| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S1097-2765(01)00204-0 |
| P698 | PubMed publication ID | 11463382 |
| P2093 | author name string | Lee PL | |
| Hastings PJ | |||
| Rosenberg SM | |||
| Lombardo MJ | |||
| McKenzie GJ | |||
| P2860 | cites work | High mutation frequencies among Escherichia coli and Salmonella pathogens | Q48057867 |
| Adaptive amplification: an inducible chromosomal instability mechanism | Q50117945 | ||
| Evolutionary implications of the frequent horizontal transfer of mismatch repair genes | Q50117948 | ||
| A direct role for DNA polymerase III in adaptive reversion of a frameshift mutation in Escherichia coli. | Q54567733 | ||
| Adaptive mutation by deletions in small mononucleotide repeats. | Q54630365 | ||
| Recombination in adaptive mutation. | Q54635736 | ||
| Highly Variable Mutation Rates in Commensal and Pathogenic Escherichia coli | Q56944671 | ||
| Repeat-associated phase variable genes in the complete genome sequence of Neisseria meningitidis strain MC58 | Q57976193 | ||
| Autodigestion and RecA-dependent cleavage of Ind- mutant LexA proteins | Q69566227 | ||
| The dinB gene encodes a novel E. coli DNA polymerase, DNA pol IV, involved in mutagenesis | Q72994394 | ||
| Toxin-antitoxin systems homologous with relBE of Escherichia coli plasmid P307 are ubiquitous in prokaryotes | Q77901497 | ||
| Complete Genome Sequence of Neisseria meningitidis Serogroup B Strain MC58 | Q22065549 | ||
| Complete DNA sequence of a serogroup A strain of Neisseria meningitidis Z2491 | Q22122399 | ||
| All three SOS-inducible DNA polymerases (Pol II, Pol IV and Pol V) are involved in induced mutagenesis | Q24597093 | ||
| Multiple pathways for SOS-induced mutagenesis in Escherichia coli: an overexpression of dinB/dinP results in strongly enhancing mutagenesis in the absence of any exogenous treatment to damage DNA | Q24628966 | ||
| Methods for generating precise deletions and insertions in the genome of wild-type Escherichia coli: application to open reading frame characterization | Q24676777 | ||
| Mismatch repair in replication fidelity, genetic recombination, and cancer biology | Q29616483 | ||
| The distribution of the numbers of mutants in bacterial populations | Q29620123 | ||
| The beta clamp targets DNA polymerase IV to DNA and strongly increases its processivity | Q30641251 | ||
| Adaptive mutation sequences reproduced by mismatch repair deficiency | Q33640315 | ||
| Role of the dinB gene product in spontaneous mutation in Escherichia coli with an impaired replicative polymerase | Q33792439 | ||
| Determining mutation rates in bacterial populations | Q33803752 | ||
| Mechanisms of stationary phase mutation: a decade of adaptive mutation | Q33847662 | ||
| Genome-wide hypermutation in a subpopulation of stationary-phase cells underlies recombination-dependent adaptive mutation | Q33886793 | ||
| The SOS response regulates adaptive mutation | Q33903483 | ||
| Escherichia coli DNA polymerase IV mutator activity: genetic requirements and mutational specificity | Q33994529 | ||
| Proofreading-defective DNA polymerase II increases adaptive mutation in Escherichia coli. | Q34019746 | ||
| Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday | Q34229913 | ||
| High frequency of hypermutable Pseudomonas aeruginosa in cystic fibrosis lung infection. | Q34508854 | ||
| Mismatch repair protein MutL becomes limiting during stationary-phase mutation | Q35190848 | ||
| Role of RecA protein in untargeted UV mutagenesis of bacteriophage lambda: evidence for the requirement for the dinB gene | Q35608675 | ||
| Nonadaptive mutations occur on the F' episome during adaptive mutation conditions in Escherichia coli | Q35620439 | ||
| The many faces of DNA polymerases: strategies for mutagenesis and for mutational avoidance | Q36099918 | ||
| The role of transient hypermutators in adaptive mutation in Escherichia coli | Q36384221 | ||
| DNA-damaging agents stimulate gene expression at specific loci in Escherichia coli | Q36389606 | ||
