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Regional replication of the bacterial chromosome induced by derepression of prophage lambda

III. Role of the replication in escape synthesis of gal operon

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Summary

Recent evidence suggests that the escape synthesis of gal operon following derepression of the prophage λ in Escherichia coli K 12 involves transcription originating at the λ promoter (PL) to extend through gal under the conditions in which λ DNA replication is prevented. Whether the observed expression of gal is due to transcription initiating at PL or at the bacterial promoter for gal (Pgal) was examined in the case of λ DNA replication being normal. The experiments are based on that two types of transcription are distinguished from each other by the following properties: 1. Pgal-promoted transcription is inhibited by chloramphenicol, while PL-promoted transcription is not. 2. PL-promoted transcription suppresses the polar effect caused by nonsense mutation in a bacterial gene, while Pgal-promoted transcription does not do so. The results have suggested that gal escape synthesis in λ-induced lysogen results from transcription which initiates not only at PL but also at Pgal. The Pgal-promoted transcription may be a consequence, direct or indirect, of the concomitant replication of gal DNA.

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References

  • Adhya, S., Gottesman, M., de Crombrugghe, B.: Release of polarity in Escherichia coli by gene N of phage λ: Termination and antitermination of transcription. Proc. nat. Acad. Sci. (Wash.) 71, 2534–2538 (1974)

    Google Scholar 

  • Bachmann, B.J., Low, K.B., Taylor, A.L.: Recalibrated linkage map of Escherichia coli K-12. Bact. Rev. 40, 116–167 (1976)

    Google Scholar 

  • Besemer, J., Herpers, M.: Suppression of polarity of insertion mutations within the gal operon of Escherichia coli. Molec. gen. Genet. 151, 295–304 (1977)

    Google Scholar 

  • Bøvre, K., Szybalski, W.: Multistep DNA-RNA hybridization techniques. In: Methods in enzymology (Grossman, L. and Moldave, K., eds.), Vol. 21, pp. 350–383. New York: Academic Press 1971

    Google Scholar 

  • Buttin, G.: Mécanismes régulateurs dans la biosynthèse des enzymes du métabolism du galactose chez Escherichia coli K12. II. Le déterminisme génétique de la régulation. J. molec. Biol. 7, 183–205 (1963a)

    Google Scholar 

  • Buttin, G.: Mécanismes régulateurs dans la biosynthèse des enzymes du métabolism du galactose chez Escherichia coli K12. III. L' Effet de dérepression provoqué par le développement des bactériophages λ chez Escherichia coli K12. J. molec. Biol. 7, 610–631 (1963b)

    Google Scholar 

  • Buttin, G., Jacob, F., Monod, J.: Synthèse constitutive de galactokinase en conséquence au dévelopement de bactériophage λ chez Escherichia coli K12. C.R. Acad. Sci. (Paris) 250, 2471–2473 (1960)

    Google Scholar 

  • de Crombrugghe, B., Adhya, S., Gottesman, M., Pastan, I.: Effect of rho on transcription of bacterial operon. Nature (Lond.) New Biol. 241, 260–264 (1973)

    Google Scholar 

  • Franklin, N.C.: The N operon of lambda: Extent and regulation as observed in fusions to the tryptophan operon of Escherichia coli. In: The bacteriophage lambda (Hershey, A.D., ed.), pp. 621–638. New York: Cold Spring Harbor Laboratory 1971

    Google Scholar 

  • Franklin, N.C.: Altered reading of genetic signals fused to the N operon of bacteriophage λ: Genetic evidence for modification of polymerase by the protein product of the N gene. J. molec. Biol. 89, 33–48 (1974)

    Google Scholar 

  • Gornall, A.G., Bardawill, C.J., David, M.M.: Determination of serum proteins by means of the biuret reaction. J. biol. Chem. 177, 751–766 (1949)

    Google Scholar 

  • Hirai, K., Fukasawa, T.: Regional replication of the bacterial chromosome induced by derepression of prophage lambda. II. Direction and origin. Molec. gen. Genet. 147, 71–78 (1976)

    Google Scholar 

  • Ikemura, T., Ozeki, H.: Gross mapping of tRNA genes in E. coli. Jap. J. Genet. 51, 410–411 (1976) (Abstract), in Japanese

    Google Scholar 

  • Imae, Y.: On the mechanism of derepression of gal operon following induction of prophage λ in Escherichia coli K12. Ph.D. Thesis, Osaka Univ. (1969) (in Japanese)

  • Imae, Y., Fukasawa, T.: On the mechanism of derepression of host galactose operon following induction of bacteriophage λ in Escherichia coli strain K12. Biochem. biophys. Res. Commun. 28, 38–43 (1967)

    Google Scholar 

  • Imae, Y., Fukusawa, T.: Regional replication of the bacterial chromosome induced by derepression of prophage lambda. J. molec. Biol. 54, 585–597 (1970)

