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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1974 Jan;71(1):144–147. doi: 10.1073/pnas.71.1.144

Indirect Ultraviolet-Reactivation of Phage λ

Jacqueline George 1,*, Raymond Devoret 1, Miroslav Radman 1,
PMCID: PMC387953  PMID: 4589889

Abstract

When an F- recipient Escherichia coli K12 bacterium receives Hfr or F-lac+ DNA from an ultraviolet-irradiated donor, its capacity to promote DNA repair and mutagenesis of ultraviolet-damaged phage λ is substantially increased.

We call this phenomenon indirect ultraviolet-reactivation, since its features are essentially the same as those of ultraviolet-reactivation; this repair process occurs in pyrimidine dimer excision-deficient strains and produces clear plaque mutations of the restored phage. Moreover, this process is similar to indirect ultraviolet-induction of prophage λ, since it is promoted by conjugation. However, contrarily to indirect induction, it is produced by Hfr donors and occurs in recipients restricting the incoming ultraviolet-damaged donor DNA.

The occurrence of indirect ultraviolet-reactivation provides evidence for the existence in E. coli of an inducible error-prone mechanism for the repair of DNA.

Keywords: mutagenesis, repair of DNA, bacterial conjugation, Escherichia coli

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Blanco M., Devoret R. Repair mechanisms involved in prophage reactivation and UV reactivation of UV-irradiated phage lambda. Mutat Res. 1973 Mar;17(3):293–305. doi: 10.1016/0027-5107(73)90001-8. [DOI] [PubMed] [Google Scholar]
  2. Borek E., Ryan A. THE TRANSFER OF IRRADIATION-ELICITED INDUCTION IN A LYSOGENIC ORGANISM. Proc Natl Acad Sci U S A. 1958 May;44(5):374–377. doi: 10.1073/pnas.44.5.374. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Boyle J. M., Setlow R. B. Correlations between host-cell reactivation, ultraviolet reactivation and pyrimidine dimer excision in the DNA of bacteriophage lambda. J Mol Biol. 1970 Jul 14;51(1):131–144. doi: 10.1016/0022-2836(70)90275-5. [DOI] [PubMed] [Google Scholar]
  4. Brooks K., Clark A. J. Behavior of lambda bacteriophage in a recombination deficienct strain of Escherichia coli. J Virol. 1967 Apr;1(2):283–293. doi: 10.1128/jvi.1.2.283-293.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Castellazzi M., George J., Buttin G. Prophage induction and cell division in E. coli. I. Further characterization of the thermosensitive mutation tif-1 whose expression mimics the effect of UV irradiation. Mol Gen Genet. 1972;119(2):139–152. doi: 10.1007/BF00269133. [DOI] [PubMed] [Google Scholar]
  6. Defais M., Fauquet P., Radman M., Errera M. Ultraviolet reactivation and ultraviolet mutagenesis of lambda in different genetic systems. Virology. 1971 Feb;43(2):495–503. doi: 10.1016/0042-6822(71)90321-7. [DOI] [PubMed] [Google Scholar]
  7. Demerec M., Adelberg E. A., Clark A. J., Hartman P. E. A proposal for a uniform nomenclature in bacterial genetics. Genetics. 1966 Jul;54(1):61–76. doi: 10.1093/genetics/54.1.61. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Devoret R., George J. Induction indirecte du prophage lambda par le rayonnement ultraviolet. Mutat Res. 1967 Nov-Dec;4(6):713–734. doi: 10.1016/0027-5107(67)90081-4. [DOI] [PubMed] [Google Scholar]
  9. Donch J., Greenberg J., Green M. H. Repression of induction by U.V. of lambda phage by exrA mutations in Escherichia coli. Genet Res. 1970 Feb;15(1):87–97. doi: 10.1017/s0016672300001397. [DOI] [PubMed] [Google Scholar]
  10. George J. Corrélation entre la disparition de l'induction indirecte du prophage lambda et la restriction du DNA transmis à la bactérie réceptrice inductible dans un croisement F+ XFhétérospécifique. C R Acad Sci Hebd Seances Acad Sci D. 1966 Apr 18;262(16):1805–1808. [PubMed] [Google Scholar]
