Generation and Repair of Postreplication Gaps in Escherichia coli

When replication forks encounter template lesions, one result is lesion skipping, where the stalled DNA polymerase transiently stalls, disengages, and then reinitiates downstream to leave the lesion behind in a postreplication gap. Despite considerable attention in the 6 decades since postreplication gaps were discovered, the mechanisms by which postreplication gaps are generated and repaired remain highly enigmatic. SUMMARY When replication forks encounter template lesions, one result is lesion skipping, where the stalled DNA polymerase transiently stalls, disengages, and then reinitiates downstream to leave the lesion behind in a postreplication gap. Despite considerable attention in the 6 decades since postreplication gaps were discovered, the mechanisms by which postreplication gaps are generated and repaired remain highly enigmatic. This review focuses on postreplication gap generation and repair in the bacterium Escherichia coli. New information to address the frequency and mechanism of gap generation and new mechanisms for their resolution are described. There are a few instances where the formation of postreplication gaps appears to be programmed into particular genomic locations, where they are triggered by novel genomic elements.

[1]  M. Cox,et al.  RecF protein targeting to postreplication (daughter strand) gaps I: DNA binding by RecF and RecFR , 2023, Nucleic acids research.

[2]  Antoine M. van Oijen,et al.  RecF protein targeting to post-replication (daughter strand) gaps II: RecF interaction with replisomes , 2023, Nucleic acids research.

[3]  M. Cox,et al.  RecA and SSB genome-wide distribution in ssDNA gaps and ends in Escherichia coli , 2023, Nucleic acids research.

[4]  J. Keck,et al.  Interaction with single-stranded DNA-binding protein modulates Escherichia coli RadD DNA repair activities , 2022, bioRxiv.

[5]  S. Lovett,et al.  Characterization of the Escherichia coli XPD/Rad3 iron-sulfur helicase YoaA in complex with the DNA polymerase III clamp loader subunit chi (χ) , 2022, The Journal of biological chemistry.

[6]  Antoine M. van Oijen,et al.  Host cell RecA activates a mobile element-encoded mutagenic DNA polymerase , 2022, Nucleic acids research.

[7]  Vincent Pagès,et al.  Single strand gap repair: The presynaptic phase plays a pivotal role in modulating lesion tolerance pathways , 2022, PLoS genetics.

[8]  K. Satyshur,et al.  X-ray crystal structure of the Escherichia coli RadD DNA repair protein bound to ADP reveals a novel zinc ribbon domain , 2022, PloS one.

[9]  A. Kozlov,et al.  How Glutamate Promotes Liquid-liquid Phase Separation and DNA Binding Cooperativity of E. coli SSB Protein. , 2022, Journal of molecular biology.

[10]  Lyle A. Simmons,et al.  Bacterial DNA excision repair pathways , 2022, Nature Reviews Microbiology.

[11]  M. Cox,et al.  RadD is a RecA-dependent accessory protein that accelerates DNA strand exchange , 2022, Nucleic acids research.

[12]  M. Cox,et al.  Genomic landscape of single-stranded DNA gapped intermediates in Escherichia coli , 2021, Nucleic acids research.

[13]  Kanika Jain,et al.  The rarA gene as part of an expanded RecFOR recombination pathway: Negative epistasis and synthetic lethality with ruvB, recG, and recQ , 2021, PLoS genetics.

[14]  Lingling Wu,et al.  Genetic Analysis of DinG Family Helicase YoaA and Its Interaction with Replication Clamp Loader Protein HolC in Escherichia coli , 2021, Journal of bacteriology.

[15]  H. Ulrich,et al.  Daughter-strand gaps in DNA replication - substrates of lesion processing and initiators of distress signalling. , 2021, DNA repair.

[16]  Sander K. Govers,et al.  Interconnecting solvent quality, transcription, and chromosome folding in Escherichia coli , 2021, Cell.

[17]  R. Woodgate,et al.  The SOS Error-Prone DNA Polymerase V Mutasome and β-Sliding Clamp Acting in Concert on Undamaged DNA and during Translesion Synthesis , 2021, Cells.

[18]  Camille Henry,et al.  Elucidating Recombination Mediator Function Using Biophysical Tools , 2021, Biology.

[19]  A. Doherty,et al.  Repriming DNA synthesis: an intrinsic restart pathway that maintains efficient genome replication , 2021, Nucleic acids research.

[20]  D. Vertommen,et al.  Redox controls RecA protein activity via reversible oxidation of its methionine residues , 2021, eLife.

[21]  S. Lovett,et al.  Alternative complexes formed by the Escherichia coli clamp loader accessory protein HolC (x) with replication protein HolD (ψ) and repair protein YoaA. , 2021, DNA repair.

[22]  Kanika Jain,et al.  RecA‐independent recombination: Dependence on the Escherichia coli RarA protein , 2020, Molecular microbiology.

[23]  M. Cox,et al.  Resolving Toxic DNA repair intermediates in every E. coli replication cycle: critical roles for RecG, Uup and RadD , 2020, Nucleic acids research.

[24]  R. Fuchs,et al.  A Comprehensive View of Translesion Synthesis in Escherichia coli , 2020, Microbiology and Molecular Biology Reviews.

[25]  K. Marians,et al.  Two components of DNA replication-dependent LexA cleavage , 2020, The Journal of Biological Chemistry.

[26]  S. Jergic,et al.  Development of a single-stranded DNA-binding protein fluorescent fusion toolbox , 2020, Nucleic acids research.

[27]  Nam Ki Lee,et al.  Single-molecule observation of ATP-independent SSB displacement by RecO in Deinococcus radiodurans , 2020, eLife.

[28]  S. Verma,et al.  Architecture of the Escherichia coli nucleoid , 2019, PLoS genetics.

[29]  David C. Grainger,et al.  Chromosome organization in bacteria: mechanistic insights into genome structure and function , 2019, Nature Reviews Genetics.

[30]  Antoine M. van Oijen,et al.  Frequent template switching in postreplication gaps: suppression of deleterious consequences by the Escherichia coli Uup and RadD proteins , 2019, Nucleic Acids Research.

[31]  J. Nguyen,et al.  Super‐resolution imaging reveals changes in Escherichia coli SSB localization in response to DNA damage , 2019, Genes to cells : devoted to molecular & cellular mechanisms.

[32]  K. Tárnok,et al.  Phase separation by ssDNA binding protein controlled via protein−protein and protein−DNA interactions , 2019, Proceedings of the National Academy of Sciences.

[33]  Cynthia J. Sakofsky,et al.  Repair of multiple simultaneous double-strand breaks causes bursts of genome-wide clustered hypermutation , 2019, PLoS biology.

[34]  A. Kozlov,et al.  Are the intrinsically disordered linkers involved in SSB binding to accessory proteins? , 2019, Nucleic acids research.

[35]  C. Dorman DNA supercoiling and transcription in bacteria: a two-way street , 2019, BMC Molecular and Cell Biology.

[36]  Wei Yang,et al.  Replisome structure suggests mechanism for continuous fork progression and post-replication repair. , 2019, DNA repair.

[37]  J. Loparo,et al.  A gatekeeping function of the replicative polymerase controls pathway choice in the resolution of lesion-stalled replisomes , 2019, Proceedings of the National Academy of Sciences.

[38]  J. Nguyen,et al.  Super-resolution imaging reveals changes in Escherichia coli SSB localization in response to DNA damage , 2019, bioRxiv.

[39]  R. Reyes-Lamothe,et al.  Replisome activity slowdown after exposure to ultraviolet light in Escherichia coli , 2019, Proceedings of the National Academy of Sciences.

[40]  R. Austin,et al.  Gamblers: An Antibiotic-Induced Evolvable Cell Subpopulation Differentiated by Reactive-Oxygen-Induced General Stress Response. , 2019, Molecular cell.

[41]  J. Xu,et al.  A Double-Strand Break Does Not Promote Neisseria gonorrhoeae Pilin Antigenic Variation , 2019, Journal of bacteriology.

[42]  Stephan Uphoff,et al.  DNA ADP-Ribosylation Stalls Replication and Is Reversed by RecF-Mediated Homologous Recombination and Nucleotide Excision Repair , 2019, Cell reports.

[43]  A. V. van Oijen,et al.  RecFOR epistasis group: RecF and RecO have distinct localizations and functions in Escherichia coli , 2019, Nucleic acids research.

[44]  A. Kuzminov,et al.  Near-continuously synthesized leading strands in Escherichia coli are broken by ribonucleotide excision , 2019, Proceedings of the National Academy of Sciences.

[45]  I. Grainge,et al.  Replication fork collapse at a protein‐DNA roadblock leads to fork reversal, promoted by the RecQ helicase , 2018, Molecular microbiology.

[46]  Andrew Robinson,et al.  Recycling of single-stranded DNA-binding protein by the bacterial replisome , 2018, bioRxiv.

[47]  R. Fuchs,et al.  Chronological Switch from Translesion Synthesis to Homology-Dependent Gap Repair In Vivo , 2018, Toxicological research.

[48]  R. Stein,et al.  Movement of the RecG Motor Domain upon DNA Binding Is Required for Efficient Fork Reversal , 2018, International journal of molecular sciences.

[49]  Antoine M. van Oijen,et al.  Spatial and temporal organization of RecA in the Escherichia coli DNA-damage response , 2018, bioRxiv.

