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. 1997 Nov;179(22):7016–7024. doi: 10.1128/jb.179.22.7016-7024.1997

Dual function of the copR gene product of plasmid pIP501.

S Brantl 1, E G Wagner 1
PMCID: PMC179642  PMID: 9371448

Abstract

Replication of plasmid pIP501 is regulated at a step subsequent to transcription initiation by an antisense RNA (RNAIII) and transcriptionally by a repressor protein, CopR. Previously, it had been shown that CopR binds to a 44-bp DNA fragment upstream of and overlapping the repR promoter pII. Subsequently, we found that high-copy-number pIP501 derivatives lacking copR and low-copy-number derivatives containing copR produced the same intracellular amounts of RNAIII. This suggested a second, hitherto-unknown function of CopR. In this report, we show that CopR does not affect the half-life of RNAIII. Instead, we demonstrate in vivo that, in the presence of both pII and pIII, CopR provided in cis or in trans causes an increase in the intracellular concentration of RNAIII and that this effect is due to the function of the protein rather than its mRNA. We suggest that, in the absence of CopR, the increased (derepressed) RNAII transcription interferes, in cis, with initiation of transcription of RNAIII (convergent transcription), resulting in a lower RNAIII/plasmid ratio. When CopR is present, the pII promoter is repressed to >90%, so that convergent transcription is mostly abolished and RNAIII/plasmid ratios are high. The hypothesis that RNAII transcription influences promoter pIII through induced changes in DNA supercoiling is supported by the finding that the gyrase inhibitor novobiocin affects the accumulation of both sense and antisense RNA. The dual role of CopR in repression of RNAII transcription and in prevention of convergent transcription is discussed in the context of replication control of pIP501.

