Error-Prone DNA Polymerases

DNA Repair and Mutagenesis

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DNA repair and mutagenesis

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DNA Replication Fidelity

Kunkel, T. A., & Bebenek, K. (2000) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.69.1.497 · Cited by 1,003

The Y-Family of DNA Polymerases

Ohmori, H., Friedberg, E. C., Fuchs, R. P., Goodman, M. F., Hanaoka, F., Hinkle, D. C., Kunkel, T. A., Lawrence, C. W., Livneh, Z., Nohmi, T., et al. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00278-7 · Cited by 882

Excision of Deoxyribose Phosphate Residues by DNA Polymerase β During DNA Repair

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Crystal Structure of a Y-Family DNA Polymerase in Action

Ling, H., Boudsocq, F., Woodgate, R., & Yang, W. (2001) · Cell · doi:10.1016/s0092-8674(01)00515-3 · Cited by 610

Roles of E. coli DNA polymerases IV and V in lesion-targeted and untargeted SOS mutagenesis

Tang, M., Pham, P., Shen, X., Taylor, J.-S., O'Donnell, M., Woodgate, R., & Goodman, M. F. (2000) · Nature · doi:10.1038/35010020 · Cited by 443

Low fidelity DNA synthesis by human DNA polymerase-η

Matsuda, T., Bebenek, K., Masutani, C., Hanaoka, F., & Kunkel, T. A. (2000) · Nature · doi:10.1038/35010014 · Cited by 372

Efficient and accurate replication in the presence of 7,8-dihydro-8-oxoguanine by DNA polymerase η

Haracska, L., Yu, S.-L., Johnson, R. E., Prakash, L., & Prakash, S. (2000) · Nature Genetics · doi:10.1038/78169 · Cited by 356

Structure of the Catalytic Core of S. cerevisiae DNA Polymerase η

Trincão, J., Johnson, R. E., Escalante, C. R., Prakash, S., Prakash, L., & Aggarwal, A. K. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00306-9 · Cited by 348

DNA Replication Fidelity

Kunkel, T. A. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.r400006200 · Cited by 754

Specialized DNA Polymerases, Cellular Survival, and the Genesis of Mutations

Friedberg, E. C., Wagner, R., & Radman, M. (2002) · Science · doi:10.1126/science.1070236 · Cited by 443

Mechanisms of transcription-coupled DNA repair

Svejstrup, J. Q. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm703 · Cited by 380

Dial 9–1–1 for DNA damage: the Rad9–Hus1–Rad1 (9–1–1) clamp complex

Parrilla-Castellar, E. R., Arlander, S. J. H., & Karnitz, L. (2004) · DNA Repair · doi:10.1016/j.dnarep.2004.03.032 · Cited by 342

Structures of Mismatch Replication Errors Observed in a DNA Polymerase

Johnson, S. J., & Beese, L. S. (2004) · Cell · doi:10.1016/s0092-8674(04)00252-1 · Cited by 300

Suffering in silence: the tolerance of DNA damage

Friedberg, E. C. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1781 · Cited by 271

Functions of DNA polymerases

Bebenek, K., & Kunkel, T. A. (2004) · Advances in Protein Chemistry · doi:10.1016/s0065-3233(04)69005-x · Cited by 258

Structural basis for recruitment of translesion DNA polymerase Pol IV/DinB to the β‐clamp

Bunting, K. A., Roe, S. M., & Pearl, L. H. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg568 · Cited by 225

Origins of Spontaneous Mutations: Specificity and Directionality of Base-Substitution, Frameshift, and Sequence-Substitution Mutageneses

Maki, H. (2002) · Annual Review of Genetics · doi:10.1146/annurev.genet.36.042602.094806 · Cited by 198

Quantitative Analysis of Translesion DNA Synthesis across a Benzo[a]pyrene-Guanine Adduct in Mammalian Cells

Avkin, S., Goldsmith, M., Velasco-Miguel, S., Geacintov, N. E., Friedberg, E. C., & Livneh, Z. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m409155200 · Cited by 177

Anti-tumour compounds illudin S and Irofulven induce DNA lesions ignored by global repair and exclusively processed by transcription- and replication-coupled repair pathways

