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. 1994 Sep;176(18):5814–5819. doi: 10.1128/jb.176.18.5814-5819.1994

An unusual gene containing a dnaJ N-terminal box flanks the putative origin of replication of Mycoplasma genitalium.

C C Bailey 1, K F Bott 1
PMCID: PMC196786  PMID: 8083173

Abstract

Origins of replication are known to be highly conserved among widely divergent microbial species, with the gene order in those regions being dnaA-dnaN-recF-gyrB. On the basis of sequence identities to entries in GenBank, the gene order of a 6-kb fragment of Mycoplasma genitalium DNA was determined to be dnaN-orf311-gyrB-gyrA-serS, which is structurally similar to the ancestral origin of replication. We have directly linked the dnaN gene to the M. genitalium dnaA gene by PCR amplification. However, we found a novel open reading frame, designated orf311, in place of an expected sequence encoding recF. Orf311 contains a DnaJ box motif at its N terminus, but it has no overall homology to any other protein or sequence in the database. We are unable to detect any recF homolog in M. genitalium by hybridization or during a random sequencing survey of the genome.

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Selected References

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

  1. Alonso J. C., Lüder G., Tailor R. H. Characterization of Bacillus subtilis recombinational pathways. J Bacteriol. 1991 Jul;173(13):3977–3980. doi: 10.1128/jb.173.13.3977-3980.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bork P., Sander C., Valencia A., Bukau B. A module of the DnaJ heat shock proteins found in malaria parasites. Trends Biochem Sci. 1992 Apr;17(4):129–129. doi: 10.1016/0968-0004(92)90319-5. [DOI] [PubMed] [Google Scholar]
  3. Brockbank S. M., Barth P. T. Cloning, sequencing, and expression of the DNA gyrase genes from Staphylococcus aureus. J Bacteriol. 1993 Jun;175(11):3269–3277. doi: 10.1128/jb.175.11.3269-3277.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Caplan A. J., Cyr D. M., Douglas M. G. Eukaryotic homologues of Escherichia coli dnaJ: a diverse protein family that functions with hsp70 stress proteins. Mol Biol Cell. 1993 Jun;4(6):555–563. doi: 10.1091/mbc.4.6.555. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Colman S. D., Hu P. C., Bott K. F. Mycoplasma pneumoniae DNA gyrase genes. Mol Microbiol. 1990 Jul;4(7):1129–1134. doi: 10.1111/j.1365-2958.1990.tb00687.x. [DOI] [PubMed] [Google Scholar]
  6. Colman S. D., Hu P. C., Litaker W., Bott K. F. A physical map of the Mycoplasma genitalium genome. Mol Microbiol. 1990 Apr;4(4):683–687. doi: 10.1111/j.1365-2958.1990.tb00638.x. [DOI] [PubMed] [Google Scholar]
  7. Davies C. J., Hutchison C. A., 3rd A directed DNA sequencing strategy based upon Tn3 transposon mutagenesis: application to the ADE1 locus on Saccharomyces cerevisiae chromosome I. Nucleic Acids Res. 1991 Oct 25;19(20):5731–5738. doi: 10.1093/nar/19.20.5731. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Devereux J., Haeberli P., Smithies O. A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. 1984 Jan 11;12(1 Pt 1):387–395. doi: 10.1093/nar/12.1part1.387. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Dybvig K., Hollingshead S. K., Heath D. G., Clewell D. B., Sun F., Woodard A. Degenerate oligonucleotide primers for enzymatic amplification of recA sequences from gram-positive bacteria and mycoplasmas. J Bacteriol. 1992 Apr;174(8):2729–2732. doi: 10.1128/jb.174.8.2729-2732.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Lai C. Y., Baumann P. Genetic analysis of an aphid endosymbiont DNA fragment homologous to the rnpA-rpmH-dnaA-dnaN-gyrB region of eubacteria. Gene. 1992 Apr 15;113(2):175–181. doi: 10.1016/0378-1119(92)90393-4. [DOI] [PubMed] [Google Scholar]