[50]  J. Xu,et al.  Analysis of Pilin Antigenic Variation in Neisseria meningitidis by Next-Generation Sequencing , 2018, Journal of bacteriology.

[51]  R. G. Lloyd,et al.  Chromosomal over-replication in Escherichia coli recG cells is triggered by replication fork fusion and amplified if replichore symmetry is disturbed , 2018, Nucleic acids research.

[52]  Jun Xia,et al.  Bacteria-to-Human Protein Networks Reveal Origins of Endogenous DNA Damage , 2018, Cell.

[53]  K. Marians Lesion Bypass and the Reactivation of Stalled Replication Forks. , 2018, Annual review of biochemistry.

[54]  B. Michel,et al.  Replication Fork Breakage and Restart in Escherichia coli , 2018, Microbiology and Molecular Biology Reviews.

[55]  A. Oijen,et al.  Specialised DNA polymerases in Escherichia coli: roles within multiple pathways , 2018, Current Genetics.

[56]  C. Jacobs-Wagner,et al.  Subcellular Organization: A Critical Feature of Bacterial Cell Replication , 2018, Cell.

[57]  Xiao-Xue Yan,et al.  ATP-dependent conformational change in ABC-ATPase RecF serves as a switch in DNA repair , 2018, Scientific Reports.

[58]  Antoine M. van Oijen,et al.  DNA polymerase IV primarily operates outside of DNA replication forks in Escherichia coli , 2018, PLoS genetics.

[59]  J. Loparo,et al.  Single-molecule imaging reveals multiple pathways for the recruitment of translesion polymerases after DNA damage , 2017, Nature Communications.

[60]  M. Lamers,et al.  Single-molecule studies contrast ordered DNA replication with stochastic translesion synthesis , 2017, eLife.

[61]  B. Michel,et al.  Division-induced DNA double strand breaks in the chromosome terminus region of Escherichia coli lacking RecBCD DNA repair enzyme , 2017, PLoS genetics.

[62]  A. Kozlov,et al.  Glutamate promotes SSB protein-protein Interactions via intrinsically disordered regions. , 2017, Journal of molecular biology.

[63]  J. A. Halliday,et al.  The transcription fidelity factor GreA impedes DNA break repair , 2017, Nature.

[64]  S. Lovett Template-switching during replication fork repair in bacteria. , 2017, DNA repair.

[65]  Yen‐Hua Huang,et al.  Staphylococcus aureus single-stranded DNA-binding protein SsbA can bind but cannot stimulate PriA helicase , 2017, PloS one.

[66]  S. Boulton,et al.  Mechanisms of DNA–protein crosslink repair , 2017, Nature Reviews Molecular Cell Biology.

[67]  C. Rapisarda,et al.  Bacterial RadA is a DnaB-type helicase interacting with RecA to promote bidirectional D-loop extension , 2017, Nature Communications.

[68]  M. Osborne,et al.  PCNA ubiquitylation ensures timely completion of unperturbed DNA replication in fission yeast , 2017, PLoS genetics.

[69]  D. Branzei,et al.  Building up and breaking down: mechanisms controlling recombination during replication , 2017, Critical reviews in biochemistry and molecular biology.

[70]  N. Shoresh,et al.  Antibiotic tolerance facilitates the evolution of resistance , 2017, Science.

[71]  M. Cox,et al.  DNA flap creation by the RarA/MgsA protein of Escherichia coli , 2017, Nucleic acids research.

[72]  J. A. Halliday,et al.  Holliday junction trap shows how cells use recombination and a junction-guardian role of RecQ helicase , 2016, Science Advances.

[73]  M. Cox,et al.  Escherichia coli RadD Protein Functionally Interacts with the Single-stranded DNA-binding Protein* , 2016, The Journal of Biological Chemistry.

[74]  R. Fuchs Tolerance of lesions in E. coli: Chronological competition between Translesion Synthesis and Damage Avoidance. , 2016, DNA repair.

[75]  R. Woodgate,et al.  Insights into the complex levels of regulation imposed on Escherichia coli DNA polymerase V. , 2016, DNA repair.

[76]  T. Paz-Elizur,et al.  High-resolution genomic assays provide insight into the division of labor between TLS and HDR in mammalian replication of damaged DNA. , 2016, DNA repair.

[77]  R. Fuchs,et al.  A defect in homologous recombination leads to increased translesion synthesis in E. coli , 2016, Nucleic acids research.

[78]  M. Cox,et al.  DNA Metabolism in Balance: Rapid Loss of a RecA-Based Hyperrec Phenotype , 2016, PloS one.

[79]  Y. Hua,et al.  Figures and figure supplements Structural basis for DNA 5 ́-end resection by RecJ Kaiying , 2016 .

[80]  R. G. Lloyd,et al.  25 years on and no end in sight: a perspective on the role of RecG protein , 2016, Current Genetics.

[81]  S. Lovett,et al.  Recombinational branch migration by the RadA/Sms paralog of RecA in Escherichia coli , 2016, eLife.

[82]  D. Leach,et al.  RecG Directs DNA Synthesis during Double-Strand Break Repair , 2016, PLoS genetics.

[83]  D. Sherratt,et al.  MatP regulates the coordinated action of topoisomerase IV and MukBEF in chromosome segregation , 2016, Nature Communications.

[84]  J. Loparo,et al.  Exchange between Escherichia coli polymerases II and III on a processivity clamp , 2015, Nucleic acids research.

[85]  T. Kunkel,et al.  Eukaryotic Mismatch Repair in Relation to DNA Replication. , 2015, Annual review of genetics.

[86]  R. Fuchs,et al.  Bacterial Proliferation: Keep Dividing and Don't Mind the Gap , 2015, PLoS genetics.

[87]  S. Lovett,et al.  Connecting Replication and Repair: YoaA, a Helicase-Related Protein, Promotes Azidothymidine Tolerance through Association with Chi, an Accessory Clamp Loader Protein , 2015, PLoS Genetics.

[88]  C. Myers,et al.  Genetic Interactions Implicating Postreplicative Repair in Okazaki Fragment Processing , 2015, PLoS genetics.

[89]  N. Rai,et al.  Mycobacterium tuberculosis class II apurinic/apyrimidinic‐endonuclease/3′‐5′ exonuclease III exhibits DNA regulated modes of interaction with the sliding DNA β‐clamp , 2015, Molecular microbiology.

[90]  S. Kowalczykowski,et al.  Imaging and energetics of single SSB-ssDNA molecules reveal intramolecular condensation and insight into RecOR function , 2015, eLife.

[91]  Antoine M. van Oijen,et al.  Regulation of Mutagenic DNA Polymerase V Activation in Space and Time , 2015, PLoS genetics.

[92]  M. Glickman,et al.  RecF and RecR Play Critical Roles in the Homologous Recombination and Single-Strand Annealing Pathways of Mycobacteria , 2015, Journal of bacteriology.

[93]  S. Sandler,et al.  Directed Evolution of RecA Variants with Enhanced Capacity for Conjugational Recombination , 2015, PLoS genetics.

[94]  Antoine M. van Oijen,et al.  Mutations for Worse or Better: Low-Fidelity DNA Synthesis by SOS DNA Polymerase V Is a Tightly Regulated Double-Edged Sword. , 2016, Biochemistry.

[95]  T. Lohman,et al.  Active displacement of RecA filaments by UvrD translocase activity , 2015, Nucleic acids research.

[96]  M. Cox,et al.  Escherichia coli radD (yejH) gene: a novel function involved in radiation resistance and double‐strand break repair , 2015, Molecular microbiology.

[97]  R. Woodgate,et al.  A RecA Protein Surface Required for Activation of DNA Polymerase V , 2015, PLoS genetics.

[98]  R. Pappu,et al.  Intrinsically disordered C-terminal tails of E. coli single-stranded DNA binding protein regulate cooperative binding to single-stranded DNA. , 2015, Journal of molecular biology.

[99]  S. Lovett,et al.  Genetic analysis of Escherichia coli RadA: functional motifs and genetic interactions , 2015, Molecular microbiology.

[100]  S. Kowalczykowski,et al.  RecQ helicase and RecJ nuclease provide complementary functions to resect DNA for homologous recombination , 2014, Proceedings of the National Academy of Sciences.

[101]  P. McGlynn,et al.  Recombination and replication. , 2014, Cold Spring Harbor perspectives in biology.

[102]  Joseph T. P. Yeeles,et al.  Replisome-mediated Translesion Synthesis and Leading Strand Template Lesion Skipping Are Competing Bypass Mechanisms* , 2014, The Journal of Biological Chemistry.

[103]  Joseph T. P. Yeeles,et al.  Regression of Replication Forks Stalled by Leading-strand Template Damage , 2014, The Journal of Biological Chemistry.

[104]  Cindy Follonier,et al.  Visualization of recombination–mediated damage-bypass by template switching , 2014, Nature Structural &Molecular Biology.

[105]  H. Maki,et al.  DNA polymerase IV mediates efficient and quick recovery of replication forks stalled at N2-dG adducts , 2014, Nucleic acids research.

[106]  R. Sorenson,et al.  RecO and RecR Are Necessary for RecA Loading in Response to DNA Damage and Replication Fork Stress , 2014, Journal of bacteriology.

