarretxena-Belandia I. Aggarwal A.K. Structure and mechanism of B-family DNA polymerase ζ specialized for translesion DNA synthesis.Nat. Struct. Mol. Biol. 2020; 27: 913-924Crossref PubMed Scopus (20) Google Scholar), and genetic evidence accrued from TLS studies opposite a number of DNA lesions in human cells aligns with such a Polζ role (5Yoon J.H. McArthur M.J. Park J. Basu D. Wakamiya M. Prakash L. Prakash S. Error-prone replication through UV lesions by DNA polymerase theta protects against skin cancers.Cell. 2019; 176: 1295-1309Abstract Full Text Full Text PDF PubMed Scopus (47) Google Scholar, 6Yoon J.-H. Prakash L. Prakash S. Highly error-free role of DNA polymerase η in the replicative bypass of UV induced pyrimidine dimers in mouse and human cells.Proc. Natl. Acad. Sci. U. S. A. 2009; 106: 18219-18224Crossref PubMed Scopus (115) Google Scholar, 11Yoon J.H. Johnson R.E. Prakash L. Prakash S. DNA polymerase theta accomplishes translesion synthesis opposite 1,N(6)-ethenodeoxyadenosine with a remarkably high fidelity in human cells.Genes Dev. 2019; 33: 282-287Crossref PubMed Scopus (6) Google Scholar, 12Yoon J.-H. Bhatia G. Prakash S. Prakash L. Error-free replicative bypass of thymine glycol by the combined action of DNA polymerases κ and ζ in human cells.Proc. Natl. Acad. Sci. U. S. A. 2010; 107: 14116-14122Crossref PubMed Scopus (54) Google Scholar). In yeast or cancer cells, Rev1 functions as a scaffolding component of Polζ and TLS by Rev1-Polζ operates in a highly error-prone manner (13Acharya N. Johnson R.E. Prakash S. Prakash L. Complex formation with Rev1 enhances the proficiency of yeast DNA polymerase ζ for mismatch extension and for extension opposite from DNA lesions.Mol. Cell. Biol. 2006; 26: 9555-9563Crossref PubMed Scopus (106) Google Scholar, 14Baynton K. Bresson-Roy A. Fuchs R.P.P. Analysis of damage tolerance pathways in Saccharomyces cerevisiae: A requirement for Rev3 DNA polymerase in translesion synthesis.Mol. Cell. Biol. 1998; 18: 960-966Crossref PubMed Scopus (74) Google Scholar, 15Doles J. Oliver T.G. Cameron E.R. Hsu G. Jacks T. Walker G.C. Hemann M.T. Suppression of Rev3, the catalytic subunit of Polζ, sensitizes drug-resistant lung tumors to chemotherapy.Proc. Natl. Acad. Sci. U. S. A. 2010; 107: 20786-20791Crossref PubMed Scopus (137) Google Scholar, 16Gibbs P.E.M. McDonald J. Woodgate R. Lawrence C.W. The relative roles in vivo of Saccharomyces cerevisiae Polη, Polζ, Rev1 protein and Pol32 in the bypass and mutation inductiion of an abasic site, T-T (6-4) photoadduct and T-T cis-syn cyclobutane dimer.Genetics. 2005; 169: 575-582Crossref PubMed Scopus (155) Google Scholar, 17Nelson J.R. Gibbs P.E.M. Nowicka A.M. Hinkle D.C. Lawrence C.W. Evidence for a second function for Saccharomyces cerevisiae Rev1p.Mol. Microbiol. 2000; 37: 549-554Crossref PubMed Scopus (179) Google Scholar, 18Xie K. Doles J. Hemann M.T. Walker G.C. Error-prone translesion synthesis mediates acquired chemoresistance.Proc. Natl. Acad. Sci. U. S. A. 2010; 107: 20792-20797Crossref PubMed Scopus (150) Google Scholar). In normal human cells, however, Rev1 functions as an indispensable scaffolding component of the Y-family Pols η, ι, and κ; and TLS studies opposite a number of DNA lesions have indicated that Rev1-dependent TLS by Y-family Pols operates in a much more error-free manner in human cells than indicated from the fidelity of the purified pols (11Yoon J.H. Johnson R.E. Prakash L. Prakash S. DNA polymerase theta accomplishes translesion synthesis opposite 1,N(6)-ethenodeoxyadenosine with a remarkably high fidelity in human cells.Genes Dev. 2019; 33: 282-287Crossref PubMed Scopus (6) Google Scholar, 19Yoon J.H. Hodge R.P. Hackfeld L.C. Park J. Roy Choudhury J. Prakash S. Prakash L. Genetic control of predominantly error-free replication through an acrolein-derived minor-groove DNA adduct.J. Biol. Chem. 2018; 293: 2949-2958Abstract Full Text Full Text PDF PubMed Scopus (6) Google Scholar, 20Yoon J.H. Park J. Conde J. Wakamiya M. Prakash L. Prakash S. Rev1 promotes replication through UV lesions in conjunction with DNA polymerases η, ι, and κ but not DNA polymerase ζ.Genes Dev. 2015; 29: 2588-2662Crossref PubMed Google Scholar, 21Yoon J.H. Roy Choudhury J. Park J. Prakash S. Prakash L. Translesion synthesis DNA polymerases promote error-free replication through the minor-groove DNA adduct 3-deaza-3-methyladenine.J. Biol. Chem. 2017; 292: 18682-18688Abstract Full Text Full Text PDF PubMed Scopus (19) Google Scholar). Furthermore, in a recent study we provided evidence for an indispensable role of Polλ as a scaffolding component of Polζ; and from TLS studies opposite a number of DNA lesions, we inferred that Polλ-dependent TLS by Polζ operates in a predominantly error-free manner in human cells (22Yoon J.H. Basu D. Sellamuthu K. Johnson R.E. Prakash S. Prakash L. A novel role of DNA polymerase lambda in translesion synthesis in conjunction with DNA polymerase zeta.Life Sci. Alliance. 