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Immediate cessation of transcription of an operator-proximal segment of the tryptophan operon in Escherichia coli following repression of the operon

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Summary

Transcription of the E gene (the first gene) of the tryptophan operon of Escherichia coli is abruptly reduced immediately after the onset of repression. This reduction arises from two sources: the inhibition of transcription which is in progress over an operator-proximal segment of the operon and the failure of initiation of transcription at the promoter site. Regarding the former phenomenon, kinetic analysis shows that inhibition occurs within 20 seconds after repression under conditions where it takes about 8 minutes to complete the first round of transcription of the operon. The length of the transcription region that is blocked immediately by the onset of repression is approximately the operator-proximal 4 percent of the operon. The possibility is excluded that the apparent inhibition of transcription is caused by selective and quick degradation of the operator-proximal region of the trp mRNA.

These findings support the hypothesis that the repressor inhibits transcription which is in progress over the initial protion of the operator-proximal region of the operon, thereby indirectly preventing additional RNA polymerase molecules from attaching at the promoter.

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References

  • Baker, R. F., Yanofsky, C.: The periodicity of RNA polymerase initiations: A new regulatory feature of transcription. Proc. nat. Acad. Sci. (Wash.) 60, 313 (1968).

    Google Scholar 

  • Daives, J., Jacob, F.: Genetic mapping of the regulator and operator genes of the lac operon. J. molec. Biol. 36, 413 (1968).

    Google Scholar 

  • Deeb, S. S., Okamoto, K., Hall, B. D.: Isolation and characterization of non-defective transducing elements of bacteriophage Ø80. Virology 31, 289 (1967).

    Google Scholar 

  • Geiduschek, E. P., Haselkorn, R.: Messenger RNA. Ann. Rev. Biochem. 38, 647 (1969).

    Google Scholar 

  • Hiraga, S.: Operator mutants of the tryptophan operon in Escherichia coli. J. Molec. Biol. 39, 159 (1969).

    Google Scholar 

  • Imamoto, F.: On the initiation of transcription of the tryptophan operon in Escherichia coli. Proc. nat. Acad. Sci. (Wash.) 60, 305 (1968a).

    Google Scholar 

  • —: Immediate cessation of transcription of the operator-proximal region of the tryptophan operon in E. coli after repression of the operon. Nature (Lond.) 220, 31 (1968b).

    Google Scholar 

  • —: Unimpaired repressibility of transcription of the operator-proximal eighth of the first (E)gene of the tryptophan operon in Escherichia coli. Molec. Gen. Genetics 105, 298–305 (1965).

    Google Scholar 

  • —, Morikawa, N., Sato, K.: On the transcription of the tryptophan operon in Escherichia coli III. Multicistronic mRNA and polarity for transcription. J. molec. Biol. 13, 169 (1965).

    Google Scholar 

  • —, Mishima, S., Nishimura, T., Matsushiro, A.: On the transcription of the tryptophan operon in Escherichia coli II. Production of the specific messenger RNA. J. molec. Biol. 13, 157 (1965).

    Google Scholar 

  • —, Yanofsky, C.: Transcription of the tryptophan operon in polarity mutants of Escherichia coli I. Characterization of the tryptophan mRNA of polar mutants. J. molec. Biol. 28, 1 (1967).

    Google Scholar 

  • Ippen, K., Miller, J. H., Scaife, J. G., Beckwith, J. R.: New controlling element in the lac operon of E. coli. Nature (Lond.) 217, 825 (1968).

    Google Scholar 

  • Ito, F., Imamoto, F.: Sequential derepression and repression of the tryptophan operon in E. coli. Nature (Lond.) 220, 441 (1968).

    Google Scholar 

  • Jacob, F., Ullman, A., Monod, J.: Le promoteur, élément genetique necéssaire a l'expression d'un opéron. C. R. Acad. Sci. (Paris) 258, 3125 (1964).

    Google Scholar 

  • —: Deletions fusionant l'Opéron Lactose et un Opéron Purine chez Escherichia coli. J. molec. Biol. 13, 704 (1965).

    Google Scholar 

  • Kaiser, A. D., Hogness, D. S.: The transformation of Escherichia coli with deoxyribonucleic acid isolated from bacteriophage λ dg. J. molec. Biol. 2, 392 (1960).

    Google Scholar 

  • Martin, R. G.: Control of gene expression. Ann. Rev. Genet. 3, (1969) (in press).

  • Matsushiro, A., Sato, K., Ito, J., Kida, S., Imamoto, F.: On the transcription of the tryptophan operon in Escherichia coli I. The tryptophan operator. J. molec. Biol. 11, 54 (1965).

    Google Scholar 

  • Miller, J. H., Ippen, D., Scaife, J. G., Beckwith, J. R.: The promoter-operator region of the lac operon of Escherichia coli. J. molec. Biol. 38, 413 (1968).

    Google Scholar 

  • Morikawa, N., Imamoto, F.: On the degradation of messenger RNA for tryptophan operon in Escherichia coli. Nature (Lond.) 223, 37 (1969).

    Google Scholar 

  • Morse, D. E., Mosteller, R., Baker, R. F., Yanofsky, C.: The direction of in vivo degradation of tryptophan messenger RNA—a correction—degradation is initiated at the 5′ end of the messenger. Nature (Lond.) 223, 40 (1969).

    Google Scholar 

  • Nygaard, A. P., Hall, B. D.: A method for the detection of RNA-DNA complex. Biochem. biophys. Res. Commun. 12, 98 (1963).

    Google Scholar 

  • —: Formation and properties of RNA-DNA complex. J. molec. Biol. 9, 125 (1964).

    Google Scholar 

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

    Google Scholar 

  • Smith, O. H.: Structure of the trpC cistron specifying indoleglycerol phosphate synthetase, and its localization in the tryptophan operon of Escherichia coli. Genetics 57, 95 (1967).

    Google Scholar 

  • Vogel, H., Bonner, D. M.: Acetylornithinase of Escherichia coli: Partial purification and some properties. J. biol. Chem. 218, 97 (1956).

    Google Scholar 

  • Yanofsky, C., Carlton, B., Guest, J. R., Helinski, D. R., Henning, U.: On the colinearity of gene structure and protein structure. Proc. nat. Acad. Sci. (Wash.) 51, 226 (1964).

    Google Scholar 

  • — Ito, J.: Nonsense codons and polarity in the tryptophan operon. J. molec. Biol. 21, 313 (1966).

    Google Scholar 

  • —, Lennox, E. S.: Transduction and recombination study of linkage relationship among the genes controlling tryptophan synthesis in Escherichia coli. Virology 8, 425 (1959).

    Google Scholar 

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Communicated by Jun-ichi Tomizawa

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Imamoto, F. Immediate cessation of transcription of an operator-proximal segment of the tryptophan operon in Escherichia coli following repression of the operon. Molec. Gen. Genet. 106, 123–138 (1970). https://doi.org/10.1007/BF00323831

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