Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1995 Apr;177(8):2118–2124. doi: 10.1128/jb.177.8.2118-2124.1995

Transcriptional analysis of a region of the Enterococcus faecalis plasmid pCF10 involved in positive regulation of conjugative transfer functions.

J W Chung 1, G M Dunny 1
PMCID: PMC176856  PMID: 7536732

Abstract

The prgB gene encodes aggregation substance (Asc10) which is essential for transfer of the pheromone-inducible conjugative plasmid pCF10 in Enterococcus faecalis. The prgQ and prgS regions, located 4 kb upstream of prgB, are required for the expression of prgB. Complementation studies indicated that the prgQ region functions in cis and in an orientation-dependent manner relative to the prgB gene (J. W. Chung and G. M. Dunny, Proc. Natl. Acad. Sci. USA 89:9020-9024, 1992). Analysis of transcriptional fusions in this study, using a promoterless lacZ gene in several locations between prgQ and prgB, confirmed that the prgQ region does not carry a promoter for the expression of prgB and that prgB does not comprise an operon with prgA (which encodes the surface exclusion protein Sec10), the gene immediately upstream from prgB. Northern (RNA) blot analysis demonstrated that two distinct transcripts (Qs RNA and QL RNA), much larger than the prgQ gene, were expressed in the prgQ region. QS RNA was produced constitutively, whereas QL RNA was produced inducibly by pheromone. The lack of any other open reading frame in QL RNA and significant sequence complementarity between the 3' end of QL RNA and the promoter region of prgB suggested that the functional products of the prgQ region might be RNA molecules rather than proteins. A mutation in prgS completely abolished the production of QL RNA. A model for transcriptional activation of prgB is presented.

