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. 1991 Dec;129(4):1007–1020. doi: 10.1093/genetics/129.4.1007

Recombinagenic Processing of Uv-Light Photoproducts in Nonreplicating Phage DNA by the Escherichia Coli Methyl-Directed Mismatch Repair System

W Y Feng 1, E Lee 1, J B Hays 1
PMCID: PMC1204766  PMID: 1838344

Abstract

Nonreplicating λ phage DNA in homoimmune Escherichia coli lysogens provides a useful model system for study of processes that activate DNA for homologous recombination. We measured recombination by extracting phage DNA from infected cells, using it to transfect recA recipient cells, and scoring the frequency of recombinant infective centers. With unirradiated phage, recombinant frequencies were less than 0.1%. However, recombination could be increased over 300-fold by prior UV irradiation of the phages. The dependence of recombination on UvrA function varied greatly with UV dose. With phage irradiated to 20 J/m(2), recombinant frequencies in repressed infections of uvr(+) bacteria were one-fifth those in uvrA infections; with phages irradiated to 100 J/m(2), frequencies in uvr(+) infections were thirty times higher than in uvrA infections. Most UV-stimulated recombination in uvrA infections appeared to depend on the bacterial methyl-directed mismatch-repair system: frequencies were depressed 5-20-fold in uvrA bacteria also lacking MutH, MutL or MutS functions, and recombinant frequencies decreased with increasing GATC-adenine methylation of phage stocks. The biological activity of nonreplicating UV-irradiated phage DNA declined with time after infection of uvrA cells; this decline was photoproduct-dependent, more marked for undermethylated than overmethylated phage DNA, and depended on host MutHLS functions. In uvr(+) bacteria, where the UvrABC system provided an alternative, apparently less efficient, route to recombinagenic DNA, UV-stimulated recombinant frequencies were about twice as high in mutH or mutLS as in mut(+) cells, in agreement with hyper-rec mut effects previously described by others.