2021; 4e202000900Crossref PubMed Google Scholar). In that study we analyzed Polλ’s role in TLS opposite the UV lesions CPDs and (6–4) pyrimidine-pyrimidone photoproducts (6–4) PPs, the oxidative DNA lesion thymine glycol (Tg), and the 1,N6-ethenodeoxyadenosine (εdA) lesion—formed in DNA through interaction with aldehydes derived from lipid peroxidation. In TLS opposite CPD, Tg, and εdA, Polζ extends synthesis from the nt inserted opposite the lesion site by another DNA Pol; and although Polλ is indispensable for Polζ’s role in TLS opposite these DNA lesions, its DNA polymerase activity is not required. Thus, for TLS opposite these DNA lesions, only Polλ’s scaffolding activity is required (22Yoon J.H. Basu D. Sellamuthu K. Johnson R.E. Prakash S. Prakash L. A novel role of DNA polymerase lambda in translesion synthesis in conjunction with DNA polymerase zeta.Life Sci. Alliance. 2021; 4e202000900Crossref PubMed Google Scholar). For TLS opposite (6–4) PPs, however, Polλ’s polymerase activity is also required, and Polλ promotes error-free replication through this lesion in human and mouse cells (22Yoon J.H. Basu D. Sellamuthu K. Johnson R.E. Prakash S. Prakash L. A novel role of DNA polymerase lambda in translesion synthesis in conjunction with DNA polymerase zeta.Life Sci. Alliance. 2021; 4e202000900Crossref PubMed Google Scholar). Since (6–4) TT PP induces a large structural distortion in DNA and since it impairs the ability of the 3’T to form a normal Watson–Crick (W-C) base pair with the correct nt (23Kemmink J. Boelens R. Koning T. van der Marel G.A. van Boom J.H. Kaptein R. 1H NMR study of the exchangeable protons of the duplex d(GCGTTGCG).d(CGCAACGC) containing a thymine photodimer.Nucleic Acids Res. 1987; 15: 4645-4653Crossref PubMed Scopus (97) Google Scholar, 24Kim J.-K. Choi B.-S. The solution structure of DNA duplex-decamer containing the (6-4) photoproduct of thymidyl(3′->5′)thymidine by NMR and relaxation matrix refinement.Eur. J. Biochem. 1995; 228: 849-854Crossref PubMed Scopus (96) Google Scholar, 25Kim J.-K. Patel D. Choi B.-S. Contrasting structural impacts induced by cis-syn cyclobutane dimer and (6-4) adduct in DNA duplex decamers: Implication in mutagenesis and repair activity.Photochem. Photobiol. 1995; 62: 44-50Crossref PubMed Scopus (187) Google Scholar, 26Lee J.-H. Hwang G.-S. Choi B.-S. Solution structure of a DNA decamer duplex containing the stable 3′ T.G base pair of the pyrimidine(6-4)pyrimidone photoproduct [(6-4) adduct]: Implications for the highly specific 3′ T -> C transition of the (6-4) adduct.Proc. Natl. Acad. Sci. U. S. A. 1999; 96: 6632-6636Crossref PubMed Scopus (53) Google Scholar), it remains unclear how Polλ, which uses W-C base pairing for normal DNA synthesis, manages error-free TLS opposite this DNA lesion. N1-methyl-deoxyadenosine (1-MeA) is repaired by direct demethylation, primarily by the ABH2 enzyme in human cells (27Ringvoli J. Nordstrand L.M. Vagbo C.B. Talstad V. Reite K. Aas P.A. Lauritzen K.H. Liabakk N.B. Bjork A. Doughty R.W. Falnes P.O. Krokan H.E. Klungland A. Repair deficient mice reveal mABH2 as the primary oxidative demethylase for repairing 1meA and 3meC lesions in DNA.EMBO J. 2006; 25: 2189-2198Crossref PubMed Scopus (145) Google Scholar). The evidence that 1-MeA residues accumulate over time in the genomic DNA of the livers from ABH2 null mice has indicated that endogenous DNA methylation contributes to their formation (27Ringvoli J. Nordstrand L.M. Vagbo C.B. Talstad V. Reite K. Aas P.A. Lauritzen K.H. Liabakk N.B. Bjork A. Doughty R.W. Falnes P.O. Krokan H.E. Klungland A. Repair deficient mice reveal mABH2 as the primary oxidative demethylase for repairing 1meA and 3meC lesions in DNA.EMBO J. 2006; 25: 2189-2198Crossref PubMed Scopus (145) Google Scholar). In human cells, TLS through the 1-MeA adduct is mediated via three independent pathways in which Polι and Polθ function in one pathway and Pols η and ζ function in the other two pathways, respectively (28Conde J. Yoon J.H. Roy Choudhury J. Prakash L. Prakash S. Genetic control of replication through N1-methyladenine in human cells.J. Biol. Chem. 2015; 290: 29794-29800Abstract Full Text Full Text PDF PubMed Scopus (17) Google Scholar). TLS by all three pathways operates in a predominantly error-free manner in human cells. For the Polι/Polθ pathway, following nt insertion by Polι opposite 1-MeA by forming a Hoogsteen base pair with the T residue (29Jain R. Choudhury J.R. Buku A. Johnson R.E. Prakash L. Prakash S. Aggarwal A.K. Mechanism of error-free DNA synthesis across N1-methyl-deoxyadenosine