| Dominant mutations (lex) in Escherichia coli K-12 which affect radiation sensitivity and frequency of ultraviolet lght-induced mutations | Q36834871 | ||
| Frameshift mutation: determinants of specificity | Q37794682 | ||
| SOS functions, cancer and inducible evolution | Q40313397 | ||
| Chapter 1 Measuring Spontaneous Mutation Rates in Yeast | Q40936432 | ||
| Adaptive reversion of a frameshift mutation in Escherichia coli by simple base deletions in homopolymeric runs | Q41572901 | ||
| Mutation for survival | Q41703503 | ||
| Roles of E. coli DNA polymerases IV and V in lesion-targeted and untargeted SOS mutagenesis | Q41734679 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 571-579 | |
| P577 | publication date | 2001-03-01 | |
| P1433 | published in | Molecular Cell | Q3319468 |
| P1476 | title | SOS mutator DNA polymerase IV functions in adaptive mutation and not adaptive amplification | |
| P478 | volume | 7 |
| Q30669971 | A DNA repair system specific for thermophilic Archaea and bacteria predicted by genomic context analysis |
| Q36966953 | A novel mutator of Escherichia coli carrying a defect in the dgt gene, encoding a dGTP triphosphohydrolase. |
| Q46890960 | A single amino acid governs enhanced activity of DinB DNA polymerases on damaged templates. |
| Q27677020 | A strategically located serine residue is critical for the mutator activity of DNA polymerase IV from Escherichia coli |
| Q24796250 | Adaptive amplification and point mutation are independent mechanisms: evidence for various stress-inducible mutation mechanisms |
| Q89115553 | Adaptive laboratory evolution resolves energy depletion to maintain high aromatic metabolite phenotypes in Escherichia coli strains lacking the Phosphotransferase System |
| Q59757712 | Adaptive mutation in Escherichia coli |
| Q36689838 | Adaptive mutation: General mutagenesis is not a programmed response to stress but results from rare coamplification of dinB with lac |
| Q35893213 | Adaptive mutation: how growth under selection stimulates Lac(+) reversion by increasing target copy number |
| Q41073516 | Adaptive point mutation and adaptive amplification pathways in the Escherichia coli Lac system: stress responses producing genetic change |
| Q34436201 | Adaptive, or stationary-phase, mutagenesis, a component of bacterial differentiation in Bacillus subtilis |
| Q21092806 | After 30 years of study, the bacterial SOS response still surprises us |
| Q34599104 | Amplification of lac cannot account for adaptive mutation to Lac+ in Escherichia coli. |
| Q34012598 | Amplification-mutagenesis: evidence that "directed" adaptive mutation and general hypermutability result from growth with a selected gene amplification |
| Q24647468 | An SOS-regulated type 2 toxin-antitoxin system |
| Q35189852 | An underlying mechanism for the increased mutagenesis of lagging-strand genes in Bacillus subtilis |
| Q54516027 | Analysis of translesion replication across an abasic site by DNA polymerase IV of Escherichia coli |
| Q47652171 | Antibiotic resistance mutations induced in growing cells of Bacillus-related thermophiles. |
| Q53939141 | Bacterial multicellularity as a possible source of antibiotic resistance. |
| Q35097340 | Between genotype and phenotype: protein chaperones and evolvability |
| Q36905565 | Causes and consequences of DNA repair activity modulation during stationary phase in Escherichia coli |
| Q35013064 | Cell-selfish modes of evolution and mutations directed after transcriptional bypass |
| Q34248796 | Characterization of three mycobacterial DinB (DNA polymerase IV) paralogs highlights DinB2 as naturally adept at ribonucleotide incorporation |
| Q33594339 | Competition of Escherichia coli DNA polymerases I, II and III with DNA Pol IV in stressed cells |
| Q36878608 | Competitive fitness during feast and famine: how SOS DNA polymerases influence physiology and evolution in Escherichia coli |
