Literature DB >> 3006102

The EcoR124 and EcoR124/3 restriction and modification systems: cloning the genes.

K Firman, C Price, S W Glover.   

Abstract

The Escherichia coli plasmid R124 codes for a type I restriction and modification system EcoR124 and carries genetic information, most probably in the form of a "silent copy," for the expression of a different R-M specificity R124/3. Characteristic DNA rearrangements have been shown to accompany the switch in specificity from R124 to R124/3 and vice versa. We have cloned a 14.2-kb HindIII fragment from R124 and shown that it contains the hsdR, hsdM, and hsdS genes which code for the EcoR124 R-M system. An equivalent fragment from the plasmid R124/3 following the switch in R-M specificity has also been cloned and shown to contain the genes coding for the EcoR124/3 R-M system. These fragments, however, lack a component present on the wild-type plasmid essential for the switch in specificity. Restriction fragment maps and preliminary heteroduplex analysis indicate the near identity of the genes that encode the two different DNA recognition specificities. Transposon mutagenesis was used to locate the positions of the hsdR, hsdM, and hsdS genes on the cloned fragments in conjunction with complementation tests for gene function. Indirect evidence indicates that hsdR is expressed from its own promoter and that hsdM and hsdS are expressed from a single promoter, unidirectionally.

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Year:  1985        PMID: 3006102     DOI: 10.1016/0147-619x(85)90006-x

Source DB:  PubMed          Journal:  Plasmid        ISSN: 0147-619X            Impact factor:   3.466


  13 in total

1.  Identification of the EcoKI and EcoR124I Type I restriction--modification enzyme subunits by non-equilibrium pH gradient two-dimensional gel electrophoresis.

Authors:  L D Nguyen; K Cajthamlová; H T Nguyen; J Weiser; I Holubová; M Weiserová
Journal:  Folia Microbiol (Praha)       Date:  2002       Impact factor: 2.099

2.  The HsdR subunit of R.EcoR124II: cloning and over-expression of the gene and unexpected properties of the subunit.

Authors:  V Zinkevich; L Popova; V Kryukov; A Abadjieva; I Bogdarina; P Janscak; K Firman
Journal:  Nucleic Acids Res       Date:  1997-02-01       Impact factor: 16.971

3.  A deletion mutant of the type IC restriction endonuclease EcoR1241 expressing a novel DNA specificity.

Authors:  A Abadjieva; J Patel; M Webb; V Zinkevich; K Firman
Journal:  Nucleic Acids Res       Date:  1993-09-25       Impact factor: 16.971

4.  Complementation and hybridization evidence for additional families of type I DNA restriction and modification genes in Salmonella serotypes.

Authors:  J Ryu; P T Rajadas; L R Bullas
Journal:  J Bacteriol       Date:  1988-12       Impact factor: 3.490

5.  The effect of recA mutation on the expression of EcoKI and EcoR124I hsd genes cloned in a multicopy plasmid.

Authors:  J Hubácek; I Holubová; M Weiserová
Journal:  Folia Microbiol (Praha)       Date:  1998       Impact factor: 2.099

Review 6.  EcoR124I: from plasmid-encoded restriction-modification system to nanodevice.

Authors:  James Youell; Keith Firman
Journal:  Microbiol Mol Biol Rev       Date:  2008-06       Impact factor: 11.056

7.  Restriction endonucleases R.EcoKI and R.EcoR124I are probably located in different environments within the bacterial cell.

Authors:  J Hubácek; M Weiserová; P Janscák; K Firman
Journal:  Folia Microbiol (Praha)       Date:  1994       Impact factor: 2.099

8.  Increased protein flexibility leads to promiscuous protein--DNA interactions in type IC restriction-modification systems.

Authors:  M Gubler; T A Bickle
Journal:  EMBO J       Date:  1991-04       Impact factor: 11.598

9.  Recombination of constant and variable modules alters DNA sequence recognition by type IC restriction-modification enzymes.

Authors:  M Gubler; D Braguglia; J Meyer; A Piekarowicz; T A Bickle
Journal:  EMBO J       Date:  1992-01       Impact factor: 11.598

10.  HsdR subunit of the type I restriction-modification enzyme EcoR124I: biophysical characterisation and structural modelling.

Authors:  Agnieszka Obarska-Kosinska; James E Taylor; Philip Callow; Jerzy Orlowski; Janusz M Bujnicki; G Geoff Kneale
Journal:  J Mol Biol       Date:  2007-11-17       Impact factor: 5.469

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