by human DNA polymerase-iota.Sci. Rep. 2017; 7: 43904Crossref PubMed Scopus (9) Google Scholar), Polθ would extend synthesis, whereas in the Polη pathway, Polη would perform both the steps of TLS (28Conde J. Yoon J.H. Roy Choudhury J. Prakash L. Prakash S. Genetic control of replication through N1-methyladenine in human cells.J. Biol. Chem. 2015; 290: 29794-29800Abstract Full Text Full Text PDF PubMed Scopus (17) Google Scholar). Our evidence for the requirement of Polλ as an indispensable scaffolding component of Polζ strongly suggested that it would be required for Polζ-dependent TLS opposite 1-MeA; further, it raised the possibility that Polλ may insert the correct nt opposite 1-MeA from which Polζ could extend synthesis. Here we provide genetic and biochemical evidence for the role of Polλ in conjunction with Polζ in mediating error-free replication through 1-MeA by inserting the correct nt opposite it. We discuss how by adopting Hoogsteen base pairing as a mechanism for inserting the correct nt opposite 1-MeA, Polλ could promote error-free replication through this adduct. In our previous analyses of the genetic control of TLS opposite 1-MeA in human cells, we identified the involvement of three independent Polι/Polθ, Polη, and Polζ pathways (28Conde J. Yoon J.H. Roy Choudhury J. Prakash L. Prakash S. Genetic control of replication through N1-methyladenine in human cells.J. Biol. Chem. 2015; 290: 29794-29800Abstract Full Text Full Text PDF PubMed Scopus (17) Google Scholar). In the Polζ pathway, however, the identity of the Pol that could insert an nt opposite 1-MeA had remained unknown. To determine whether Polλ functions together with Polζ, we analyzed the effects of siRNA depletion of Polλ alone and in combination with depletion of other TLS Pols on TLS frequency opposite 1-MeA carried on the leading strand template in the duplex plasmid in which bidirectional replication initiates from an origin of replication (28Conde J. Yoon J.H. Roy Choudhury J. Prakash L. Prakash S. Genetic control of replication through N1-methyladenine in human cells.J. Biol. Chem. 2015; 290: 29794-29800Abstract Full Text Full Text PDF PubMed Scopus (17) Google Scholar). As shown in Table 1, TLS in normal human fibroblasts (HFs) treated with control (NC) siRNA occurs with a frequency of ∼63%. In Polη depleted cells, TLS frequency is reduced to ∼53% and depletion of Polι, Polθ, Rev3, or Polλ reduced TLS frequency to 40 to 46%. Our evidence that codepletion of Polλ with Polη, Polι, or Polθ reduces TLS frequency nearly to ∼27% indicated a role for Polλ in a TLS pathway independent of Polη or Polι/Polθ pathways, and our observation that TLS frequency remains the same in cells codepleted for Polλ and Rev3 (∼42%) as in cells depleted for either Pol alone implicated a role for Polλ in TLS in conjunction with Polζ.Table 1Effects of siRNA knockdowns of Polλ and other TLS Pols on replicative bypass of 1-MeA carried on the leading DNA strand template in normal human fibroblastssiRNANumber of Kan+ coloniesNumber of blue colonies among Kan+ coloniesTLS (%)NC40725863.4Polη36819653.3Polι35616546.3Polθ47518939.8Rev334415745.6Polλ43620446.8Polη + Polλ39010426.7Polι + Polλ40811427.9Polθ + Polλ41711226.9Rev3 + Polλ31713442.3 Open table in a new tab To provide further evidence for the role of Polλ in TLS with Polζ, we analyzed the effects or Polλ depletion alone and in combination with the depletion of other TLS Pols in XPV HFs (Table 2). In control siRNA-treated XPV HFs, TLS opposite 1-MeA occurs with a frequency of ∼47% and as expected from the role of Polι/Polθ and Polλ/Polζ in Polη-independent pathways, TLS frequency is reduced to ∼30% in XPV HFs depleted for Polι, Polθ, Rev3, or Polλ (Table 2). Our results that TLS frequency is reduced to ∼5% in XPV HFs codepleted for Polλ either with Polι or with Polθ and that TLS frequency remains nearly the same (∼29%) in XPV HFs codepleted for Polλ and Rev3 as in cells depleted for either Pol alone add further support for the role of Polλ in TLS opposite 1-MeA together with Polζ and independent of Polι and Polθ. Altogether from TLS analyses in WT HFs and XPV HFs, we conclude that TLS through 1-MeA operates via three independent Polι/Polθ, Polη, and Polλ/Polζ pathways (Fig. 1).Table 2Effects of siRNA knockdowns of Polλ and other TLS Pols on replicative bypass of 1-MeA carried on the leading DNA strand template in XPV human fibroblastssiRNANumber of Kan+ coloniesNumber of blue colonies among Kan+ coloniesTLS (%)NC39618045.5Polι41012430.2Polθ39511027.8Rev342612930.3Polλ50214528.9Polι + Polλ230114.8Polθ + Polλ426235.4Rev3 + Polλ47213628.8 Open table in a new tab To determine if Polλ’s polymerase activity was required for TLS opposite 1-MeA, we analyzed the effects of the D427A, D429A