Home LiteratureArticle Details
PMID: 3294000 Published · ppublish English Journal Article

Resolution of ColE1 dimers requires a DNA sequence implicated in the three-dimensional organization of the cer site.

The EMBO journal ·Vol. 7 ·No. 3 ·1988-03-00 ·Pages 851-8

Summers DK, Sherratt DJ

Abstract

Plasmid ColE1 specifies a recombination site (cer) which participates in the conversion of plasmid dimers to monomers. The uncontrolled accumulation of dimers (and higher oligomeric forms) would otherwise lead to plasmid instability. Exonuclease III-generated deletions have been used to define the left-hand boundary of the cer site. Deletions which have lost up to 60 bp adjacent to the boundary no longer mediate the conversion of plasmid dimers to monomers, but still recombine with a wild-type site. Although this boundary region is essential for dimer resolution, its DNA sequence is poorly conserved among multimer resolution sites in related plasmids. We present evidence that its function is to influence the three-dimensional organization of the site and suggest that it may be required for the formation of a condensed nucleoprotein complex.

MeSH Terms
Chromosome Deletion DNA, Bacterial/genetics,metabolism Escherichia coli Molecular Conformation Plasmids Recombination, Genetic Sequence Homology, Nucleic Acid
Chemicals
DNA, Bacterial
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Summers D K
University of Cambridge, Department of Genetics, UK.
Sherratt D J
References (27)
27 references, click to expand
  1. Induction of colicin production by high temperature or inhibition of protein synthesis.
    J Bacteriol. 1971 Oct;108(1):10-9 PMID: 4941551
  2. Bacteriophage lambda int protein recognizes two classes of sequence in the phage att site: characterization of arm-type sites.
    Proc Natl Acad Sci U S A. 1982 Dec;79(24):7724-8 PMID: 6218502
  3. Pedigrees of some mutant strains of Escherichia coli K-12.
    Bacteriol Rev. 1972 Dec;36(4):525-57 PMID: 4568763
  4. DNA sequencing with chain-terminating inhibitors.
    Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463-7 PMID: 271968
  5. Sequence analysis of the DNA encoding the Eco RI endonuclease and methylase.
    J Biol Chem. 1981 Mar 10;256(5):2143-53 PMID: 6257703
  6. A system for shotgun DNA sequencing.
    Nucleic Acids Res. 1981 Jan 24;9(2):309-21 PMID: 6259625
  7. A rapid boiling method for the preparation of bacterial plasmids.
    Anal Biochem. 1981 Jun;114(1):193-7 PMID: 6269464
  8. recA-independent general genetic recombination of plasmids.
    Nature. 1981 Nov 12;294(5837):184-6 PMID: 7029308
  9. Oligonucleotide-directed mutagenesis using M13-derived vectors: an efficient and general procedure for the production of point mutations in any fragment of DNA.
    Nucleic Acids Res. 1982 Oct 25;10(20):6487-500 PMID: 6757864
  10. A new pair of M13 vectors for selecting either DNA strand of double-digest restriction fragments.
    Gene. 1982 Oct;19(3):269-76 PMID: 6295880
  11. Requirement for an upstream element for optimal transcription of a bacterial tRNA gene.
    Nature. 1983 Sep 15-21;305(5931):248-50 PMID: 6350894
  12. Maintenance of multicopy plasmid Clo DF13 in E. coli cells: evidence for site-specific recombination at parB.
    Cell. 1984 Jan;36(1):203-9 PMID: 6319008
  13. Multimerization of high copy number plasmids causes instability: CoIE1 encodes a determinant essential for plasmid monomerization and stability.
    Cell. 1984 Apr;36(4):1097-103 PMID: 6323019
  14. Construction of improved M13 vectors using oligodeoxynucleotide-directed mutagenesis.
    Gene. 1983 Dec;26(1):101-6 PMID: 6323249
  15. Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing.
    Gene. 1984 Jun;28(3):351-9 PMID: 6235151
  16. Site-specific recombination in transposition and plasmid stability.
    Cold Spring Harb Symp Quant Biol. 1984;49:227-33 PMID: 6099237
  17. Improved oligonucleotide site-directed mutagenesis using M13 vectors.
    Nucleic Acids Res. 1985 Jun 25;13(12):4431-43 PMID: 2989795
  18. Nucleotide sequence and gene organization of ColE1 DNA.
    J Biol Chem. 1985 Jul 25;260(15):8925-35 PMID: 2991225
  19. Sequence-induced DNA curvature at the bacteriophage lambda origin of replication.
    Nature. 1985 Oct 3-9;317(6036):451-3 PMID: 2995831
  20. Nucleotide sequence of the partition function of Escherichia coli plasmid ColE1.
    DNA. 1985 Oct;4(5):351-5 PMID: 3908032
  21. Multimer resolution systems of ColE1 and ColK: localisation of the crossover site.
    Mol Gen Genet. 1985;201(2):334-8 PMID: 3003536
  22. DNA bending and its relation to nucleosome positioning.
    J Mol Biol. 1985 Dec 20;186(4):773-90 PMID: 3912515
  23. Host protein requirements for in vitro site-specific DNA inversion.
    Cell. 1986 Aug 15;46(4):531-9 PMID: 3524854
  24. Multiple DNA-protein interactions governing high-precision DNA transactions.
    Science. 1986 Sep 5;233(4768):1050-6 PMID: 2943018
  25. Sequence periodicities in chicken nucleosome core DNA.
    J Mol Biol. 1986 Oct 20;191(4):659-75 PMID: 3806678
  26. A system to study promoter and terminator signals recognized by Escherichia coli RNA polymerase.
    Gene Amplif Anal. 1981;2:383-415 PMID: 6101056
  27. Nonchromosomal antibiotic resistance in bacteria: genetic transformation of Escherichia coli by R-factor DNA.
    Proc Natl Acad Sci U S A. 1972 Aug;69(8):2110-4 PMID: 4559594
Article Info
Journal
The EMBO journal
Abbr.
EMBO J
ISSN
0261-4189
Published
1988-03-00
Pages
851-8
Language
English
Region
England
NLM ID
8208664
PMCID
PMC454402
Subset
IM
Databases
GENBANK
X07185
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com