Error-Prone Repair DNA Polymerases in Prokaryotes and Eukaryotes

Class Switch Recombination and Hypermutation Require Activation-Induced Cytidine Deaminase (AID), a Potential RNA Editing Enzyme

Muramatsu, M., Kinoshita, K., Fagarasan, S., Yamada, S., Shinkai, Y., & Honjo, T. (2000) · Cell · doi:10.1016/s0092-8674(00)00078-7 · Cited by 3,475

Ultraviolet mutagenesis and inducible DNA repair in Escherichia coli

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Activation-Induced Cytidine Deaminase (AID) Deficiency Causes the Autosomal Recessive Form of the Hyper-IgM Syndrome (HIGM2)

Revy, P., Muto, T., Lévy, Y., Geissmann, F., Plebani, A., Sanal, Ö., Catalan, N., Forveille, M., Dufourcq-Lagelouse, R., Gennery, A. R., et al. (2000) · Cell · doi:10.1016/s0092-8674(00)00079-9 · Cited by 1,645

The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase η

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Biochemistry of homologous recombination in Escherichia coli

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The importance of repairing stalled replication forks

Cox, M. M., Goodman, M. F., Kreuzer, K. N., Sherratt, D. J., Sandler, S. J., & Marians, K. J. (2000) · Nature · doi:10.1038/35003501 · Cited by 1,044

Hypermutation of multiple proto-oncogenes in B-cell diffuse large-cell lymphomas

Pasqualucci, L., Neumeister, P., Goossens, T., Nanjangud, G., Chaganti, R. S. K., Küppers, R., & Dalla-Favera, R. (2001) · Nature · doi:10.1038/35085588 · Cited by 1,032

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

Recombinational Repair of DNA Damage in Escherichia coli and Bacteriophage λ

Kuzminov, A. (1999) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.63.4.751-813.1999 · Cited by 897

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

Deciphering cellular states of innate tumor drug responses

Graudens, E., Boulanger, V., Mollard, C., Mariage, R., Barlet, X., Grémy, G., Couillault, C., Lajémi, M., Piatier‐Tonneau, D., Zaborski, P., et al. (2006) · Genome biology · doi:10.1186/gb-2006-7-3-r19 · Cited by 130

Molecular Design and Functional Organization of the RecA Protein

McGrew, D. A., & Knight, K. L. (2003) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409230390242489 · Cited by 127

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

Repair of DNA Damage Induced by Solar UV

Britt, A. B. (2004) · Photosynthesis Research · doi:10.1023/b:pres.0000035035.12340.58 · Cited by 124

A Water-Mediated and Substrate-Assisted Catalytic Mechanism forSulfolobus solfataricusDNA Polymerase IV

Wang, L., Yu, X., Hu, P., Broyde, S. B., & Zhang, Y. (2007) · Journal of the American Chemical Society · doi:10.1021/ja068821c · Cited by 124

DNA Repair Synthesis Facilitates RAD52-Mediated Second-End Capture during DSB Repair

McIlwraith, M. J., & West, S. C. (2008) · Molecular Cell · doi:10.1016/j.molcel.2007.11.037 · Cited by 123

Lysine 63-Polyubiquitination Guards against Translesion Synthesis–Induced Mutations

Chiu, R. K., Brun, J., Ramaekers, C. H. M. A., Theys, J., Weng, L., Lambin, P., Gray, D. A., & Wouters, B. G. (2005) · PLoS Genetics · doi:10.1371/journal.pgen.0020116 · Cited by 128

Cleavage of Model Replication Forks by Fission Yeast Mus81-Eme1 and Budding Yeast Mus81-Mms4

Whitby, M. C., Osman, F., & Dixon, J. E. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m210006200 · Cited by 122

Exo1 competes with repair synthesis, converts NER intermediates to long ssDNA gaps, and promotes checkpoint activation

