Literature DB >> 9157244

The type IC hsd loci of the enterobacteria are flanked by DNA with high homology to the phage P1 genome: implications for the evolution and spread of DNA restriction systems.

C Tyndall1, H Lehnherr, U Sandmeier, E Kulik, T A Bickle.   

Abstract

EcoR124l, EcoDXXl and Ecoprrl are the known members of the type IC family of DNA restriction and modification systems. The first three are carried on large, conjugative plasmids, while Ecoprrl is chromosomally encoded. The enzymes are coded by three genes, hsdR, hsdM and hsdS. Analysis of the DNA sequences upstream and downstream of the type IC hsd loci shows that all are highly homologous to each other and also to sequences present in the bacteriophage P1 genome. The upstream sequences include functional phd and doc genes, which encode an addiction system that stabilizes the P1 prophage state, and extend to and beyond pac, the site at which phage DNA packaging begins. Downstream of the hsd loci, P1 DNA sequences begin at exactly the same place for all of the systems. For EcoDXXl and Ecoprrl the P1 homology extends for thousands of base pairs while for EcoR124l and IS1 insertion and an associated deletion have removed most of the P1-homologous sequences. The significance of these results for the evolution of DNA restriction and modification systems is discussed.

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Year:  1997        PMID: 9157244     DOI: 10.1046/j.1365-2958.1997.2531622.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  14 in total

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Authors:  K Gerdes
Journal:  J Bacteriol       Date:  2000-02       Impact factor: 3.490

2.  Modular organization of the Phd repressor/antitoxin protein.

Authors:  Jeremy Allen Smith; Roy David Magnuson
Journal:  J Bacteriol       Date:  2004-05       Impact factor: 3.490

3.  Hypothetical functions of toxin-antitoxin systems.

Authors:  Roy David Magnuson
Journal:  J Bacteriol       Date:  2007-07-06       Impact factor: 3.490

4.  A species barrier between bacteriophages T2 and T4: exclusion, join-copy and join-cut-copy recombination and mutagenesis in the dCTPase genes.

Authors:  T P Gary; N E Colowick; G Mosig
Journal:  Genetics       Date:  1998-04       Impact factor: 4.562

5.  A prediction of the amino acids and structures involved in DNA recognition by type I DNA restriction and modification enzymes.

Authors:  S S Sturrock; D T Dryden
Journal:  Nucleic Acids Res       Date:  1997-09-01       Impact factor: 16.971

6.  When Competing Viruses Unify: Evolution, Conservation, and Plasticity of Genetic Identities.

Authors:  Luis P Villarreal; Guenther Witzany
Journal:  J Mol Evol       Date:  2015-05-27       Impact factor: 2.395

7.  Evidence for horizontal transfer of the EcoT38I restriction-modification gene to chromosomal DNA by the P2 phage and diversity of defective P2 prophages in Escherichia coli TH38 strains.

Authors:  Keiko Kita; Hideaki Kawakami; Hiroaki Tanaka
Journal:  J Bacteriol       Date:  2003-04       Impact factor: 3.490

8.  Families of restriction enzymes: an analysis prompted by molecular and genetic data for type ID restriction and modification systems.

Authors:  A J Titheradge; J King; J Ryu; N E Murray
Journal:  Nucleic Acids Res       Date:  2001-10-15       Impact factor: 16.971

9.  Sequence of conjugative plasmid pIP1206 mediating resistance to aminoglycosides by 16S rRNA methylation and to hydrophilic fluoroquinolones by efflux.

Authors:  Bruno Périchon; Pierre Bogaerts; Thierry Lambert; Lionel Frangeul; Patrice Courvalin; Marc Galimand
Journal:  Antimicrob Agents Chemother       Date:  2008-05-05       Impact factor: 5.191

10.  Genome comparison and context analysis reveals putative mobile forms of restriction-modification systems and related rearrangements.

Authors:  Yoshikazu Furuta; Kentaro Abe; Ichizo Kobayashi
Journal:  Nucleic Acids Res       Date:  2010-01-12       Impact factor: 16.971

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