Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1995 Jul;177(13):3781–3787. doi: 10.1128/jb.177.13.3781-3787.1995

The pilE gene of Neisseria gonorrhoeae MS11 is transcribed from a sigma 70 promoter during growth in vitro.

J A Fyfe 1, C S Carrick 1, J K Davies 1
PMCID: PMC177096  PMID: 7601844

Abstract

Type 4 pili are essential for virulence in Neisseria gonorrhoeae. The gonococcal pilin subunit is encoded by pilE, upstream of which three putative promoter sequences (P1, P2, and P3) have been identified. P1 and P2 are sigma 70-like promoters and are functional when a PpiE::cat transcriptional fusion is expressed in Escherichia coli DH5 alpha. P3 is sigma 54 dependent and overlaps the P1 sequence. Site-directed mutagenesis of the pilE promoters followed by transcriptional analysis in E. coli indicated that in the absence of an appropriate activator protein, binding of RNA polymerase-sigma 54 to P3 inhibits transcription from P1 on the order of 30-fold. Transcription from P3 was undetectable in E. coli. However, PilR-dependent, P3-associated expression was detected in Pseudomonas aeruginosa PAK containing a PpilE::cat fusion, with P3 the only intact promoter. A similar analysis was performed on gonococcal reporter strains containing wild-type and mutated PpilE::cat cassettes recombined into the chromosome. In such piliated gonococcal recombinants cultured in vitro, P1 was responsible for cat expression and almost certainly for transcription of pilE. Transcription from P2 and P3 was not detectable under these conditions. Inhibition of transcription from P1 by sigma 54 binding to P3 was not apparent in N. gonorrhoeae MS11-A, suggesting that sigma 54 was either absent or unable to bind to P3 in these cells.

Full Text

The Full Text of this article is available as a PDF (393.3 KB).