Giannattasio, M., Follonier, C., Tourrière, H., Puddu, F., Lazzaro, F., Pasero, P., Lopes, M., Plevani, P., & Muzi-Falconi, M. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.004 · Cited by 121

Induction of frameshift and base pair substitution mutations by the major DNA adduct of the endogenous carcinogen malondialdehyde

VanderVeen, L. A., Hashim, M. F., Shyr, Y., & Marnett, L. J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2332176100 · Cited by 120

Essential roles for imuA ′- and imuB -encoded accessory factors in DnaE2-dependent mutagenesis in Mycobacterium tuberculosis

Warner, D. F., Ndwandwe, D. E., Abrahams, G. L., Kana, B. D., Machowski, E. E., Venclovas, Č., & Mizrahi, V. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002614107 · Cited by 120

Correlated mutations: Advances and limitations. A study on fusion proteins and on the Cohesin‐Dockerin families

Halperin, I., Wolfson, H. J., & Nussinov, R. (2006) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.20933 · Cited by 119

UmuD and RecA Directly Modulate the Mutagenic Potential of the Y Family DNA Polymerase DinB

Godoy, V. G., Jarosz, D. F., Simon, S. M., Abyzov, A. S., Ilyin, V., & Walker, G. C. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.10.025 · Cited by 118

Functional Uncoupling of Twin Polymerases

McInerney, P., & O’Donnell, M. E. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m401649200 · Cited by 118

Transcriptional mutagenesis: causes and involvement in tumour development

Brégeon, D., & Doetsch, P. W. (2011) · Nature reviews. Cancer · doi:10.1038/nrc3006 · Cited by 120

The 9-1-1 Checkpoint Clamp Physically Interacts with Polζ and Is Partially Required for Spontaneous Polζ-dependent Mutagenesis in Saccharomyces cerevisiae

Sabbioneda, S., Minesinger, B. K., Giannattasio, M., Plevani, P., Muzi-Falconi, M., & Jinks-Robertson, S. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m507638200 · Cited by 116

Pre-Steady-State Kinetic Studies of the Fidelity of Sulfolobus solfataricus P2 DNA Polymerase IV

Fiala, K. A., & Suo, Z. (2004) · Biochemistry · doi:10.1021/bi0357457 · Cited by 115

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

Crystal Structure of the Catalytic Core of Human DNA Polymerase Kappa

Uljon, S., Johnson, R. E., Edwards, T. A., Prakash, S., Prakash, L., & Aggarwal, A. K. (2004) · Structure · doi:10.1016/j.str.2004.05.011 · Cited by 114

Adaptive Translation as a Mechanism of Stress Response and Adaptation

Pan, T. (2013) · Annual Review of Genetics · doi:10.1146/annurev-genet-111212-133522 · Cited by 115

Switching from high-fidelity replicases to low-fidelity lesion-bypass polymerases

Plosky, B. S., & Woodgate, R. (2004) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2004.02.002 · Cited by 110

DNA polymerase θ contributes to the generation of C/G mutations during somatic hypermutation of Ig genes

Masuda, K., Ouchida, R., Takeuchi, A., Saito, T., Koseki, H., Kawamura, K., Tagawa, M., Tokuhisa, T., Azuma, T., & Wang, J. O. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505636102 · Cited by 110

Human DNA polymerase iota protects cells against oxidative stress

Lajus, T. B. P., Nakajima, S., Zlatanou, A., Despras, E., Couvé, S., Ishchenko, A. A., Sarasin, A. R., Yasui, A., & Kannouche, P. L. (2008) · The EMBO Journal · doi:10.1038/emboj.2008.210 · Cited by 115

Adaptive Mutation in Escherichia coliPreprint

Foster, P. L. (2000) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2000.65.21 · Cited by 108

Human DNA Polymerase κ Bypasses and Extends beyond Thymine Glycols during Translesion Synthesis in Vitro, Preferentially Incorporating Correct Nucleotides

