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Hyperproduction of the sigma subunit of RNA polymerase in a mutant of Escherichia coli

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Summary

A mutant of Escherichia coli K12 is described in which σ and α subunits of the DNA-dependent RNA polymerase (EC 2.7.7.6) are produced at the rates much higher than in the normal strain. The rate of synthesis for σ subunit was found to be at least 10-times higher, though the rapid degradation of σ polypeptides accompanied with the accelerated synthesis precludes accurate estimation of the extent of hyperproduction. The α subunit synthesis was about 5-times higher in this mutant than in the control, and excess α polypeptides produced were as stable as the bulk of protein under the conditions employed. Genetic analyses of the mutant by conjugation and by transduction with phage P1 revealed that at least three distinct but closely linked mutations are responsible for hyperproduction of the σ subunit; one (sig-1) is located very close to rif, and the others (sig-2 and sig-3) at the argH-bfe and metB regions, respectively. The results further indicate that the accelerated synthesis of α subunit is due to a mutation also located at the metB region. The present finding suggests that the synthesis of σ subunit is subject to a complex control that can be affected by a number of cellular processes. The possible involvement of the core polymerase in determining the rate of synthesis of σ subunit is discussed.

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References

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

    Google Scholar 

  • Doi, R. H., Nagata, T., Yura, T.: Studies on RNA polymerase mutants in Escherichia coli. IV. Rifampicin-resistant amber mutants. Ann. Rept. Inst. Virus Res., Kyoto Univ. 15, 53–54 (1972)

    Google Scholar 

  • Errington, L., Glass, R. E., Hayward, R. S., Scaife, J. G.: Structure and orientation of an RNA polymerase operon in Escherichia coli. Nature (Lond.) 249, 519–522 (1974)

    Google Scholar 

  • Hayward, R. S., Austin, S. J., Scaife, J. G.: The effect of gene dosage on the synthesis and stability of RNA polymerase subunits in Escherichia coli. Molec. gen. Genet. 131, 173–180 (1974)

    Google Scholar 

  • Hayward, R. S., Tittawella, I. P. B., Scaife, J. G.: Evidence for specific control of RNA polymerase synthesis in Escherichia coli. Nature (Lond.) 243, 6–9 (1973)

    Google Scholar 

  • Ikeda, H., Tomizawa, J.: Transducing fragments in generalized transduction by phage P1. I. Molecular origin of the fragments. J. molec. Biol. 14, 85–109 (1965)

    Google Scholar 

  • Ikeuchi, T., Yura, T., Yamagishi, H.: Genetic and physical studies of lambda transducing phage carrying the β subunit gene of Escherichia coli RNA polymerase. J. Bact. 122, 1247–1256 (1975)

    Google Scholar 

  • Iwakura, Y., Ishihama, A.: Biosynthesis of RNA polymerase in Escherichia coli. II. Control of RNA polymerase synthesis during nutritional shift up and down. Molec. gen. Genet. in press (1975)

  • Iwakura, Y., Ito, K., Ishihama, A.: Biosynthesis of RNA polymerase in Escherichia coli. I. Control of RNA polymerase content at various growth rates. Molec. gen. Genet. 133, 1–23 (1974)

    Google Scholar 

  • Kirschbaum, J. B.: Regulation of subunit synthesis of Escherichia coli RNA polymerase. Proc. nat. Acad. Sci. (Wash.) 70, 2651–2655 (1973)

    Google Scholar 

  • Kirschbaum, J. B., Scaife, J.: Evidence for a λ transducing phage carrying the genes for the β and β′ subunits of Escherichia coli RNA polymerase. Molec. gen. Genet. 132, 193–201 (1974)

    Google Scholar 

  • Matzura, H., Hansen, R. S., Zeuthen, J.: Biosynthesis of the β and β′ subunits of RNA polymerase in Escherichia coli. J. molec. Biol. 74, 9–20 (1973)

    Google Scholar 

  • Matzura, H., Molin, S., Maaløe, O.: Sequential biosynthesis of the β and β′ subunits of the DNA-dependent RNA polymerase from Escherichia coli. J. molec. Biol. 59, 17–25 (1971)

    Google Scholar 

  • Nakamura, Y., Yura, T.: Localization of the structural gene for the β′ subunit of RNA polymerase in Escherichia coli. Biochem. biophys. Res. Commun. 53, 645–652 (1973)

    Google Scholar 

  • Nakamura, Y., Yura, T.: Evidence for a positive regulation of RNA polymerase synthesis in Escherichia coli. J. molec. Biol. in press (1975a)

  • Nakamura, Y., Yura, T.: Effects of rifampicin on the synthesis and activity of the DNA-dependent RNA polymerase in Escherichia coli (in preparation) (1975b)

  • Panny, S. R., Heil, A., Mazus, B., Palm, P., Zillig, W., Mindlin, S. Z., Ilyina, T. S., Khesin, R. S.: A temperature sensitive mutation of the β′-subunit of DNA-dependent RNA polymerase from E. coli T16. FEBS Lett. 48, 241–245 (1974)

    Google Scholar 

  • Taylor, A. L., Trotter, C. D.: Linkage map of Escherichia coli strain K12. Bact. Rev. 36, 504–524 (1972)

    Google Scholar 

  • Travers, A.: Exchange of the sigma subunit of RNA polymerase. FEBS Lett. 53, 76–79 (1975)

    Google Scholar 

  • Wolf, J. L., Mason, G., Honig, G. R.: Regulation of hemoglobin β-chain synthesis in bone marrow erythroid cells by α chains. Proc. nat. Acad. Sci. (Wash.) 70, 3405–3409 (1973)

    Google Scholar 

  • Yarmolinsky, M. B., Wiesmayer, H.: Regulation by coliphage λ 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 E. Bautz

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Nakamura, Y., Yura, T. Hyperproduction of the sigma subunit of RNA polymerase in a mutant of Escherichia coli . Molec. Gen. Genet. 141, 97–111 (1975). https://doi.org/10.1007/BF00267677

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