| Q36961674 | Controlling mutation: intervening in evolution as a therapeutic strategy |
| Q33804889 | Coral-mucus-associated Vibrio integrons in the Great Barrier Reef: genomic hotspots for environmental adaptation |
| Q27634747 | Crystal structure of a DinB lesion bypass DNA polymerase catalytic fragment reveals a classic polymerase catalytic domain |
| Q27635332 | Crystal structure of a Y-family DNA polymerase in action: a mechanism for error-prone and lesion-bypass replication |
| Q37358566 | DNA damage tolerance and a web of connections with DNA repair at Yale |
| Q48207182 | DNA polymerase IV primarily operates outside of DNA replication forks in Escherichia coli |
| Q54446139 | DNA polymerase V allows bypass of toxic guanine oxidation products in vivo. |
| Q37188497 | DNA polymerase switching: effects on spontaneous mutagenesis in Escherichia coli |
| Q37396897 | DNA polymerases are error-prone at RecA-mediated recombination intermediates. |
| Q35978843 | DNA polymerases eta and iota |
| Q36194928 | DNA repair and genome maintenance in Bacillus subtilis |
| Q35555900 | DNA shuffling: induced molecular breeding to produce new generation long-lasting vaccines. |
| Q43264411 | Degradation of nitroaromatic compounds: a model to study evolution of metabolic pathways |
| Q36268415 | Determinants of spontaneous mutation in the bacterium Escherichia coli as revealed by whole-genome sequencing |
| Q35806050 | Development of a stress-induced mutagenesis module for autonomous adaptive evolution of Escherichia coli to improve its stress tolerance |
| Q39680847 | Different spectra of stationary-phase mutations in early-arising versus late-arising mutants of Pseudomonas putida: involvement of the DNA repair enzyme MutY and the stationary-phase sigma factor RpoS. |
| Q37173424 | DinB upregulation is the sole role of the SOS response in stress-induced mutagenesis in Escherichia coli |
| Q36178618 | Diversify or die: generation of diversity in response to stress. |
| Q35746786 | Double-Strand Break Repair and Holliday Junction Processing Are Required for Chromosome Processing in Stationary-Phase Escherichia coli Cells |
| Q47609306 | Effect of deletion of SOS-induced polymerases, pol II, IV, and V, on spontaneous mutagenesis in Escherichia coli mutD5. |
| Q43816434 | Efficiency and accuracy of SOS-induced DNA polymerases replicating benzo[a]pyrene-7,8-diol 9,10-epoxide A and G adducts |
| Q41915989 | Elevated mutation frequency in surviving populations of carbon-starved rpoS-deficient Pseudomonas putida is caused by reduced expression of superoxide dismutase and catalase |
| Q35058954 | Environmental regulation of mutation rates at specific sites. |
| Q33700107 | Error-prone DNA polymerase IV is regulated by the heat shock chaperone GroE in Escherichia coli |
| Q39753960 | Error-prone polymerase, DNA polymerase IV, is responsible for transient hypermutation during adaptive mutation in Escherichia coli. |
| Q34049897 | Error‐prone DNA polymerase IV is controlled by the stress‐response sigma factor, RpoS, in Escherichia coli |
| Q43104148 | Escherichia coli DNA polymerase IV contributes to spontaneous mutagenesis at coding sequences but not microsatellite alleles |
| Q34907780 | Escherichia coli Rep DNA helicase and error-prone DNA polymerase IV interact physically and functionally |
| Q24542676 | Evidence that selected amplification of a bacterial lac frameshift allele stimulates Lac(+) reversion (adaptive mutation) with or without general hypermutability |
| Q34297067 | Evolving responsively: adaptive mutation |
| Q51246704 | Expression of the F plasmid ccd toxin-antitoxin system in Escherichia coli cells under nutritional stress. |
| Q44049947 | Fidelity of Escherichia coli DNA polymerase IV. Preferential generation of small deletion mutations by dNTP-stabilized misalignment |
| Q39714248 | Formation of an F' plasmid by recombination between imperfectly repeated chromosomal Rep sequences: a closer look at an old friend (F'(128) pro lac). |