Jaspers, N. G. J., Raams, A., Kelner, M. J., Ng, J. M. Y., Yamashita, Y. M., Takeda, S., McMorris, T. C., & Hoeijmakers, J. H. J. (2002) · DNA repair · doi:10.1016/s1568-7864(02)00166-0 · Cited by 161

Structural Insights into the Origins of DNA Polymerase Fidelity

Beard, W. A., & Wilson, S. H. (2003) · Structure · doi:10.1016/s0969-2126(03)00051-0 · Cited by 157

A/T mutagenesis in hypermutated immunoglobulin genes strongly depends on PCNAK164 modification

Langerak, P., Nygren, A. O. H., Krijger, P. H. L., van den Berk, P. C. M., & Jacobs, H. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070902 · Cited by 166

The structure of T. aquaticus DNA polymerase III is distinct from eukaryotic replicative DNA polymerases.

Bailey, S., Wing, R. A., & Steitz, T. (2006) · Cell · doi:10.1016/j.cell.2006.07.027 · Cited by 145

Tuberculosis Chemotherapy: the Influence of Bacillary Stress and Damage Response Pathways on Drug Efficacy

Warner, D. F., & Mizrahi, V. (2006) · Clinical Microbiology Reviews · doi:10.1128/cmr.00060-05 · Cited by 135

Efficiency of Correct Nucleotide Insertion Governs DNA Polymerase Fidelity

Beard, W. A., Shock, D. D., Vande Berg, B. J., & Wilson, S. H. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m210036200 · Cited by 129

Role of DNA Polymerase η in the UV Mutation Spectrum in Human Cells

Stary, A., Kannouche, P. L., Lehmann, A. R., & Sarasin, A. R. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m211838200 · Cited by 133

Functions of human DNA polymerases η, κ and ι suggested by their properties, including fidelity with undamaged DNA templates

Kunkel, T. A., Pavlov, Y. I., & Bebenek, K. (2003) · DNA Repair · doi:10.1016/s1568-7864(02)00224-0 · Cited by 125

Altered DNA Polymerase ι Expression in Breast Cancer Cells Leads to a Reduction in DNA Replication Fidelity and a Higher Rate of Mutagenesis

Jin, Y., Chen, Z., Liu, Y., Hickey, R. J., & Malkas, L. H. (2004) · Cancer Research · doi:10.1158/0008-5472.can-04-0603 · Cited by 115

Mechanism of DNA Polymerization Catalyzed by Sulfolobus solfataricus P2 DNA Polymerase IV

Fiala, K. A., & Suo, Z. (2004) · Biochemistry · doi:10.1021/bi035746z · Cited by 114

Replication of damaged DNA in mammalian cells: new solutions to an old problem

Lehmann, A. R. (2002) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(02)00227-0 · Cited by 112

Increased Susceptibility to UV-Induced Skin Carcinogenesis in Polymerase η–deficient Mice

Lin, Q., Clark, A. B., McCulloch, S. D., Yuan, T., Bronson, R. T., Kunkel, T. A., & Kucherlapati, R. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-1862 · Cited by 95

Yeast MPH1 Gene Functions in an Error-Free DNA Damage Bypass Pathway That Requires Genes From Homologous Recombination, but Not From Postreplicative Repair

Schürer, K. A., Rudolph, C. J., Ulrich, H. D., & Kramer, W. (2004) · Genetics · doi:10.1534/genetics.166.4.1673 · Cited by 99

Enzymatic switching for efficient and accurate translesion DNA replication.

McCulloch, S. D., Kokoska, R., Chilkova, O., Welch, C. M., Johansson, E., Burgers, P., & Kunkel, T. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh777 · Cited by 97

A non-catalytic role of DNA polymerase η in recruiting Rad18 and promoting PCNA monoubiquitination at stalled replication forks

Durando, M., Tateishi, S., & Vaziri, C. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt016 · Cited by 91

Preferential Misincorporation of Purine Nucleotides by Human DNA Polymerase η Opposite Benzo[a]pyrene 7,8-Diol 9,10-Epoxide Deoxyguanosine Adducts

Chiapperino, D., Kroth, H., Kramarczuk, I. H., Sayer, J. M., Masutani, C., Hanaoka, F., Jerina, D. M., & Cheh, A. M. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m112139200 · Cited by 87