Full Text

The Full Text of this article is available as a PDF (377.0 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bensing B. A., Dunny G. M. Cloning and molecular analysis of genes affecting expression of binding substance, the recipient-encoded receptor(s) mediating mating aggregate formation in Enterococcus faecalis. J Bacteriol. 1993 Nov;175(22):7421–7429. doi: 10.1128/jb.175.22.7421-7429.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Brendel V., Hamm G. H., Trifonov E. N. Terminators of transcription with RNA polymerase from Escherichia coli: what they look like and how to find them. J Biomol Struct Dyn. 1986 Feb;3(4):705–723. doi: 10.1080/07391102.1986.10508457. [DOI] [PubMed] [Google Scholar]
  3. Christie P. J., Dunny G. M. Identification of regions of the Streptococcus faecalis plasmid pCF-10 that encode antibiotic resistance and pheromone response functions. Plasmid. 1986 May;15(3):230–241. doi: 10.1016/0147-619x(86)90041-7. [DOI] [PubMed] [Google Scholar]
  4. Christie P. J., Kao S. M., Adsit J. C., Dunny G. M. Cloning and expression of genes encoding pheromone-inducible antigens of Enterococcus (Streptococcus) faecalis. J Bacteriol. 1988 Nov;170(11):5161–5168. doi: 10.1128/jb.170.11.5161-5168.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Chung J. W., Bensing B. A., Dunny G. M. Genetic analysis of a region of the Enterococcus faecalis plasmid pCF10 involved in positive regulation of conjugative transfer functions. J Bacteriol. 1995 Apr;177(8):2107–2117. doi: 10.1128/jb.177.8.2107-2117.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Chung J. W., Dunny G. M. Cis-acting, orientation-dependent, positive control system activates pheromone-inducible conjugation functions at distances greater than 10 kilobases upstream from its target in Enterococcus faecalis. Proc Natl Acad Sci U S A. 1992 Oct 1;89(19):9020–9024. doi: 10.1073/pnas.89.19.9020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Clewell D. B., Pontius L. T., An F. Y., Ike Y., Suzuki A., Nakayama J. Nucleotide sequence of the sex pheromone inhibitor (iAD1) determinant of Enterococcus faecalis conjugative plasmid pAD1. Plasmid. 1990 Sep;24(2):156–161. doi: 10.1016/0147-619x(90)90019-9. [DOI] [PubMed] [Google Scholar]
  8. Dunny G. M., Brown B. L., Clewell D. B. Induced cell aggregation and mating in Streptococcus faecalis: evidence for a bacterial sex pheromone. Proc Natl Acad Sci U S A. 1978 Jul;75(7):3479–3483. doi: 10.1073/pnas.75.7.3479. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Dunny G. M., Clewell D. B. Transmissible toxin (hemolysin) plasmid in Streptococcus faecalis and its mobilization of a noninfectious drug resistance plasmid. J Bacteriol. 1975 Nov;124(2):784–790. doi: 10.1128/jb.124.2.784-790.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dunny G. M., Craig R. A., Carron R. L., Clewell D. B. Plasmid transfer in Streptococcus faecalis: production of multiple sex pheromones by recipients. Plasmid. 1979 Jul;2(3):454–465. doi: 10.1016/0147-619x(79)90029-5. [DOI] [PubMed] [Google Scholar]
  11. Dunny G. M., Leonard B. A., Hedberg P. J. Pheromone-inducible conjugation in Enterococcus faecalis: interbacterial and host-parasite chemical communication. J Bacteriol. 1995 Feb;177(4):871–876. doi: 10.1128/jb.177.4.871-876.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Dunny G., Funk C., Adsit J. Direct stimulation of the transfer of antibiotic resistance by sex pheromones in Streptococcus faecalis. Plasmid. 1981 Nov;6(3):270–278. doi: 10.1016/0147-619x(81)90035-4. [DOI] [PubMed] [Google Scholar]
  13. Galli D., Friesenegger A., Wirth R. Transcriptional control of sex-pheromone-inducible genes on plasmid pAD1 of Enterococcus faecalis and sequence analysis of a third structural gene for (pPD1-encoded) aggregation substance. Mol Microbiol. 1992 May;6(10):1297–1308. doi: 10.1111/j.1365-2958.1992.tb00851.x. [DOI] [PubMed] [Google Scholar]
  14. Kao S. M., Olmsted S. B., Viksnins A. S., Gallo J. C., Dunny G. M. Molecular and genetic analysis of a region of plasmid pCF10 containing positive control genes and structural genes encoding surface proteins involved in pheromone-inducible conjugation in Enterococcus faecalis. J Bacteriol. 1991 Dec;173(23):7650–7664. doi: 10.1128/jb.173.23.7650-7664.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. LeBlanc D. J., Inamine J. M., Lee L. N. Broad geographical distribution of homologous erythromycin, kanamycin, and streptomycin resistance determinants among group D streptococci of human and animal origin. Antimicrob Agents Chemother. 1986 Apr;29(4):549–555. doi: 10.1128/aac.29.4.549. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Mori M., Sakagami Y., Ishii Y., Isogai A., Kitada C., Fujino M., Adsit J. C., Dunny G. M., Suzuki A. Structure of cCF10, a peptide sex pheromone which induces conjugative transfer of the Streptococcus faecalis tetracycline resistance plasmid, pCF10. J Biol Chem. 1988 Oct 5;263(28):14574–14578. [PubMed] [Google Scholar]
  17. Muscholl A., Galli D., Wanner G., Wirth R. Sex pheromone plasmid pAD1-encoded aggregation substance of Enterococcus faecalis is positively regulated in trans by traE1. Eur J Biochem. 1993 May 15;214(1):333–338. doi: 10.1111/j.1432-1033.1993.tb17928.x. [DOI] [PubMed] [Google Scholar]
  18. Nakayama J., Ruhfel R. E., Dunny G. M., Isogai A., Suzuki A. The prgQ gene of the Enterococcus faecalis tetracycline resistance plasmid pCF10 encodes a peptide inhibitor, iCF10. J Bacteriol. 1994 Dec;176(23):7405–7408. doi: 10.1128/jb.176.23.7405-7408.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Novick R. P., Ross H. F., Projan S. J., Kornblum J., Kreiswirth B., Moghazeh S. Synthesis of staphylococcal virulence factors is controlled by a regulatory RNA molecule. EMBO J. 1993 Oct;12(10):3967–3975. doi: 10.1002/j.1460-2075.1993.tb06074.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Olmsted S. B., Kao S. M., van Putte L. J., Gallo J. C., Dunny G. M. Role of the pheromone-inducible surface protein Asc10 in mating aggregate formation and conjugal transfer of the Enterococcus faecalis plasmid pCF10. J Bacteriol. 1991 Dec;173(23):7665–7672. doi: 10.1128/jb.173.23.7665-7672.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Pontius L. T., Clewell D. B. Conjugative transfer of Enterococcus faecalis plasmid pAD1: nucleotide sequence and transcriptional fusion analysis of a region involved in positive regulation. J Bacteriol. 1992 May;174(10):3152–3160. doi: 10.1128/jb.174.10.3152-3160.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Tanimoto K., Clewell D. B. Regulation of the pAD1-encoded sex pheromone response in Enterococcus faecalis: expression of the positive regulator TraE1. J Bacteriol. 1993 Feb;175(4):1008–1018. doi: 10.1128/jb.175.4.1008-1018.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Trotter K. M., Dunny G. M. Mutants of Enterococcus faecalis deficient as recipients in mating with donors carrying pheromone-inducible plasmids. Plasmid. 1990 Jul;24(1):57–67. doi: 10.1016/0147-619x(90)90025-8. [DOI] [PubMed] [Google Scholar]
  24. Weaver K. E., Clewell D. B. Regulation of the pAD1 sex pheromone response in Enterococcus faecalis: effects of host strain and traA, traB, and C region mutants on expression of an E region pheromone-inducible lacZ fusion. J Bacteriol. 1990 May;172(5):2633–2641. doi: 10.1128/jb.172.5.2633-2641.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Wirth R., An F. Y., Clewell D. B. Highly efficient protoplast transformation system for Streptococcus faecalis and a new Escherichia coli-S. faecalis shuttle vector. J Bacteriol. 1986 Mar;165(3):831–836. doi: 10.1128/jb.165.3.831-836.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES