Literature DB >> 10476036

Norfloxacin-induced DNA cleavage occurs at the dif resolvase locus in Escherichia coli and is the result of interaction with topoisomerase IV.

A Hojgaard1, H Szerlong, C Tabor, P Kuempel.   

Abstract

The dif locus is a site-specific recombination site located within the terminus region of the chromosome of Escherichia coli. Recombination at dif resolves circular dimer chromosomes to monomers, and this recombination requires the XerC, XerD and FtsK proteins, as well as cell division. In order to characterize other enzymes that interact at dif, we tested whether quinolone-induced cleavage occurs at this site. Quinolone drugs, such as norfloxacin, inhibit the type 2 topoisomerases, DNA gyrase and topoisomerase IV, and can cleave DNA at sites where these enzymes interact with the chromosome. Using strains in which either DNA gyrase or topoisomerase IV, or both, were resistant to norfloxacin, we determined that specific interactions between dif and topoisomerase IV caused cleavage at that site. This interaction required XerC and XerD, but did not require the C-terminal region of FtsK or cell division.

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Year:  1999        PMID: 10476036     DOI: 10.1046/j.1365-2958.1999.01545.x

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


  16 in total

1.  FtsK functions in the processing of a Holliday junction intermediate during bacterial chromosome segregation.

Authors:  F X Barre; M Aroyo; S D Colloms; A Helfrich; F Cornet; D J Sherratt
Journal:  Genes Dev       Date:  2000-12-01       Impact factor: 11.361

Review 2.  DNA replication meets genetic exchange: chromosomal damage and its repair by homologous recombination.

Authors:  A Kuzminov
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

3.  Decatenation of DNA circles by FtsK-dependent Xer site-specific recombination.

Authors:  Stephen C Y Ip; Migena Bregu; François-Xavier Barre; David J Sherratt
Journal:  EMBO J       Date:  2003-12-01       Impact factor: 11.598

4.  The two Escherichia coli chromosome arms locate to separate cell halves.

Authors:  Xindan Wang; Xun Liu; Christophe Possoz; David J Sherratt
Journal:  Genes Dev       Date:  2006-07-01       Impact factor: 11.361

5.  A gyrase mutant with low activity disrupts supercoiling at the replication terminus.

Authors:  Zhenhua Pang; Ray Chen; Dipankar Manna; N Patrick Higgins
Journal:  J Bacteriol       Date:  2005-11       Impact factor: 3.490

6.  Actin homolog MreB affects chromosome segregation by regulating topoisomerase IV in Escherichia coli.

Authors:  Ram Madabhushi; Kenneth J Marians
Journal:  Mol Cell       Date:  2009-01-30       Impact factor: 17.970

7.  Unlinking chromosome catenanes in vivo by site-specific recombination.

Authors:  Ian Grainge; Migena Bregu; Mariel Vazquez; Viknesh Sivanathan; Stephen C Y Ip; David J Sherratt
Journal:  EMBO J       Date:  2007-09-06       Impact factor: 11.598

8.  A MatP-divisome interaction coordinates chromosome segregation with cell division in E. coli.

Authors:  Olivier Espéli; Romain Borne; Pauline Dupaigne; Axel Thiel; Emmanuelle Gigant; Romain Mercier; Frédéric Boccard
Journal:  EMBO J       Date:  2012-05-11       Impact factor: 11.598

9.  A defined terminal region of the E. coli chromosome shows late segregation and high FtsK activity.

Authors:  Marie Deghorain; Carine Pagès; Jean-Christophe Meile; Mathieu Stouf; Hervé Capiaux; Romain Mercier; Christian Lesterlin; Bernard Hallet; François Cornet
Journal:  PLoS One       Date:  2011-07-20       Impact factor: 3.240

10.  Rates of gyrase supercoiling and transcription elongation control supercoil density in a bacterial chromosome.

Authors:  Nikolay Rovinskiy; Andrews Akwasi Agbleke; Olga Chesnokova; Zhenhua Pang; N Patrick Higgins
Journal:  PLoS Genet       Date:  2012-08-16       Impact factor: 5.917

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