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. 1995 Aug;177(15):4350–4355. doi: 10.1128/jb.177.15.4350-4355.1995

Characterization of the functional sites in the oriT region involved in DNA transfer promoted by sex factor plasmid R100.

T Abo 1, E Ohtsubo 1
PMCID: PMC177183  PMID: 7635820

Abstract

We have previously identified three sites, named sbi, ihfA, and sbyA, specifically recognized or bound by the TraI, IHF, and TraY proteins, respectively; these sites are involved in nicking at the origin of transfer, oriT, of plasmid R100. In the region next to these sites, there exists the sbm region, which consists of four sites, sbmA, sbmB, sbmC, and sbmD; this region is specifically bound by the TraM protein, which is required for DNA transfer. Between sbmB and sbmC in this region, there exists another IHF-binding site, ihfB. The region containing all of these sites is located in the proximity of the tra region and is referred to as the oriT region. To determine whether these sites are important for DNA transfer in vivo, we constructed plasmids with various mutations in the oriT region and tested their mobilization in the presence of R100-1, a transfer-proficient mutant of R100. Plasmids with either deletions in the sbi-ihfA-sbyA region or substitution mutations introduced into each specific site in this region were mobilized at a greatly reduced frequency, showing that all of these sites are essential for DNA transfer. By binding to ihfA, IHF, which is known to bend DNA, may be involved in the formation of a complex (which may be called oriT-some) consisting of TraI, IHF, and TraY that efficiently introduces a nick at oriT. Plasmids with either deletions in the sbm-ihfB region or substitution mutations introduced into each specific site in this region were mobilized at a reduced frequency, showing that this region is also important for DNA transfer. By binding to ihfB, IHF may also be involved in the formation of another complex (which may be called the TraM-IHF complex) consisting of TraM and IHF that ensures DNA transfer with a high level of efficiency. Several-base-pair insertions into the positions between sbyA and sbmA affected the frequency of transfer in a manner dependent upon the number of base pairs, indicating that the phasing between sbyA and sbmA is important. This in turn suggests that both oriT-some and the TraM-IHF complex should be in an appropriate position spatially to facilitate DNA transfer.

