Skip to main content
Log in

Prophage λ induction caused by mini-F plasmid genes

  • Published:
Molecular and General Genetics MGG Aims and scope Submit manuscript

Summary

When bacterial cells harboring a temperaturesensitive replication plasmid, which carries the particular ccd segment of a mini-F plasmid, are transferred to 42°C, cell division is inhibited after incubation for an appropriate time. The inhibition occurs, when the copy number of the plasmid decreases to become critically low, about one per cell (Ogura and Hiraga 1983 b). In λ phage lysogens carrying this type of plasmid, the prophage is induced in a small portion of the cell population under the same conditions, in addition to the inhibition of cell division in most of cells. The prophage induction, but not the inhibition of normal cell division, depends on normal recA function. Both induction of prophage and inhibition of cell division are suppressed by the simultaneous presence of a replication proficient plasmid carrying the ccdA gene. We discuss molecular mechanisms of the ccd function that couples host cell division to plasmid proliferation and induces the prophage. Additionally, we propose a hypothesis that the ccd mechanism of F plasmid contributes to indirect induction of prophage λ by an F plasmid damaged by UV-irradiation and then introduced into a lysogen via conjugation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

kb:

kilobase pairs. m.o.i., multiplicity of infection

References

  • Bex F, Karoui H, Rokeach L, Dréze P, Garcia L, Couturier M (1983) Mini-F encoded proteins: identification of a new 10.5 kilodalton species. The EMBO J 2:1853–1861

    Google Scholar 

  • Bolivar F, Rodriguez RL, Greene PJ, Betlach MC, Heyneker HL, Boyer HW, Crosa JH, Falkow S (1977) Construction and characterization of new cloning vehicles. II. A multipurpose cloning system. Gene 2:95–113

    Google Scholar 

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

    Google Scholar 

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

    Google Scholar 

  • Capage MA, Scott JR (1983) SOS induction by P1 Km miniplasmids. J Bacteriol 155:473–480

    Google Scholar 

  • Casaregola S, D'Ari R, Huisman O (1982) Role of DNA replication in the induction and turn-off of the SOS response in Escherichia coli. Mol Gen Genet 185:440–444

    Google Scholar 

  • Cohen A, Fisher WD, Curtiss III R, Adler HI (1968) The properties of DNA transferred to minicells during conjugation. Cold Spring Harbor Symp Quant Biol 33:635–641

    Google Scholar 

  • D'Ari R, Huisman O (1983) Novel mechanism of cell division inhibition associated with the SOS response in Escherichia coli. J Bacteriol 156:243–250

    Google Scholar 

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

    Google Scholar 

  • George J, Devoret R, Radman M (1974) Indirect ultraviolet-reactivation of phage λ. Proc Natl Acad Sci USA 71:144–147

    Google Scholar 

  • Hashimoto-Gotoh T, Franklin FCH, Nordheim A, Timmis KN (1981) Specific-purpose plasmid cloning vectors. I. Low copy number, temperature-sensitive, mobilization-defective pSC101-derived containment vectors. Gene 16:227–235

    Google Scholar 

  • Hiraga S, Saitoh T (1975) F deoxyribonucleic acid transferred to recipient cells in the presence of refampin. J Bacteriol 121:1000–1006

    Google Scholar 

  • Inoue M (1971) Pleiotropic effect of the recA gene of Escherichia coli: Uncoupling of cell division from deoxyribonucleic acid replication. J Bacteriol 106:539–542

    Google Scholar 

  • Karoui H, Bex F, Dréze P, Couturier M (1983) Ham22, a mini-F mutation which is lethal to host cell and promotes recA-dependent induction of lambdoid prophage. The EMBO J 2:1863–1868

    Google Scholar 

  • Lane HED (1981) Replication and incompatibility of F and plasmids in the incFI group. Plasmid 5:100–126

    Google Scholar 

  • Little JW, Mount DW (1982) The SOS regulatory system of Escherichia coli. Cell 29:11–22

    Google Scholar 

  • MacQueen HA, Donachie WD (1977) Intracellular localization and effects on cell division of a plasmid blocked in deoxyribonucleic acid replication. J Bacteriol 132:392–397

    Google Scholar 

  • Monk M (1969) Induction of phage λ by transferred irradiated coll DNA. Mol Gen Genet 106:14–24

    Google Scholar 

  • Monk M, Gross J (1971) Induction of prophage λ in a mutant of E. coli K12 defective in initiation of DNA replication at high temperature. Mol Gen Genet 110:299–306

    Google Scholar 

  • Moreau PL, Pelico JV, Devoret R (1982) Cleavage of λ repressor and synthesis of RecA protein induced by transferred UV-damaged F sex factor. Mol Gen Genet 186:170–179

    Google Scholar 

  • Murotsu T, Matsubara K, Sugisaki H, Takanami M (1981) Nine unique repeating sequences in a region essential for replication and incompatibility of the mini-F plasmid. Gene 15:257–271

    Google Scholar 

  • Ogura T, Hiraga S (1983a) Partition mechanism of F plasmid: Two plasmid gene-encoded products and a cis-acting region are involved in partition. Cell 32:351–360

    Google Scholar 

  • Ogura T, Hiraga S (1983b) Mini-F plasmid genes that coupled host cell division to plasmid proliferation. Proc Natl Acad Sci USA 80:4784–4788

    Google Scholar 

  • Ohki M, Tomizawa J (1968) Asymmetric transfer of DNA strands in bacterial conjugation. Cold Spring Harbor Symp Quant Biol 33:651–658

    Google Scholar 

  • Oishi M, Smith CL (1978) Inactivation of phage repressor in a permeable cell system: Role of recBC DNase in induction. Proc Natl Acad Sci USA 75:3569–3573

    Google Scholar 

  • Rosner JL, Kass LR, Yarmolinsky MB (1968) Parallel behavior of F and P1 in causing indirect induction of lysogenic bacteria. Cold Spring Harbor Symp Quant Biol 33:785–789

    Google Scholar 

  • Rupp WD, Ihler G (1968) Strand selection during bacterial mating. Cold Spring Harbor Symp Quant Biol 33:647–650

    Google Scholar 

  • Saitoh T, Hiraga S (1975) F deoxyribonucleic acid superinfected into phenocopies of donor strains. J Bacteriol 121:1007–1012

    Google Scholar 

  • Schuster H, Beyersmann D, Mikolajczyk M, Schlicht M (1973) Prophage induction by high temperature in thermosensitive dna mutants lysogenic for bacteriophage lambda. J Virol 11:879–885

    Google Scholar 

  • Timmis K, Cabello F, Cohen SN (1975) Cloning, isolation, and characterization of replication regions of complex plasmid genomes. Proc Natl Acad Sci USA 72:2242–2246

    Google Scholar 

  • Yarmolinsky MB, Stevens E (1983) Replication-control function block the induction of an SOS response by a damaged P1 bacteriophage. Mol Gen Genet 192:140–148

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by W. Arber

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mori, H., Ogura, T. & Hiraga, S. Prophage λ induction caused by mini-F plasmid genes. Mol Gen Genet 196, 185–193 (1984). https://doi.org/10.1007/BF00328049

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00328049

Keywords

Navigation