  11. Lampe M. F., Bott K. F. Genetic and physical organization of the cloned gyrA and gyrB genes of Bacillus subtilis. J Bacteriol. 1985 Apr;162(1):78–84. doi: 10.1128/jb.162.1.78-84.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Madiraju M. V., Clark A. J. Evidence for ATP binding and double-stranded DNA binding by Escherichia coli RecF protein. J Bacteriol. 1992 Dec;174(23):7705–7710. doi: 10.1128/jb.174.23.7705-7710.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Miyata M., Sano K., Okada R., Fukumura T. Mapping of replication initiation site in Mycoplasma capricolum genome by two-dimensional gel-electrophoretic analysis. Nucleic Acids Res. 1993 Oct 11;21(20):4816–4823. doi: 10.1093/nar/21.20.4816. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Ogasawara N., Yoshikawa H. Genes and their organization in the replication origin region of the bacterial chromosome. Mol Microbiol. 1992 Mar;6(5):629–634. doi: 10.1111/j.1365-2958.1992.tb01510.x. [DOI] [PubMed] [Google Scholar]
  15. Old I. G., Margarita D., Saint Girons I. Unique genetic arrangement in the dnaA region of the Borrelia burgdorferi linear chromosome: nucleotide sequence of the dnaA gene. FEMS Microbiol Lett. 1993 Jul 15;111(1):109–114. doi: 10.1111/j.1574-6968.1993.tb06369.x. [DOI] [PubMed] [Google Scholar]
  16. Peterson S. N., Hu P. C., Bott K. F., Hutchison C. A., 3rd A survey of the Mycoplasma genitalium genome by using random sequencing. J Bacteriol. 1993 Dec;175(24):7918–7930. doi: 10.1128/jb.175.24.7918-7930.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Peterson S. N., Schramm N., Hu P. C., Bott K. F., Hutchison C. A., 3rd A random sequencing approach for placing markers on the physical map of Mycoplasma genitalium. Nucleic Acids Res. 1991 Nov 11;19(21):6027–6031. doi: 10.1093/nar/19.21.6027. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Razin S. Molecular biology and genetics of mycoplasmas (Mollicutes). Microbiol Rev. 1985 Dec;49(4):419–455. doi: 10.1128/mr.49.4.419-455.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Reece R. J., Maxwell A. DNA gyrase: structure and function. Crit Rev Biochem Mol Biol. 1991;26(3-4):335–375. doi: 10.3109/10409239109114072. [DOI] [PubMed] [Google Scholar]
  20. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Smith D. W., Yee T. W., Baird C., Krishnapillai V. Pseudomonad replication origins: a paradigm for bacterial origins? Mol Microbiol. 1991 Nov;5(11):2581–2587. doi: 10.1111/j.1365-2958.1991.tb01966.x. [DOI] [PubMed] [Google Scholar]
  22. Smith G. E., Summers M. D. The bidirectional transfer of DNA and RNA to nitrocellulose or diazobenzyloxymethyl-paper. Anal Biochem. 1980 Nov 15;109(1):123–129. doi: 10.1016/0003-2697(80)90019-6. [DOI] [PubMed] [Google Scholar]
  23. Smith G. R. Homologous recombination in procaryotes. Microbiol Rev. 1988 Mar;52(1):1–28. doi: 10.1128/mr.52.1.1-28.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
  25. Tamura J. K., Gellert M. Characterization of the ATP binding site on Escherichia coli DNA gyrase. Affinity labeling of Lys-103 and Lys-110 of the B subunit by pyridoxal 5'-diphospho-5'-adenosine. J Biol Chem. 1990 Dec 5;265(34):21342–21349. [PubMed] [Google Scholar]
  26. Woese C. R., Maniloff J., Zablen L. B. Phylogenetic analysis of the mycoplasmas. Proc Natl Acad Sci U S A. 1980 Jan;77(1):494–498. doi: 10.1073/pnas.77.1.494. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Zweiger G., Shapiro L. Expression of Caulobacter dnaA as a function of the cell cycle. J Bacteriol. 1994 Jan;176(2):401–408. doi: 10.1128/jb.176.2.401-408.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]

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