mutations, which inactivate this activity. For these studies, we stably expressed siRNA-resistant wild-type human Polλ or the D427A, D429A catalytic mutant Polλ in WT HFs. As shown in Table 3, TLS opposite 1-MeA in Polλ-depleted HFs harboring the vector plasmid occurs with a frequency of ∼45%, and the frequency rises to ∼64% in cells expressing WT Polλ. Our results that TLS frequency is reduced to the same level (∼45%) in cells expressing the D427A, D429A catalytic mutant as in cells harboring the vector plasmid establish the requirement of Polλ’s polymerase activity for TLS through 1-MeA in human cells. Additionally, we confirmed the requirement of Polλ’s polymerase activity for TLS through this adduct in Polλ−/− MEFs (Table 4).Table 3Effects of catalytically active (WT) Polλ, catalytically inactive D427A, D429A Polλ, N-terminally deleted (245–575) Polλ, catalytically active (WT) Rev1, catalytically inactive D570A, E571A Rev1, catalytically active (WT) Rev3, or catalytically inactive D2781A, D2783A Rev3 on TLS opposite 1-MeA carried on the leading DNA strand template in normal human fibroblastsVector expressingsiRNANumber of Kan+ coloniesNumber of blue colonies among Kan+ coloniesTLS (%)No Polλ (control)Polλ37216644.6WT (1–575) PolλPolλ32620863.8D427A, D429A PolλPolλ30613845.1(245–575) PolλPolλ33421664.7No Rev3 (control)Rev329412442.2WT Rev3Rev324216166.5D2781A, D2783A Rev3Rev340918044.0No Rev1 (control)Rev135410629.9WT Rev1Rev148430262.4D570A, E571A Rev1Rev124815863.7 Open table in a new tab Table 4Effects of catalytically active (WT) Polλ, catalytically inactive D427A, D429A Polλ, or N-terminally deleted (245–575) Polλ on TLS opposite 1-MeA carried on the leading DNA strand template in Polλ−/− MEFsVector expressingNumber of Kan+ coloniesNumber of blue colonies among Kan+ coloniesTLS (%)No Polλ (control)34014642.9WT Polλ31819461.0D427A, D429A Polλ37515340.8(245–575) Polλ27617061.6 Open table in a new tab Polλ is a 575 residue polypeptide that contains an N-terminal BRCT domain. We have shown previously that N-terminally deleted Polλ comprised of residues 245 to 575, which lacks the BRCT domain and the proline-rich region, physically interacts with the Rev7 subunit of Polζ and that this N-terminally deleted Polλ supports TLS through (6–4) TT photoproduct in human cells (22Yoon J.H. Basu D. Sellamuthu K. Johnson R.E. Prakash S. Prakash L. A novel role of DNA polymerase lambda in translesion synthesis in conjunction with DNA polymerase zeta.Life Sci. Alliance. 2021; 4e202000900Crossref PubMed Google Scholar). Our results that expression of (245–575) Polλ in HFs supports WT levels of TLS (Table 3) confirm that the N-terminal BRCT domain and the adjoining proline-rich region are also not required for Polλ’s role in TLS through 1-MeA in HFs (Table 3); additionally, we confirmed these results in Polλ−/− MEFs (Table 4). The requirement of Polλ’s polymerase activity for TLS through the 1-MeA adduct in conjunction with Polζ in human cells suggested that Polλ would insert an nt opposite 1-MeA from which Polζ would extend synthesis. Hence, we examined purified Polλ for its ability to insert dATP, dTTP, dGTP, or dCTP opposite 1-MeA and to synthesize DNA through the adduct in the presence of all four dNTPs. As shown in Figure 2, Polλ replicates through the undamaged template residue A by inserting a T. Opposite 1-MeA also Polλ inserts a T and then extends synthesis similar to that on undamaged DNA. The high proficiency of Polλ for inserting the correct nt opposite 1-MeA stands in sharp contrast to the error-proneness of purified Polι or Polη opposite this adduct (28Conde J. Yoon J.H. Roy Choudhury J. Prakash L. Prakash S. Genetic control of replication through N1-methyladenine in human cells.J. Biol. Chem. 2015; 290: 29794-29800Abstract Full Text Full Text PDF PubMed Scopus (17) Google Scholar). Thus in addition to the insertion of a T, Polι inserts an A or a C opposite 1-MeA, and steady-state kinetic analyses have indicated that it does so with only an ∼100-fold lower catalytic efficiency than for the insertion of correct T (29Jain R. Choudhury J.R. Buku A. Johnson R.E. Prakash L. Prakash S. Aggarwal A.K. Mechanism of error-free DNA synthesis across N1-methyl-deoxyadenosine by human DNA polymerase-iota.Sci. Rep. 2017; 7: 43904Crossref PubMed Scopus (9) Google Scholar). Likewise, compared with the catalytic efficiency for the insertion of a T, Polη inserts an A or a G opposite 1-MeA with only an ∼40-fold reduction in catalytic efficiency, and it inserts a C opposite 1-MeA with only an ∼100-fold reduction in catalytic efficiency (Table 5). Nevertheless, in spite of their error-proneness in vitro, both these Pols conduct predominantly error-free TLS through 1-MeA in human cells (28Conde J. Yoon J.H. Roy Choudhury