J Courcelle

Summary

Affiliation: Mississippi State University
Country: USA

Publications

  1. ncbi DNA damage-induced replication fork regression and processing in Escherichia coli
    Justin Courcelle
    Department of Biological Sciences, Box GY, Mississippi State University, Mississippi State, MS 39762, USA
    Science 299:1064-7. 2003
  2. ncbi When replication travels on damaged templates: bumps and blocks in the road
    Justin Courcelle
    Department of Biological Sciences, Box GY, Mississippi State University, Mississippi State, MS 39762, USA
    Res Microbiol 155:231-7. 2004
  3. ncbi Comparative gene expression profiles following UV exposure in wild-type and SOS-deficient Escherichia coli
    J Courcelle
    Department of Biochemistry, Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA
    Genetics 158:41-64. 2001
  4. ncbi Therefore, what are recombination proteins there for?
    J Courcelle
    Department of Biological Sciences Mississippi State University, 39762, USA
    Bioessays 23:463-70. 2001
  5. ncbi Participation of recombination proteins in rescue of arrested replication forks in UV-irradiated Escherichia coli need not involve recombination
    J Courcelle
    Department of Biological Sciences, Mississippi State University, P O Box GY, Mississippi State, MS 39762 5759, USA
    Proc Natl Acad Sci U S A 98:8196-202. 2001
  6. ncbi RecA-dependent recovery of arrested DNA replication forks
    Justin Courcelle
    Department of Biological Sciences, Box GY, Mississippi State University, Mississippi State, Mississippi 39762, USA
    Annu Rev Genet 37:611-46. 2003
  7. ncbi RecQ and RecJ process blocked replication forks prior to the resumption of replication in UV-irradiated Escherichia coli
    J Courcelle
    Biological Sciences, Stanford University, CA 94305, USA
    Mol Gen Genet 262:543-51. 1999
  8. ncbi recF and recR are required for the resumption of replication at DNA replication forks in Escherichia coli
    J Courcelle
    Department of Biological Sciences, Stanford University, CA 94305 5020, USA
    Proc Natl Acad Sci U S A 94:3714-9. 1997
  9. ncbi Recovery of DNA replication in UV-irradiated Escherichia coli requires both excision repair and recF protein function
    J Courcelle
    Department of Biological Sciences, Stanford University, Stanford, California 94305, USA
    J Bacteriol 181:916-22. 1999
  10. ncbi Requirement for uracil-DNA glycosylase during the transition to late-phase cytomegalovirus DNA replication
    C T Courcelle
    Department of Microbiology and Immunology, Stanford University, Stanford, California 94305, USA
    J Virol 75:7592-601. 2001

Collaborators

Detail Information

Publications20

  1. ncbi DNA damage-induced replication fork regression and processing in Escherichia coli
    Justin Courcelle
    Department of Biological Sciences, Box GY, Mississippi State University, Mississippi State, MS 39762, USA
    Science 299:1064-7. 2003
    ..We propose that fork regression allows repair enzymes to gain access to the replication-blocking lesion, allowing processive replication to resume once the blocking lesion is removed...
  2. ncbi When replication travels on damaged templates: bumps and blocks in the road
    Justin Courcelle
    Department of Biological Sciences, Box GY, Mississippi State University, Mississippi State, MS 39762, USA
    Res Microbiol 155:231-7. 2004
    ....
  3. ncbi Comparative gene expression profiles following UV exposure in wild-type and SOS-deficient Escherichia coli
    J Courcelle
    Department of Biochemistry, Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA
    Genetics 158:41-64. 2001
    ..These newly identified UV-responsive genes are discussed with respect to their possible roles in cellular recovery following exposure to UV irradiation...
  4. ncbi Therefore, what are recombination proteins there for?
    J Courcelle
    Department of Biological Sciences Mississippi State University, 39762, USA
    Bioessays 23:463-70. 2001
    ....
  5. ncbi Participation of recombination proteins in rescue of arrested replication forks in UV-irradiated Escherichia coli need not involve recombination
    J Courcelle
    Department of Biological Sciences, Mississippi State University, P O Box GY, Mississippi State, MS 39762 5759, USA
    Proc Natl Acad Sci U S A 98:8196-202. 2001
    ....
  6. ncbi RecA-dependent recovery of arrested DNA replication forks
    Justin Courcelle
    Department of Biological Sciences, Box GY, Mississippi State University, Mississippi State, Mississippi 39762, USA
    Annu Rev Genet 37:611-46. 2003
    ..In this review, we examine the significant experimental approaches that have led to our current understanding of the RecA-mediated processes that restore replication following encounters with DNA damage...
  7. ncbi RecQ and RecJ process blocked replication forks prior to the resumption of replication in UV-irradiated Escherichia coli
    J Courcelle
    Biological Sciences, Stanford University, CA 94305, USA
    Mol Gen Genet 262:543-51. 1999
    ....
  8. ncbi recF and recR are required for the resumption of replication at DNA replication forks in Escherichia coli
    J Courcelle
    Department of Biological Sciences, Stanford University, CA 94305 5020, USA
    Proc Natl Acad Sci U S A 94:3714-9. 1997
    ..Current biochemical and genetic data on the conditions under which recF-mediated recombination occurs suggest that the recombinational intermediate also may mimic the structure of a disrupted replication fork...
  9. ncbi Recovery of DNA replication in UV-irradiated Escherichia coli requires both excision repair and recF protein function
    J Courcelle
    Department of Biological Sciences, Stanford University, Stanford, California 94305, USA
    J Bacteriol 181:916-22. 1999
    ....
  10. ncbi Requirement for uracil-DNA glycosylase during the transition to late-phase cytomegalovirus DNA replication
    C T Courcelle
    Department of Microbiology and Immunology, Stanford University, Stanford, California 94305, USA
    J Virol 75:7592-601. 2001
    ..The process of uracil incorporation and excision may introduce strand breaks to facilitate the transition from early-phase replication to late-phase amplification...
  11. ncbi Inactivation of the DnaB helicase leads to the collapse and degradation of the replication fork: a comparison to UV-induced arrest
    Jerilyn J Belle
    Department of Biological Sciences, Mississippi State University, Mississippi State, Mississippi 39762, USA
    J Bacteriol 189:5452-62. 2007
    ..We discuss these observations in relation to potential models for both UV-induced and DnaB(Ts)-mediated replication inhibition...
  12. ncbi Structural conservation of RecF and Rad50: implications for DNA recognition and RecF function
    Olga Koroleva
    Edward A Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, St Louis, MO 63104, USA
    EMBO J 26:867-77. 2007
    ..The RecF structure, mutagenesis of conserved motifs and ATP-dependent dimerization of RecF are discussed with respect to its role in promoting presynaptic complex formation at DNA damage sites...
  13. ncbi RuvABC is required to resolve holliday junctions that accumulate following replication on damaged templates in Escherichia coli
    Janet R Donaldson
    Department of Biology, Portland State University, Portland, Oregon 97207, USA
    J Biol Chem 281:28811-21. 2006
    ..A model is proposed in which RuvABC is required to resolve junctions that arise during the repair of a subset of nonarresting lesions after replication has passed through the template...
  14. ncbi Monitoring DNA replication following UV-induced damage in Escherichia coli
    Charmain T Courcelle
    Department of Biology, Portland State University, Oregon, USA
    Methods Enzymol 409:425-41. 2006
    ..This chapter describes three techniques that can be used to monitor the progression, degradation, and structural properties of replication forks following UV-induced DNA damage in Escherichia coli...
  15. ncbi Nascent DNA processing by RecJ favors lesion repair over translesion synthesis at arrested replication forks in Escherichia coli
    Charmain T Courcelle
    Department of Biology, Portland State University, Box 751, Portland, OR 97207 0751, USA
    Proc Natl Acad Sci U S A 103:9154-9. 2006
    ..In the absence of nascent DNA processing, polymerase V can synthesize past the lesion to prevent lethality, although this occurs with slower kinetics and a higher frequency of mutagenesis...
  16. ncbi Nucleotide excision repair or polymerase V-mediated lesion bypass can act to restore UV-arrested replication forks in Escherichia coli
    Charmain T Courcelle
    Department of Biology, P O Box 751, Portland State University, Portland, OR 97207 0751, USA
    J Bacteriol 187:6953-61. 2005
    ..We discuss a model in which cells first use DNA repair to process replication-arresting UV lesions before resorting to mutagenic pathways such as translesion DNA synthesis to bypass these impediments to replication progression...
  17. ncbi Recs preventing wrecks
    Justin Courcelle
    Portland State University, Department of Biology, P O Box 751, Portland, OR 97207 0751, USA
    Mutat Res 577:217-27. 2005
    ....
  18. ncbi RuvAB and RecG are not essential for the recovery of DNA synthesis following UV-induced DNA damage in Escherichia coli
    Janet R Donaldson
    Department of Biological Sciences, Mississippi State University, Mississippi State, Mississippi 39762, USA
    Genetics 166:1631-40. 2004
    ..The data presented here indicate that RecG- or RuvAB-catalyzed fork regression is not essential for DNA synthesis to resume following arrest by UV-induced DNA damage in vivo...
  19. ncbi RecO acts with RecF and RecR to protect and maintain replication forks blocked by UV-induced DNA damage in Escherichia coli
    Kin Hoe Chow
    Department of Biological Science, Mississippi State University, Mississippi State, Mississippi 39762, USA
    J Biol Chem 279:3492-6. 2004
    ....
  20. ncbi RecBCD and RecJ/RecQ initiate DNA degradation on distinct substrates in UV-irradiated Escherichia coli
    Kin Hoe Chow
    Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah 84112, USA
    Radiat Res 168:499-506. 2007
    ..In addition, they demonstrate that RecBCD initiates degradation at a site(s) other than the arrested replication fork directly...