Structural and Functional Elucidation of the Mechanism Promoting Error-prone Synthesis by Human DNA Polymerase κ Opposite the 7,8-Dihydro-8-oxo-2′-deoxyguanosine Adduct

Irimia, A., Eoff, R. L., Guengerich, F. P., & Egli, M. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.003905 · Cited by 85

DNA mismatch repair and p53 function are major determinants of the rate of development of cisplatin resistance

Lin, X., & Howell, S. B. (2006) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-05-0491 · Cited by 89

Structure of a High Fidelity DNA Polymerase Bound to a Benzo[a]pyrene Adduct That Blocks Replication

Hsu, G. W., Huang, X., Luneva, N. P., Geacintov, N. E., & Beese, L. S. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m411276200 · Cited by 82

Two-step error-prone bypass of the (+)- and (−)-trans-anti-BPDE-N2-dG adducts by human DNA polymerases η and κ

Zhang, Y., Wu, X., Guo, D., Rechkoblit, O., Geacintov, N. E., & Wang, Z. (2002) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(02)00249-x · Cited by 78

Role of DNA polymerase in the bypass of abasic sites in yeast cells

Zhao, B. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh710 · Cited by 79

Diversify or Die: Generation of Diversity in Response to Stress

Aertsen, A., & Michiels, C. W. (2005) · Critical Reviews in Microbiology · doi:10.1080/10408410590921718 · Cited by 74

Involvement of Error-Prone DNA Polymerase IV in Stationary-Phase Mutagenesis in Pseudomonas putida

Tegova, R., Tover, A., Tarassova, K., Tark‐Dame, M., & Kivisaar, M. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.9.2735-2744.2004 · Cited by 74

Observing Translesion Synthesis of an Aromatic Amine DNA Adduct by a High-fidelity DNA Polymerase

Hsu, G. W., Kiefer, J. R., Burnouf, D., Bécherel, O. J., Fuchs, R. P., & Beese, L. S. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m409224200 · Cited by 72

Nucleotide insertion opposite a cis-syn thymine dimer by a replicative DNA polymerase from bacteriophage T7

Li, Y., Dutta, S., Doublié, S., Bdour, H. M., Taylor, J., & Ellenberger, T. (2004) · Nature Structural & Molecular Biology · doi:10.1038/nsmb792 · Cited by 69

Lesion Bypass Activities of Human DNA Polymerase μ

Zhang, Y., Wu, X., Guo, D., Rechkoblit, O., Taylor, J., Geacintov, N. E., & Wang, Z. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m207297200 · Cited by 68

Functions of Eukaryotic DNA Polymerases

Shcherbakova, P. V., Bębenek, K., & Kunkel, T. A. (2003) · Science of Aging Knowledge Environment · doi:10.1126/sageke.2003.8.re3 · Cited by 69

Aspergillus nidulans as a model system to characterize the DNA damage response in eukaryotes

Goldman, G. H., & Käfer, E. (2004) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2003.12.001 · Cited by 67

CpG dinucleotides and the mutation rate of non-CpG DNAPreprint

Walser, J., Ponger, L., & Furano, A. V. (2008) · Genome Research · doi:10.1101/gr.076455.108 · Cited by 64

Sequence context-dependent replication of DNA templates containing UV-induced lesions by human DNA polymerase ι

Vaisman, A., Frank, E. G., Iwai, S., Ohashi, E., Ohmori, H., Hanaoka, F., & Woodgate, R. (2003) · DNA repair · doi:10.1016/s1568-7864(03)00094-6 · Cited by 59

Considering the cancer consequences of altered DNA polymerase function

Kunkel, T. A. (2003) · Cancer Cell · doi:10.1016/s1535-6108(03)00027-8 · Cited by 55

DNA polymerase I acts in translesion synthesis mediated by the Y‐polymerases in Bacillus subtilis

Duigou, S., Ehrlich, S. D., Noirot, P. H., & Noirot‐Gros, M. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04725.x · Cited by 54

Local Deformations Revealed by Dynamics Simulations of DNA Polymerase β with DNA Mismatches at the Primer Terminus

Yang, L., Beard, W. A., Wilson, S. H., Roux, B., Broyde, S. B., & Tamar Schlick, A. (2002) · Journal of Molecular Biology · doi:10.1016/s0022-2836(02)00617-4 · Cited by 53