Fischhaber, P. L., Gerlach, V. L., Feaver, W. J., Hatahet, Z., Wallace, S. S., & Friedberg, E. C. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m206027200 · Cited by 106

Recombinase, chromosomal translocations and lymphoid neoplasia: Targeting mistakes and repair failures

Marculescu, R., Vanura, K., Montpellier, B., Roulland, S., Le, T., Navarro, J., Jaeger, U., McBlane, F., & Nadel, B. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.05.015 · Cited by 105

A small indel mutation in an anthocyanin transporter causes variegated colouration of peach flowers

Cheng, J., Liao, L., Zhou, H., Gu, C., Wang, L., & Han, Y. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv419 · Cited by 104

DNA Polymerase V and RecA Protein, a Minimal Mutasome

Schlacher, K., Leslie, K. D., Wyman, C., Woodgate, R., Cox, M. M., & Goodman, M. F. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.01.006 · Cited by 102

New structural and mechanistic insight into the A-rule and the instructional and non-instructional behavior of DNA photoproducts and other lesions

Taylor, J. (2002) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(02)00252-x · Cited by 102

Computer simulations of protein functions: Searching for the molecular origin of the replication fidelity of DNA polymerases

Florián, J., Goodman, M. F., & Warshel, A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0408173102 · Cited by 102

DNA polymerase POLQ and cellular defense against DNA damage

Yousefzadeh, M. J., & Wood, R. D. (2012) · DNA repair · doi:10.1016/j.dnarep.2012.10.004 · Cited by 109

Properties and Functions of Escherichia Coli: Pol IV and Pol V

Fuchs, R. P., Fujii, S., & Wagner, J. (2004) · Advances in Protein Chemistry · doi:10.1016/s0065-3233(04)69008-5 · Cited by 100

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

Spontaneous mutation rate is a plastic trait associated with population density across domains of life

Krašovec, R., Richards, H., Gifford, D. R., Hatcher, C., Faulkner, K. J., Belavkin, R. V., Channon, A., Aston, E., McBain, A. J., & Cg, K. (2017) · PLoS Biology · doi:10.1371/journal.pbio.2002731 · Cited by 100

The gp38 Adhesins of the T4 Superfamily: A Complex Modular Determinant of the Phage’s Host Specificity

Trojet, S. N., Caumont‐Sarcos, A., Perrody, E., Comeau, A., & Krisch, H. M. (2011) · Genome Biology and Evolution · doi:10.1093/gbe/evr059 · Cited by 97

A Dynamic Polymerase Exchange with Escherichia coli DNA Polymerase IV Replacing DNA Polymerase III on the Sliding Clamp*

Furukohri, A., Goodman, M. F., & Maki, H. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m709689200 · Cited by 96

RecA acts in trans to allow replication of damaged DNA by DNA polymerase V

Schlacher, K., Cox, M. M., Woodgate, R., & Goodman, M. F. (2006) · Nature · doi:10.1038/nature05042 · Cited by 96

Modifying the β,γ Leaving-Group Bridging Oxygen Alters Nucleotide Incorporation Efficiency, Fidelity, and the Catalytic Mechanism of DNA Polymerase β

Sucato, C. A., Upton, T. G., Kashemirov, B. A., Batra, V. K., Martínek, V., Xiang, Y., Beard, W. A., Pedersen, L. C., Wilson, S. H., McKenna, C. E., et al. (2006) · Biochemistry · doi:10.1021/bi061517b · Cited by 96

Addendum

Kannouche, P. L., de Henestrosa, A. R. F., Coull, B. J., Vidal, A. E., Gray, C., Zicha, D., Woodgate, R., & Lehmann, A. R. (2003) · The EMBO Journal · doi:10.1093/emboj/7595006 · Cited by 98

All living cells are cognitive

Shapiro, J. A. (2020) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.08.120 · Cited by 100