J. Prakash L. Prakash S. Genetic control of replication through N1-methyladenine in human cells.J. Biol. Chem. 2015; 290: 29794-29800Abstract Full Text Full Text PDF PubMed Scopus (17) Google Scholar).Table 5Steady-state kinetic analyses of nucleotide incorporation opposite undamaged A or 1-MeA by human PolηTemplate residueIncoming nucleotidekcat (min−1)Km (μM)kcat/KmCatalytic efficiency relative to TAT7.4 ± 0.20.39 ± 0.08191A2.2 ± 0.12.4 ± 0.40.95 × 10−2G2.9 ± 0.25.3 ± 1.30.543 × 10−2C2.2 ± 0.1813.46 ± 20.160.8 × 10−21-MeAT5.8 ± 0.31.05 ± 0.25.81A2.3 ± 0.514.99 ± 60.152.6 × 10−2G1.6 ± 0.210.58 ± 3.70.152.6 × 10−2C1.9 ± 0.0935.9 ± 5.30.051 × 10−2Polη (0.25 nM) was incubated with primer:template DNA substrate (10 nM) and increasing concentrations of dNTPs for 10 min, at 37 °C. The nucleotide incorporation rate was plotted against dNTP concentration and the data were fit to the Michaelis–Menten equation. Apparent Km and kcat values were obtained from the fit and used to calculate the efficiency of deoxynucleotide incorporation (kcat/Km). Open table in a new tab Polη (0.25 nM) was incubated with primer:template DNA substrate (10 nM) and increasing concentrations of dNTPs for 10 min, at 37 °C. The nucleotide incorporation rate was plotted against dNTP concentration and the data were fit to the Michaelis–Menten equation. Apparent Km and kcat values were obtained from the fit and used to calculate the efficiency of deoxynucleotide incorporation (kcat/Km). The ability of purified Polλ for replicating through the 1-MeA adduct with nearly the same proficiency as for replicating undamaged DNA raised the question of whether Polζ’s polymerase activity was required for TLS through this adduct in human cells. To examine this, we expressed full-length WT Rev3, or the D2781A, D2783A mutant Rev3, defective in its polymerase activity, in HFs. In Rev3-depleted HFs harboring the vector plasmid, TLS opposite 1-MeA occurs with a frequency of ∼42% and TLS frequency rises to ∼66% in cells expressing WT Rev3. Our results that in cells expressing the D2781A, D2783A Rev3 catalytic mutant, TLS is reduced to the same level (∼44%) as in cells harboring the vector control (Table 3) confirm that the Rev3 DNA polymerase activity is, in fact, required for TLS through 1-MeA in human cells. In previous studies opposite a number of DNA lesions, we have provided evidence for a scaffolding role of Rev1 in TLS by Y-family Pols (11Yoon J.H. Johnson R.E. Prakash L. Prakash S. DNA polymerase theta accomplishes translesion synthesis opposite 1,N(6)-ethenodeoxyadenosine with a remarkably high fidelity in human cells.Genes Dev. 2019; 33: 282-287Crossref PubMed Scopus (6) Google Scholar, 19Yoon J.H. Hodge R.P. Hackfeld L.C. Park J. Roy Choudhury J. Prakash S. Prakash L. Genetic control of predominantly error-free replication through an acrolein-derived minor-groove DNA adduct.J. Biol. Chem. 2018; 293: 2949-2958Abstract Full Text Full Text PDF PubMed Scopus (6) Google Scholar, 20Yoon J.H. Park J. Conde J. Wakamiya M. Prakash L. Prakash S. Rev1 promotes replication through UV lesions in conjunction with DNA polymerases η, ι, and κ but not DNA polymerase ζ.Genes Dev. 2015; 29: 2588-2662Crossref PubMed Google Scholar, 21Yoon J.H. Roy Choudhury J. Park J. Prakash S. Prakash L. Translesion synthesis DNA polymerases promote error-free replication through the minor-groove DNA adduct 3-deaza-3-methyladenine.J. Biol. Chem. 2017; 292: 18682-18688Abstract Full Text Full Text PDF PubMed Scopus (19) Google Scholar). To confirm that Rev1 plays a similar role in TLS by Polι and Polη opposite 1-MeA, we analyzed the epistatic relationship of Rev1 with these Pols. Our results that TLS occurs at the same frequency in Rev1 depleted HFs (∼30%) as in cells depleted for Rev1 together with Polη or with Polι and that TLS frequency is reduced to ∼6% in cells depleted for Rev1 together with Rev3 or with Polλ (Table 6) concur with a role of Rev1 in TLS in Polι and Polη-dependent pathways that operate independently or Polλ/Polζ pathway. To confirm that Rev1’s polymerase activity is not required for TLS opposite 1-MeA, we expressed full-length WT Rev1, or D570A, E571A Rev1 defective in its DNA polymerase activity, in HFs. Our results that the catalytic mutant Rev1 supports the same level of TLS (∼64%) as the WT Rev1 (∼62%) (Table 3) confirmed that Rev1’s polymerase activity was not required. Thus, only the scaffolding role of Rev1 is required for the Polι and Polη TLS pathways.Table 6Effects of siRNA knockdowns of Rev1 and other TLS Pols on replicative bypass of 1-MeA carried on the leading DNA strand template in normal human fibroblastssiRNANumber of Kan+ coloniesNumber of blue colonies among Kan+ coloniesTLS (%)NC47630764.5Rev134010430.6Polη + Rev137811229.6Polι + Rev140212029.9Rev3 + Rev1382225.8Polλ + Rev1420245.7 Open table in a new tab Since the addition of a methyl group to the N1 atom of deoxyadenosine disrupts W-C base pairing (29Jain R. Choudhury J.R. Buku A. Johnson R.E. Prakash L. Prakash S. Aggarwal A.K. Mechanism of error-free DNA synthesis across N1-methyl-deoxyadenosine by human DNA polymerase-iota.Sci. Rep. 2017; 7: 43904Crossref PubMed Scopus (9) Google Scholar), the insertion of T opposite 1-MeA by Polλ could occur only if the adduct is accommodated in a syn conformation in its active site and the adduct forms a Hoogsteen base pair with T. Thus Polλ active site, which normally accommodates template residues in an anti conformation and forms a W-C base pair with the incoming nt (30Garcia-Diaz M. Bebenek K. Krahn J.M. Kunkel T.A. Pedersen L.C. A closed conformation for the Pol lambda catalytic cycle.Nat. Struct. Mol. Biol. 2005; 12: 97-98Crossref PubMed Scopus (130) Google Scholar), would stabilize 1-MeA in a syn conformation. Such an ability of Polλ active site to accommodate a W-C impairing DNA lesion in a syn conformation would add another novel aspect to Polλ’s function in TLS—in addition to its role as a scaffolding component of Polζ for TLS in human cells. Even though purified Polλ inserts a T opposite 1-MeA and extends synthesis, Polζ’s polymerase activity is still required for replication through 1-MeA in human cells. The requirement of both the Polλ and Polζ polymerase activities strongly suggests that their polymerase activities are restrained to act at the nt insertion or the extension step of TLS in human cells. We presume that in the multiprotein ensemble of Polλ-Polζ, the action mechanism of the two Pols is restrained such that Polλ’s action is limited to inserting a T opposite 1-MeA and Polζ functions at the extension step. The decipherment of the action mechanism of these Pols in human cells would require the identification of the components of the Polλ-Polζ multiprotein ensemble and biochemical analyses of Polλ’s and Polζ’s role in TLS opposite 1-MeA in the Polλ-Polζ ensemble. Our evidence that similar to the requirement of Rev1 as a scaffolding component of Y-family Pols for TLS opposite CPDs, (6–4) PPs, 3-methyl deoxyadenosine, εdA, and other DNA lesions, Rev1’s scaffolding role is required for TLS opposite 1-MeA by Polι and Polη suggests that Rev1 would effect the assembly of these Y-family Pols with the other protein components and that the fidelity of Polι and Polη for TLS opposite 1-MeA would be elevated in the respective multiprotein ensemble thus formed. Polι differs from other Y-family Pols in that its active site accommodates a template purine A or G in a syn conformation, which then forms a Hoogsteen base pair with the incoming nt (31Nair D.T. Johnson R.E. Prakash L. Prakash S. Aggarwal A.K. Human DNA polymerase ι incorporates dCTP opposite template G via a G.C+ Hoogsteen base pair.Structure. 2005; 13: 1569-1577Abstract Full Text Full Text PDF PubMed Scopus (112) Google Scholar, 32Nair D.T. Johnson R.E. Prakash S. Prakash L. Aggarwal A.K. Replication by human DNA polymerase ι occurs via Hoogsteen base-pairing.Nature. 2004; 430: 377-380Crossref PubMed Scopus (249) Google Scholar, 33Nair D.T. Johnson R.E. Prakash S. Prakash L. Aggarwal A.K. An incoming nucleotide imposes an anti to syn conformational change on the templating purine in the human DNA polymerase-ι active site.Structure. 2006; 14: 749-755Abstract Full Text Full Text PDF PubMed Scopus (54) Google Scholar). This allows Polι to accommodate DNA lesions, such as εdA, which impair W-C base pairing, in a syn conformation and to form a Hoogsteen base pair with the incoming nt (9Nair D.T. Johnson R.E. Prakash L. Prakash S. Aggarwal A.K. Hoogsteen base pair formation promotes synthesis opposite the 1,N6-ethenodeoxyadenosine lesion by human DNA polymerase iota.Nat. Struct. Mol. Biol. 2006; 13: 619-625Crossref PubMed Scopus (94) Google Scholar). However, biochemical studies with Polι have indicated that it can insert not only the correct nt T opposite εdA but also the incorrect nt C with only a few-fold reduction in catalytic efficiency, and structure studies have shown that εdA in Polι active site adopts a syn conformation and that it Hoogsteen base pairs with the incoming dTTP or dCTP (9Nair D.T. Johnson R.E. Prakash L. Prakash S. Aggarwal A.K. Hoogsteen base pair formation promotes synthesis opposite the 1,N6-ethenodeoxyadenosine lesion by human DNA polymerase iota.Nat. Struct. Mol. Biol. 2006; 13: 619-625Crossref PubMed Scopus (94) Google Scholar). Nevertheless, in spite of the penchant of Polι for inserting a C opposite εdA, Polι conducts error-free TLS opposite this adduct in human cells (11Yoon J.H. Johnson R.E. Prakash L. Prakash S. DNA polymerase theta accomplishes