[107]  J. Loparo,et al.  Polymerase exchange on single DNA molecules reveals processivity clamp control of translesion synthesis , 2014, Proceedings of the National Academy of Sciences.

[108]  K. Skarstad,et al.  DNA compaction in the early part of the SOS response is dependent on RecN and RecA. , 2014, Microbiology.

[109]  David H Burkhardt,et al.  Quantifying Absolute Protein Synthesis Rates Reveals Principles Underlying Allocation of Cellular Resources , 2014, Cell.

[110]  A. Kuzminov The Precarious Prokaryotic Chromosome , 2014, Journal of bacteriology.

[111]  A. Sarasin,et al.  Gap-filling and bypass at the replication fork are both active mechanisms for tolerance of low-dose ultraviolet-induced DNA damage in the human genome. , 2014, DNA repair.

[112]  T. Ha,et al.  Structural mechanisms of PriA-mediated DNA replication restart , 2013, Proceedings of the National Academy of Sciences.

[113]  Joseph T. P. Yeeles,et al.  Dynamics of leading-strand lesion skipping by the replisome. , 2013, Molecular cell.

[114]  J. A. Halliday,et al.  Engineered proteins detect spontaneous DNA breakage in human and bacterial cells , 2013, eLife.

[115]  M. O’Donnell,et al.  DNA polymerases are error-prone at RecA-mediated recombination intermediates , 2013, Cell cycle.

[116]  R. Woodgate,et al.  Translesion DNA polymerases. , 2013, Cold Spring Harbor perspectives in biology.

[117]  J. Courcelle,et al.  Fate of the replisome following arrest by UV-induced DNA damage in Escherichia coli , 2013, Proceedings of the National Academy of Sciences.

[118]  S. Finkel,et al.  Competitive Fitness During Feast and Famine: How SOS DNA Polymerases Influence Physiology and Evolution in Escherichia coli , 2013, Genetics.

[119]  J. Imlay,et al.  The molecular mechanisms and physiological consequences of oxidative stress: lessons from a model bacterium , 2013, Nature Reviews Microbiology.

[120]  Zhihao Zhuang,et al.  Regulatory role of ubiquitin in eukaryotic DNA translesion synthesis. , 2013, Biochemistry.

[121]  P. Pasero,et al.  Rescuing stalled or damaged replication forks. , 2013, Cold Spring Harbor perspectives in biology.

[122]  M. O’Donnell,et al.  Preferential D-loop Extension by a Translesion DNA Polymerase Underlies Error-Prone Recombination , 2013, Nature Structural &Molecular Biology.

[123]  R. S. Grand,et al.  Genome conformation capture reveals that the Escherichia coli chromosome is organized by replication and transcription , 2013, Nucleic acids research.

[124]  T. Ha,et al.  PriC-mediated DNA Replication Restart Requires PriC Complex Formation with the Single-stranded DNA-binding Protein* , 2013, The Journal of Biological Chemistry.

[125]  S. Boiteux,et al.  DNA Repair Mechanisms and the Bypass of DNA Damage in Saccharomyces cerevisiae , 2013, Genetics.

[126]  V. Godoy,et al.  Antibiotic Resistance Acquired through a DNA Damage-Inducible Response in Acinetobacter baumannii , 2013, Journal of bacteriology.

[127]  C. McHenry,et al.  The PriA Replication Restart Protein Blocks Replicase Access Prior to Helicase Assembly and Directs Template Specificity through Its ATPase Activity* , 2012, The Journal of Biological Chemistry.

[128]  D. Sherratt,et al.  Chromosome replication and segregation in bacteria. , 2012, Annual review of genetics.

[129]  S. Kowalczykowski,et al.  Direct imaging of RecA nucleation and growth on single molecules of SSB-coated ssDNA , 2012, Nature.

[130]  G. Rudenko,et al.  Microbial antigenic variation mediated by homologous DNA recombination. , 2012, FEMS microbiology reviews.

[131]  B. Michel,et al.  Replication Fork Reversal after Replication–Transcription Collision , 2012, PLoS genetics.

[132]  A. Kuzminov,et al.  Replication Forks Stalled at Ultraviolet Lesions Are Rescued via RecA and RuvABC Protein-catalyzed Disintegration in Escherichia coli* , 2011, The Journal of Biological Chemistry.

[133]  M. O’Donnell,et al.  Single-molecule studies reveal the function of a third polymerase in the replisome , 2011, Nature Structural &Molecular Biology.

[134]  Joseph T. P. Yeeles,et al.  The Escherichia coli Replisome Is Inherently DNA Damage Tolerant , 2011, Science.

[135]  N. de Wind,et al.  DNA damage bypass operates in the S and G2 phases of the cell cycle and exhibits differential mutagenicity , 2011, Nucleic acids research.

[136]  C. Shee,et al.  Impact of a stress-inducible switch to mutagenic repair of DNA breaks on mutation in Escherichia coli , 2011, Proceedings of the National Academy of Sciences.

[137]  P. Plevani,et al.  Mind the gap: Keeping UV lesions in check , 2011, DNA repair.

[138]  M. Bichara,et al.  Postreplication repair mechanisms in the presence of DNA adducts in Escherichia coli. , 2011, Mutation research.

[139]  S. Korolev,et al.  Mechanism of RecO recruitment to DNA by single-stranded DNA binding protein , 2011, Nucleic acids research.

[140]  S. Lovett,et al.  Toxicity and tolerance mechanisms for azidothymidine, a replication gap-promoting agent, in Escherichia coli. , 2011, DNA repair.

[141]  J. Keck,et al.  Structure and Biochemical Activities of Escherichia coli MgsA*♦ , 2011, The Journal of Biological Chemistry.

[142]  T. Shibata,et al.  A Mechanism for Single-stranded DNA-binding Protein (SSB) Displacement from Single-stranded DNA upon SSB-RecO Interaction* , 2010, The Journal of Biological Chemistry.

[143]  F. Lecointe,et al.  The C-Terminal Domain of the Bacterial SSB Protein Acts as a DNA Maintenance Hub at Active Chromosome Replication Forks , 2010, PLoS genetics.

[144]  W. Heyer,et al.  Regulation of homologous recombination in eukaryotes. , 2010, Annual review of genetics.

[145]  D. Branzei,et al.  Replication and Recombination Factors Contributing to Recombination-Dependent Bypass of DNA Lesions by Template Switch , 2010, PLoS genetics.

[146]  M. Vijayan,et al.  X-ray and molecular-dynamics studies on Mycobacterium leprae single-stranded DNA-binding protein and comparison with other eubacterial SSB structures. , 2010, Acta crystallographica. Section D, Biological crystallography.

[147]  R. G. Lloyd,et al.  RecG Protein and Single-Strand DNA Exonucleases Avoid Cell Lethality Associated With PriA Helicase Activity in Escherichia coli , 2010, Genetics.

[148]  M. Cox,et al.  Less Is More: Neisseria gonorrhoeae RecX Protein Stimulates Recombination by Inhibiting RecA* , 2010, The Journal of Biological Chemistry.

[149]  D. Sherratt,et al.  Stoichiometry and Architecture of Active DNA Replication Machinery in Escherichia coli , 2010, Science.

[150]  T. Kelly,et al.  Postreplication gaps at UV lesions are signals for checkpoint activation , 2010, Proceedings of the National Academy of Sciences.

[151]  S. Rosenberg,et al.  RecQ-dependent death-by-recombination in cells lacking RecG and UvrD. , 2010, DNA repair.

[152]  Z. Livneh,et al.  Multiple two-polymerase mechanisms in mammalian translesion DNA synthesis , 2010, Cell cycle.

[153]  N. de Wind,et al.  Mammalian polymerase zeta is essential for post-replication repair of UV-induced DNA lesions. , 2009, DNA repair.

[154]  M. O’Donnell,et al.  The clamp loader assembles the beta clamp onto either a 3' or 5' primer terminus: the underlying basis favoring 3' loading. , 2009, The Journal of biological chemistry.

[155]  R. G. Lloyd,et al.  Replication fork collisions cause pathological chromosomal amplification in cells lacking RecG DNA translocase , 2009, Molecular microbiology.

[156]  Z. Livneh,et al.  Repair of gaps opposite lesions by homologous recombination in mammalian cells , 2009, Nucleic acids research.

[157]  R. Woodgate,et al.  The active form of DNA polymerase V is UmuD′2C–RecA–ATP , 2009, Nature.

[158]  R. G. Lloyd,et al.  Pathological replication in cells lacking RecG DNA translocase , 2009, Molecular microbiology.

[159]  D. Romero,et al.  The Extent of Migration of the Holliday Junction Is a Crucial Factor for Gene Conversion in Rhizobium etli , 2009, Journal of bacteriology.

[160]  Yuh-Ju Sun,et al.  Single-stranded DNA-binding protein complex from Helicobacter pylori suggests an ssDNA-binding surface. , 2009, Journal of molecular biology.

[161]  M. Radman,et al.  Recombination and Replication in DNA Repair of Heavily Irradiated Deinococcus radiodurans , 2009, Cell.

[162]  Mary Ellen Wiltrout,et al.  Eukaryotic Translesion Polymerases and Their Roles and Regulation in DNA Damage Tolerance , 2009, Microbiology and Molecular Biology Reviews.