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Selected References

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  1. Anagnostopoulos C., Spizizen J. REQUIREMENTS FOR TRANSFORMATION IN BACILLUS SUBTILIS. J Bacteriol. 1961 May;81(5):741–746. doi: 10.1128/jb.81.5.741-746.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Behnke D., Gilmore M. S., Ferretti J. J. Plasmid pGB301, a new multiple resistance streptococcal cloning vehicle and its use in cloning of a gentamicin/kanamycin resistance determinant. Mol Gen Genet. 1981;182(3):414–421. doi: 10.1007/BF00293929. [DOI] [PubMed] [Google Scholar]
  3. Behnke D., Malke H., Hartmann M., Walter F. Post-transformational rearrangement of an in vitro reconstructed group-A streptococcal erythromycin resistance plasmid. Plasmid. 1979 Oct;2(4):605–616. doi: 10.1016/0147-619x(79)90058-1. [DOI] [PubMed] [Google Scholar]
  4. Blomberg P., Wagner E. G., Nordström K. Control of replication of plasmid R1: the duplex between the antisense RNA, CopA, and its target, CopT, is processed specifically in vivo and in vitro by RNase III. EMBO J. 1990 Jul;9(7):2331–2340. doi: 10.1002/j.1460-2075.1990.tb07405.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bowater R. P., Chen D., Lilley D. M. Elevated unconstrained supercoiling of plasmid DNA generated by transcription and translation of the tetracycline resistance gene in eubacteria. Biochemistry. 1994 Aug 9;33(31):9266–9275. doi: 10.1021/bi00197a030. [DOI] [PubMed] [Google Scholar]
  6. Bowater R. P., Chen D., Lilley D. M. Modulation of tyrT promoter activity by template supercoiling in vivo. EMBO J. 1994 Dec 1;13(23):5647–5655. doi: 10.1002/j.1460-2075.1994.tb06903.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Brantl S., Behnke D., Alonso J. C. Molecular analysis of the replication region of the conjugative Streptococcus agalactiae plasmid pIP501 in Bacillus subtilis. Comparison with plasmids pAM beta 1 and pSM19035. Nucleic Acids Res. 1990 Aug 25;18(16):4783–4790. doi: 10.1093/nar/18.16.4783. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Brantl S., Behnke D. Copy number control of the streptococcal plasmid pIP501 occurs at three levels. Nucleic Acids Res. 1992 Feb 11;20(3):395–400. doi: 10.1093/nar/20.3.395. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Brantl S., Behnke D. The amount of RepR protein determines the copy number of plasmid pIP501 in Bacillus subtilis. J Bacteriol. 1992 Aug;174(16):5475–5478. doi: 10.1128/jb.174.16.5475-5478.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Brantl S., Birch-Hirschfeld E., Behnke D. RepR protein expression on plasmid pIP501 is controlled by an antisense RNA-mediated transcription attenuation mechanism. J Bacteriol. 1993 Jul;175(13):4052–4061. doi: 10.1128/jb.175.13.4052-4061.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Brantl S. The copR gene product of plasmid pIP501 acts as a transcriptional repressor at the essential repR promoter. Mol Microbiol. 1994 Nov;14(3):473–483. doi: 10.1111/j.1365-2958.1994.tb02182.x. [DOI] [PubMed] [Google Scholar]
  12. Brantl S., Wagner E. G. An unusually long-lived antisense RNA in plasmid copy number control: in vivo RNAs encoded by the streptococcal plasmid pIP501. J Mol Biol. 1996 Jan 19;255(2):275–288. doi: 10.1006/jmbi.1996.0023. [DOI] [PubMed] [Google Scholar]
  13. Brantl S., Wagner E. G. Antisense RNA-mediated transcriptional attenuation occurs faster than stable antisense/target RNA pairing: an in vitro study of plasmid pIP501. EMBO J. 1994 Aug 1;13(15):3599–3607. doi: 10.1002/j.1460-2075.1994.tb06667.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Clewell D. B., Yagi Y., Dunny G. M., Schultz S. K. Characterization of three plasmid deoxyribonucleic acid molecules in a strain of Streptococcus faecalis: identification of a plasmid determining erythromycin resistance. J Bacteriol. 1974 Jan;117(1):283–289. doi: 10.1128/jb.117.1.283-289.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Free A., Dorman C. J. Escherichia coli tyrT gene transcription is sensitive to DNA supercoiling in its native chromosomal context: effect of DNA topoisomerase IV overexpression on tyrT promoter function. Mol Microbiol. 1994 Oct;14(1):151–161. doi: 10.1111/j.1365-2958.1994.tb01275.x. [DOI] [PubMed] [Google Scholar]
  16. Horodniceanu T., Bouanchaud D. H., Bieth G., Chabbert Y. A. R plasmids in Streptococcus agalactiae (group B). Antimicrob Agents Chemother. 1976 Nov;10(5):795–801. doi: 10.1128/aac.10.5.795. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kawamura F., Doi R. H. Construction of a Bacillus subtilis double mutant deficient in extracellular alkaline and neutral proteases. J Bacteriol. 1984 Oct;160(1):442–444. doi: 10.1128/jb.160.1.442-444.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kok J., van der Vossen J. M., Venema G. Construction of plasmid cloning vectors for lactic streptococci which also replicate in Bacillus subtilis and Escherichia coli. Appl Environ Microbiol. 1984 Oct;48(4):726–731. doi: 10.1128/aem.48.4.726-731.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Le Chatelier E., Ehrlich S. D., Jannière L. Countertranscript-driven attenuation system of the pAM beta 1 repE gene. Mol Microbiol. 1996 Jun;20(5):1099–1112. doi: 10.1111/j.1365-2958.1996.tb02550.x. [DOI] [PubMed] [Google Scholar]
  20. Le Chatelier E., Ehrlich S. D., Jannière L. The pAM beta 1 CopF repressor regulates plasmid copy number by controlling transcription of the repE gene. Mol Microbiol. 1994 Nov;14(3):463–471. doi: 10.1111/j.1365-2958.1994.tb02181.x. [DOI] [PubMed] [Google Scholar]
  21. Light J., Riise E., Molin S. Transcription and its regulation in the basic replicon region of plasmid R1. Mol Gen Genet. 1985;198(3):503–508. doi: 10.1007/BF00332947. [DOI] [PubMed] [Google Scholar]
  22. Liu L. F., Wang J. C. Supercoiling of the DNA template during transcription. Proc Natl Acad Sci U S A. 1987 Oct;84(20):7024–7027. doi: 10.1073/pnas.84.20.7024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Nordström K., Molin S., Light J. Control of replication of bacterial plasmids: genetics, molecular biology, and physiology of the plasmid R1 system. Plasmid. 1984 Sep;12(2):71–90. doi: 10.1016/0147-619x(84)90054-4. [DOI] [PubMed] [Google Scholar]
  24. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Spirito F., Bossi L. Long-distance effect of downstream transcription on activity of the supercoiling-sensitive leu-500 promoter in a topA mutant of Salmonella typhimurium. J Bacteriol. 1996 Dec;178(24):7129–7137. doi: 10.1128/jb.178.24.7129-7137.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Steiner K., Malke H. Transcription termination of the streptokinase gene of Streptococcus equisimilis H46A: bidirectionality and efficiency in homologous and heterologous hosts. Mol Gen Genet. 1995 Feb 6;246(3):374–380. doi: 10.1007/BF00288611. [DOI] [PubMed] [Google Scholar]
  27. Stougaard P., Light J., Molin S. Convergent transcription interferes with expression of the copy number control gene, copA, from plasmid R1. EMBO J. 1982;1(3):323–328. doi: 10.1002/j.1460-2075.1982.tb01168.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. del Solar G., Acebo P., Espinosa M. Replication control of plasmid pLS1: efficient regulation of plasmid copy number is exerted by the combined action of two plasmid components, CopG and RNA II. Mol Microbiol. 1995 Dec;18(5):913–924. doi: 10.1111/j.1365-2958.1995.18050913.x. [DOI] [PubMed] [Google Scholar]
  29. del Solar G., Acebo P., Espinosa M. Replication control of plasmid pLS1: the antisense RNA II and the compact rnaII region are involved in translational regulation of the initiator RepB synthesis. Mol Microbiol. 1997 Jan;23(1):95–108. doi: 10.1046/j.1365-2958.1997.1981561.x. [DOI] [PubMed] [Google Scholar]
  30. del Solar G., Espinosa M. The copy number of plasmid pLS1 is regulated by two trans-acting plasmid products: the antisense RNA II and the repressor protein, RepA. Mol Microbiol. 1992 Jan;6(1):83–94. doi: 10.1111/j.1365-2958.1992.tb00840.x. [DOI] [PubMed] [Google Scholar]

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