translesion synthesis opposite 1,N(6)-ethenodeoxyadenosine with a remarkably high fidelity in human cells.Genes Dev. 2019; 33: 282-287Crossref PubMed Scopus (6) Google Scholar). Similar to εdA, 1-MeA is accommodated in a syn conformation in Polι’s active site, and it forms a Hoogsteen base pair with T (29Jain R. Choudhury J.R. Buku A. Johnson R.E. Prakash L. Prakash S. Aggarwal A.K. Mechanism of error-free DNA synthesis across N1-methyl-deoxyadenosine by human DNA polymerase-iota.Sci. Rep. 2017; 7: 43904Crossref PubMed Scopus (9) Google Scholar); however, even though purified Polι misincorporates an A or a C at a frequency of ∼10−2 (29Jain R. Choudhury J.R. Buku A. Johnson R.E. Prakash L. Prakash S. Aggarwal A.K. Mechanism of error-free DNA synthesis across N1-methyl-deoxyadenosine by human DNA polymerase-iota.Sci. Rep. 2017; 7: 43904Crossref PubMed Scopus (9) Google Scholar), it promotes error-free TLS through 1-MeA in human cells. The adoption of entirely error-free TLS opposite εdA and of predominantly error-free TLS opposite 1-MeA in human cells could be explained if Polι’s error-proneness is annulled in the multiprotein ensemble that the scaffolding role of Rev1 would assemble. Polη uses W-C base pairing for replicating undamaged DNA (34Washington M.T. Helquist S.A. Kool E.T. Prakash L. Prakash S. Requirement of Watson-Crick hydrogen bonding for DNA synthesis by yeast DNA polymerase η.Mol. Cell. Biol. 2003; 23: 5107-5112Crossref PubMed Scopus (79) Google Scholar) and for replicating through the two covalently linked pyrimidines of a CPD (2Johnson R.E. Prakash S. Prakash L. Efficient bypass of a thymine-thymine dimer by yeast DNA polymerase, Polη.Science. 1999; 283: 1001-1004Crossref PubMed Scopus (677) Google Scholar, 4Masutani C. Kusumoto R. Yamada A. Dohmae N. Yokoi M. Yuasa M. Araki M. Iwai S. Takio K. Hanaoka F. The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase η.Nature. 1999; 399: 700-704Crossref PubMed Scopus (1117) Google Scholar, 35Biertumpfel C. Zhao Y. Kondo Y. Ramon-Maiques S. Gregory M. Lee J.Y. Masutani C. Lehmann A.R. Hanaoka F. Yang W. Structure and mechanism of human DNA polymerase η.Nature. 2010; 465: 1044-1048Crossref PubMed Scopus (240) Google Scholar, 36Johnson R.E. Prakash L. Prakash S. Distinct mechanisms of cis-syn thymine dimer bypass by Dpo4 and DNA polymerase η.Proc. Natl. Acad. Sci. U. S. A. 2005; 102: 12359-12364Crossref PubMed Scopus (30) Google Scholar, 37Silverstein T.D. Johnson R.E. Jain R. Prakash L. Prakash S. Aggarwal A.K. Structural basis for the suppression of skin cancers by DNA polymerase eta.Nature. 2010; 465: 1039-1043Crossref PubMed Scopus (117) Google Scholar). And Polη can replicate through both the guanines of a cisplatin GG intrastrand cross-link with both the Gs in the cross-link forming a W-C base pair with the incoming dCTP (38Ummat A. Rechkoblit O. Jain R. Roy Choudhury J. Johnson R.E. Silverstein T.D. Buku A. Lone S. Prakash L. Prakash S. Aggarwal A.K. Structural basis for cisplatin DNA damage tolerance by human polymerase eta during cancer chemotherapy.Nat. Struct. Mol. Biol. 2012; 19: 628-632Crossref PubMed Scopus (67) Google Scholar, 39Zhao Y. Biertumpfel C. Gregory M.T. Hua Y.J. Hanaoka F. Yang W. Structural basis of human DNA polymerase eta-mediated chemoresistance to cisplatin.Proc. Natl. Acad. Sci. U. S. A. 2012; 109: 7269-7274Crossref PubMed Scopus (118) Google Scholar). Hence, the hallmark of Polη has been its ability to accommodate two template residues in its active site and to form a W-C base pair with the incoming nt. The proficiency of purified Polη for incorporating a T opposite 1-MeA and the genetic evidence that Polη replicates through this adduct in human cells strongly suggest that Polη accommodates 1-MeA in its active site in a syn conformation, which then Hoogsteen base pairs with the correct nt T or with incorrect nts. We presume that the intrinsic error-proneness of Polη for TLS through 1-MeA is attenuated in the Polη multiprotein ensemble. The heteroduplex vectors containing 1-MeA on the leading or the lagging strand template were constructed as described previously (28Conde J. Yoon J.H. Roy Choudhury J. Prakash L. Prakash S. Genetic control of replication through N1-methyladenine in human cells.J. Biol. Chem. 2015; 290: 29794-29800Abstract Full Text Full Text PDF PubMed Scopus (17) Google Scholar). Normal human fibroblasts (Coriell Institute Cell Repository, GM00637), XPV fibroblasts (Coriell Institute Cell Repository, GM03617), Polλ−/− MEFs, and big blue mouse embryonic fibroblasts (Agilent) were grown in DMEM medium (GenDEPOT) containing 10% fetal bovine serum (GenDEPOT) and 1% antibiotic-antimycotic (GenDEPOT). Cells were grown on plastic culture dishes at 37 °C in a humidified incubator with 5% CO2. The siRNA sequences, the siRNA knockdown efficiency of TLS Pols, as well as the detailed methods for TLS assays and for mutational analyses have been described previously (6Yoon J.