[163]  S. Butcher,et al.  Identification of the SSB binding site on E. coli RecQ reveals a conserved surface for binding SSB's C terminus. , 2009, Journal of molecular biology.

[164]  M. Cox,et al.  RecFOR and RecOR as Distinct RecA Loading Pathways* , 2009, Journal of Biological Chemistry.

[165]  S. Korolev,et al.  RecR-mediated Modulation of RecF Dimer Specificity for Single- and Double-stranded DNA* , 2009, Journal of Biological Chemistry.

[166]  S. Sandler,et al.  UvrD303, a Hyperhelicase Mutant That Antagonizes RecA-Dependent SOS Expression by a Mechanism That Depends on Its C Terminus , 2008, Journal of bacteriology.

[167]  P. Bianco,et al.  RecG interacts directly with SSB: implications for stalled replication fork regression , 2008, Nucleic acids research.

[168]  Stéphane Robin,et al.  The MatP/matS Site-Specific System Organizes the Terminus Region of the E. coli Chromosome into a Macrodomain , 2008, Cell.

[169]  Hao Li,et al.  Defective Dissociation of a “Slow” RecA Mutant Protein Imparts an Escherichia coli Growth Defect* , 2008, Journal of Biological Chemistry.

[170]  A. Mathieu,et al.  Unveiling Novel RecO Distant Orthologues Involved in Homologous Recombination , 2008, PLoS genetics.

[171]  T. Shibata,et al.  RecR forms a ring-like tetramer that encircles dsDNA by forming a complex with RecF , 2008, Nucleic acids research.

[172]  Catherine Suski,et al.  Resolution of converging replication forks by RecQ and topoisomerase III. , 2008, Molecular cell.

[173]  M. Cox,et al.  SSB Antagonizes RecX-RecA Interaction* , 2008, Journal of Biological Chemistry.

[174]  J. Sale,et al.  PCNA ubiquitination and REV1 define temporally distinct mechanisms for controlling translesion synthesis in the avian cell line DT40. , 2008, Molecular cell.

[175]  N. Pavletich,et al.  Mechanism of homologous recombination from the RecA–ssDNA/dsDNA structures , 2008, Nature.

[176]  D. Sherratt,et al.  Independent Positioning and Action of Escherichia coli Replisomes in Live Cells , 2008, Cell.

[177]  A. Kozlov,et al.  SSB as an Organizer/Mobilizer of Genome Maintenance Complexes , 2008 .

[178]  M. O’Donnell,et al.  Replisome Fate upon Encountering a Leading Strand Block and Clearance from DNA by Recombination Proteins* , 2007, Journal of Biological Chemistry.

[179]  O. Kuipers,et al.  Search for Genes Essential for Pneumococcal Transformation: the RadA DNA Repair Protein Plays a Role in Genomic Recombination of Donor DNA , 2007, Journal of bacteriology.

[180]  B. Michel,et al.  Recombination proteins and rescue of arrested replication forks. , 2007, DNA repair.

[181]  J. Keck,et al.  A Central Role for SSB in Escherichia coli RecQ DNA Helicase Function* , 2007, Journal of Biological Chemistry.

[182]  R. G. Lloyd,et al.  Ring Structure of the Escherichia coli DNA-binding Protein RdgC Associated with Recombination and Replication Fork Repair* , 2007, Journal of Biological Chemistry.

[183]  M. Cox,et al.  SSB Protein Limits RecOR Binding onto Single-stranded DNA* , 2007, Journal of Biological Chemistry.

[184]  R. G. Lloyd,et al.  Replication fork stalling and cell cycle arrest in UV-irradiated Escherichia coli. , 2007, Genes & development.

[185]  J. Courcelle,et al.  Structural conservation of RecF and Rad50: implications for DNA recognition and RecF function , 2007, The EMBO journal.

[186]  M. Cox Motoring along with the bacterial RecA protein , 2007, Nature Reviews Molecular Cell Biology.

[187]  R. Woodgate,et al.  Characterization of polVR391: a Y‐family polymerase encoded by rumA′B from the IncJ conjugative transposon, R391 , 2007, Molecular microbiology.

[188]  S. Sandler,et al.  UvrD Limits the Number and Intensities of RecA-Green Fluorescent Protein Structures in Escherichia coli K-12 , 2007, Journal of bacteriology.

[189]  S. Lovett,et al.  RecA-independent recombination is efficient but limited by exonucleases , 2007, Proceedings of the National Academy of Sciences.

[190]  M. Cox Regulation of Bacterial RecA Protein Function , 2007, Critical reviews in biochemistry and molecular biology.

[191]  A. Lehmann,et al.  Gaps and forks in DNA replication: Rediscovering old models. , 2006, DNA repair.

[192]  R. Heller,et al.  Replisome assembly and the direct restart of stalled replication forks , 2006, Nature Reviews Molecular Cell Biology.

[193]  Z. Dauter,et al.  Structure of the single-stranded DNA-binding protein SSB from Thermus aquaticus. , 2006, Acta crystallographica. Section D, Biological crystallography.

[194]  S. Lovett Microbiology: Resurrecting a broken genome , 2006, Nature.

[195]  M. O’Donnell,et al.  DNA replication: keep moving and don't mind the gap. , 2006, Molecular cell.

[196]  T. Shibata,et al.  Identification of the RecR Toprim Domain as the Binding Site for both RecF and RecO , 2006, Journal of Biological Chemistry.

[197]  J. Jiricny The multifaceted mismatch-repair system , 2006, Nature Reviews Molecular Cell Biology.

[198]  S. Lovett,et al.  DNA repeat rearrangements mediated by DnaK-dependent replication fork repair. , 2006, Molecular cell.

[199]  M. Cox,et al.  Inhibition of RecA Protein Function by the RdgC Protein from Escherichia coli* , 2006, Journal of Biological Chemistry.

[200]  S. Lovett,et al.  RecJ exonuclease: substrates, products and interaction with SSB , 2006, Nucleic acids research.

[201]  R. Heller,et al.  Replication fork reactivation downstream of a blocked nascent leading strand , 2006, Nature.

[202]  M. Cox,et al.  The RecF protein antagonizes RecX function via direct interaction. , 2006, Molecular cell.

[203]  M. Lopes,et al.  Multiple mechanisms control chromosome integrity after replication fork uncoupling and restart at irreparable UV lesions. , 2006, Molecular cell.

[204]  G. Walker,et al.  Two processivity clamp interactions differentially alter the dual activities of UmuC , 2006, Molecular microbiology.

[205]  E. Rocha,et al.  Comparative and Evolutionary Analysis of the Bacterial Homologous Recombination Systems , 2005, PLoS genetics.

[206]  R. G. Lloyd,et al.  AFM studies on the role of the protein RdgC in bacterial DNA recombination. , 2005, Journal of molecular biology.

[207]  F. Boccard,et al.  Spatial arrangement and macrodomain organization of bacterial chromosomes , 2005, Molecular microbiology.

[208]  T. Kunkel,et al.  DNA mismatch repair. , 2005, Annual review of biochemistry.

[209]  D. Hall,et al.  Crystal structure and DNA‐binding analysis of RecO from Deinococcus radiodurans , 2005, The EMBO journal.

[210]  H. Shinagawa,et al.  Functional overlap between RecA and MgsA (RarA) in the rescue of stalled replication forks in Escherichia coli , 2005, Genes to cells : devoted to molecular & cellular mechanisms.

[211]  K. Brčić-Kostić,et al.  Effects of recJ, recQ, and recFOR Mutations on Recombination in Nuclease-Deficient recB recD Double Mutants of Escherichia coli , 2005, Journal of bacteriology.

[212]  A. Emili,et al.  Interaction network containing conserved and essential protein complexes in Escherichia coli , 2005, Nature.

[213]  M. Cox,et al.  Organized Unidirectional Waves of ATP Hydrolysis within a RecA Filament , 2005, PLoS biology.

[214]  F. Fabre,et al.  UvrD helicase, unlike Rep helicase, dismantles RecA nucleoprotein filaments in Escherichia coli , 2005, The EMBO journal.

[215]  M. Cox,et al.  The DinI and RecX Proteins Are Competing Modulators of RecA Function* , 2004, Journal of Biological Chemistry.

[216]  M. Cox,et al.  Inhibition of RecA Protein by the Escherichia coli RecX Protein , 2004, Journal of Biological Chemistry.

[217]  Kendric C. Smith Recombinational DNA repair: the ignored repair systems. , 2004, BioEssays : news and reviews in molecular, cellular and developmental biology.

[218]  M. Rossignol,et al.  Macrodomain organization of the Escherichia coli chromosome , 2004, The EMBO journal.

[219]  C. Bell,et al.  Crystal structures of Escherichia coli RecA in a compressed helical filament. , 2004, Journal of molecular biology.

[220]  D. Grandgenett,et al.  A novel structure of DNA repair protein RecO from Deinococcus radiodurans. , 2004, Structure.

[221]  M. Cox,et al.  A RecA filament capping mechanism for RecX protein. , 2004, Molecular cell.

[222]  M. Cozar,et al.  Genetic Recombination in Bacillus subtilis 168: Contribution of Holliday Junction Processing Functions in Chromosome Segregation , 2004, Journal of bacteriology.

