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. 1997 Nov 3;16(21):6574–6583. doi: 10.1093/emboj/16.21.6574

DnaA protein binding to individual DnaA boxes in the Escherichia coli replication origin, oriC.

C Weigel 1, A Schmidt 1, B Rückert 1, R Lurz 1, W Messer 1
PMCID: PMC1170261  PMID: 9351837

Abstract

The formation of nucleoprotein complexes between the Escherichia coli initiator protein DnaA and the replication origin oriC was analysed in vitro by band-shift assays and electron microscopy. DnaA protein binds equally well to linear and supercoiled oriC substrates as revealed by analysis of the binding preference to individual DnaA boxes (9-mer repeats) in oriC, and by a competition band-shift assay. DnaA box R4 (oriC positions 260-268) binds DnaA preferentially and in the oriC context with higher affinity than expected from its binding constant. This effect depends on oriC positions 249 to 274, is enhanced by the wild-type sequence in the DnaA box R3 region, but is not dependent on Dam methylation or the curved DNA segment to the right of oriC. DnaA binds randomly to the DnaA boxes R1, M, R2 and R3 in oriC with no apparent cooperativity: the binding preference of DnaA to these sites was not altered for templates with mutated DnaA box R4. In the oriC context, DnaA box R1 binds DnaA with lower affinity than expected from its binding constant, i.e. the affinity is reduced to approximately that of DnaA box R2. Higher protein concentrations were required to observe binding to DnaA box M, making this low-affinity site a novel candidate for a regulatory dnaA box.