Translesion synthesis of 7,8-dihydro-8-oxo-2′-deoxyguanosine by DNA polymerase eta in vivo

Lee, D.-H., & Pfeifer, G. P. (2008) · Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis · doi:10.1016/j.mrfmmm.2008.02.006 · Cited by 53

Common structural features of nucleic acid polymerases

Cramer, P. (2002) · BioEssays · doi:10.1002/bies.10127 · Cited by 50

Mutagenesis of Benzo[a]pyrene Diol Epoxide in Yeast: Requirement for DNA Polymerase ζ and Involvement of DNA Polymerase η

Xie, Z., Braithwaite, E. K., Guo, D., Zhao, B., Geacintov, N. E., & Wang, Z. (2003) · Biochemistry · doi:10.1021/bi0346704 · Cited by 46

Cognizance of Molecular Methods for the Generation of Mutagenic Phage Display Antibody Libraries for Affinity Maturation

Lim, C. C., Choong, Y. S., & Lim, T. S. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20081861 · Cited by 44

The Role of Polymerase η in Somatic Hypermutation Determined by Analysis of Mutations in a Patient with Xeroderma Pigmentosum Variant

Yavuz, Ş., Yavuz, A. S., Kraemer, K. H., & Lipsky, P. E. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.7.3825 · Cited by 43

The unexpected landscape of in vivo somatic mutation in a human epithelial cell lineage

Colgin, L. M., Hackmann, A. F. M., Emond, M. J., & Monnat, R. J. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.032655699 · Cited by 43

Effect of manganese on in vitro replication of damaged DNA catalyzed by the herpes simplex virus type-1 DNA polymerase

Villani, G. (2002) · Nucleic Acids Research · doi:10.1093/nar/gkf463 · Cited by 40

The p-benzoquinone DNA adducts derived from benzene are highly mutagenic

Xie, Z., Zhang, Y., Guliaev, A. B., Shen, H., Hang, B., Singer, B. C., & Wang, Z. (2005) · DNA repair · doi:10.1016/j.dnarep.2005.08.012 · Cited by 40

tRNA‐nucleotidyltransferases: Highly unusual RNA polymerases with vital functions

Vörtler, S., & Mörl, M. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.10.078 · Cited by 38

polι-dependent lesion bypass in vitro

Vaisman, A., Frank, E. G., McDonald, J. P., Tissier, A., & Woodgate, R. (2002) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(02)00248-8 · Cited by 38

Pol , Pol and Rev1 together are required for G to T transversion mutations induced by the (+)- and (-)-trans-anti-BPDE-N2-dG DNA adducts in yeast cells

Zhao, B. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkj446 · Cited by 38

A RecA Protein Surface Required for Activation of DNA Polymerase V

Gruber, A. J., Erdem, A. L., Sabat, G., Karata, K., Jaszczur, M. M., Vo, D. D., Olsen, T. M., Woodgate, R., Goodman, M. F., & Cox, M. M. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005066 · Cited by 37

In vivo deamination of cytosine-containing cyclobutane pyrimidine dimers in E. coli: a feasible part of UV-mutagenesis

Burger, A., Fix, D. F., Liu, H., Hays, J. B., & Bockrath, R. C. (2003) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(02)00310-x · Cited by 33

An Active Site Aromatic Triad in Escherichia coli DNA Pol IV Coordinates Cell Survival and Mutagenesis in Different DNA Damaging Agents

Benson, R. W., Norton, M., Lin, I., Comb, W. D., & Godoy, V. G. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019944 · Cited by 31

The Use of Non‐natural Nucleotides to Probe Template‐Independent DNA Synthesis

Berdis, A. J., & McCutcheon, D. C. (2007) · ChemBioChem · doi:10.1002/cbic.200700096 · Cited by 31

Tissue-specific time courses of spontaneous mutation frequency and deviations in mutation pattern are observed in middle to late adulthood in Big Blue mice

Hill, K. A., Halangoda, A., Heinmöller, P., Hagman, K. D. F., Chitaphan, C., Longmate, J., Scaringe, W. A., Wang, J., & Sommer, S. S. (2005) · Environmental and Molecular Mutagenesis · doi:10.1002/em.20119 · Cited by 32

