RuvABC-dependent double-strand breaks in dnaBts mutants require RecA

Molecular Microbiology

Volumn 38, Issue 3, 2000, Pages 565-574

  Seigneur, M ^a   Ehrlich, S D ^a   Michel, B ^a  

^a CEMAGREF   (France)

Author keywords

[No Author keywords available]

Indexed keywords

HELICASE; RECA PROTEIN; RESOLVASE;

ARTICLE; DNA STRAND BREAKAGE; ENZYME ACTIVITY; ESCHERICHIA COLI; GENETIC RECOMBINATION; HOLLIDAY JUNCTION; NONHUMAN; PRIORITY JOURNAL; SOS CHROMOTEST;

BACTERIAL PROTEINS; DNA DAMAGE; DNA HELICASES; DNA REPAIR; DNA REPLICATION; DNA, BACTERIAL; DNA-BINDING PROTEINS; DNAB HELICASES; ELECTROPHORESIS, POLYACRYLAMIDE GEL; ENDODEOXYRIBONUCLEASES; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; MUTATION; REC A RECOMBINASES; RECOMBINATION, GENETIC; SOS RESPONSE (GENETICS);

EID: 0033710452     PISSN: 0950382X     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2958.2000.02152.x     Document Type: Article

References (47)

1. Unraveling a region-specific hyper-recombination phenomenon: Genetic control and modalities of terminal recombination in Escherichia coli
2. RecQ and RecJ process blocked replication forks prior to the resumption of replication in UV-irradiated Escherichia coli
3. recF and recR are required for the resumption of replication at DNA replication forks in Escherichia coli
4. The importance of repairing stalled forks
5. Elimination of replication block protein Fob1 extends the life span of yeast mother cells
6. The chi psi subunits of DNA polymerase III holoenzyme bind to single-stranded DNA-binding protein (SSB) and facilitate replication of an SSB-coated template
7. DNA recombination: The replication connection
8. Initiation of bidirectional replication at the chromosomal origin is directed by the interaction between helicase and primase
9. Double-strand break repair in yeast requires both leading and lagging strand DNA polymerases
10. The phi X174-type primosome promotes replisome assembly at the site of recombination in bacteriophage Mu transposition
11. Duplex opening by primosome protein PriA for replisome assembly on a recombination intermediate
12. Devoted to the lagging strand - The chi subunit of DNA polymerase III holoenzyme contacts SSB to promote processive elongation and sliding clamp assembly
13. Mechanism of transient inhibition of DNA synthesis in ultraviolet- Irradiated E. coli: Inhibition is independent of recA whilst recovery requires RecA protein itself and an additional, inducible SOS function
14. Coupling of a replicative polymerase and helicase: A tau-DnaB interaction mediates rapid replication fork movement
15. Expansion and contraction of ribosomal DNA repeats in Saccharomyces cerevisiae: Requirement of replication fork blocking (Fob1) protein and the role of RNA polymerase I
16. Stable DNA replication: Interplay between DNA replication, homologous recombination, and transcription
17. The DNA replication priming protein, PriA, is required for homologous recombination and double-strand break repair
18. Biochemistry of homologous recombination in Escherichia coli
19. Double-strand end repair via the RecBC pathway in Escherichia coli primes DNA replication
20. The rep mutation. IV. Slower movement of replication forks in Escherichia coli rep strains
21. Replication fork assembly at recombination intermediates is required for bacterial growth
22. Homologous recombination
23. Modulation of RNA polymerase by (p)ppGpp reveals a RecG-dependent mechanism for replication fork progression
24. Properties of a mutant recA-encoded protein reveal a possible role for Escherichia coli recF-encoded protein in genetic recombination
25. Holliday junction resolvases encoded by homologous rusA genes in Escherichia coli K-12 and phage 82
26. Resolution of holliday intermediates in recombination and DNA repair - Indirect suppression of ruvA, ruvB, and ruvC mutations
27. DNA helicases - Enzymes with essential roles in all aspects of DNA metabolism
28. Replication fork arrest and DNA recombination
29. DNA doublestrand breaks caused by replication arrest
30. Double-strand-break repair recombination in Escherichia coli: Physical evidence for a DNA replication mechanism in vivo
31. Use of bacteriophage lambda recombination functions to promote gene replacement in Escherichia coli
32. Hyper-recombination and Bloom's syndrome: Microbes again provide clues about cancer
33. Replication fork pausing and recombination or 'gimme a break'
34. Biochemical characterization of Escherichia coli temperature-sensitive dnaB mutants dnaBS, dnaB252, dnaB70, dnaB43, and dnaB454
35. Role of PriA in replication fork reactivation in Escherichia coli
36. Differential suppression of priA2::kan phenotypes in Escherichia coli K-12 by mutations in priA, lexA, and dnaC
37. Tandem repeat recombination induced by replication fork defects in Escherichia coli requires a novel factor, RadC
38. RuvAB acts at arrested replication forks
39. UmuD'(2)C is an errorprone DNA polymerase, Escherichia coli pol V
40. Identification of a domain of Escherichia coli primase required for functional interaction with the DnaB helicase at the replication fork
41. Biochemical interaction of the Escherichia coli RecF, RecO, and RecR proteins with RecA protein and single-stranded DNA binding protein
42. Lethality of rep recB and rep recC double mutants of Escherichia coli
43. The SOS response of Escherichia coli
44. Processing of recombination intermediates by the RuvABC proteins
45. Trading places on DNA-A three-point switch underlies primer handoff from primase to the replicative DNA polymerase
46. Holliday junctions accumulate in replication mutants via a RecA homolog-independent mechanism