    Google Scholar 

  • Imae, Y., Morikawa, N., Kurahashi, K.: Purification and properties of uridine diphosphoglucose 4-epimerase from Escherichia coli. J. Biochem. (Tokyo) 56, 138–144 (1964)

    Google Scholar 

  • Imamoto, F.: Diversity of regulation of genetic transcription. I. Effect of antibiotics which inhibit the process of translocation on RNA metabolizm in Escherichia coli. J. molec. Biol. 74, 113–136 (1973)

    Google Scholar 

  • Joyner, A., Isaacs, L.N., Echols, H., Sly, W.S.: DNA replication and messenger RNA production after induction of wild type λ bacteriophage and λ mutants. J. molec. Biol. 19, 174–186 (1966)

    Google Scholar 

  • Krell, K., Gottesman, M.E., Parks, J.S.: Escape synthesis of the biotin operon in induced λb2 lysogens. J. molec. Biol. 68, 69–82 (1972)

    Google Scholar 

  • Morse, D.E.: Polarity induced by chloramphenicol and relief by suA. J. molec. Biol. 55, 113–118 (1971)

    Google Scholar 

  • Nakamura, Y., Ikeuchi, T., Imai, M., Yura, T.: Escape synthesis of RNA polymerase subunits and termination factor rho following induction of prophage lambda in Escherichia coli. Molec. gen. Genet. 150, 317–324 (1977)

    Google Scholar 

  • Ogawa, T., Tomizawa, J.: Replication of bacteriophage DNA. I. Replication of DNA of lambda phage defective in early function. J. molec. Biol. 38, 217–225 (1968)

    Google Scholar 

  • Okamoto, K., Sugino, Y., Nomura, M.: Synthesis and turnover of phage messenger RNA in E. coli infected with bacteriophage T4 in the presence of chloromycetin. J. molec. Biol. 5, 527–534 (1962)

    Google Scholar 

  • Revel, H.R., Luria, S.E.: Biosynthesis of β-D-galactosidase controlled by phage-carried genes. II. The behavior of phage-transduced z +genes toward regulatory mechanisms. Proc. nat. Acad. Sci. (Wash.) 47, 1968–1974 (1961)

    Google Scholar 

  • Saedler, H., Gullon, A., Fiethen, L., Starlinger, P.: Negative control of the galactose operon in E. coli. Molec. gen. Genet. 102, 79–88 (1968)

    Google Scholar 

  • Schleif, R., Greenblatt, J., Davis, R.W.: Dual control of arabinose genes on transducing phage λdara. J. molec. Biol. 59, 127–150 (1971)

    Google Scholar 

  • Segawa, T., Imamoto, F.: Diversity of regulation of genetic transcription: II. Specific relaxation of polarity in read-through transcription of the translocated trp operon in bacteriophage lambda trp. J. molec. Biol. 87, 741–754 (1974)

    Google Scholar 

  • Skalka, A.: Multiple units of transcription in phage lambda. Cold Spr. Harb. Symp. quant. Biol. 31, 377–379 (1966)

    Google Scholar 

  • Skalka, A., Butler, B., Echols, H.: Genetic control of transcription during development of phage λ. Proc. nat. Acad. Sci. (Wash.) 58, 576–583 (1967)

    Google Scholar 

  • Sly, W., Echols, H., Adler, J.: Control of viral messenger RNA after lambda phage infection and induction. Proc. nat. Acad. Sci. (Wash.) 53, 378–384 (1965)

    Google Scholar 

  • Taylor, K., Hradecna, Z., Szybalski, W.: Asymmetric distribution of the transcribing regions on the complementary strands of coliphage λ DNA. Proc. nat. Acad. Sci. (Wash.) 57, 1618–1625 (1967)

    Google Scholar 

  • Vermus, H.E., Perlman, R.L., Pastan, I.: Regulation of lac transcription in antibiotic-treated E. coli. Nature (Lond.) New Biol. 230, 41–44 (1971)

    Google Scholar 

  • Willard, M., Echols, H.: Role of bacteriophage DNA replication in λdg escape synthesis. J. molec. Biol. 32, 37–46 (1968)

    Google Scholar 

  • Wilson, D., Hogness, D.: Galactokinase and uridine diphosphogalactose 4-epimerase from Escherichia coli. In: Methods in enzymology (Newfield, E. and Ginsberg, V., eds.), Vol. 8, pp. 229–240. New York: Academic Press 1966

    Google Scholar 

  • Yarmolinsky, M.B., Wiesmeyer, H.: Regulation by coliphage lambda of the expression of the capacity to synthesize a sequence of host enzymes. Proc. nat. Acad. Sci. (Wash.) 46, 1626–1645 (1960)

    Google Scholar 

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Communicated by T. Yura

The second article of this series is in Molec. gen. Genet. 147, 71–78 (1976)

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Fukasawa, T., Obonai, K. Regional replication of the bacterial chromosome induced by derepression of prophage lambda. Molec. Gen. Genet. 159, 185–190 (1978). https://doi.org/10.1007/BF00270892

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  • DOI: https://doi.org/10.1007/BF00270892

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