-H. Prakash L. Prakash S. Highly error-free role of DNA polymerase η in the replicative bypass of UV induced pyrimidine dimers in mouse and human cells.Proc. Natl. Acad. Sci. U. S. A. 2009; 106: 18219-18224Crossref PubMed Scopus (115) Google Scholar, 11Yoon J.H. Johnson R.E. Prakash L. Prakash S. DNA polymerase theta accomplishes translesion synthesis opposite 1,N(6)-ethenodeoxyadenosine with a remarkably high fidelity in human cells.Genes Dev. 2019; 33: 282-287Crossref PubMed Scopus (6) Google Scholar, 22Yoon J.H. Basu D. Sellamuthu K. Johnson R.E. Prakash S. Prakash L. A novel role of DNA polymerase lambda in translesion synthesis in conjunction with DNA polymerase zeta.Life Sci. Alliance. 2021; 4e202000900Crossref PubMed Google Scholar, 40Yoon J.-H. Prakash L. Prakash S. Error-free replicative bypass of (6-4) photoproducts by DNA polymerase ζ in mouse and human cells.Genes Dev. 2010; 24: 123-128Crossref PubMed Scopus (64) Google Scholar). Stable expression of siRNA resistant WT or D570A E571A mutant Rev1 has been described previously (19Yoon J.H. Hodge R.P. Hackfeld L.C. Park J. Roy Choudhury J. Prakash S. Prakash L. Genetic control of predominantly error-free replication through an acrolein-derived minor-groove DNA adduct.J. Biol. Chem. 2018; 293: 2949-2958Abstract Full Text Full Text PDF PubMed Scopus (6) Google Scholar). Stable expressions of siRNA-resistant WT Polλ, catalytic mutant (D427A D429A) Polλ, N-terminally deleted (245–575) Polλ, and of siRNA-resistant WT Rev3 or catalytic mutant (D2781A D2783A) were done as described (22Yoon J.H. Basu D. Sellamuthu K. Johnson R.E. Prakash S. Prakash L. A novel role of DNA polymerase lambda in translesion synthesis in conjunction with DNA polymerase zeta.Life Sci. Alliance. 2021; 4e202000900Crossref PubMed Google Scholar). The template 75-mer oligonucleotide contained the sequence 5′ AGC AAG TCA CCA ATG TCT AAG AGT TCG TAT AAT GCC TAC ACT GGA GTA CCG GAG CAT CGT CGT GAC TGG GAA AAC-3′, and it harbored an undamaged A or a 1-MeA at the underlined position. For examining the incorporation of dATP, dTTP, dCTP, or dGTP nucleotides individually, or of all four dNTPs, a 44 mer primer 5′ GTT TTC CCA GTC ACG ACG ATG CTC CGG TAC TCC AGT GTA GGC AT-3′ was annealed to the abovementioned 75 mer template. The specific details of DNA synthesis assays are stated in Figure 2 legend, and the general methods for DNA synthesis assays were as described before (22Yoon J.H. Basu D. Sellamuthu K. Johnson R.E. Prakash S. Prakash L. A novel role of DNA polymerase lambda in translesion synthesis in conjunction with DNA polymerase zeta.Life Sci. Alliance. 2021; 4e202000900Crossref PubMed Google Scholar, 28Conde J. Yoon J.H. Roy Choudhury J. Prakash L. Prakash S. Genetic control of replication through N1-methyladenine in human cells.J. Biol. Chem. 2015; 290: 29794-29800Abstract Full Text Full Text PDF PubMed Scopus (17) Google Scholar). Steady-state kinetic analyses for deoxynucleotide incorporation opposite undamaged A or 1-MeA by Polη were performed as described (21Yoon J.H. Roy Choudhury J. Park J. Prakash S. Prakash L. Translesion synthesis DNA polymerases promote error-free replication through the minor-groove DNA adduct 3-deaza-3-methyladenine.J. Biol. Chem. 2017; 292: 18682-18688Abstract Full Text Full Text PDF PubMed Scopus (19) Google Scholar, 41Johnson R.E. Prakash L. Prakash S. Yeast and human translesion DNA synthesis polymerases: Expression, purification, and biochemical characterization.Methods Enzymol. 2006; 408: 390-407Crossref PubMed Scopus (42) Google Scholar). The specific details for kinetic analyses are described in Table 5 legend. All relevant data are contained within the article. The authors declare that they have no conflicts of interest with the contents of this article. This work was supported by grants from the National Institutes of Health ( R01 GM126087 ). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. J.-H. Y., J. R. C., and S. P. formal analysis; J.-H. Y., D. B., J. R. C., and S. P. investigation; J.-H. Y. methodology; J.-H. Y., D. B., J. R. C., S. P., and L. P. writing-review and editing; S. P. and L. P. conceptualization; S. P. and L. P. supervision; S. P. validation; S. P. writing-original draft; S. P. and L. P. project administration; L. P. funding acquisition." @default.
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• W3171107472 title "DNA polymerase λ promotes error-free replication through Watson–Crick impairing N1-methyl-deoxyadenosine adduct in conjunction with DNA polymerase ζ" @default.
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