| Q34778532 | Fragile DNA motifs trigger mutagenesis at distant chromosomal loci in saccharomyces cerevisiae |
| Q34643555 | General stress response regulator RpoS in adaptive mutation and amplification in Escherichia coli |
| Q22122504 | Genome sequence of Bacillus cereus and comparative analysis with Bacillus anthracis |
| Q37513651 | Genomic changes arising in long-term stab cultures of Escherichia coli |
| Q42325513 | Gross chromosomal rearrangement mediated by DNA replication in stressed cells: evidence from Escherichia coli |
| Q42969505 | Identity and function of a large gene network underlying mutagenic repair of DNA breaks |
| Q35037445 | In pursuit of a molecular mechanism for adaptive gene amplification |
| Q35913829 | Interactions and Localization of Escherichia coli Error-Prone DNA Polymerase IV after DNA Damage |
| Q47448190 | Investigating the role of the little finger domain of Y-family DNA polymerases in low fidelity synthesis and translesion replication. |
| Q42126464 | Involvement of Escherichia coli DNA polymerase IV in tolerance of cytotoxic alkylating DNA lesions in vivo. |
| Q34697729 | Involvement of Y-family DNA polymerases in mutagenesis caused by oxidized nucleotides in Escherichia coli |
| Q40763644 | Involvement of error-prone DNA polymerase IV in stationary-phase mutagenesis in Pseudomonas putida |
| Q43937118 | Low fidelity DNA synthesis by a y family DNA polymerase due to misalignment in the active site. |
| Q38330433 | Lupus autoantibodies to native DNA preferentially bind DNA presented on PolIV. |
| Q35864947 | MsDpo4-a DinB Homolog from Mycobacterium smegmatis-Is an Error-Prone DNA Polymerase That Can Promote G:T and T:G Mismatches |
| Q37512348 | Multiple strategies for translesion synthesis in bacteria |
| Q33373675 | Mutability and importance of a hypermutable cell subpopulation that produces stress-induced mutants in Escherichia coli |
| Q92256237 | Mutation and Recombination Rates Vary Across Bacterial Chromosome |
| Q35869358 | Mutation as a stress response and the regulation of evolvability |
| Q53158429 | Mutational signatures indicative of environmental stress in bacteria. |
| Q34077193 | Mutator phenotype resulting from DNA polymerase IV overproduction in Escherichia coli: preferential mutagenesis on the lagging strand |
| Q34489588 | Mycobacterium smegmatis DinB2 misincorporates deoxyribonucleotides and ribonucleotides during templated synthesis and lesion bypass |
| Q34940893 | Novel autoproteolytic and DNA-damage sensing components in the bacterial SOS response and oxidized methylcytosine-induced eukaryotic DNA demethylation systems |
| Q33239373 | On the mechanism of gene amplification induced under stress in Escherichia coli |
| Q37323159 | Oncogene homologue Sch9 promotes age-dependent mutations by a superoxide and Rev1/Polzeta-dependent mechanism |
| Q46325763 | Origins of cancer symposium 2016: exploring tumor complexity |
| Q42412527 | Oxidative DNA damage defense systems in avoidance of stationary-phase mutagenesis in Pseudomonas putida |
| Q47558874 | Oxygen and RNA in stress-induced mutation. |
| Q38670044 | Persistent damaged bases in DNA allow mutagenic break repair in Escherichia coli |
| Q42045562 | Phenotype switching is a natural consequence of Staphylococcus aureus replication |
| Q39741226 | Phenotypes of lexA mutations in Salmonella enterica: evidence for a lethal lexA null phenotype due to the Fels-2 prophage |
| Q34471714 | Plasmid copy number underlies adaptive mutability in bacteria |
| Q33694470 | Polymerase exchange on single DNA molecules reveals processivity clamp control of translesion synthesis |
| Q37424859 | Polymerases leave fingerprints: analysis of the mutational spectrum in Escherichia coli rpoB to assess the role of polymerase IV in spontaneous mutation |
| Q42125442 | Polyphosphate kinase regulates error-prone replication by DNA polymerase IV in Escherichia coli |
| Q36936978 | Preferential D-loop extension by a translesion DNA polymerase underlies error-prone recombination |