DNA polymerases and human diseases

Sweasy, J. B., Lauper, J. M., & Eckert, K. A. (2006) · Radiation Research · doi:10.1667/rr0706.1 · Cited by 93

The RAD6 Pathway: Control of DNA Damage Bypass and Mutagenesis by Ubiquitin and SUMO

Ulrich, H. D. (2005) · ChemBioChem · doi:10.1002/cbic.200500139 · Cited by 96

Replication through an abasic DNA lesion: structural basis for adenine selectivity

Obeid, S., Blatter, N., Kranaster, R., Schnur, A., Diederichs, K., Welte, W., & Marx, A. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.64 · Cited by 96

Inactivation of Human MAD2B in Nasopharyngeal Carcinoma Cells Leads to Chemosensitization to DNA-Damaging Agents

Cheung, H. W., Chun, A. C. S., Wang, Q., Deng, W., Hu, L., Guan, X., Nicholls, J. M., Ling, M., Wong, Y. C., Tsao, S. W., et al. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-3602 · Cited by 91

Recombination, repair and replication in the pathogenic Neisseriae: the 3 R′s of molecular genetics of two human‐specific bacterial pathogens

Kline, K. A., Sechman, E. V., Skaar, E. P., & Seifert, H. S. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03679.x · Cited by 90

Adduct Size Limits Efficient and Error-free Bypass Across Bulky N2-Guanine DNA Lesions by Human DNA Polymerase η

Choi, J., & Guengerich, F. P. (2005) · Journal of Molecular Biology · doi:10.1016/j.jmb.2005.06.079 · Cited by 89

Snapshots of a Y-Family DNA Polymerase in Replication: Substrate-induced Conformational Transitions and Implications for Fidelity of Dpo4

Wong, J. H. Y., Fiala, K. A., Suo, Z., & Ling, H. (2008) · Journal of Molecular Biology · doi:10.1016/j.jmb.2008.03.038 · Cited by 89

DNA polymerase θ (POLQ) can extend from mismatches and from bases opposite a (6-4) photoproduct

Seki, M., & Wood, R. D. (2007) · DNA repair · doi:10.1016/j.dnarep.2007.08.005 · Cited by 89

Structure–function studies of DNA polymerase lambda

García–Díaz, M., Bębenek, K., Gao, G., Pedersen, L. C., London, R. E., & Kunkel, T. A. (2005) · DNA repair · doi:10.1016/j.dnarep.2005.09.001 · Cited by 89

The DinI Protein Stabilizes RecA Protein Filaments

Lusetti, S. L., Voloshin, O. N., Inman, R. B., Camerini‐Otero, R. D., & Cox, M. M. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m403064200 · Cited by 89

Error-prone polymerase activity causes multinucleotide mutations in humansPreprint

Harris, K., & Nielsen, R. (2014) · Genome Research · doi:10.1101/gr.170696.113 · Cited by 91

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

Central Role of the Holliday Junction Helicase RuvAB in vlsE Recombination and Infectivity of Borrelia burgdorferi

Lin, T., Gao, L., Edmondson, D. G., Jacobs, M. B., Philipp, M. T., & Norris, S. J. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000679 · Cited by 84

Stationary phase mutagenesis: mechanisms that accelerate adaptation of microbial populations under environmental stress

Kivisaar, M. (2003) · Environmental Microbiology · doi:10.1046/j.1462-2920.2003.00488.x · Cited by 87

An error-prone family Y DNA polymerase (DinB homolog from Sulfolobus solfataricus) uses a 'steric gate' residue for discrimination against ribonucleotides

DeLucia, A. M. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg417 · Cited by 83

An underlying mechanism for the increased mutagenesis of lagging-strand genes in Bacillus subtilis

Million‐Weaver, S., Samadpour, A. N., Moreno-Habel, D. A., Nugent, P., Brittnacher, M., Weiss, E. J., Hayden, H. S., Miller, S. I., Liachko, I., & Merrikh, H. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1416651112 · Cited by 82

