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. 1995 Feb;177(3):558–565. doi: 10.1128/jb.177.3.558-565.1995

Two enhancer elements for DNA replication of pSC101, par and a palindromic binding sequence of the Rep protein.

S Ohkubo 1, K Yamaguchi 1
PMCID: PMC176628  PMID: 7836287

Abstract

The minimal replication origin (ori) of the plasmid pSC101 has been previously defined as an approximately 220-bp region by using plasmids defective in the par region, which is a cis-acting determinant of plasmid stability. This ori region contains the DnaA binding sequence, three repeated sequences (iterons), and an inverted repeat (IR) element (IR-1), one of the binding sites of an initiator protein, Rep (or RepA). In the present study, we show that plasmids containing par can replicate at a nearly normal copy number in the absence of IR-1 but still require a region (the downstream region) between the third iteron and IR-1. Because par is dispensable in plasmids retaining IR-1, par and IR-1 can compensate each other for efficient replication. The region from the DnaA box to the downstream region can support DNA replication at a reduced frequency, and it is designated "core-ori." Addition of either IR-1 or par to core-ori increases the copy number of the plasmid up to a nearly normal level. However, the IR-1 element must be located downstream of the third iteron (or upstream of the rep gene) to enhance replication of the plasmid, while the par region, to which DNA gyrase can bind, functions optimally regardless of its location. Furthermore, the enhancer activity of IR-1 is dependent on the helical phase of the DNA double helix, suggesting that the Rep protein bound to IR-1 stimulates the activation of ori via its interaction with another factor or factors capable of binding to individual loci within ori.