Selected References

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

  1. Black C. G., Fyfe J. A., Davies J. K. A promoter associated with the neisserial repeat can be used to transcribe the uvrB gene from Neisseria gonorrhoeae. J Bacteriol. 1995 Apr;177(8):1952–1958. doi: 10.1128/jb.177.8.1952-1958.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bolivar F., Rodriguez R. L., Greene P. J., Betlach M. C., Heyneker H. L., Boyer H. W., Crosa J. H., Falkow S. Construction and characterization of new cloning vehicles. II. A multipurpose cloning system. Gene. 1977;2(2):95–113. [PubMed] [Google Scholar]
  3. Boyle-Vavra S., Seifert H. S. Shuttle mutagenesis: two mini-transposons for gene mapping and for lacZ transcriptional fusions in Neisseria gonorrhoeae. Gene. 1993 Jul 15;129(1):51–57. doi: 10.1016/0378-1119(93)90695-y. [DOI] [PubMed] [Google Scholar]
  4. Boyle-Vavra S., So M., Seifert H. S. Transcriptional control of gonococcal pilE expression: involvement of an alternate sigma factor. Gene. 1993 Dec 31;137(2):233–236. doi: 10.1016/0378-1119(93)90012-r. [DOI] [PubMed] [Google Scholar]
  5. Busby S., Ebright R. H. Promoter structure, promoter recognition, and transcription activation in prokaryotes. Cell. 1994 Dec 2;79(5):743–746. doi: 10.1016/0092-8674(94)90063-9. [DOI] [PubMed] [Google Scholar]
  6. Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem. 1987 Apr;162(1):156–159. doi: 10.1006/abio.1987.9999. [DOI] [PubMed] [Google Scholar]
  7. Duncan L., Losick R. SpoIIAB is an anti-sigma factor that binds to and inhibits transcription by regulatory protein sigma F from Bacillus subtilis. Proc Natl Acad Sci U S A. 1993 Mar 15;90(6):2325–2329. doi: 10.1073/pnas.90.6.2325. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Elleman T. C., Hoyne P. A., Stewart D. J., McKern N. M., Peterson J. E. Expression of pili from Bacteroides nodosus in Pseudomonas aeruginosa. J Bacteriol. 1986 Nov;168(2):574–580. doi: 10.1128/jb.168.2.574-580.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Freundlich M., Ramani N., Mathew E., Sirko A., Tsui P. The role of integration host factor in gene expression in Escherichia coli. Mol Microbiol. 1992 Sep;6(18):2557–2563. doi: 10.1111/j.1365-2958.1992.tb01432.x. [DOI] [PubMed] [Google Scholar]
  10. Fyfe J. A., Strugnell R. A., Davies J. K. Control of gonococcal pilin-encoding gene expression in Escherichia coli. Gene. 1993 Jan 15;123(1):45–50. doi: 10.1016/0378-1119(93)90537-d. [DOI] [PubMed] [Google Scholar]
  11. Goodman S. D., Scocca J. J. Identification and arrangement of the DNA sequence recognized in specific transformation of Neisseria gonorrhoeae. Proc Natl Acad Sci U S A. 1988 Sep;85(18):6982–6986. doi: 10.1073/pnas.85.18.6982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Heckels J. E. Structure and function of pili of pathogenic Neisseria species. Clin Microbiol Rev. 1989 Apr;2 (Suppl):S66–S73. doi: 10.1128/cmr.2.suppl.s66. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hobbs M., Collie E. S., Free P. D., Livingston S. P., Mattick J. S. PilS and PilR, a two-component transcriptional regulatory system controlling expression of type 4 fimbriae in Pseudomonas aeruginosa. Mol Microbiol. 1993 Mar;7(5):669–682. doi: 10.1111/j.1365-2958.1993.tb01158.x. [DOI] [PubMed] [Google Scholar]
  14. Hobbs M., Dalrymple B. P., Cox P. T., Livingstone S. P., Delaney S. F., Mattick J. S. Organization of the fimbrial gene region of Bacteroides nodosus: class I and class II strains. Mol Microbiol. 1991 Mar;5(3):543–560. doi: 10.1111/j.1365-2958.1991.tb00726.x. [DOI] [PubMed] [Google Scholar]
  15. Horton R. M., Hunt H. D., Ho S. N., Pullen J. K., Pease L. R. Engineering hybrid genes without the use of restriction enzymes: gene splicing by overlap extension. Gene. 1989 Apr 15;77(1):61–68. doi: 10.1016/0378-1119(89)90359-4. [DOI] [PubMed] [Google Scholar]
  16. Hoyne P. A., Haas R., Meyer T. F., Davies J. K., Elleman T. C. Production of Neisseria gonorrhoeae pili (fimbriae) in Pseudomonas aeruginosa. J Bacteriol. 1992 Nov;174(22):7321–7327. doi: 10.1128/jb.174.22.7321-7327.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Ishimoto K. S., Lory S. Formation of pilin in Pseudomonas aeruginosa requires the alternative sigma factor (RpoN) of RNA polymerase. Proc Natl Acad Sci U S A. 1989 Mar;86(6):1954–1957. doi: 10.1073/pnas.86.6.1954. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Ishimoto K. S., Lory S. Identification of pilR, which encodes a transcriptional activator of the Pseudomonas aeruginosa pilin gene. J Bacteriol. 1992 Jun;174(11):3514–3521. doi: 10.1128/jb.174.11.3514-3521.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Jin S., Ishimoto K. S., Lory S. PilR, a transcriptional regulator of piliation in Pseudomonas aeruginosa, binds to a cis-acting sequence upstream of the pilin gene promoter. Mol Microbiol. 1994 Dec;14(5):1049–1057. doi: 10.1111/j.1365-2958.1994.tb01338.x. [DOI] [PubMed] [Google Scholar]