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Selected References

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  1. Bachmann B. J. Pedigrees of some mutant strains of Escherichia coli K-12. Bacteriol Rev. 1972 Dec;36(4):525–557. doi: 10.1128/br.36.4.525-557.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Becker A., Gold M. Isolation of the bacteriophage lambda A-gene protein. Proc Natl Acad Sci U S A. 1975 Feb;72(2):581–585. doi: 10.1073/pnas.72.2.581. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Biek D. P., Cohen S. N. Identification and characterization of recD, a gene affecting plasmid maintenance and recombination in Escherichia coli. J Bacteriol. 1986 Aug;167(2):594–603. doi: 10.1128/jb.167.2.594-603.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Connolly B., West S. C. Genetic recombination in Escherichia coli: Holliday junctions made by RecA protein are resolved by fractionated cell-free extracts. Proc Natl Acad Sci U S A. 1990 Nov;87(21):8476–8480. doi: 10.1073/pnas.87.21.8476. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cunningham R. P., Wu A. M., Shibata T., DasGupta C., Radding C. M. Homologous pairing and topological linkage of DNA molecules by combined action of E. coli RecA protein and topoisomerase I. Cell. 1981 Apr;24(1):213–223. doi: 10.1016/0092-8674(81)90517-1. [DOI] [PubMed] [Google Scholar]
  6. Dohet C., Wagner R., Radman M. Repair of defined single base-pair mismatches in Escherichia coli. Proc Natl Acad Sci U S A. 1985 Jan;82(2):503–505. doi: 10.1073/pnas.82.2.503. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Doutriaux M. P., Wagner R., Radman M. Mismatch-stimulated killing. Proc Natl Acad Sci U S A. 1986 Apr;83(8):2576–2578. doi: 10.1073/pnas.83.8.2576. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Fishel R. A., Siegel E. C., Kolodner R. Gene conversion in Escherichia coli. Resolution of heteroallelic mismatched nucleotides by co-repair. J Mol Biol. 1986 Mar 20;188(2):147–157. doi: 10.1016/0022-2836(86)90300-1. [DOI] [PubMed] [Google Scholar]
  9. Franklin W. A., Lo K. M., Haseltine W. A. Alkaline lability of fluorescent photoproducts produced in ultraviolet light-irradiated DNA. J Biol Chem. 1982 Nov 25;257(22):13535–13543. [PubMed] [Google Scholar]
  10. HOWARD-FLANDERS P., THERIOT L. A method for selecting radiation-sensitive mutants of Escherichia coli. Genetics. 1962 Sep;47:1219–1224. doi: 10.1093/genetics/47.9.1219. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Hays J. B., Boehmer S. Antagonists of DNA gyrase inhibit repair and recombination of UV-irradiated phage lambda. Proc Natl Acad Sci U S A. 1978 Sep;75(9):4125–4129. doi: 10.1073/pnas.75.9.4125. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hays J. B., Duncan B. K., Boehmer S. Recombination of uracil-containing lambda bacteriophages. J Bacteriol. 1981 Jan;145(1):306–320. doi: 10.1128/jb.145.1.306-320.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hays J. B., Lee E. Repair and recombination of nonreplicating UV-irradiated phage DNA in E. coli III. Enhancement of excision repair in UV-treated bacteria. Mol Gen Genet. 1985;201(3):402–408. doi: 10.1007/BF00331330. [DOI] [PubMed] [Google Scholar]
  14. Hays J. B., Martin S. J., Bhatia K. Repair of nonreplicating UV-irradiated DNA: cooperative dark repair by Escherichia coli uvr and phr functions. J Bacteriol. 1985 Feb;161(2):602–608. doi: 10.1128/jb.161.2.602-608.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Herman G. E., Modrich P. Escherichia coli dam methylase. Physical and catalytic properties of the homogeneous enzyme. J Biol Chem. 1982 Mar 10;257(5):2605–2612. [PubMed] [Google Scholar]
  16. Holmes J., Jr, Clark S., Modrich P. Strand-specific mismatch correction in nuclear extracts of human and Drosophila melanogaster cell lines. Proc Natl Acad Sci U S A. 1990 Aug;87(15):5837–5841. doi: 10.1073/pnas.87.15.5837. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Hutchinson F., Yamamoto K., Stein J., Wood R. D. Effect of photoreactivation on mutagenesis of lambda phage by ultraviolet light. J Mol Biol. 1988 Aug 5;202(3):593–601. doi: 10.1016/0022-2836(88)90289-6. [DOI] [PubMed] [Google Scholar]
  18. Jones M., Wagner R., Radman M. Repair of a mismatch is influenced by the base composition of the surrounding nucleotide sequence. Genetics. 1987 Apr;115(4):605–610. doi: 10.1093/genetics/115.4.605. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Kobayashi I., Ikeda H. Formation of recombinant DNA of bacteriophage lambda by recA function of Escherichia coli without duplication, transcription, translation, and maturation. Mol Gen Genet. 1977 Jun 24;153(3):237–245. doi: 10.1007/BF00431589. [DOI] [PubMed] [Google Scholar]
  20. Konforti B. B., Davis R. W. DNA substrate requirements for stable joint molecule formation by the RecA and single-stranded DNA-binding proteins of Escherichia coli. J Biol Chem. 1991 Jun 5;266(16):10112–10121. [PubMed] [Google Scholar]
  21. Konrad E. B. Method for the isolation of Escherichia coli mutants with enhanced recombination between chromosomal duplications. J Bacteriol. 1977 Apr;130(1):167–172. doi: 10.1128/jb.130.1.167-172.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Korba B. E., Hays J. B. Novel mutants of Escherichia coli that produce recombinogenic lesions in DNA. II. Properties of recombinogenic lambda phages grown on bacteria carrying arl mutations. J Mol Biol. 1980 May 25;139(3):473–489. doi: 10.1016/0022-2836(80)90142-4. [DOI] [PubMed] [Google Scholar]
  23. Lacks S. A., Dunn J. J., Greenberg B. Identification of base mismatches recognized by the heteroduplex-DNA-repair system of Streptococcus pneumoniae. Cell. 1982 Dec;31(2 Pt 1):327–336. doi: 10.1016/0092-8674(82)90126-x. [DOI] [PubMed] [Google Scholar]