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Selected References

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  1. Armstrong K. A., Acosta R., Ledner E., Machida Y., Pancotto M., McCormick M., Ohtsubo H., Ohtsubo E. A 37 X 10(3) molecular weight plasmid-encoded protein is required for replication and copy number control in the plasmid pSC101 and its temperature-sensitive derivative pHS1. J Mol Biol. 1984 May 25;175(3):331–348. doi: 10.1016/0022-2836(84)90352-8. [DOI] [PubMed] [Google Scholar]
  2. Beaucage S. L., Miller C. A., Cohen S. N. Gyrase-dependent stabilization of pSC101 plasmid inheritance by transcriptionally active promoters. EMBO J. 1991 Sep;10(9):2583–2588. doi: 10.1002/j.1460-2075.1991.tb07799.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Biek D. P., Cohen S. N. Propagation of pSC101 plasmids defective in binding of integration host factor. J Bacteriol. 1992 Feb;174(3):785–792. doi: 10.1128/jb.174.3.785-792.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Churchward G., Linder P., Caro L. The nucleotide sequence of replication and maintenance functions encoded by plasmid pSC101. Nucleic Acids Res. 1983 Aug 25;11(16):5645–5659. doi: 10.1093/nar/11.16.5645. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. DasGupta S., Mukhopadhyay G., Papp P. P., Lewis M. S., Chattoraj D. K. Activation of DNA binding by the monomeric form of the P1 replication initiator RepA by heat shock proteins DnaJ and DnaK. J Mol Biol. 1993 Jul 5;232(1):23–34. doi: 10.1006/jmbi.1993.1367. [DOI] [PubMed] [Google Scholar]
  6. Fueki T., Yamaguchi K. A single-stranded region located downstream of the repeated sequence in the ori region of pSC101 is required for binding of the Rep protein in vitro. J Biochem. 1991 Nov;110(5):775–779. doi: 10.1093/oxfordjournals.jbchem.a123658. [DOI] [PubMed] [Google Scholar]
  7. Ingmer H., Cohen S. N. Excess intracellular concentration of the pSC101 RepA protein interferes with both plasmid DNA replication and partitioning. J Bacteriol. 1993 Dec;175(24):7834–7841. doi: 10.1128/jb.175.24.7834-7841.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Ingmer H., Cohen S. N. The pSC101 par locus alters protein-DNA interactions in vivo at the plasmid replication origin. J Bacteriol. 1993 Sep;175(18):6046–6048. doi: 10.1128/jb.175.18.6046-6048.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Ishiai M., Wada C., Kawasaki Y., Yura T. Replication initiator protein RepE of mini-F plasmid: functional differentiation between monomers (initiator) and dimers (autogenous repressor). Proc Natl Acad Sci U S A. 1994 Apr 26;91(9):3839–3843. doi: 10.1073/pnas.91.9.3839. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Linder P., Churchward G., Caro L. Plasmid pSC101 replication mutants generated by insertion of the transposon Tn1000. J Mol Biol. 1983 Oct 25;170(2):287–303. doi: 10.1016/s0022-2836(83)80149-1. [DOI] [PubMed] [Google Scholar]
  11. Linder P., Churchward G., Xia G. X., Yu Y. Y., Caro L. An essential replication gene, repA, of plasmid pSC101 is autoregulated. J Mol Biol. 1985 Feb 5;181(3):383–393. doi: 10.1016/0022-2836(85)90227-x. [DOI] [PubMed] [Google Scholar]
  12. Manen D., Goebel T., Caro L. The par region of pSC101 affects plasmid copy number as well as stability. Mol Microbiol. 1990 Nov;4(11):1839–1846. doi: 10.1111/j.1365-2958.1990.tb02032.x. [DOI] [PubMed] [Google Scholar]
  13. Manen D., Upegui-Gonzalez L. C., Caro L. Monomers and dimers of the RepA protein in plasmid pSC101 replication: domains in RepA. Proc Natl Acad Sci U S A. 1992 Oct 1;89(19):8923–8927. doi: 10.1073/pnas.89.19.8923. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Manen D., Xia G., Caro L. A locus involved in the regulation of replication in plasmid pSC101. Mol Microbiol. 1994 Mar;11(5):875–884. doi: 10.1111/j.1365-2958.1994.tb00366.x. [DOI] [PubMed] [Google Scholar]
  15. Meacock P. A., Cohen S. N. Partitioning of bacterial plasmids during cell division: a cis-acting locus that accomplishes stable plasmid inheritance. Cell. 1980 Jun;20(2):529–542. doi: 10.1016/0092-8674(80)90639-x. [DOI] [PubMed] [Google Scholar]
  16. Miller C. A., Beaucage S. L., Cohen S. N. Role of DNA superhelicity in partitioning of the pSC101 plasmid. Cell. 1990 Jul 13;62(1):127–133. doi: 10.1016/0092-8674(90)90246-b. [DOI] [PubMed] [Google Scholar]
  17. Miller C. A., Cohen S. N. The partition (par) locus of pSC101 is an enhancer of plasmid incompatibility. Mol Microbiol. 1993 Aug;9(4):695–702. doi: 10.1111/j.1365-2958.1993.tb01730.x. [DOI] [PubMed] [Google Scholar]
  18. Miller C. A., Tucker W. T., Meacock P. A., Gustafsson P., Cohen S. N. Nucleotide sequence of the partition locus of Escherichia coli plasmid pSC101. Gene. 1983 Oct;24(2-3):309–315. doi: 10.1016/0378-1119(83)90091-4. [DOI] [PubMed] [Google Scholar]