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Selected References

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  1. Abo T., Inamoto S., Ohtsubo E. Specific DNA binding of the TraM protein to the oriT region of plasmid R100. J Bacteriol. 1991 Oct;173(20):6347–6354. doi: 10.1128/jb.173.20.6347-6354.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Abo T., Ohtsubo E. Repression of the traM gene of plasmid R100 by its own product and integration host factor at one of the two promoters. J Bacteriol. 1993 Jul;175(14):4466–4474. doi: 10.1128/jb.175.14.4466-4474.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Achtman M., Manning P. A., Edelbluth C., Herrlich P. Export without proteolytic processing of inner and outer membrane proteins encoded by F sex factor tra cistrons in Escherichia coli minicells. Proc Natl Acad Sci U S A. 1979 Oct;76(10):4837–4841. doi: 10.1073/pnas.76.10.4837. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chung C. T., Niemela S. L., Miller R. H. One-step preparation of competent Escherichia coli: transformation and storage of bacterial cells in the same solution. Proc Natl Acad Sci U S A. 1989 Apr;86(7):2172–2175. doi: 10.1073/pnas.86.7.2172. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Dempsey W. B. Integration host factor and conjugative transfer of the antibiotic resistance plasmid R100. J Bacteriol. 1987 Sep;169(9):4391–4392. doi: 10.1128/jb.169.9.4391-4392.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Di Laurenzio L., Frost L. S., Paranchych W. The TraM protein of the conjugative plasmid F binds to the origin of transfer of the F and ColE1 plasmids. Mol Microbiol. 1992 Oct;6(20):2951–2959. doi: 10.1111/j.1365-2958.1992.tb01754.x. [DOI] [PubMed] [Google Scholar]
  7. Friedman D. I. Integration host factor: a protein for all reasons. Cell. 1988 Nov 18;55(4):545–554. doi: 10.1016/0092-8674(88)90213-9. [DOI] [PubMed] [Google Scholar]
  8. Frost L. S., Ippen-Ihler K., Skurray R. A. Analysis of the sequence and gene products of the transfer region of the F sex factor. Microbiol Rev. 1994 Jun;58(2):162–210. doi: 10.1128/mr.58.2.162-210.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Fu Y. H., Tsai M. M., Luo Y. N., Deonier R. C. Deletion analysis of the F plasmid oriT locus. J Bacteriol. 1991 Feb;173(3):1012–1020. doi: 10.1128/jb.173.3.1012-1020.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Gamas P., Caro L., Galas D., Chandler M. Expression of F transfer functions depends on the Escherichia coli integration host factor. Mol Gen Genet. 1987 May;207(2-3):302–305. doi: 10.1007/BF00331593. [DOI] [PubMed] [Google Scholar]
  11. Gao Q., Luo Y., Deonier R. C. Initiation and termination of DNA transfer at F plasmid oriT. Mol Microbiol. 1994 Feb;11(3):449–458. doi: 10.1111/j.1365-2958.1994.tb00326.x. [DOI] [PubMed] [Google Scholar]
  12. Inamoto S., Fukuda H., Abo T., Ohtsubo E. Site- and strand-specific nicking at oriT of plasmid R100 in a purified system: enhancement of the nicking activity of TraI (helicase I) with TraY and IHF. J Biochem. 1994 Oct;116(4):838–844. doi: 10.1093/oxfordjournals.jbchem.a124604. [DOI] [PubMed] [Google Scholar]
  13. Inamoto S., Ohtsubo E. Specific binding of the TraY protein to oriT and the promoter region for the traY gene of plasmid R100. J Biol Chem. 1990 Apr 15;265(11):6461–6466. [PubMed] [Google Scholar]
  14. Inamoto S., Yoshioka Y., Ohtsubo E. Identification and characterization of the products from the traJ and traY genes of plasmid R100. J Bacteriol. 1988 Jun;170(6):2749–2757. doi: 10.1128/jb.170.6.2749-2757.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Inamoto S., Yoshioka Y., Ohtsubo E. Site- and strand-specific nicking in vitro at oriT by the traY-traI endonuclease of plasmid R100. J Biol Chem. 1991 Jun 5;266(16):10086–10092. [PubMed] [Google Scholar]
  16. Kano Y., Imamoto F. Requirement of integration host factor (IHF) for growth of Escherichia coli deficient in HU protein. Gene. 1990 Apr 30;89(1):133–137. doi: 10.1016/0378-1119(90)90216-e. [DOI] [PubMed] [Google Scholar]
  17. Kunkel T. A. Rapid and efficient site-specific mutagenesis without phenotypic selection. Proc Natl Acad Sci U S A. 1985 Jan;82(2):488–492. doi: 10.1073/pnas.82.2.488. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Machida Y., Machida C., Ohtsubo E. A novel type of transposon generated by insertion element IS102 present in a pSC101 derivative. Cell. 1982 Aug;30(1):29–36. doi: 10.1016/0092-8674(82)90008-3. [DOI] [PubMed] [Google Scholar]
  19. Matson S. W., Morton B. S. Escherichia coli DNA helicase I catalyzes a site- and strand-specific nicking reaction at the F plasmid oriT. J Biol Chem. 1991 Aug 25;266(24):16232–16237. [PubMed] [Google Scholar]
  20. Raleigh E. A., Murray N. E., Revel H., Blumenthal R. M., Westaway D., Reith A. D., Rigby P. W., Elhai J., Hanahan D. McrA and McrB restriction phenotypes of some E. coli strains and implications for gene cloning. Nucleic Acids Res. 1988 Feb 25;16(4):1563–1575. doi: 10.1093/nar/16.4.1563. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Reygers U., Wessel R., Müller H., Hoffmann-Berling H. Endonuclease activity of Escherichia coli DNA helicase I directed against the transfer origin of the F factor. EMBO J. 1991 Sep;10(9):2689–2694. doi: 10.1002/j.1460-2075.1991.tb07812.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Schmid M. B. More than just "histone-like" proteins. Cell. 1990 Nov 2;63(3):451–453. doi: 10.1016/0092-8674(90)90438-k. [DOI] [PubMed] [Google Scholar]
  23. Schwab M., Gruber H., Högenauer G. The TraM protein of plasmid R1 is a DNA-binding protein. Mol Microbiol. 1991 Feb;5(2):439–446. doi: 10.1111/j.1365-2958.1991.tb02127.x. [DOI] [PubMed] [Google Scholar]
  24. Takeshita S., Sato M., Toba M., Masahashi W., Hashimoto-Gotoh T. High-copy-number and low-copy-number plasmid vectors for lacZ alpha-complementation and chloramphenicol- or kanamycin-resistance selection. Gene. 1987;61(1):63–74. doi: 10.1016/0378-1119(87)90365-9. [DOI] [PubMed] [Google Scholar]
  25. Vieira J., Messing J. Production of single-stranded plasmid DNA. Methods Enzymol. 1987;153:3–11. doi: 10.1016/0076-6879(87)53044-0. [DOI] [PubMed] [Google Scholar]
  26. Yanisch-Perron C., Vieira J., Messing J. Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. Gene. 1985;33(1):103–119. doi: 10.1016/0378-1119(85)90120-9. [DOI] [PubMed] [Google Scholar]
  27. Yoshioka Y., Ohtsubo H., Ohtsubo E. Repressor gene finO in plasmids R100 and F: constitutive transfer of plasmid F is caused by insertion of IS3 into F finO. J Bacteriol. 1987 Feb;169(2):619–623. doi: 10.1128/jb.169.2.619-623.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]

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