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Selected References

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  1. Baker T. A., Funnell B. E., Kornberg A. Helicase action of dnaB protein during replication from the Escherichia coli chromosomal origin in vitro. J Biol Chem. 1987 May 15;262(14):6877–6885. [PubMed] [Google Scholar]
  2. Bates D. B., Asai T., Cao Y., Chambers M. W., Cadwell G. W., Boye E., Kogoma T. The DnaA box R4 in the minimal oriC is dispensable for initiation of Escherichia coli chromosome replication. Nucleic Acids Res. 1995 Aug 25;23(16):3119–3125. doi: 10.1093/nar/23.16.3119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bramhill D., Kornberg A. Duplex opening by dnaA protein at novel sequences in initiation of replication at the origin of the E. coli chromosome. Cell. 1988 Mar 11;52(5):743–755. doi: 10.1016/0092-8674(88)90412-6. [DOI] [PubMed] [Google Scholar]
  4. Buhk H. J., Messer W. The replication origin region of Escherichia coli: nucleotide sequence and functional units. Gene. 1983 Oct;24(2-3):265–279. doi: 10.1016/0378-1119(83)90087-2. [DOI] [PubMed] [Google Scholar]
  5. Cassler M. R., Grimwade J. E., Leonard A. C. Cell cycle-specific changes in nucleoprotein complexes at a chromosomal replication origin. EMBO J. 1995 Dec 1;14(23):5833–5841. doi: 10.1002/j.1460-2075.1995.tb00271.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Crooke E., Thresher R., Hwang D. S., Griffith J., Kornberg A. Replicatively active complexes of DnaA protein and the Escherichia coli chromosomal origin observed in the electron microscope. J Mol Biol. 1993 Sep 5;233(1):16–24. doi: 10.1006/jmbi.1993.1481. [DOI] [PubMed] [Google Scholar]
  7. Fuller R. S., Funnell B. E., Kornberg A. The dnaA protein complex with the E. coli chromosomal replication origin (oriC) and other DNA sites. Cell. 1984 Oct;38(3):889–900. doi: 10.1016/0092-8674(84)90284-8. [DOI] [PubMed] [Google Scholar]
  8. Fuller R. S., Kaguni J. M., Kornberg A. Enzymatic replication of the origin of the Escherichia coli chromosome. Proc Natl Acad Sci U S A. 1981 Dec;78(12):7370–7374. doi: 10.1073/pnas.78.12.7370. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Funnell B. E., Baker T. A., Kornberg A. In vitro assembly of a prepriming complex at the origin of the Escherichia coli chromosome. J Biol Chem. 1987 Jul 25;262(21):10327–10334. [PubMed] [Google Scholar]
  10. Gille H., Messer W. Localized DNA melting and structural pertubations in the origin of replication, oriC, of Escherichia coli in vitro and in vivo. EMBO J. 1991 Jun;10(6):1579–1584. doi: 10.1002/j.1460-2075.1991.tb07678.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Holz A., Schaefer C., Gille H., Jueterbock W. R., Messer W. Mutations in the DnaA binding sites of the replication origin of Escherichia coli. Mol Gen Genet. 1992 May;233(1-2):81–88. doi: 10.1007/BF00587564. [DOI] [PubMed] [Google Scholar]
  12. Hsu J., Bramhill D., Thompson C. M. Open complex formation by DnaA initiation protein at the Escherichia coli chromosomal origin requires the 13-mers precisely spaced relative to the 9-mers. Mol Microbiol. 1994 Mar;11(5):903–911. doi: 10.1111/j.1365-2958.1994.tb00369.x. [DOI] [PubMed] [Google Scholar]
  13. Hwang D. S., Kornberg A. Opening of the replication origin of Escherichia coli by DnaA protein with protein HU or IHF. J Biol Chem. 1992 Nov 15;267(32):23083–23086. [PubMed] [Google Scholar]
  14. Kimura T., Asai T., Imai M., Takanami M. Methylation strongly enhances DNA bending in the replication origin region of the Escherichia coli chromosome. Mol Gen Genet. 1989 Oct;219(1-2):69–74. doi: 10.1007/BF00261159. [DOI] [PubMed] [Google Scholar]
  15. Kline B. C., Kogoma T., Tam J. E., Shields M. S. Requirement of the Escherichia coli dnaA gene product for plasmid F maintenance. J Bacteriol. 1986 Oct;168(1):440–443. doi: 10.1128/jb.168.1.440-443.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Langer U., Richter S., Roth A., Weigel C., Messer W. A comprehensive set of DnaA-box mutations in the replication origin, oriC, of Escherichia coli. Mol Microbiol. 1996 Jul;21(2):301–311. doi: 10.1046/j.1365-2958.1996.6481362.x. [DOI] [PubMed] [Google Scholar]
  17. Margulies C., Kaguni J. M. Ordered and sequential binding of DnaA protein to oriC, the chromosomal origin of Escherichia coli. J Biol Chem. 1996 Jul 19;271(29):17035–17040. doi: 10.1074/jbc.271.29.17035. [DOI] [PubMed] [Google Scholar]
  18. Marszalek J., Kaguni J. M. DnaA protein directs the binding of DnaB protein in initiation of DNA replication in Escherichia coli. J Biol Chem. 1994 Feb 18;269(7):4883–4890. [PubMed] [Google Scholar]
  19. Matsui M., Oka A., Takanami M., Yasuda S., Hirota Y. Sites of dnaA protein-binding in the replication origin of the Escherichia coli K-12 chromosome. J Mol Biol. 1985 Aug 5;184(3):529–533. doi: 10.1016/0022-2836(85)90299-2. [DOI] [PubMed] [Google Scholar]
  20. Messer W., Hartmann-Kühlein H., Langer U., Mahlow E., Roth A., Schaper S., Urmoneit B., Woelker B. The complex for replication initiation of Escherichia coli. Chromosoma. 1992;102(1 Suppl):S1–S6. doi: 10.1007/BF02451779. [DOI] [PubMed] [Google Scholar]
  21. Parada C. A., Marians K. J. Mechanism of DNA A protein-dependent pBR322 DNA replication. DNA A protein-mediated trans-strand loading of the DNA B protein at the origin of pBR322 DNA. J Biol Chem. 1991 Oct 5;266(28):18895–18906. [PubMed] [Google Scholar]
  22. Pérez-Martín J., del Solar G. H., Lurz R., de la Campa A. G., Dobrinski B., Espinosa M. Induced bending of plasmid pLS1 DNA by the plasmid-encoded protein RepA. J Biol Chem. 1989 Dec 15;264(35):21334–21339. [PubMed] [Google Scholar]
  23. Roth A., Messer W. The DNA binding domain of the initiator protein DnaA. EMBO J. 1995 May 1;14(9):2106–2111. doi: 10.1002/j.1460-2075.1995.tb07202.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Samitt C. E., Hansen F. G., Miller J. F., Schaechter M. In vivo studies of DnaA binding to the origin of replication of Escherichia coli. EMBO J. 1989 Mar;8(3):989–993. doi: 10.1002/j.1460-2075.1989.tb03462.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Schaper S., Messer W. Interaction of the initiator protein DnaA of Escherichia coli with its DNA target. J Biol Chem. 1995 Jul 21;270(29):17622–17626. doi: 10.1074/jbc.270.29.17622. [DOI] [PubMed] [Google Scholar]
  26. Sekimizu K., Bramhill D., Kornberg A. Sequential early stages in the in vitro initiation of replication at the origin of the Escherichia coli chromosome. J Biol Chem. 1988 May 25;263(15):7124–7130. [PubMed] [Google Scholar]
  27. Sekimizu K., Yung B. Y., Kornberg A. The dnaA protein of Escherichia coli. Abundance, improved purification, and membrane binding. J Biol Chem. 1988 May 25;263(15):7136–7140. [PubMed] [Google Scholar]
  28. Seufert W., Messer W. Start sites for bidirectional in vitro DNA replication inside the replication origin, oriC, of Escherichia coli. EMBO J. 1987 Aug;6(8):2469–2472. doi: 10.1002/j.1460-2075.1987.tb02527.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Skarstad K., Boye E. The initiator protein DnaA: evolution, properties and function. Biochim Biophys Acta. 1994 Mar 1;1217(2):111–130. doi: 10.1016/0167-4781(94)90025-6. [DOI] [PubMed] [Google Scholar]
  30. Woelker B., Messer W. The structure of the initiation complex at the replication origin, oriC, of Escherichia coli. Nucleic Acids Res. 1993 Nov 11;21(22):5025–5033. doi: 10.1093/nar/21.22.5025. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Yoshikawa H., Ogasawara N. Structure and function of DnaA and the DnaA-box in eubacteria: evolutionary relationships of bacterial replication origins. Mol Microbiol. 1991 Nov;5(11):2589–2597. doi: 10.1111/j.1365-2958.1991.tb01967.x. [DOI] [PubMed] [Google Scholar]
  32. Zakrzewska-Czerwińska J., Schrempf H. Characterization of an autonomously replicating region from the Streptomyces lividans chromosome. J Bacteriol. 1992 Apr;174(8):2688–2693. doi: 10.1128/jb.174.8.2688-2693.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]

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