  19. Nordström K. Control of plasmid replication--how do DNA iterons set the replication frequency? Cell. 1990 Dec 21;63(6):1121–1124. doi: 10.1016/0092-8674(90)90405-4. [DOI] [PubMed] [Google Scholar]
  20. Schleif R. DNA looping. Annu Rev Biochem. 1992;61:199–223. doi: 10.1146/annurev.bi.61.070192.001215. [DOI] [PubMed] [Google Scholar]
  21. Stenzel T. T., MacAllister T., Bastia D. Cooperativity at a distance promoted by the combined action of two replication initiator proteins and a DNA bending protein at the replication origin of pSC101. Genes Dev. 1991 Aug;5(8):1453–1463. doi: 10.1101/gad.5.8.1453. [DOI] [PubMed] [Google Scholar]
  22. Stenzel T. T., Patel P., Bastia D. The integration host factor of Escherichia coli binds to bent DNA at the origin of replication of the plasmid pSC101. Cell. 1987 Jun 5;49(5):709–717. doi: 10.1016/0092-8674(87)90547-2. [DOI] [PubMed] [Google Scholar]
  23. Sugiura S., Nakatani S., Mizukami Y., Hase T., Hirokawa H., Masamune Y. Characterization of a mini plasmid isolated from Shigella sonnei. J Biochem. 1984 Oct;96(4):1193–1204. doi: 10.1093/oxfordjournals.jbchem.a134937. [DOI] [PubMed] [Google Scholar]
  24. Sugiura S., Ohkubo S., Yamaguchi K. Minimal essential origin of plasmid pSC101 replication: requirement of a region downstream of iterons. J Bacteriol. 1993 Sep;175(18):5993–6001. doi: 10.1128/jb.175.18.5993-6001.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Sugiura S., Tanaka M., Masamune Y., Yamaguchi K. DNA binding properties of purified replication initiator protein (Rep) encoded by plasmid pSC101. J Biochem. 1990 Mar;107(3):369–376. doi: 10.1093/oxfordjournals.jbchem.a123052. [DOI] [PubMed] [Google Scholar]
  26. Sugiura S., Yamaguchi K. A pseudo-symmetric DNA binding motif of purified Rep dimer of plasmid pSC101. J Biochem. 1993 Oct;114(4):547–552. doi: 10.1093/oxfordjournals.jbchem.a124214. [DOI] [PubMed] [Google Scholar]
  27. Tucker W. T., Miller C. A., Cohen S. N. Structural and functional analysis of the par region of the pSC 10 1 plasmid. Cell. 1984 Aug;38(1):191–201. doi: 10.1016/0092-8674(84)90540-3. [DOI] [PubMed] [Google Scholar]
  28. Uhlin B. E., Nordström K. R plasmid gene dosage effects in Escherichia coli K-12: copy mutants of the R plasmic R1drd-19. Plasmid. 1977 Nov;1(1):1–7. doi: 10.1016/0147-619x(77)90003-8. [DOI] [PubMed] [Google Scholar]
  29. Vocke C., Bastia D. DNA-protein interaction at the origin of DNA replication of the plasmid pSC101. Cell. 1983 Dec;35(2 Pt 1):495–502. doi: 10.1016/0092-8674(83)90183-6. [DOI] [PubMed] [Google Scholar]
  30. Vocke C., Bastia D. Primary structure of the essential replicon of the plasmid pSC101. Proc Natl Acad Sci U S A. 1983 Nov;80(21):6557–6561. doi: 10.1073/pnas.80.21.6557. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Vocke C., Bastia D. The replication initiator protein of plasmid pSC101 is a transcriptional repressor of its own cistron. Proc Natl Acad Sci U S A. 1985 Apr;82(8):2252–2256. doi: 10.1073/pnas.82.8.2252. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Wahle E., Kornberg A. The partition locus of plasmid pSC101 is a specific binding site for DNA gyrase. EMBO J. 1988 Jun;7(6):1889–1895. doi: 10.1002/j.1460-2075.1988.tb03022.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Wickner S., Hoskins J., McKenney K. Function of DnaJ and DnaK as chaperones in origin-specific DNA binding by RepA. Nature. 1991 Mar 14;350(6314):165–167. doi: 10.1038/350165a0. [DOI] [PubMed] [Google Scholar]
  34. Wickner S., Hoskins J., McKenney K. Monomerization of RepA dimers by heat shock proteins activates binding to DNA replication origin. Proc Natl Acad Sci U S A. 1991 Sep 15;88(18):7903–7907. doi: 10.1073/pnas.88.18.7903. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Wickner S., Skowyra D., Hoskins J., McKenney K. DnaJ, DnaK, and GrpE heat shock proteins are required in oriP1 DNA replication solely at the RepA monomerization step. Proc Natl Acad Sci U S A. 1992 Nov 1;89(21):10345–10349. doi: 10.1073/pnas.89.21.10345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Yamaguchi K., Masamune Y. Autogenous regulation of synthesis of the replication protein in plasmid pSC101. Mol Gen Genet. 1985;200(3):362–367. doi: 10.1007/BF00425718. [DOI] [PubMed] [Google Scholar]
  37. Yamaguchi K., Tomizawa J. Establishment of Escherichia coli cells with an integrated high copy number plasmid. Mol Gen Genet. 1980;178(3):525–533. doi: 10.1007/BF00337857. [DOI] [PubMed] [Google Scholar]
  38. Yamaguchi K., Yamaguchi M. The replication origin of pSC101: the nucleotide sequence and replication functions of the ori region. Gene. 1984 Jul-Aug;29(1-2):211–219. doi: 10.1016/0378-1119(84)90181-1. [DOI] [PubMed] [Google Scholar]
  39. 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]

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