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Indirect ultraviolet induction and curing in E. coli cells lysogenic for bacteriophage λ

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Summary

Indirect ultraviolet induction of prophage λ occurs when lysogenic E. coli K12 cells are mated with ultraviolet-irradiated donor strains carrying a transmissible episome such as F lac +. Indirect induction occurs in wild type, uvrA, or recB recipient lysogens, but not in recA lysogens. When nonpermissive lysogens carrying prophages λ susO or λ susP are similarly mated, the defective prophages are induced and indirect curing takes place.

Although indirect induction is independent of the capacity of the lysogen for repair by pyrimidine dimer excision, indirect curing (and hence indirect induction) is subject to photoreactivation when the recipient lysogen is exposed to visible light after mating. This confirms that the structure initiating indirect ultraviolet induction is a damaged transferred episome consisting of one DNA strand containing ultraviolet photoproducts and a newly synthesized discontinuous DNA strand such that pyrimidine dimers remain in single-stranded regions.

F- lac + recombinants are formed in either nonlysogenic or lysogenic Lac- cells receiving damaged F lac + episomes from ultraviolet irradiated F lac + donors. λ prophage induction occurs more frequently in zygotes that form Lac+ recombinants than in zygotes that remain Lac-. In contrast, cells receiving intact (undamaged) episomes are converted to F lac + secondary donors, but are rarely induced or cured.

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References

  • Adelberg, E. A., Burns, S. N.: Genetic variation in the sex factor of Escherichia coli. J. Bact. 79, 321–330 (1960).

    Google Scholar 

  • Borek, E., Ryan, A.: The transfer of irradiation-elicited induction in a lysogenic organism. Proc. nat. Acad. Sci. (Wash.) 44, 374–377 (1958).

    Google Scholar 

  • Borek, E., Ryan, A.: The transfer of a biologically active irradiation product from cell to cell. Biochim. biophys. Acta (Amst.) 41, 67–73 (1960).

    Google Scholar 

  • Brooks, K., Clark, A. J.: Behavior of λ bacteriophage in a recombination deficient strain of Escherichia coli. J. Virol. 1, 283–293 (1967).

    Google Scholar 

  • Campbell, A.: Sensitive mutants of bacteriophage λ. Virology 14, 22–32 (1961).

    Google Scholar 

  • Cole, R. S.: Properties of F′ factor deoxyribonucleic acid transferred from ultraviolet-irradiated donors: Photoreactivation in the recipient and the influence of recA, recB, recC, and uur genes. J. Bact. 106, 143–149 (1971).

    Google Scholar 

  • Cross, R. A., Lieb, M.: Heat inducible λ phage V. Induction of prophages with mutations in genes O, P, and R. Genetics 57, 549–560 (1967).

    Google Scholar 

  • Devoret, R., George, J.: Induction indirecte du prophage λ par le rayonnement ultraviolet. Mutation Res. 4, 713–734 (1967).

    Google Scholar 

  • Devoret, R., Monk, M., George, J.: Indirect ultraviolet induction of prophage λ and the colicin I factor. Z. Bakteriol. 196, 193–207 (1965).

    Google Scholar 

  • Dove, W.: Strains of phage λ in current use. Virology 38, 349–350 (1969).

    Google Scholar 

  • Eisen, H. A., Fuerst, C. R., Siminovitch, L., Thomas, R., Lambert, L., Piera da Silva, L., Jacob, F.: Genetics and physiology of defective lysogeny in K12 (λ): Studies of early mutants. Virology 30, 224–241 (1966).

    Google Scholar 

  • Eisen, H. A., Siminovitch, L., Mohide, P. T.: Excision of lambda prophage: Effects on host survival. Virology 34, 97–103 (1968).

    Google Scholar 

  • George, J.: Corrélation entra la disparition de l'induction indirect du prophage λ et la restriction du DNA transmis à la bactérie receptrice inducible dans un croissement F+×F- hetero-specifique. Comptes Rendus 262, 1805–1808 (1966).

    Google Scholar 

  • George, J., Devoret, R.: Conjugal transfer of UV-damaged F-prime sex factors and indirect induction of prophage λ. Molec. gen. Genet. 111, 103 (1971).

    Google Scholar 

  • Hall, J. D., Howard-Flanders, P.: Recombinant F′ factors from Escherichia coli K12 strains carrying recB or recC. J. Bact. 110, 578 (1972).

    Google Scholar 

  • Howard-Flanders, P., Boyce, R.: DNA repair and genetic recombination: Studies on mutants of E. coli defective in these processes. Radiat. Res., Suppl. 6, 156–184 (1966).

