Home LiteratureArticle Details
PMID: 6310572 Published · ppublish English Journal Article

DNA inversions in the chromosome of Escherichia coli and in bacteriophage Mu: relationship to other site-specific recombination systems.

Plasterk RH, Brinkman A, van de Putte P

Abstract

The gene product of bacteriophage Mu gin catalyzes a 3,000-base-pair inversion in the DNA of the phage, thus changing its host range. In some strains of Escherichia coli there is a function that can complement Mu gin mutations. This function (pin) was cloned and shown to catalyze an inversion of 1,800 base pairs in the adjacent E. coli DNA (P region). pin- derivatives carry the P region frozen in the (+) or (-) orientation. The function of the switch is not yet clear. The sequences of gin and pin were determined; they exhibit 70% homology. The sequences around the recombination sites of Gin and Pin are also largely homologous; a consensus sequence is derived for the recombination sites of Gin and Pin, and of Hin in Salmonella typhimurium. The amino acid sequences of Gin, Pin, Hin, and TnpR are compared, and the evolutionary relationship between these prokaryotic site-specific recombination systems is discussed.

MeSH Terms
Amino Acid Sequence Bacterial Proteins/genetics Base Sequence Chromosomes, Bacterial/physiology Cloning, Molecular Coliphages/genetics DNA, Bacterial/genetics DNA, Recombinant/metabolism DNA, Viral/genetics Escherichia coli/genetics Genes Genes, Bacterial Genes, Viral Plasmids Viral Proteins/genetics
Chemicals
Bacterial Proteins DNA, Bacterial DNA, Recombinant DNA, Viral Viral Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Plasterk R H
Brinkman A
van de Putte P
References (25)
25 references, click to expand
  1. Inversions of specific DNA segments in flagellar phase variation of Salmonella and inversion systems of bacteriophages P1 and Mu.
    Proc Natl Acad Sci U S A. 1980 Dec;77(12):7338-41 PMID: 7012837
  2. Analysis of the nucleotide sequence of an invertible controlling element.
    Proc Natl Acad Sci U S A. 1980 Jul;77(7):4196-200 PMID: 6933466
  3. Identification of the gin protein of bacteriophage mu.
    Virology. 1981 Oct 15;114(1):291-6 PMID: 6456594
  4. Transposon-mediated site-specific recombination: a defined in vitro system.
    Cell. 1981 Sep;25(3):713-9 PMID: 6269755
  5. Transposon-mediated site-specific recombination in vitro: DNA cleavage and protein-DNA linkage at the recombination site.
    Cell. 1981 Sep;25(3):721-8 PMID: 6269756
  6. The relationship of two invertible segments in bacteriophage Mu and Salmonella typhimurium DNA.
    Mol Gen Genet. 1981;184(3):564-6 PMID: 7038403
  7. G inversion in bacteriophage Mu: a novel way of gene splicing.
    Nature. 1982 May 27;297(5864):339-42 PMID: 6210848
  8. Transposon-mediated site-specific recombination: identification of three binding sites for resolvase at the res sites of gamma delta and Tn3.
    Cell. 1982 Aug;30(1):19-27 PMID: 6290077
  9. 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
  10. Transcription initiation of Mu mom depends on methylation of the promoter region and a phage-coded transactivator.
    Nature. 1983 Jan 27;301(5898):344-7 PMID: 6218410
  11. Site-specific recombination by Gin of bacteriophage Mu: inversions and deletions.
    Virology. 1983 May;127(1):24-36 PMID: 6305017
  12. A site-specific, conservative recombination system carried by bacteriophage P1. Mapping the recombinase gene cin and the cross-over sites cix for the inversion of the C segment.
    EMBO J. 1982;1(11):1445-53 PMID: 6327269
  13. Structure of inserted bacteriophage Mu-1 DNA and physical mapping of bacterial genes by Mu-1 DNA insertion.
    Proc Natl Acad Sci U S A. 1972 Oct;69(10):2823-7 PMID: 4562742
  14. A colony bank containing synthetic Col El hybrid plasmids representative of the entire E. coli genome.
    Cell. 1976 Sep;9(1):91-9 PMID: 788919
  15. The invertible DNA segments of coliphages Mu and P1 are identical.
    Virology. 1976 Oct 1;74(1):242-8 PMID: 982820
  16. Inversion of the G DNA segment of phage Mu controls phage infectivity.
    Nature. 1978 Feb 9;271(5645):577-80 PMID: 622196
  17. DNA sequencing with chain-terminating inhibitors.
    Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463-7 PMID: 271968
  18. The use of thin acrylamide gels for DNA sequencing.
    FEBS Lett. 1978 Mar 1;87(1):107-10 PMID: 631324
  19. In vitro constructed plasmids containing both ends of bacteriophage Mu DNA express phage functions.
    Mol Gen Genet. 1979 Jan 16;169(1):97-105 PMID: 286147
  20. A rapid alkaline extraction procedure for screening recombinant plasmid DNA.
    Nucleic Acids Res. 1979 Nov 24;7(6):1513-23 PMID: 388356
  21. DNA sequence analysis of the transposon Tn3: three genes and three sites involved in transposition of Tn3.
    Cell. 1979 Dec;18(4):1153-63 PMID: 391406
  22. Covalent bonds between protein and DNA. Formation of phosphotyrosine linkage between certain DNA topoisomerases and DNA.
    J Biol Chem. 1980 Jun 25;255(12):5560-5 PMID: 6155377
  23. Invertible DNA determines host specificity of bacteriophage mu.
    Nature. 1980 Jul 17;286(5770):218-22 PMID: 6250048
  24. Phase variation: evolution of a controlling element.
    Science. 1980 Sep 19;209(4463):1370-4 PMID: 6251543
  25. Resolution of cointegrates between transposons gamma delta and Tn3 defines the recombination site.
    Proc Natl Acad Sci U S A. 1981 Jun;78(6):3428-32 PMID: 6267590
Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1983-09-00
Pages
5355-8
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC384254
Subset
IM
Databases
GENBANK
K00676, K00677, V01463
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: [email protected]