Detours to Replication: Functions of Specialized DNA Polymerases during Oncogene-induced Replication Stress

Tsao, W.-C., & Eckert, K. A. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19103255 · Cited by 32

Multiple Strategies for Translesion Synthesis in Bacteria

Ippoliti, P. J., DeLateur, N. A., Jones, K. M., & Beuning, P. J. (2012) · Cells · doi:10.3390/cells1040799 · Cited by 28

Conformational Changes during Nucleotide Selection by Sulfolobus solfataricus DNA Polymerase Dpo4

Eoff, R. L., Sánchez-Ponce, R., & Guengerich, F. P. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.009506 · Cited by 28

Y586F mutation in murine leukemia virus reverse transcriptase decreases fidelity of DNA synthesis in regions associated with adenine–thymine tracts

Zhang, W., Svarovskaia, E. S., Barr, R., & Pathak, V. K. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.152186199 · Cited by 28

The L561A Substitution in the Nascent Base-Pair Binding Pocket of RB69 DNA Polymerase Reduces Base Discrimination

Zhang, H., Rhee, C., Bębenek, A., Drake, J. W., Wang, J., & Konigsberg, W. H. (2006) · Biochemistry · doi:10.1021/bi052099y · Cited by 27

Rational Attempts to Optimize Non-Natural Nucleotides for Selective Incorporation Opposite an Abasic Site

Zhang, X., Donnelly, A. C., Lee, I., & Berdis, A. J. (2006) · Biochemistry · doi:10.1021/bi060418v · Cited by 27

Examining the potential role of DNA polymerases η and ζ in triplet repeat instability in yeast

Dixon, M. J. (2002) · DNA repair · doi:10.1016/s1568-7864(02)00095-2 · Cited by 26

Spontaneous multiple mutations show both proximal spacing consistent with chronocoordinate events and alterations with p53-deficiency

Hill, K. A., Wang, J., Hagman, K. D. F., Scaringe, W. A., & Sommer, S. S. (2004) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2004.05.005 · Cited by 24

Exploring the Effects of Active Site Constraints on HIV-1 Reverse Transcriptase DNA Polymerase Fidelity

Cramer, J., Strerath, M., Marx, A., & Restle, T. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m207854200 · Cited by 22

Adaptation to Endoplasmic Reticulum Stress Enhances Resistance of Oral Cancer Cells to Cisplatin by Up-Regulating Polymerase η and Increasing DNA Repair Efficiency

Chen, C.-Y., Kawasumi, M., Lan, T.-Y., Poon, C.-L., Lin, Y.-S., Wu, P.-J., Chen, Y.-C., Chen, B., Wu, C., Lo, J., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms22010355 · Cited by 22

The DinB•RecA complex of Escherichia coli mediates an efficient and high‐fidelity response to ubiquitous alkylation lesions

Cafarelli, T. M., Rands, T. J., & Godoy, V. G. (2013) · Environmental and Molecular Mutagenesis · doi:10.1002/em.21826 · Cited by 21

Lesion bypass DNA polymerases replicate across non-DNA segments

Maor-Shoshani, A., Ben-Ari, V., & Livneh, Z. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2433503100 · Cited by 20

A Review of Stable Isotope Labeling and Mass Spectrometry Methods to Distinguish Exogenous from Endogenous DNA Adducts and Improve Dose–Response Assessments

Lü, K., Hsiao, Y.-C., Liu, C., Schoeny, R. S., Gentry, R., & Starr, T. B. (2021) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.1c00212 · Cited by 17

Accommodation of a 1S-(−)-Benzo[c]phenanthrenyl-N6-dA Adduct in the Y-Family Dpo4 DNA Polymerase Active Site: Structural Insights through Molecular Dynamics Simulations

Wang, L., Wu, M., Yan, S. F., Patel, D. J., Geacintov, N. E., & Broyde, S. B. (2005) · Chemical Research in Toxicology · doi:10.1021/tx049786v · Cited by 17

Residues in the fingers domain of the translesion DNA polymerase DinB enable its unique participation in error-prone double-strand break repair