    Google Scholar 

  • Howard-Flanders, P., Boyce, R. P., Theriot, L.: Three loci in Escherichia coli K12 that control the excision of pyrimidine dimers and certain other mutagen products from DNA. Genetics 53, 1119–1136 (1966).

    Google Scholar 

  • Howard-Flanders, P., Rupp, W. D., Wilkins, B. M., Cole, R. S.: DNA replication and recombination after UV-irradiation. Cold Spr. Harb. Symp. quant. Biol. 33, 195–205 (1968).

    Google Scholar 

  • Howard-Flanders, P., Theriot, L.: Mutants of Escherichia coli K12 defective in DNA repair and in genetic recombination. Genetics 53, 1137–1150 (1966).

    Google Scholar 

  • Jacob, F., Campbell, A.: Sur le systeme de repression assurant l'immonite chez les bacteries lysogenes. C. R. Acad. Sci. (Paris) 248, 3219–3225 (1959).

    Google Scholar 

  • Jacob, F., Wollman, E.: Sexuality and the genetics of bacteria, p. 303. New York: Academic Press 1961.

    Google Scholar 

  • Lieb, M.: Studies of heat-inducible λ phage III. Mutation in cistron N affecting heat induction. Genetics 54, 835–844 (1966).

    Google Scholar 

  • Matsubara, K.: Properties of sex factor and related episomes isolated from purified E. coli zygote cells. J. molec. Biol. 38, 89–108 (1968).

    Google Scholar 

  • Mattern, J. E., Winden, M. P. van, Rorsch, A.: The range of action of genes controlling radiation sensitivity in E. coli. Mutation Res. 2, 111–135 (1965).

    Google Scholar 

  • Meselson, M., Weigle, J. J.: Chromosome breakage accompanying genetic recombination in bacteriophage. Proc. nat. Acad. Sci. (Wash.) 47, 857–868 (1961).

    Google Scholar 

  • Monk, M.: Induction of phage λ by transferred irradiated col I DNA. Molec. gen. genet. 106, 14–24 (1969).

    Google Scholar 

  • Monk, M., Devoret, R.: Induction ultraviolette par conjugaison du prophage λ par l'intermediaire du facteur colidinogene I. Ann. Inst. Pasteur. 107, 163–170 (1964).

    Google Scholar 

  • Monk, M., Peacey, M., Gross, J.: Repair of damage induced by ultraviolet light in DNA polymerase-defective E. coli cells. J. molec. Biol. 58, 623 (1971).

    Google Scholar 

  • Ohki, M., Tomizawa, J.-I.: Asymmetric transfer of DNA strands in bacterial conjugation. Cold Spr. Harb. Symp. quant. Biol. 33, 651–658 (1968).

    Google Scholar 

  • Pardee, A. B., Prestidge, L. S.: Ultraviolet-sensitive targets in the enzyme-synthesizing apparatus of Escherichia coli. J. Bact. 93, 1210–1215 (1967).

    Google Scholar 

  • Pritchard, R. H., Barth, P. T., Collins, J.: Control of DNA synthesis in bacteria. Symp. Soc. Gen. Microbiol. 19, 263–297 (1969).

    Google Scholar 

  • Rosner, J. L., Kass, L. R., Yarmolinsky, M. B.: Parallel behavior of F and Pl in causing indirect induction of lysogenic bacteria. Cold Spr. Harb. Symp. quant. Biol. 33, 785–798 (1968).

    Google Scholar 

  • Rupp, W. D., Howard-Flanders, P.: Discontinuities in the DNA synthesized in an excision-defective strain of Escherichia coli following ultraviolet irradiation. J. molec. Biol. 31, 291–304 (1968).

    Google Scholar 

  • Rupp, W. D., Wilde, C. E. III, Reno, D. L., Howard-Flanders, P.: Exchanges between DNA strands in ultraviolet-irradiated Escherichia coli. J. molec. Biol. 61, 25–44 (1971).

    Google Scholar 

  • Vapnek, D., Rupp, W. D.: Asymmetric segregation of the complementary sexfactor DNA strands during conjugation in Escherichia coli. J. molec. Biol. 60, 413 (1971).

    Google Scholar 

  • Wilkins, B. M.: Chromosome transfer from F-lac + strains of Escherichia coli K-12 mutant at recA, recB or recC. J. Bact. 98, 599–604 (1969).

    Google Scholar 

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Communicated by G. Bertani

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Benbow, R.M., Devoret, R. & Howard-Flanders, P. Indirect ultraviolet induction and curing in E. coli cells lysogenic for bacteriophage λ. Molec. Gen. Genet. 120, 355–368 (1973). https://doi.org/10.1007/BF00268149

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