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Autoregulation of the ccd operon in the F plasmid

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Summary

Mini-F sequences, including the promoter and portions of the ccd region, were inserted upstream of lacZ in promoterless lacZ vectors, and β-galactosidase specific activities were measured. The results showed that the H (ccdA), G (ccdB) and D genes, together with a promoter, comprise an operon. Ccd operon expression was shown to be regulated at the level of transcription by the G gene product, probably in concert with the H gene product. Thus expression is autoregulated. Expression of the D gene was largely dependent on the ccd promoter, although low levels of transcription from another promoter within the ccd coding region were detected.

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References

  • Austin S, Wierzbicki A (1983) Two mini-F-encoded proteins are essential for equipartition. Plasmid 10:73–81

    Google Scholar 

  • Bailone A, Sommer S, Devoret R (1985) Mini-F plasmid-induced SOS signal in Escherichia coli is RecBC dependent. Proc Natl Acad Sci USA 82:5973–5977

    Google Scholar 

  • Bergquist PL, Adelberg EA (1972) Abnormal excision and transfer of chromosomal segments by a strain of Escherichia coli K12. J Bacteriol 111:119–128

    Google Scholar 

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

    Google Scholar 

  • Birnboim MC, Doly J (1979) A rapid alkaline lysis extraction procedure for screening recombinant DNA. Nucleic Acids Res 7:1513–1523

    Google Scholar 

  • Brandenburger A, Bailone A, Lévine A, Devoret R (1984) Gratuitous induction. J Mol Biol 179:571–576

    Google Scholar 

  • Caughey P (1986) PhD Thesis, University of Auckland, New Zealand

  • Francis S (1985) MSc Thesis, University of Auckland, New Zealand

  • Gerdes K, Rasmussen PB, Molin S (1986) Unique type of plasmid maintenance function: post segregational killing of plasmid-free cells. Proc Natl Acad Sci USA 83:3116–3120

    Google Scholar 

  • Jaffé A, Ogura T, Hiraga S (1985) Effects of ccd function of the plasmid on bacterial growth. J Bacteriol 163:841–849

    Google Scholar 

  • Lane D, Gardner RC (1979) Second EcoRI fragment of F capable of self replication. J Bacteriol 139:141–151

    Google Scholar 

  • Lane D, de Feyter R, Kennedy M, Phua S-H, Semon D (1986) D protein of Mini F plasmid acts as a repressor of transcription and as a site-specific resolvase. Nucleic Acids Res 14:9713–9728

    Google Scholar 

  • Loh SM, Cram DS, Skurray RA (1988) Nucleotide sequence and transcriptional analysis of a third function (Flm) involved in F plasmid maintenance. Gene 66:259–268

    Google Scholar 

  • Masson L, Ray DS (1986) Mechanism of autonomous control of the Escherichia coli F plasmid: different complexes of the initiator/repressor protein are bound to its operator and to an F plasmid replication origin. Nucleic Acids Res 14:5693–5711

    Google Scholar 

  • Maxam AM, Gilbert W (1980) Sequencing end-labelled DNA with base-specific chemical cleavages. Methods Enzymol 65:499–560

    Google Scholar 

  • Miki T, Yoshioka K, Horiuchi T (1984) Control of cell division by sex factor F in Escherichia coli I. The 42.84-43.6F segment couples cell division of the host bacteria with replication of plasmid DNA. J Mol Biol 174:605–625

    Google Scholar 

  • Miller JF, Malamy MH (1983) Identification of the pifC gene and its role in negative control of F factor pif gene expression. J Bacteriol 156:338–347

    Google Scholar 

  • Miller JH (1972) Experiments in Molecular Genetics. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York

    Google Scholar 

  • Mori H, Ogura T, Hiraga S (1984) Prophage λ induction caused by mini-F plasmid genes. Mol Gen Genet 196:185–193

    Google Scholar 

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

    Google Scholar 

  • Shapira SK, Chou J, Richaud FV, Casadaban MJ (1983) New versatile plasmid vectors for expression of hybrid proteins coded by a cloned gene fused to lacZ gene sequences encoding an enzymatically active carboxy-terminal portion of β-galactosidase. Gene 25:71–82

    Google Scholar 

  • Søgaard-Andersen L, Rokeach LA, Molin S (1984) Regulated expression of a gene important for replication of plasmid F in E. coli. EMBO J 3:257–262

    Google Scholar 

  • Sommer S, Bailone A, Devoret R (1985) SOS induction by thermosensitive replication mutants of miniF plasmid. Mol Gen Genet 198:456–464

    Google Scholar 

  • Stoker NG, Fairweather NF, Spratt BG (1982) Versatile low copy number plasmid vectors for cloning in Escherichia coli. Gene 18:335–341

    Google Scholar 

  • Vieira J, Messing J (1982) The pUC plasmids, an M13mp7-derived system for insertional mutagenesis and sequencing with synthetic universal primers. Gene 19:259–268

    Google Scholar 

  • Watson LA, Phua S-H, Bergquist PL, Lane HED (1982) An Mr 29,000 protein is essential for mini-F maintenance in E. coli. Gene 19:173–178

    Google Scholar 

  • Yang J, Pittard J (1987) Molecular analysis of the regulatory region of the Escherichia coli K12 tyrB gene. J Bacteriol 169:4710–4715

    Google Scholar 

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Communicated by R. Devoret

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de Feyter, R., Wallace, C. & Lane, D. Autoregulation of the ccd operon in the F plasmid. Mol Gen Genet 218, 481–486 (1989). https://doi.org/10.1007/BF00332413

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  • DOI: https://doi.org/10.1007/BF00332413

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