| Q41090654 | Processing closely spaced lesions during Nucleotide Excision Repair triggers mutagenesis in E. coli. |
| Q35978849 | Properties and functions of Escherichia coli: Pol IV and Pol V. |
| Q37025967 | R-loops and nicks initiate DNA breakage and genome instability in non-growing Escherichia coli |
| Q51136979 | Rapid evolution of acetic acid-detoxifying Escherichia coli under phosphate starvation conditions requires activation of the cryptic PhnE permease and induction of translesion synthesis DNA polymerases. |
| Q41763723 | Rebuttal: adaptive mutation in Escherichia coli (Foster) |
| Q42793523 | Rebuttal: growth under selection stimulates Lac(+) reversion (Roth and Andersson). |
| Q38262646 | Regenerant Arabidopsis lineages display a distinct genome-wide spectrum of mutations conferring variant phenotypes |
| Q36761497 | Regulation of bacterial RecA protein function |
| Q43944895 | Replication restart in UV-irradiated Escherichia coli involving pols II, III, V, PriA, RecA and RecFOR proteins |
| Q77322177 | Resolving a fidelity paradox: why Escherichia coli DNA polymerase II makes more base substitution errors in AT- compared with GC-rich DNA |
| Q35130259 | Role of DNA polymerase IV in Escherichia coli SOS mutator activity |
| Q35271644 | Role of Escherichia coli DNA polymerase IV in in vivo replication fidelity |
| Q42324867 | Role of Ribonucleotide Reductase in Bacillus subtilis Stress-Associated Mutagenesis |
| Q33769195 | Role of the DinB homologs Rv1537 and Rv3056 in Mycobacterium tuberculosis |
| Q24631035 | Roles of DNA polymerases V and II in SOS-induced error-prone and error-free repair in Escherichia coli |
| Q34470485 | Roles of E. coli double-strand-break-repair proteins in stress-induced mutation |
| Q36365259 | Roles of Nucleoid-Associated Proteins in Stress-Induced Mutagenic Break Repair in Starving Escherichia coli |
| Q34810207 | Roles of YqjH and YqjW, homologs of the Escherichia coli UmuC/DinB or Y superfamily of DNA polymerases, in stationary-phase mutagenesis and UV-induced mutagenesis of Bacillus subtilis |
| Q42738196 | RpoS, the stress response sigma factor, plays a dual role in the regulation of Escherichia coli's error-prone DNA polymerase IV. |
| Q24530758 | SOS-induced DNA polymerases enhance long-term survival and evolutionary fitness |
| Q50186955 | Selection-Enhanced Mutagenesis of lac Genes Is Due to Their Co-amplification with dinB Encoding an Error-Prone DNA Polymerase |
| Q34119281 | Separate DNA Pol II- and Pol IV-dependent pathways of stress-induced mutation during double-strand-break repair in Escherichia coli are controlled by RpoS. |
| Q34514283 | Single-strand-specific exonucleases prevent frameshift mutagenesis by suppressing SOS induction and the action of DinB/DNA polymerase IV in growing cells |
| Q38346395 | Situational repair of replication forks: roles of RecG and RecA proteins |
| Q88488940 | Specialised DNA polymerases in Escherichia coli: roles within multiple pathways |
| Q33796363 | Spontaneous DNA breakage in single living Escherichia coli cells |
| Q36961669 | Stationary phase mutagenesis in B. subtilis: a paradigm to study genetic diversity programs in cells under stress |
| Q35544150 | Stationary phase mutagenesis: mechanisms that accelerate adaptation of microbial populations under environmental stress |
| Q37096423 | Stationary-phase mutation in the bacterial chromosome: recombination protein and DNA polymerase IV dependence |
| Q36914336 | Steric and electrostatic effects in DNA synthesis by the SOS-induced DNA polymerases II and IV of Escherichia coli |
| Q37274991 | Steric gate variants of UmuC confer UV hypersensitivity on Escherichia coli. |
| Q46463787 | Stochasticity and determinism in cancer creation and progression |
| Q35986593 | Stress responses and genetic variation in bacteria. |
| Q40459862 | Stress-Induced Mutagenesis. |
| Q64389723 | Stress-Induced Mutagenesis: Implications in Cancer and Drug Resistance |