[223]  B. Michel,et al.  Multiple pathways process stalled replication forks. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[224]  Oleg N. Voloshin,et al.  The DinI Protein Stabilizes RecA Protein Filaments* , 2004, Journal of Biological Chemistry.

[225]  S. Savvides,et al.  The C‐terminal domain of full‐length E. coli SSB is disordered even when bound to DNA , 2004, Protein science : a publication of the Protein Society.

[226]  A. Sancar,et al.  Molecular mechanisms of mammalian DNA repair and the DNA damage checkpoints. , 2004, Annual review of biochemistry.

[227]  J. Keck,et al.  Crystal structure of the Deinococcus radiodurans single-stranded DNA-binding protein suggests a mechanism for coping with DNA damage. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[228]  N. Larebeke,et al.  Endogenous DNA damage in humans: a review of quantitative data , 2004 .

[229]  J. Courcelle,et al.  When replication travels on damaged templates: bumps and blocks in the road. , 2004, Research in microbiology.

[230]  B. Michel,et al.  Requirement for RecFOR‐mediated recombination in priA mutant , 2004, Molecular microbiology.

[231]  J. Courcelle,et al.  RecO Acts with RecF and RecR to Protect and Maintain Replication Forks Blocked by UV-induced DNA Damage in Escherichia coli* , 2004, Journal of Biological Chemistry.

[232]  M. Cox The bacterial RecA protein as a motor protein. , 2003, Annual review of microbiology.

[233]  J. Courcelle,et al.  RecA-dependent recovery of arrested DNA replication forks. , 2003, Annual review of genetics.

[234]  H. Krokan,et al.  The interacting pathways for prevention and repair of oxidative DNA damage. , 2003, Mutation research.

[235]  E. Egelman,et al.  Complexes of RecA with LexA and RecX differentiate between active and inactive RecA nucleoprotein filaments. , 2003, Journal of molecular biology.

[236]  M. Vijayan,et al.  Structure of Mycobacterium tuberculosis single-stranded DNA-binding protein. Variability in quaternary structure and its implications. , 2003, Journal of molecular biology.

[237]  R. Fuchs,et al.  Uncoupling of Leading- and Lagging-Strand DNA Replication During Lesion Bypass in Vivo , 2003, Science.

[238]  P. Hanawalt,et al.  Who's on first in the cellular response to DNA damage? , 2003, Nature Reviews Molecular Cell Biology.

[239]  S. Kowalczykowski,et al.  RecFOR proteins load RecA protein onto gapped DNA to accelerate DNA strand exchange: a universal step of recombinational repair. , 2003, Molecular cell.

[240]  Wilson Dm rd,et al.  Repair mechanisms for oxidative DNA damage. , 2003 .

[241]  A. Kuzminov,et al.  Chromosomal lesion suppression and removal in Escherichia coli via linear DNA degradation. , 2003, Genetics.

[242]  R. Fuchs,et al.  recX, a new SOS gene that is co-transcribed with the recA gene in Escherichia coli. , 2003, DNA repair.

[243]  R. G. Lloyd,et al.  The RdgC protein of Escherichia coli binds DNA and counters a toxic effect of RecFOR in strains lacking the replication restart protein PriA , 2003, The EMBO journal.

[244]  R. G. Lloyd,et al.  PriA supports two distinct pathways for replication restart in UV‐irradiated Escherichia coli cells , 2003, Molecular microbiology.

[245]  Joel P. Brockman,et al.  Escherichia coli RecX Inhibits RecA Recombinase and Coprotease Activities in Vitro and in Vivo * , 2003, The Journal of Biological Chemistry.

[246]  M. Cox The nonmutagenic repair of broken replication forks via recombination. , 2002, Mutation research.

[247]  S. Lovett,et al.  Role for radA/sms in Recombination Intermediate Processing in Escherichia coli , 2002, Journal of bacteriology.

[248]  R. G. Lloyd,et al.  Genome stability and the processing of damaged replication forks by RecG. , 2002, Trends in genetics : TIG.

[249]  Bethany Yeiser,et al.  SOS-induced DNA polymerases enhance long-term survival and evolutionary fitness , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[250]  S. Lovett,et al.  Crossing over between regions of limited homology in Escherichia coli. RecA-dependent and RecA-independent pathways. , 2002, Genetics.

[251]  R. G. Lloyd,et al.  Direct rescue of stalled DNA replication forks via the combined action of PriA and RecG helicase activities. , 2002, Molecular cell.

[252]  M. Cox,et al.  The RecOR proteins modulate RecA protein function at 5′ ends of single‐stranded DNA , 2001, The EMBO journal.

[253]  R. G. Lloyd,et al.  Action of RuvAB at Replication Fork Structures* , 2001, The Journal of Biological Chemistry.

[254]  S. Kowalczykowski,et al.  A step backward in advancing DNA replication: rescue of stalled replication forks by RecG. , 2001, Molecular cell.

[255]  D. Wigley,et al.  Structural Analysis of DNA Replication Fork Reversal by RecG , 2001, Cell.

[256]  S. Sandler,et al.  PriA mutations that affect PriA–PriC function during replication restart , 2001, Molecular microbiology.

[257]  A. Kuzminov Single-strand interruptions in replicating chromosomes cause double-strand breaks , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[258]  R. G. Lloyd,et al.  Rescue of stalled replication forks by RecG: Simultaneous translocation on the leading and lagging strand templates supports an active DNA unwinding model of fork reversal and Holliday junction formation , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[259]  R. G. Lloyd,et al.  Formation of Holliday junctions by regression of nascent DNA in intermediates containing stalled replication forks: RecG stimulates regression even when the DNA is negatively supercoiled , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[260]  A. Kuzminov DNA replication meets genetic exchange: Chromosomal damage and its repair by homologous recombination , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[261]  D. Sherratt,et al.  Circles: The replication-recombination-chromosome segregation connection , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[262]  K. Keller,et al.  Survival and induction of SOS in Escherichia coli treated with cisplatin, UV-irradiation, or mitomycin C are dependent on the function of the RecBC and RecFOR pathways of homologous recombination. , 2001, Mutation research.

[263]  G. Walker,et al.  Genetic Interactions between the Escherichia coli umuDC Gene Products and the β Processivity Clamp of the Replicative DNA Polymerase , 2001, Journal of bacteriology.

[264]  S. Rosenberg,et al.  SOS mutator DNA polymerase IV functions in adaptive mutation and not adaptive amplification. , 2001, Molecular cell.

[265]  N. Kunishima,et al.  Crystal structure of the Holliday junction migration motor protein RuvB from Thermus thermophilus HB8. , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[266]  F. Harmon,et al.  Biochemical Characterization of the DNA Helicase Activity of theEscherichia coli RecQ Helicase* , 2001, The Journal of Biological Chemistry.

[267]  R. Schaaper,et al.  SOS mutator activity: unequal mutagenesis on leading and lagging strands. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[268]  M. O’Donnell,et al.  Cross-utilization of the β Sliding Clamp by Replicative Polymerases of Evolutionary Divergent Organisms* , 2000, The Journal of Biological Chemistry.

[269]  G. Waksman,et al.  Structure of the DNA binding domain of E. coli SSB bound to ssDNA , 2000, Nature Structural Biology.

[270]  D. Sherratt,et al.  Resolution of Holliday junctions by RuvABC prevents dimer formation in rep mutants and UV‐irradiated cells , 2000, Molecular microbiology.

[271]  Peter L Lee,et al.  The SOS response regulates adaptive mutation. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[272]  S. Kowalczykowski Initiation of genetic recombination and recombination-dependent replication. , 2000, Trends in biochemical sciences.

[273]  K. Marians PriA-directed replication fork restart in Escherichia coli. , 2000, Trends in biochemical sciences.

[274]  Myron F. Goodman,et al.  The importance of repairing stalled replication forks , 2000, Nature.

[275]  F. Hanaoka,et al.  [Translesion DNA polymerases]. , 2000, Seikagaku. The Journal of Japanese Biochemical Society.

[276]  T. Tsukihara,et al.  Roles of functional loops and the C-terminal segment of a single-stranded DNA binding protein elucidated by X-Ray structure analysis. , 2000, Journal of biochemistry.

[277]  S. Sandler,et al.  Role of PriA in Replication Fork Reactivation inEscherichia coli , 2000, Journal of bacteriology.

[278]  J. Courcelle,et al.  RecQ and RecJ process blocked replication forks prior to the resumption of replication in UV-irradiated Escherichia coli , 1999, Molecular and General Genetics MGG.

[279]  S. Kowalczykowski,et al.  A Single Mutation, RecBD1080A, Eliminates RecA Protein Loading but Not Chi Recognition by RecBCD Enzyme* , 1999, The Journal of Biological Chemistry.

[280]  R. G. Lloyd,et al.  Holliday Junction Processing in Bacteria: Insights from the Evolutionary Conservation of RuvABC, RecG, and RusA , 1999, Journal of bacteriology.

[281]  R. Woodgate,et al.  A phenotype for enigmatic DNA polymerase II: a pivotal role for pol II in replication restart in UV-irradiated Escherichia coli. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[282]  S. West,et al.  Assembly of the Escherichia coli RuvABC resolvasome directs the orientation of holliday junction resolution. , 1999, Genes & development.