Y‐family DNA polymerases respond to DNA damage‐independent inhibition of replication fork progression

Godoy, V. G., Jarosz, D. F., Walker, F. L., Simmons, L. A., & Walker, G. C. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7600986 · Cited by 82

Whither the replisome: Emerging perspectives on the dynamic nature of the DNA replication machinery

Langston, L. D., Indiani, C., & O’Donnell, M. E. (2009) · Cell Cycle · doi:10.4161/cc.8.17.9390 · Cited by 81

A structural gap in Dpo4 supports mutagenic bypass of a major benzo[ a ]pyrene dG adduct in DNA through template misalignment

Bauer, J., Xing, G., Yagi, H., Sayer, J. M., Jerina, D. M., & Ling, H. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700717104 · Cited by 81

The choice of nucleotide inserted opposite abasic sites formed within chromosomal DNA reveals the polymerase activities participating in translesion DNA synthesis

Chan, K., Resnick, M. A., & Gordenin, D. A. (2013) · DNA repair · doi:10.1016/j.dnarep.2013.07.008 · Cited by 83

Role of Pseudomonas aeruginosa dinB -Encoded DNA Polymerase IV in Mutagenesis

Sanders, L. H., Rockel, A. B., Lu, H., Wozniak, D. J., & Sutton, M. D. (2006) · Journal of Bacteriology · doi:10.1128/jb.01481-06 · Cited by 79

Human DNA Polymerase λ Diverged in Evolution from DNA Polymerase β toward Specific Mn++ Dependence: a Kinetic and Thermodynamic Study

Blanca, G., Shevelev, I., Ramadan, K., Villani, G., Spadari, S., Hübscher, U., & Maga, G. (2003) · Biochemistry · doi:10.1021/bi034198m · Cited by 78

NMR Structure and Dynamics of the C-Terminal Domain from Human Rev1 and Its Complex with Rev1 Interacting Region of DNA Polymerase η

Pozhidaeva, A., Pustovalova, Y., D’Souza, S., Bezsonova, I., Walker, G. C., & Korzhnev, D. M. (2012) · Biochemistry · doi:10.1021/bi300566z · Cited by 80

Natural Selection and the Emergence of a Mutation Phenotype: An Update of the Evolutionary Synthesis Considering Mechanisms that Affect Genome Variation

Caporale, L. H. (2003) · Annual Review of Microbiology · doi:10.1146/annurev.micro.57.030502.090855 · Cited by 77

Replication Bypass of the Acrolein-Mediated Deoxyguanine DNA-Peptide Cross-Links by DNA Polymerases of the DinB Family

Minko, I. G., Yamanaka, K., Kozekov, I. D., Kozekova, A., Indiani, C., O’Donnell, M. E., Jiang, Q., Goodman, M. F., Rizzo, C. J., & Lloyd, R. S. (2008) · Chemical Research in Toxicology · doi:10.1021/tx800174a · Cited by 76

High-fidelity in vivo replication of DNA base shape mimics without Watson–Crick hydrogen bonds

Delaney, J. C., Henderson, P. T., Helquist, S. A., Morales, J. C., Essigmann, J. M., & Kool, E. T. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0837277100 · Cited by 76

The DNA Damage Response

Lovett, S. T. (2014) · ASM Press eBooks · doi:10.1128/9781555816841.ch13 · Cited by 75

The Biochemical Requirements of DNA Polymerase V-mediated Translesion Synthesis Revisited

藤井, 慎., Gasser, V., & Fuchs, R. P. (2004) · Journal of Molecular Biology · doi:10.1016/j.jmb.2004.06.017 · Cited by 75

Cooperation and interplay between base and nucleotide excision repair pathways: From DNA lesions to proteins

Kumar, N., Moreno, N. C., Feltes, B. C., Menck, C. F. M., & Houten, B. V. (2020) · Genetics and Molecular Biology · doi:10.1590/1678-4685-gmb-2019-0104 · Cited by 79