  24. Lahue R. S., Au K. G., Modrich P. DNA mismatch correction in a defined system. Science. 1989 Jul 14;245(4914):160–164. doi: 10.1126/science.2665076. [DOI] [PubMed] [Google Scholar]
  25. Lahue R. S., Su S. S., Modrich P. Requirement for d(GATC) sequences in Escherichia coli mutHLS mismatch correction. Proc Natl Acad Sci U S A. 1987 Mar;84(6):1482–1486. doi: 10.1073/pnas.84.6.1482. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Lu A. L., Clark S., Modrich P. Methyl-directed repair of DNA base-pair mismatches in vitro. Proc Natl Acad Sci U S A. 1983 Aug;80(15):4639–4643. doi: 10.1073/pnas.80.15.4639. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Lu C., Scheuermann R. H., Echols H. Capacity of RecA protein to bind preferentially to UV lesions and inhibit the editing subunit (epsilon) of DNA polymerase III: a possible mechanism for SOS-induced targeted mutagenesis. Proc Natl Acad Sci U S A. 1986 Feb;83(3):619–623. doi: 10.1073/pnas.83.3.619. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Luisi-DeLuca C., Lovett S. T., Kolodner R. D. Genetic and physical analysis of plasmid recombination in recB recC sbcB and recB recC sbcA Escherichia coli K-12 mutants. Genetics. 1989 Jun;122(2):269–278. doi: 10.1093/genetics/122.2.269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Marinus M. G., Carraway M., Frey A. Z., Brown L., Arraj J. A. Insertion mutations in the dam gene of Escherichia coli K-12. Mol Gen Genet. 1983;192(1-2):288–289. doi: 10.1007/BF00327681. [DOI] [PubMed] [Google Scholar]
  30. McGraw B. R., Marinus M. G. Isolation and characterization of Dam+ revertants and suppressor mutations that modify secondary phenotypes of dam-3 strains of Escherichia coli K-12. Mol Gen Genet. 1980;178(2):309–315. doi: 10.1007/BF00270477. [DOI] [PubMed] [Google Scholar]
  31. McMilin K. D., Stahl M. M., Stahl F. W. Rec-mediated recombinational hot spot activity in bacteriophage lambda. I. Hot spot activity associated with spi-deletions and bio substitutions. Genetics. 1974 Jul;77(3):409–423. doi: 10.1093/genetics/77.3.409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Meistrich M. L., Lamola A. A. Triplet-state sensitization of thymine photodimerization in bacteriophage T4. J Mol Biol. 1972 Apr 28;66(1):83–95. doi: 10.1016/s0022-2836(72)80007-x. [DOI] [PubMed] [Google Scholar]
  33. Michaelis S., Guarente L., Beckwith J. In vitro construction and characterization of phoA-lacZ gene fusions in Escherichia coli. J Bacteriol. 1983 Apr;154(1):356–365. doi: 10.1128/jb.154.1.356-365.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Mitchell D. L. The relative cytotoxicity of (6-4) photoproducts and cyclobutane dimers in mammalian cells. Photochem Photobiol. 1988 Jul;48(1):51–57. doi: 10.1111/j.1751-1097.1988.tb02785.x. [DOI] [PubMed] [Google Scholar]
  35. Pearlman D. A., Holbrook S. R., Pirkle D. H., Kim S. H. Molecular models for DNA damaged by photoreaction. Science. 1985 Mar 15;227(4692):1304–1308. doi: 10.1126/science.3975615. [DOI] [PubMed] [Google Scholar]
  36. Porter R. D., McLaughlin T., Low B. Transduction versus "conjuduction": evidence for multiple roles for exonuclease V in genetic recombination in Escherichia coli. Cold Spring Harb Symp Quant Biol. 1979;43(Pt 2):1043–1047. doi: 10.1101/sqb.1979.043.01.113. [DOI] [PubMed] [Google Scholar]
  37. Rayssiguier C., Thaler D. S., Radman M. The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants. Nature. 1989 Nov 23;342(6248):396–401. doi: 10.1038/342396a0. [DOI] [PubMed] [Google Scholar]
  38. SUSSMAN R., JACOB F. [On a thermosensitive repression system in the Escherichia coli lambda bacteriophage]. C R Hebd Seances Acad Sci. 1962 Feb 19;254:1517–1519. [PubMed] [Google Scholar]
  39. Schellhorn H. E., Low K. B. Indirect stimulation of recombination in Escherichia coli K-12: dependence on recJ, uvrA, and uvrD. J Bacteriol. 1991 Oct;173(19):6192–6198. doi: 10.1128/jb.173.19.6192-6198.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Smith T. A., Hays J. B. Repair and recombination of nonreplicating UV-irradiated phage DNA in E. coli II. Stimulation of RecF-dependent recombination by excision repair of cyclobutane pyrimidine dimers and of other photoproducts. Mol Gen Genet. 1985;201(3):393–401. doi: 10.1007/BF00331329. [DOI] [PubMed] [Google Scholar]
  41. Su S. S., Grilley M., Thresher R., Griffith J., Modrich P. Gap formation is associated with methyl-directed mismatch correction under conditions of restricted DNA synthesis. Genome. 1989;31(1):104–111. doi: 10.1139/g89-020. [DOI] [PubMed] [Google Scholar]
  42. Tsujimura T., Maher V. M., Godwin A. R., Liskay R. M., McCormick J. J. Frequency of intrachromosomal homologous recombination induced by UV radiation in normally repairing and excision repair-deficient human cells. Proc Natl Acad Sci U S A. 1990 Feb;87(4):1566–1570. doi: 10.1073/pnas.87.4.1566. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. WOLF B., MESELSON M. REPRESSION OF THE REPLICATION OF SUPERINFECTING BACTERIOPHAGE DNA IN IMMUNE CELLS. J Mol Biol. 1963 Dec;7:636–644. doi: 10.1016/s0022-2836(63)80110-2. [DOI] [PubMed] [Google Scholar]
  44. Yanisch-Perron C., Vieira J., Messing J. Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. Gene. 1985;33(1):103–119. doi: 10.1016/0378-1119(85)90120-9. [DOI] [PubMed] [Google Scholar]
  45. Zagursky R. J., Hays J. B. Expression of the phage lambda recombination genes exo and bet under lacPO control on a multi-copy plasmid. Gene. 1983 Sep;23(3):277–292. doi: 10.1016/0378-1119(83)90018-5. [DOI] [PubMed] [Google Scholar]
  46. Zieg J., Maples V. F., Kushner S. R. Recombinant levels of Escherichia coli K-12 mutants deficient in various replication, recombination, or repair genes. J Bacteriol. 1978 Jun;134(3):958–966. doi: 10.1128/jb.134.3.958-966.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]

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