  20. Jin S., Ishimoto K., Lory S. Nucleotide sequence of the rpoN gene and characterization of two downstream open reading frames in Pseudomonas aeruginosa. J Bacteriol. 1994 Mar;176(5):1316–1322. doi: 10.1128/jb.176.5.1316-1322.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Jones D. H., Franklin F. C., Thomas C. M. Molecular analysis of the operon which encodes the RNA polymerase sigma factor sigma 54 of Escherichia coli. Microbiology. 1994 May;140(Pt 5):1035–1043. doi: 10.1099/13500872-140-5-1035. [DOI] [PubMed] [Google Scholar]
  22. Klimpel K. W., Lesley S. A., Clark V. L. Identification of subunits of gonococcal RNA polymerase by immunoblot analysis: evidence for multiple sigma factors. J Bacteriol. 1989 Jul;171(7):3713–3718. doi: 10.1128/jb.171.7.3713-3718.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  24. Merrick M. J., Coppard J. R. Mutations in genes downstream of the rpoN gene (encoding sigma 54) of Klebsiella pneumoniae affect expression from sigma 54-dependent promoters. Mol Microbiol. 1989 Dec;3(12):1765–1775. doi: 10.1111/j.1365-2958.1989.tb00162.x. [DOI] [PubMed] [Google Scholar]
  25. Meyer T. F., Billyard E., Haas R., Storzbach S., So M. Pilus genes of Neisseria gonorrheae: chromosomal organization and DNA sequence. Proc Natl Acad Sci U S A. 1984 Oct;81(19):6110–6114. doi: 10.1073/pnas.81.19.6110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Min K. T., Hilditch C. M., Diederich B., Errington J., Yudkin M. D. Sigma F, the first compartment-specific transcription factor of B. subtilis, is regulated by an anti-sigma factor that is also a protein kinase. Cell. 1993 Aug 27;74(4):735–742. doi: 10.1016/0092-8674(93)90520-z. [DOI] [PubMed] [Google Scholar]
  27. Norrander J., Kempe T., Messing J. Construction of improved M13 vectors using oligodeoxynucleotide-directed mutagenesis. Gene. 1983 Dec;26(1):101–106. doi: 10.1016/0378-1119(83)90040-9. [DOI] [PubMed] [Google Scholar]
  28. Ohnishi K., Kutsukake K., Suzuki H., Lino T. A novel transcriptional regulation mechanism in the flagellar regulon of Salmonella typhimurium: an antisigma factor inhibits the activity of the flagellum-specific sigma factor, sigma F. Mol Microbiol. 1992 Nov;6(21):3149–3157. doi: 10.1111/j.1365-2958.1992.tb01771.x. [DOI] [PubMed] [Google Scholar]
  29. Pasloske B. L., Carpenter M. R., Frost L. S., Finlay B. B., Paranchych W. The expression of Pseudomonas aeruginosa PAK pilin gene mutants in Escherichia coli. Mol Microbiol. 1988 Mar;2(2):185–195. doi: 10.1111/j.1365-2958.1988.tb00020.x. [DOI] [PubMed] [Google Scholar]
  30. Pasloske B. L., Drummond D. S., Frost L. S., Paranchych W. The activity of the Pseudomonas aeruginosa pilin promoter is enhanced by an upstream regulatory site. Gene. 1989 Sep 1;81(1):25–34. doi: 10.1016/0378-1119(89)90333-8. [DOI] [PubMed] [Google Scholar]
  31. Pohlner J., Halter R., Beyreuther K., Meyer T. F. Gene structure and extracellular secretion of Neisseria gonorrhoeae IgA protease. 1987 Jan 29-Feb 4Nature. 325(6103):458–462. doi: 10.1038/325458a0. [DOI] [PubMed] [Google Scholar]
  32. Popham D. L., Szeto D., Keener J., Kustu S. Function of a bacterial activator protein that binds to transcriptional enhancers. Science. 1989 Feb 3;243(4891):629–635. doi: 10.1126/science.2563595. [DOI] [PubMed] [Google Scholar]
  33. Pérez-Martín J., Rojo F., de Lorenzo V. Promoters responsive to DNA bending: a common theme in prokaryotic gene expression. Microbiol Rev. 1994 Jun;58(2):268–290. doi: 10.1128/mr.58.2.268-290.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Reitzer L. J., Magasanik B. Transcription of glnA in E. coli is stimulated by activator bound to sites far from the promoter. Cell. 1986 Jun 20;45(6):785–792. doi: 10.1016/0092-8674(86)90553-2. [DOI] [PubMed] [Google Scholar]
  35. Sarandopoulos S., Davies J. K. Genetic organization and evolution of the cryptic plasmid of Neisseria gonorrhoeae. Plasmid. 1993 May;29(3):206–221. doi: 10.1006/plas.1993.1023. [DOI] [PubMed] [Google Scholar]
  36. Segal E., Billyard E., So M., Storzbach S., Meyer T. F. Role of chromosomal rearrangement in N. gonorrhoeae pilus phase variation. Cell. 1985 Feb;40(2):293–300. doi: 10.1016/0092-8674(85)90143-6. [DOI] [PubMed] [Google Scholar]
  37. Taha M. K., Dupuy B., Saurin W., So M., Marchal C. Control of pilus expression in Neisseria gonorrhoeae as an original system in the family of two-component regulators. Mol Microbiol. 1991 Jan;5(1):137–148. doi: 10.1111/j.1365-2958.1991.tb01834.x. [DOI] [PubMed] [Google Scholar]
  38. Thöny B., Hennecke H. The -24/-12 promoter comes of age. FEMS Microbiol Rev. 1989 Dec;5(4):341–357. doi: 10.1016/0168-6445(89)90028-4. [DOI] [PubMed] [Google Scholar]
  39. Warrelmann J., Eitinger M., Schwartz E., Römermann D., Friedrich B. Nucleotide sequence of the rpoN (hno) gene region of Alcaligenes eutrophus: evidence for a conserved gene cluster. Arch Microbiol. 1992;158(2):107–114. doi: 10.1007/BF00245213. [DOI] [PubMed] [Google Scholar]

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

RESOURCES