[283]  S. Lovett,et al.  Expansion of DNA repeats in Escherichia coli: effects of recombination and replication functions. , 1999, Journal of molecular biology.

[284]  M. Cox,et al.  ATP Hydrolysis and DNA Binding by the Escherichia coli RecF Protein* , 1999, The Journal of Biological Chemistry.

[285]  M. Cox,et al.  Quantitative analysis of the kinetics of end-dependent disassembly of RecA filaments from ssDNA. , 1999, Journal of molecular biology.

[286]  G. Marsischky,et al.  Eukaryotic DNA mismatch repair. , 1999, Current opinion in genetics & development.

[287]  Z. Kelman,et al.  The internal workings of a DNA polymerase clamp‐loading machine , 1999, EMBO Journal.

[288]  A. Kuzminov,et al.  Double-strand end repair via the RecBC pathway in Escherichia coli primes DNA replication. , 1999, Genes & development.

[289]  Ed Zintel,et al.  Resources , 1998, IT Prof..

[290]  S C West,et al.  Coordinated actions of RuvABC in Holliday junction processing. , 1998, Journal of molecular biology.

[291]  R. G. Lloyd,et al.  Targeting Holliday Junctions by the RecG Branch Migration Protein of Escherichia coli * , 1998, The Journal of Biological Chemistry.

[292]  S. West,et al.  Formation of RuvABC–Holliday junction complexes in vitro , 1998, Current Biology.

[293]  F. Harmon,et al.  RecQ helicase, in concert with RecA and SSB proteins, initiates and disrupts DNA recombination. , 1998, Genes & development.

[294]  A. Cheng,et al.  Involvement of recF, recO, and recR Genes in UV-Radiation Mutagenesis ofEscherichia coli , 1998, Journal of bacteriology.

[295]  M. Cox,et al.  Recombinational DNA Repair: The RecF and RecR Proteins Limit the Extension of RecA Filaments beyond Single-Strand DNA Gaps , 1997, Cell.

[296]  Daniel G. Anderson,et al.  The Translocating RecBCD Enzyme Stimulates Recombination by Directing RecA Protein onto ssDNA in a χ-Regulated Manner , 1997, Cell.

[297]  R. G. Lloyd,et al.  The DNA replication protein PriA and the recombination protein RecG bind D-loops. , 1997, Journal of molecular biology.

[298]  M. Cox,et al.  RecA as a Motor Protein , 1997, The Journal of Biological Chemistry.

[299]  G. Waksman,et al.  Crystal structure of the homo-tetrameric DNA binding domain of Escherichia coli single-stranded DNA-binding protein determined by multiwavelength x-ray diffraction on the selenomethionyl protein at 2.9-A resolution. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[300]  J. Courcelle,et al.  recF and recR are required for the resumption of replication at DNA replication forks in Escherichia coli. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[301]  T. Kogoma Is RecF a DNA replication protein? , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[302]  M. Hecker,et al.  The Bacillus subtilis clpC operon encodes DNA repair and competence proteins. , 1997, Microbiology.

[303]  M. Cox,et al.  RecA protein filaments: end-dependent dissociation from ssDNA and stabilization by RecO and RecR proteins. , 1997, Journal of molecular biology.

[304]  R. G. Lloyd,et al.  Modulation of recombination and DNA repair by the RecG and PriA helicases of Escherichia coli K-12 , 1996, Journal of bacteriology.

[305]  J. Sekiguchi,et al.  Cleavage of single- and double-stranded DNAs containing an abasic residue by Escherichia coli exonuclease III (AP endonuclease VI). , 1996, Nucleic acids research.

[306]  R. G. Lloyd,et al.  Crystal Structure of DNA Recombination Protein RuvA and a Model for Its Binding to the Holliday Junction , 1996, Science.

[307]  C. Urbanke,et al.  In vitro and in vivo function of the C-terminus of Escherichia coli single-stranded DNA binding protein. , 1996, Nucleic acids research.

[308]  L. Liu,et al.  A replicational model for DNA recombination between direct repeats. , 1996, Journal of molecular biology.

[309]  S. West,et al.  The RuvABC proteins and Holliday junction processing in Escherichia coli , 1996, Journal of bacteriology.

[310]  Z. Livneh,et al.  Reconstitution of repair-gap UV mutagenesis with purified proteins from Escherichia coli: a role for DNA polymerases III and II. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[311]  S. Sandler Overlapping functions for recF and priA in cell viability and UV‐inducible SOS expression are distinguished by dnaC809 in Escherichia coli K‐12 , 1996, Molecular microbiology.

[312]  M. Cox,et al.  An Interaction between the Escherichia coli RecF and RecR Proteins Dependent on ATP and Double-stranded DNA (*) , 1995, The Journal of Biological Chemistry.

[313]  R. Kolodner Mismatch repair: mechanisms and relationship to cancer susceptibility. , 1995, Trends in biochemical sciences.

[314]  R. Bennett,et al.  RuvC protein resolves Holliday junctions via cleavage of the continuous (noncrossover) strands. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[315]  M. O’Donnell,et al.  Assembly of a Chromosomal Replication Machine: Two DNA Polymerases, a Clamp Loader, and Sliding Clamps in One Holoenzyme Particle. , 1995, The Journal of Biological Chemistry.

[316]  M. O’Donnell,et al.  Assembly of a Chromosomal Replication Machine: Two DNA Polymerases, a Clamp Loader, and Sliding Clamps in One Holoenzyme Particle. , 1995, The Journal of Biological Chemistry.

[317]  S. Lovett,et al.  Suppression of recJ exonuclease mutants of Escherichia coli by alterations in DNA helicases II (uvrD) and IV (helD). , 1995, Genetics.

[318]  A. Kuzminov Collapse and repair of replication forks in Escherichia coli , 1995, Molecular microbiology.

[319]  S. West,et al.  Structure of a multisubunit complex that promotes DNA branch migration , 1995, Nature.

[320]  R. G. Lloyd,et al.  Conjugational recombination in Escherichia coli: genetic analysis of recombinant formation in Hfr x F- crosses. , 1995, Genetics.

[321]  S. Sandler Studies on the mechanism of reduction of W-inducible sulAp expression by recF overexpression in Escherichia coli K-12 , 1994, Molecular and General Genetics MGG.

[322]  R. Kolodner,et al.  Protein interactions in genetic recombination in Escherichia coli. Interactions involving RecO and RecR overcome the inhibition of RecA by single-stranded DNA-binding protein. , 1994, The Journal of biological chemistry.

[323]  S. Lovett,et al.  Recombination between repeats in Escherichia coli by a recA-independent, proximity-sensitive mechanism , 1994, Molecular and General Genetics MGG.

[324]  R. G. Lloyd,et al.  Branch migration of Holliday junctions: identification of RecG protein as a junction specific DNA helicase. , 1994, The EMBO journal.

[325]  M. O’Donnell,et al.  An explanation for lagging strand replication: Polymerase hopping among DNA sliding clamps , 1994, Cell.

[326]  S. Kowalczykowski,et al.  Biochemistry of homologous recombination in Escherichia coli , 1994 .

[327]  T. C. Wang,et al.  Involvement of RecF pathway recombination genes in postreplication repair in UV-irradiated Escherichia coli cells. , 1994, Mutation research.

[328]  S. Sandler,et al.  RecOR suppression of recF mutant phenotypes in Escherichia coli K-12 , 1994, Journal of bacteriology.

[329]  M. Cox Why does RecA protein hydrolyse ATP? , 1994, Trends in biochemical sciences.

[330]  R. Kolodner,et al.  Homologous pairing and strand exchange promoted by the Escherichia coli RecT protein. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[331]  S. West,et al.  Processing of Holliday junctions by theEscherichia coli RuvA, RuvB, RuvC and ReeG proteins , 1994, Experientia.

[332]  L. Liu,et al.  recA-independent and recA-dependent intramolecular plasmid recombination. Differential homology requirement and distance effect. , 1994, Journal of molecular biology.

[333]  S. Lovett,et al.  A sister-strand exchange mechanism for recA-independent deletion of repeated DNA sequences in Escherichia coli. , 1993, Genetics.

[334]  S. Sandler,et al.  Use of high and low level overexpression plasmids to test mutant alleles of the recF gene of Escherichia coli K-12 for partial activity. , 1993, Genetics.

[335]  R. G. Lloyd,et al.  Reverse branch migration of holliday junctions by RecG protein: A new mechanism for resolution of intermediates in recombination and DNA repair , 1993, Cell.

[336]  R. Woodgate,et al.  A rapid method for cloning mutagenic DNA repair genes: isolation of umu-complementing genes from multidrug resistance plasmids R391, R446b, and R471a , 1993, Journal of bacteriology.

[337]  M. Altshuler Recovery of DNA replication in UV-damaged Escherichia coli. , 1993, Mutation research.

[338]  T. C. Wang,et al.  Cosuppression of recF, recR and recO mutations by mutant recA alleles in Escherichia coli cells. , 1993, Mutation research.

[339]  A. Kuzminov RuvA, RuvB and RuvC proteins: cleaning-up after recombinational repairs in E. coli. , 1993, BioEssays : news and reviews in molecular, cellular and developmental biology.

[340]  M. Tang,et al.  NUCLEOTIDE EXCISION REPAIR , 1993, Photochemistry and photobiology.