  11. George J., Devoret R. Conjugal transfer of UV-damaged F-prime sex factors and indirect induction of prophage- . Mol Gen Genet. 1971;111(2):103–119. doi: 10.1007/BF00267786. [DOI] [PubMed] [Google Scholar]
  12. Harm W. Comment on the relationship between UV reactivation and host-cell reactivation in phage. Virology. 1966 Jul;29(3):494–494. doi: 10.1016/0042-6822(66)90226-1. [DOI] [PubMed] [Google Scholar]
  13. Hart M. G., Ellison J. Ultraviolet reactivation in bacteriophage lambda. J Gen Virol. 1970 Sep;8(3):197–208. doi: 10.1099/0022-1317-8-3-197. [DOI] [PubMed] [Google Scholar]
  14. Hertman I., Luria S. E. Transduction studies on the role of a rec+ gene in the ultraviolet induction of prophage lambda. J Mol Biol. 1967 Jan 28;23(2):117–133. doi: 10.1016/s0022-2836(67)80021-4. [DOI] [PubMed] [Google Scholar]
  15. Howard-Flanders P., Boyce R. P. DNA repair and genetic recombination: studies on mutants of Escherichia coli defective in these processes. Radiat Res. 1966;(Suppl):156+–156+. [PubMed] [Google Scholar]
  16. KELLENBERGER G., WEIGLE J. Etude au moyen des rayons ultraviolets de l'interaction entre bactériophage tempéré et bactérie hote. Biochim Biophys Acta. 1958 Oct;30(1):112–124. doi: 10.1016/0006-3002(58)90247-6. [DOI] [PubMed] [Google Scholar]
  17. KONDO E., MITSUHASHI S. DRUG RESISTANCE OF ENTERIC BACTERIA. IV. ACTIVE TRANSDUCING BACTERIOPHAGE P1 CM PRODUCED BY THE COMBINATION OF R FACTOR WITH BACTERIOPHAGE P1. J Bacteriol. 1964 Nov;88:1266–1276. doi: 10.1128/jb.88.5.1266-1276.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kirby E. P., Jacob F., Goldthwait D. A. Prophage induction and filament formation in a mutant strain of Escherichia coli. Proc Natl Acad Sci U S A. 1967 Nov;58(5):1903–1910. doi: 10.1073/pnas.58.5.1903. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Kneser H. Relationship between K-reactivation and UV-reactivation of bacteriophage lambda. Virology. 1968 Oct;36(2):303–305. doi: 10.1016/0042-6822(68)90148-7. [DOI] [PubMed] [Google Scholar]
  20. Miura A., Tomizawa J. I. Studies on radiation-sensitive mutants of E. coli. 3. Participation of the rec system in induction of mutation by ultraviolet irradiation. Mol Gen Genet. 1968;103(1):1–10. doi: 10.1007/BF00271151. [DOI] [PubMed] [Google Scholar]
  21. Monk M. Induction of phage lambda by transferred irradiated colI DNA. Mol Gen Genet. 1969;106(1):14–24. doi: 10.1007/BF00332817. [DOI] [PubMed] [Google Scholar]
  22. Ogawa H., Tomizawa J. I. Ultraviolet reactivation of lambda phage: assay of infectivity of DNA molecules by spheroplast transfection. J Mol Biol. 1973 Feb 5;73(4):397–406. doi: 10.1016/0022-2836(73)90089-2. [DOI] [PubMed] [Google Scholar]
  23. Radman M., Devoret R. UV-reactivation of bacteriophage lambda in excision repair-deficient hosts: independence of red functions and attachment regions. Virology. 1971 Feb;43(2):504–506. doi: 10.1016/0042-6822(71)90322-9. [DOI] [PubMed] [Google Scholar]
  24. Rosner J. L., Kass L. R., Yarmolinsky M. B. Parallel behavior of F and Pl in causing indirect induction of lysogenic bacteria. Cold Spring Harb Symp Quant Biol. 1968;33:785–789. doi: 10.1101/sqb.1968.033.01.090. [DOI] [PubMed] [Google Scholar]
  25. Rupp W. D., Wilde C. E., 3rd, Reno D. L., Howard-Flanders P. Exchanges between DNA strands in ultraviolet-irradiated Escherichia coli. J Mol Biol. 1971 Oct 14;61(1):25–44. doi: 10.1016/0022-2836(71)90204-x. [DOI] [PubMed] [Google Scholar]
  26. Weigle J. J. Induction of Mutations in a Bacterial Virus. Proc Natl Acad Sci U S A. 1953 Jul;39(7):628–636. doi: 10.1073/pnas.39.7.628. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Witkin E. M. The mutability toward ultraviolet light of recombination-deficient strains of Escherichia coli. Mutat Res. 1969 Jul-Aug;8(1):9–14. doi: 10.1016/0027-5107(69)90135-3. [DOI] [PubMed] [Google Scholar]

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