Literature DB >> 3001318

EcoA: the first member of a new family of type I restriction modification systems. Gene organization and enzymatic activities.

B Suri, T A Bickle.   

Abstract

The characterization of the EcoA restriction-modification enzymes from Escherichia coli 15T- is described. The reactions catalysed by these enzymes are very similar to those catalysed by the classical type I restriction and modification enzymes, a family of genetically related proteins. The detailed mechanisms, particularly for DNA modification, differ. The genetic and transcriptional organizations are also very similar to those of the classical systems, despite the fact that EcoA is not allelic to the others. We demonstrate that the expression of the EcoA genes is controlled following conjugative transfer to other strains in such a way that no lethality is observed, probably because the recipient chromosome is completely modified before restriction activity is expressed.

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Year:  1985        PMID: 3001318     DOI: 10.1016/0022-2836(85)90258-x

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  24 in total

Review 1.  Type I restriction systems: sophisticated molecular machines (a legacy of Bertani and Weigle).

Authors:  N E Murray
Journal:  Microbiol Mol Biol Rev       Date:  2000-06       Impact factor: 11.056

Review 2.  Nucleoside triphosphate-dependent restriction enzymes.

Authors:  D T Dryden; N E Murray; D N Rao
Journal:  Nucleic Acids Res       Date:  2001-09-15       Impact factor: 16.971

3.  Purification and biochemical characterisation of the EcoR124 type I modification methylase.

Authors:  I Taylor; J Patel; K Firman; G Kneale
Journal:  Nucleic Acids Res       Date:  1992-01-25       Impact factor: 16.971

4.  Transfer of the genes for the StyLTI restriction-modification system of Salmonella typhimurium to strains lacking modification ability results in death of the recipient cells and degradation of their DNA.

Authors:  O De Backer; C Colson
Journal:  J Bacteriol       Date:  1991-02       Impact factor: 3.490

5.  High resolution footprinting of a type I methyltransferase reveals a large structural distortion within the DNA recognition site.

Authors:  D R Mernagh; G G Kneale
Journal:  Nucleic Acids Res       Date:  1996-12-15       Impact factor: 16.971

6.  Substrate recognition and selectivity in the type IC DNA modification methylase M.EcoR124I.

Authors:  I Taylor; D Watts; G Kneale
Journal:  Nucleic Acids Res       Date:  1993-10-25       Impact factor: 16.971

7.  Delayed expression of in vivo restriction activity following conjugal transfer of Escherichia coli hsdK (restriction-modification) genes.

Authors:  A Prakash-Cheng; J Ryu
Journal:  J Bacteriol       Date:  1993-08       Impact factor: 3.490

Review 8.  Biology of DNA restriction.

Authors:  T A Bickle; D H Krüger
Journal:  Microbiol Rev       Date:  1993-06

9.  Pathological phenotypes and in vivo DNA cleavage by unrestrained activity of a phosphorothioate-based restriction system in Salmonella.

Authors:  Bo Cao; Qiuxiang Cheng; Chen Gu; Fen Yao; Michael S DeMott; Xiaoqing Zheng; Zixin Deng; Peter C Dedon; Delin You
Journal:  Mol Microbiol       Date:  2014-07-23       Impact factor: 3.501

10.  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

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