[341]  R. Kolodner,et al.  Biochemical interaction of the Escherichia coli RecF, RecO, and RecR proteins with RecA protein and single-stranded DNA binding protein. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[342]  R. G. Lloyd,et al.  Processing of recombination intermediates by the RecG and RuvAB proteins of Escherichia coli. , 1993, Nucleic acids research.

[343]  T. Lindahl Instability and decay of the primary structure of DNA , 1993, Nature.

[344]  K. Umezu,et al.  RecQ DNA helicase of Escherichia coli. Characterization of the helix-unwinding activity with emphasis on the effect of single-stranded DNA-binding protein. , 1993, Journal of molecular biology.

[345]  M. Madiraju,et al.  Evidence for ATP binding and double-stranded DNA binding by Escherichia coli RecF protein , 1992, Journal of bacteriology.

[346]  H. Shinagawa,et al.  Escherichia coli RuvA and RuvB proteins specifically interact with Holliday junctions and promote branch migration. , 1992, Genes & development.

[347]  R. Woodgate,et al.  Mutagenesis induced by bacterial UmuDC proteins and their plasmid homologues , 1992, Molecular microbiology.

[348]  S. West,et al.  ATP-dependent branch migration of holliday junctions promoted by the RuvA and RuvB proteins of E. coli , 1992, Cell.

[349]  R. G. Lloyd,et al.  Interaction of Escherichia coli RuvA and RuvB proteins with synthetic Holliday junctions. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[350]  T. C. Wang,et al.  Similar-sized daughter-strand gaps are produced in the leading and lagging strands of DNA in UV-irradiated E. coli uvrA cells. , 1992, Biochemical and biophysical research communications.

[351]  L. Fisher,et al.  Nucleotide sequence of the Staphylococcus aureus gyrB-gyrA locus encoding the DNA gyrase A and B proteins , 1992, Journal of bacteriology.

[352]  H. Yoshikawa,et al.  Structure of the dnaA and DnaA-box region in the Mycoplasma capricolum chromosome: conservation and variations in the course of evolution. , 1992, Gene.

[353]  George Lliakis,et al.  The role of DNA double strand breaks in lonizing radiation‐induced killing of eukaryotic cells , 1991 .

[354]  R. Woodgate,et al.  Levels of chromosomally encoded Umu proteins and requirements for in vivo UmuD cleavage , 1991, Molecular and General Genetics MGG.

[355]  G. Dianov,et al.  Mechanisms of deletion formation in Escherichin coli plasmids , 1991, Molecular and General Genetics MGG.

[356]  G. Dianov,et al.  Molecular mechanisms of deletion formation in Escherichia coli plasmids , 1991, Molecular and General Genetics MGG.

[357]  G. Dianov,et al.  Mechanisms of deletion formation in Escherichia coli plasmids. II. Deletions mediated by short direct repeats. , 1991, Molecular & general genetics : MGG.

[358]  R. G. Lloyd,et al.  Resolution of Holliday junctions in vitro requires the Escherichia coli ruvC gene product. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[359]  S. Kowalczykowski Biochemical and biological function of Escherichia coli RecA protein: behavior of mutant RecA proteins. , 1991, Biochimie.

[360]  F. Macian,et al.  Positive and negative regulatory elements in the dnaA-dnaN-recF operon of Escherichia coli. , 1991, Biochimie.

[361]  S. Lovett,et al.  Nucleotide sequence of the Escherichia coli recJ chromosomal region and construction of recJ-overexpression plasmids , 1991, Journal of bacteriology.

[362]  P. Laine,et al.  The single-stranded DNA-binding protein of Escherichia coli , 1990 .

[363]  R. Kolodner,et al.  Purification and preliminary characterization of the Escherichia coli K-12 recF protein , 1990, Journal of bacteriology.

[364]  N. Kleckner,et al.  E. coli oriC and the dnaA gene promoter are sequestered from dam methyltransferase following the passage of the chromosomal replication fork , 1990, Cell.

[365]  H. Yoshikawa,et al.  Structure of the dnaA region of Micrococcus luteus: conservation and variations among eubacteria. , 1990, Gene.

[366]  K. Nakayama,et al.  Escherichia coli RecQ protein is a DNA helicase. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[367]  J. Sweasy,et al.  RecA protein of Escherichia coli has a third essential role in SOS mutator activity , 1990, Journal of bacteriology.

[368]  R. G. Lloyd,et al.  Molecular and functional analysis of the ruv region of Escherichia coli K-12 reveals three genes involved in DNA repair and recombination , 1990, Molecular and General Genetics MGG.

[369]  Kendric C. Smith,et al.  Role of ruvAB genes in UV- and γ-radiation and chemical mutagenesis in Escherichia coli , 1989 .

[370]  H. Shinagawa,et al.  Involvement in DNA repair of the ruvA gene of Escherichia coli , 1989, Molecular and General Genetics MGG.

[371]  R. Woodgate,et al.  UmuC mutagenesis protein of Escherichia coli: purification and interaction with UmuD and UmuD'. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[372]  R. G. Lloyd,et al.  The recR locus of Escherichia coli K-12: molecular cloning, DNA sequencing and identification of the gene product. , 1989, Nucleic acids research.

[373]  T. Lohman,et al.  Negative co-operativity in Escherichia coli single strand binding protein-oligonucleotide interactions. II. Salt, temperature and oligonucleotide length effects. , 1989, Journal of molecular biology.

[374]  T. Lohman,et al.  Negative co-operativity in Escherichia coli single strand binding protein-oligonucleotide interactions. I. Evidence and a quantitative model. , 1989, Journal of molecular biology.

[375]  F. Galibert,et al.  New recA mutations that dissociate the various RecA protein activities in Escherichia coli provide evidence for an additional role for RecA protein in UV mutagenesis , 1989, Journal of bacteriology.

[376]  R. G. Lloyd,et al.  Identification of the recR locus of Escherichia coli K-12 and analysis of its role in recombination and DNA repair , 1989, Molecular and General Genetics MGG.

[377]  E. Egelman,et al.  Structure of helical RecA-DNA complexes. III. The structural polarity of RecA filaments and functional polarity in the RecA-mediated strand exchange reaction. , 1988, Journal of molecular biology.

[378]  R. Knippers,et al.  Camptothecin, a specific inhibitor of type I DNA topoisomerase, induces DNA breakage at replication forks , 1988, Molecular and cellular biology.

[379]  R. Scheuermann,et al.  UmuD mutagenesis protein of Escherichia coli: overproduction, purification, and cleavage by RecA. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[380]  H. Shinagawa,et al.  RecA protein-dependent cleavage of UmuD protein and SOS mutagenesis. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[381]  J. Battista,et al.  RecA-mediated cleavage activates UmuD for mutagenesis: mechanistic relationship between transcriptional derepression and posttranslational activation. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[382]  E. Egelman,et al.  Structure of helical RecA-DNA complexes. Complexes formed in the presence of ATP-gamma-S or ATP. , 1988, Journal of molecular biology.

[383]  K. Smith,et al.  recA-dependent DNA repair in UV-irradiated Escherichia coli. , 1987, Journal of photochemistry and photobiology. B, Biology.

[384]  T. Lohman,et al.  Limited co-operativity in protein-nucleic acid interactions. A thermodynamic model for the interactions of Escherichia coli single strand binding protein with single-stranded nucleic acids in the "beaded", (SSB)65 mode. , 1987, Journal of molecular biology.

[385]  T. C. Wang,et al.  recA (Srf) suppression of recF deficiency in the postreplication repair of UV-irradiated Escherichia coli K-12 , 1986, Journal of bacteriology.

[386]  Arlen W. Johnson,et al.  Exonuclease III and endonuclease IV remove 3' blocks from DNA synthesis primers in H2O2-damaged Escherichia coli. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[387]  T. Lohman,et al.  Salt-dependent changes in the DNA binding co-operativity of Escherichia coli single strand binding protein. , 1986, Journal of molecular biology.

[388]  R. Kolodner,et al.  Genetic recombination of bacterial plasmid DNA: effect of RecF pathway mutations on plasmid recombination in Escherichia coli , 1985, Journal of bacteriology.

[389]  S. Lovett,et al.  Cloning of the Escherichia coli recJ chromosomal region and identification of its encoded proteins , 1985, Journal of bacteriology.

[390]  L. W. Ream,et al.  Molecular analysis of the recF gene of Escherichia coli. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[391]  K. Smith,et al.  recF-dependent and recF recB-independent DNA gap-filling repair processes transfer dimer-containing parental strands to daughter strands in Escherichia coli K-12 uvrB , 1984, Journal of bacteriology.

[392]  J. W. Little,et al.  Autodigestion of lexA and phage lambda repressors. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[393]  S. Lovett,et al.  Genetic analysis of the recJ gene of Escherichia coli K-12 , 1984, Journal of bacteriology.

[394]  T. C. Wang,et al.  Mechanisms for recF-dependent and recB-dependent pathways of postreplication repair in UV-irradiated Escherichia coli uvrB , 1983, Journal of bacteriology.

[395]  V. Pigiet,et al.  Polyoma virus minichromosomes: characterization of the products of in vitro DNA synthesis , 1983, Journal of virology.

[396]  S. West,et al.  Role of SSB protein in RecA promoted branch migration reactions , 1982, Molecular and General Genetics MGG.