| Q37355812 | Stress-induced beta-lactam antibiotic resistance mutation and sequences of stationary-phase mutations in the Escherichia coli chromosome. |
| Q34504117 | Stress-induced evolution and the biosafety of genetically modified microorganisms released into the environment |
| Q36961683 | Stress-induced mutagenesis in bacteria. |
| Q36496909 | Stress-induced mutation via DNA breaks in Escherichia coli: a molecular mechanism with implications for evolution and medicine |
| Q27642458 | Structural basis for recruitment of translesion DNA polymerase Pol IV/DinB to the -clamp |
| Q38296309 | Synthetic activity of Sso DNA polymerase Y1, an archaeal DinB-like DNA polymerase, is stimulated by processivity factors proliferating cell nuclear antigen and replication factor C. |
| Q64074428 | Systems Biology of Cold Adaptation in the Polyextremophilic Red Alga |
| Q35037449 | The "A" rule revisited: polymerases as determinants of mutational specificity |
| Q36588940 | The DNA polymerase III holoenzyme contains γ and is not a trimeric polymerase |
| Q41996473 | The Escherichia coli histone-like protein HU has a role in stationary phase adaptive mutation |
| Q38541782 | The Origin of Mutants Under Selection: How Natural Selection Mimics Mutagenesis (Adaptive Mutation) |
| Q27681904 | The PAD region in the mycobacterial DinB homologue MsPolIV exhibits positional heterogeneity |
| Q34491677 | The SMC-like protein complex SbcCD enhances DNA polymerase IV-dependent spontaneous mutation in Escherichia coli |
| Q39326888 | The Small RNA GcvB Promotes Mutagenic Break Repair by Opposing the Membrane Stress Response |
| Q43694249 | The TGV transgenic vectors for single-copy gene expression from the Escherichia coli chromosome |
| Q35098519 | The dinB operon and spontaneous mutation in Escherichia coli |
| Q43993329 | The effect of genomic position on reversion of a lac frameshift mutation (lacIZ33) during non-lethal selection (adaptive mutation). |
| Q42676720 | The mutational specificity of the Dbh lesion bypass polymerase and its implications |
| Q41862731 | The optimal burst of mutation to create a phenotype |
| Q24522537 | The processivity factor beta controls DNA polymerase IV traffic during spontaneous mutagenesis and translesion synthesis in vivo |
| Q34614165 | The roles of Klenow processing and flap processing activities of DNA polymerase I in chromosome instability in Escherichia coli K12 strains |
| Q34017416 | The sigma(E) stress response is required for stress-induced mutation and amplification in Escherichia coli |
| Q42916075 | The transcription elongation factor NusA is required for stress-induced mutagenesis in Escherichia coli |
| Q33621553 | Three new RelE-homologous mRNA interferases of Escherichia coli differentially induced by environmental stresses |
| Q46375749 | To slip or skip, visualizing frameshift mutation dynamics for error-prone DNA polymerases |
| Q41445233 | Transcriptional de-repression and Mfd are mutagenic in stressed Bacillus subtilis cells |
| Q34509062 | Translesion DNA Synthesis |
| Q34389241 | Translesion DNA synthesis and mutagenesis in prokaryotes. |
| Q34974987 | Tuberculosis chemotherapy: the influence of bacillary stress and damage response pathways on drug efficacy |
| Q54472760 | Two processivity clamp interactions differentially alter the dual activities of UmuC. |
| Q41887546 | UmuD and RecA directly modulate the mutagenic potential of the Y family DNA polymerase DinB. |
| Q64096919 | What is mutation? A chapter in the series: How microbes "jeopardize" the modern synthesis |
| Q37976150 | What limits the efficiency of double-strand break-dependent stress-induced mutation in Escherichia coli? |
| Q64517233 | Worming into genetic instability |
| Q36380747 | Zinc blocks SOS-induced antibiotic resistance via inhibition of RecA in Escherichia coli |
| Q36737307 | β-Lactam antibiotics promote bacterial mutagenesis via an RpoS-mediated reduction in replication fidelity |
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