Kinetic Evidence for Inefficient and Error-prone Bypass across Bulky N-Guanine DNA Adducts by Human DNA Polymerase ι

Choi, J., & Guengerich, F. P. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m600112200 · Cited by 74

Varying DNA Base-Pair Size in Subangstrom Increments: Evidence for a Loose, Not Large, Active Site in Low-Fidelity Dpo4 Polymerase

Mizukami, S., Kim, T. W., Helquist, S. A., & Kool, E. T. (2006) · Biochemistry · doi:10.1021/bi051961z · Cited by 74

Development of tRNA synthetases and connection to genetic code and disease

SCHIMMEL, P. R. (2008) · Protein Science · doi:10.1110/ps.037242.108 · Cited by 73

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

Structural insight into recruitment of translesion DNA polymerase Dpo4 to sliding clamp PCNA

Xing, G., Kirouac, K. N., Shin, Y. J., Bell, S. D., & Ling, H. (2008) · Molecular Microbiology · doi:10.1111/j.1365-2958.2008.06553.x · Cited by 73

DNA polymerase IV primarily operates outside of DNA replication forks in Escherichia coli

Henrikus, S. S., Wood, E. A., McDonald, J. P., Cox, M. M., Woodgate, R., Goodman, M. F., van Oijen, A. M., & Robinson, A. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007161 · Cited by 76

Translesion replication of benzo[a]pyrene and benzo[c]phenanthrene diol epoxide adducts of deoxyadenosine and deoxyguanosine by human DNA polymerase iota

Frank, E. G. (2002) · Nucleic Acids Research · doi:10.1093/nar/gkf643 · Cited by 72

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

Adaptive Mutation inEscherichia coli

Foster, P. L. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.15.4846-4852.2004 · Cited by 72

Controlling Mutation: Intervening in Evolution as a Therapeutic Strategy

Cirz, R. T., & Romesberg, F. E. (2007) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409230701597741 · Cited by 71

Survival versus maintenance of genetic stability: a conflict of priorities during stress

Matić, I., Taddéi, F., & Radman, M. (2004) · Research in Microbiology · doi:10.1016/j.resmic.2004.01.010 · Cited by 71

Mechanism and Stoichiometry of Interaction of DnaG Primase with DnaB Helicase of Escherichia coli in RNA Primer Synthesis

Mitkova, A. V., Khopde, S. M., & Biswas, S. B. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m308956200 · Cited by 71

Roles of DNA Polymerase V and RecA Protein in SOS Damage-Induced Mutation

Schlacher, K., Pham, P., Cox, M. M., & Goodman, M. F. (2006) · Chemical Reviews · doi:10.1021/cr0404951 · Cited by 71

Mechanistic Comparison of High-Fidelity and Error-Prone DNA Polymerases and Ligases Involved in DNA Repair

Showalter, A. K., Lamarche, B. J., Bakhtina, M., Su, M., Tang, K., & Tsai, M. (2006) · Chemical Reviews · doi:10.1021/cr040487k · Cited by 71

Role of Escherichia coli DNA Polymerase IV in In Vivo Replication Fidelity

Kuban, W., Jonczyk, P., Gaweł, D., Malanowska, K., Schaaper, R. M., & Fijałkowska, I. J. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.14.4802-4807.2004 · Cited by 71

Translesion DNA Polymerases and Cancer

Makridakis, N. M., & Reichardt, J. K. V. (2012) · Frontiers in Genetics · doi:10.3389/fgene.2012.00174 · Cited by 70

Kinetic Analysis of Translesion Synthesis Opposite Bulky N2- and O6-Alkylguanine DNA Adducts by Human DNA Polymerase REV1

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Overproduction of Escherichia coli DNA polymerase DinB (Pol IV) inhibits replication fork progression and is lethal

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