[397]  J. Griffith,et al.  Escherichia coli single-strand binding protein organizes single-stranded DNA in nucleosome-like units. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[398]  W. Diver,et al.  A mutation (radA100) in Escherichia coli that selectively sensitizes cells grown in rich medium to x- or u.v.-radiation, or methyl methanesulphonate. , 1982, International journal of radiation biology and related studies in physics, chemistry, and medicine.

[399]  S. West,et al.  Mechanism of E. coli RecA protein directed strand exchanges in post-replication repair of DNA , 1981, Nature.

[400]  I. Lehman,et al.  Directionality and polarity in recA protein-promoted branch migration. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[401]  I. Lehman,et al.  recA protein of Escherichia coli promotes branch migration, a kinetically distinct phase of DNA strand exchange. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[402]  T. Shibata,et al.  Homologous pairing and topological linkage of DNA molecules by combined action of E. coli recA protein and topoisomerase I , 1981, Cell.

[403]  T. Shibata,et al.  The topology of homologous pairing promoted by RecA protein , 1980, Cell.

[404]  A. Kornberg,et al.  A temperature-sensitive single-stranded DNA-binding protein from Escherichia coli. , 1980, The Journal of biological chemistry.

[405]  A. Kornberg,et al.  An Escherichia coli mutant defective in single-strand binding protein is defective in DNA replication. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[406]  I. Lehman,et al.  Excision repair of uracil incorporated in DNA as a result of a defect in dUTPase. , 1977, Journal of molecular biology.

[407]  Takesi Kato,et al.  Isolation and characterization of mutants of Escherichia coli deficient in induction of mutations by ultraviolet light , 1977, Molecular and General Genetics MGG.

[408]  A. Clark,et al.  Defective excision and postreplication repair of UV-damaged DNA in a recL mutant strain of E. coli K-12 , 1977, Molecular and General Genetics MGG.

[409]  A. Clark,et al.  The dependence of postreplication repair on uvrB in a recF mutant of Escherichia coli K-12 , 1977, Molecular and General Genetics MGG.

[410]  V. Mackay,et al.  Selective inhibition of the dnase activity of the recBC enzyme by the DNA binding protein from Escherichia coli. , 1976, The Journal of biological chemistry.

[411]  K. Smith,et al.  Genetic control of multiple pathways of post-replicational repair in uvrB strains of Escherichia coli K-12 , 1976, Journal of bacteriology.

[412]  T. Bonura,et al.  QUANTITATIVE EVIDENCE FOR ENZYMATICALLY‐INDUCED DNA DOUBLE‐STRAND BREAKS AS LETHAL LESIONS IN UV IRRADIATED pol+ AND polAl STRAINS OF E. COLI K‐12 , 1975, Photochemistry and photobiology.

[413]  M. Gefter,et al.  Properties of the Escherichia coli DNA-binding (unwinding) protein interaction with nucleolytic enzymes and DNA. , 1975, Journal of molecular biology.

[414]  S. Sedgwick Genetic and kinetic evidence for different types of postreplication repair in Escherichia coli B , 1975, Journal of bacteriology.

[415]  A T Diaz,et al.  Mechanism of DNA chain growth. , 1975, Journal of molecular biology.

[416]  I. R. Lehman,et al.  Novel mutants of Escherichia coli that accumulate very small DNA replicative intermediates. , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[417]  Y. Kurosawa,et al.  Mechanism of DNA chain growth. XIII. Evidence for discontinuous replication of both strands of P2 phage DNA. , 1975, Journal of molecular biology.

[418]  S. Barbour,et al.  Analysis of the Growth of Recombination-Deficient Strains of Escherichia coli K-12 , 1974, Journal of bacteriology.

[419]  S. Sedgwick,et al.  Effect of Photoreactivation on the Filling of Gaps in Deoxyribonucleic Acid Synthesized After Exposure of Escherichia coli to Ultraviolet Light , 1974, Journal of bacteriology.

[420]  Z. Horii,et al.  Genetic analysis of the recF pathway to genetic recombination in Escherichia coli K12: isolation and characterization of mutants. , 1973, Journal of molecular biology.

[421]  C. Wilde,et al.  Exchanges between DNA strands in ultraviolet-irradiated Escherichia coli. , 1971, Journal of molecular biology.

[422]  T. Okazaki,et al.  Mechanism of DNA chain growth. IV. Direction of synthesis of T4 short DNA chains as revealed by exonucleolytic degradation. , 1969, Proceedings of the National Academy of Sciences of the United States of America.

[423]  P. Howard-Flanders,et al.  Discontinuities in the DNA synthesized in an excision-defective strain of Escherichia coli following ultraviolet irradiation. , 1968, Journal of molecular biology.

[424]  OUP accepted manuscript , 2021, Nucleic Acids Research.

[425]  H. Pospiech,et al.  In vitro gap-directed translesion DNA synthesis of an abasic site involving human DNA polymerases epsilon , lambda , and beta , 2019 .

[426]  E. Nudler,et al.  A Magic Spot in Genome Maintenance. , 2017, Trends in genetics : TIG.

[427]  H. Seifert,et al.  Antigenic Variation in Bacterial Pathogens , 2016, Microbiology spectrum.

[428]  M. O’Donnell,et al.  A proposal: Source of single strand DNA that elicits the SOS response. , 2013, Frontiers in bioscience.

[429]  M. Cox The Bacterial RecA Protein: Structure, Function, and Regulation , 2006 .

[430]  J. Gulbis,et al.  Crystal structure of the chi:psi sub-assembly of the Escherichia coli DNA polymerase clamp-loader complex. , 2004, European journal of biochemistry.

[431]  N. Van Larebeke,et al.  Endogenous DNA damage in humans: a review of quantitative data. , 2004, Mutagenesis.

[432]  J. Wagner,et al.  Properties and functions of Escherichia coli: Pol IV and Pol V. , 2004, Advances in protein chemistry.

[433]  D. R. McNeill,et al.  Repair mechanisms for oxidative DNA damage. , 2003, Frontiers in bioscience : a journal and virtual library.

[434]  M. Cox,et al.  The bacterial RecA protein and the recombinational DNA repair of stalled replication forks. , 2002, Annual review of biochemistry.

[435]  I. Hickson,et al.  Cellular responses to DNA damage. , 2001, Annual review of pharmacology and toxicology.

[436]  M. Cox,et al.  Recombinational DNA repair in bacteria and the RecA protein. , 1999, Progress in nucleic acid research and molecular biology.

[437]  A. Kuzminov Recombinational repair of DNA damage in Escherichia coli and bacteriophage lambda. , 1999, Microbiology and molecular biology reviews : MMBR.

[438]  M. Cox,et al.  On the mechanism of RecA-mediated repair of double-strand breaks: no role for four-strand DNA pairing intermediates. , 1998, Molecular cell.

[439]  S. West,et al.  Processing of recombination intermediates by the RuvABC proteins. , 1997, Annual review of genetics.

[440]  A. Sancar DNA excision repair. , 1996, Annual review of biochemistry.

[441]  P. Modrich,et al.  Mismatch repair in replication fidelity, genetic recombination, and cancer biology. , 1996, Annual review of biochemistry.

[442]  T. Lohman,et al.  Escherichia coli single-stranded DNA-binding protein: multiple DNA-binding modes and cooperativities. , 1994, Annual review of biochemistry.

[443]  G. Iliakis,et al.  The role of DNA double strand breaks in ionizing radiation-induced killing of eukaryotic cells. , 1991, BioEssays : news and reviews in molecular, cellular and developmental biology.

[444]  S. West,et al.  Molecular mechanism of post-replication repair: formation and resolution of recombination intermediates in vitro. , 1990, Progress in clinical and biological research.

[445]  B. Demple Oxidative DNA damage: repair and inducible cellular responses. , 1990, Progress in clinical and biological research.

[446]  K. Smith,et al.  Role of ruvAB genes in UV- and gamma-radiation and chemical mutagenesis in Escherichia coli. , 1989, Mutation research.

[447]  J. Griffith,et al.  Visualization of SSB-ssDNA complexes active in the assembly of stable RecA-DNA filaments. , 1984, Cold Spring Harbor symposia on quantitative biology.

[448]  P C Hanawalt,et al.  DNA repair in bacteria and mammalian cells. , 1979, Annual review of biochemistry.

[449]  I. Lehman On the role of the recA protein of Escherichia coli in general recombination. , 1979, UCLA forum in medical sciences.

[450]  B. Tye,et al.  Uracil incorporation: a source of pulse-labeled DNA fragments in the replication of the Escherichia coli chromosome. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[451]  B. Tye,et al.  Transient accumulation of Okazaki fragments as a result of uracil incorporation into nascent DNA. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[452]  P. Howard-Flanders Repair by genetic recombination in bacteria: overview. , 1975, Basic life sciences.

[453]  V. Iyer,et al.  Usefulness of benzoylated naphthoylated DEAE-cellulose to distinguish and fractionate double-stranded DNA bearing different extents of single-stranded regions. , 1971, Biochimica et biophysica acta.

[454]  T. Okazaki,et al.  In Vivo Mechanism of DNA Chain Growth , 1968 .

[455]  B. Wilkins,et al.  DNA replication and recombination after UV irradiation. , 1968, Cold Spring Harbor symposia on quantitative biology.