Tashjian, T. F., Danilowicz, C., Molza, A.-E., Nguyen, B. H., Prévost, C., Prentiss, M. G., & Godoy, V. G. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.006233 · Cited by 16

Model of the developing tumorigenic phenotype in mammalian cells and the roles of sustained stress and replicative senescence

Karpinets, T. V., & Foy, B. D. (2004) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2003.11.005 · Cited by 15

Trans-Lesion DNA Polymerases May Be Involved in Yeast Meiosis

Arbel‐Eden, A., Joseph-Strauss, D., Masika, H., Printzental, O., Rachi, E., & Simchen, G. (2013) · G3 Genes Genomes Genetics · doi:10.1534/g3.113.005603 · Cited by 16

Amino Acid Substitutions at Conserved Tyrosine 52 Alter Fidelity and Bypass Efficiency of Human DNA Polymerase η

Glick, E., Chau, J. S., Vigna, K. L., McCulloch, S. D., Adman, E. T., Kunkel, T. A., & Loeb, L. A. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m300686200 · Cited by 16

BP[dG]-induced distortions to DNA polymerase and DNA duplex: A detailed mechanism of BP adducts blocking replication

Wu, Z., Peng, L., Hu, Y., Xie, T., Yan, H., Wan, H., Liu, W., Liang, L., Xie, Z., Liu, K., et al. (2020) · Food and Chemical Toxicology · doi:10.1016/j.fct.2020.111325 · Cited by 15

A new proofreading mechanism for lesion bypass by DNA polymerase‐λ

Crespan, E., Maga, G., & Hübscher, U. (2011) · EMBO Reports · doi:10.1038/embor.2011.226 · Cited by 14

Yeast POL5 Is an Evolutionarily Conserved Regulator of rDNA Transcription Unrelated to Any Known DNA Polymerases

Yang, W., Rogozin, I. B., & Koonin, E. V. (2003) · Cell Cycle · doi:10.4161/cc.2.2.329 · Cited by 14

Molecular Mechanisms of Carcinogenesis

Malejka‐Giganti, D., & Tretyakova, N. Y. (2005) · Chemical and functional properties of food components series · doi:10.1201/9781420039269.ch2 · Cited by 12

Mutagenic DNA repair potential inPseudomonasspp., and characterization of therulABPcoperon from the highly mutable strainPseudomonas cichorii302959

Zhang, S., & Sundin, G. W. (2004) · Canadian Journal of Microbiology · doi:10.1139/w03-105 · Cited by 12

Somatic microindels in human cancer: the insertions are highly error-prone and derive from nearby but not adjacent sense and antisense templates

Scaringe, W. A., Li, K., Gu, D., Hagman, K. D. F., Chen, Z., Hill, K. A., & Sommer, S. S. (2008) · Human Molecular Genetics · doi:10.1093/hmg/ddn190 · Cited by 11

A nuclear 3′–5′ exonuclease proofreads for the exonuclease-deficient DNA polymerase α

Brown, K. R., Weatherdon, K. L., Galligan, C. L., & Skalski, V. (2002) · DNA repair · doi:10.1016/s1568-7864(02)00115-5 · Cited by 11

Signal Transduction in the Escherichia coli SOS Response

Foti, J. J., Simmons, L. A., Beuning, P., & Walker, G. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-374145-5.00258-8 · Cited by 7

Multiple PolK (POLK) transcripts in mammalian testis

Guo, C., Gao, T., Confer, N., Velasco-Miguel, S., & Friedberg, E. C. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.10.006 · Cited by 10

Impact of Chemical Adducts on Translesion Synthesis in Replicative and Bypass DNA Polymerases: From Structure to Function

Eoff, R. L., Egli, M., & Guengerich, F. P. (2010) · Wiley eBooks · doi:10.1002/9783527630110.ch13 · Cited by 9

Selection of dinB Alleles Suppressing Survival Loss upon dinB Overexpression in Escherichia coli

Benson, R. W., Cafarelli, T. M., Rands, T. J., Lin, I., & Godoy, V. G. (2014) · Journal of Bacteriology · doi:10.1128/jb.01782-14 · Cited by 9

Mouse models of DNA polymerases

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On the role of proofreading exonuclease in bypass of a 1,2 d(GpG) cisplatin adduct by the herpes simplex virus-1 DNA polymerase

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