Literature DB >> 7877981

The dif resolvase locus of the Escherichia coli chromosome can be replaced by a 33-bp sequence, but function depends on location.

M Tecklenburg1, A Naumer, O Nagappan, P Kuempel.   

Abstract

The dif locus (deletion-induced filamentation) of Escherichia coli is a resolvase site, located in the terminus region of the chromosome, that reduces chromosome multimers to monomers. In strains in which this site has been deleted, a fraction of the cells is filamentous, has abnormal nucleoid structure, and exhibits elevated levels of the SOS repair system. We have demonstrated that a 33-bp sequence, which is sufficient for RecA-independent recombination and which shows similarity to the cer site of pColE1, suppresses the Dif phenotype when inserted in the terminus region. Flanking sequences were not required, since suppression occurred in strains in which dif as well as 12 kb or 173 kb of DNA had been deleted. However, location was important, and insertions at a site 118 kb away from the normal site did not suppress the Dif phenotype. These sites were otherwise still functional, and they exhibited wild-type levels of RecA-independent recombination with dif-containing plasmids and recombined with other chromosomal dif sites to cause deletions and inversions. It is proposed that the functions expressed by a dif site depend on chromosome location and structure, and analysis of these functions provides a way to examine the structure of the terminus region.

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Year:  1995        PMID: 7877981      PMCID: PMC42517          DOI: 10.1073/pnas.92.5.1352

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  21 in total

1.  New method for generating deletions and gene replacements in Escherichia coli.

Authors:  C M Hamilton; M Aldea; B K Washburn; P Babitzke; S R Kushner
Journal:  J Bacteriol       Date:  1989-09       Impact factor: 3.490

2.  Two related recombinases are required for site-specific recombination at dif and cer in E. coli K12.

Authors:  G Blakely; G May; R McCulloch; L K Arciszewska; M Burke; S T Lovett; D J Sherratt
Journal:  Cell       Date:  1993-10-22       Impact factor: 41.582

3.  Deletion of the terminus region (340 kilobase pairs of DNA) from the chromosome of Escherichia coli.

Authors:  J M Henson; P L Kuempel
Journal:  Proc Natl Acad Sci U S A       Date:  1985-06       Impact factor: 11.205

4.  In vitro insertional mutagenesis with a selectable DNA fragment.

Authors:  P Prentki; H M Krisch
Journal:  Gene       Date:  1984-09       Impact factor: 3.688

5.  Plasmid pSC101 harbors a recombination site, psi, which is able to resolve plasmid multimers and to substitute for the analogous chromosomal Escherichia coli site dif.

Authors:  F Cornet; I Mortier; J Patte; J M Louarn
Journal:  J Bacteriol       Date:  1994-06       Impact factor: 3.490

6.  Isolation and characterization of noncleavable (Ind-) mutants of the LexA repressor of Escherichia coli K-12.

Authors:  L L Lin; J W Little
Journal:  J Bacteriol       Date:  1988-05       Impact factor: 3.490

7.  Genetic mapping of nth, a gene affecting endonuclease III (thymine glycol-DNA glycosylase) in Escherichia coli K-12.

Authors:  B Weiss; R P Cunningham
Journal:  J Bacteriol       Date:  1985-05       Impact factor: 3.490

8.  Chromosomal transformation of Escherichia coli recD strains with linearized plasmids.

Authors:  C B Russell; D S Thaler; F W Dahlquist
Journal:  J Bacteriol       Date:  1989-05       Impact factor: 3.490

9.  xerB, an Escherichia coli gene required for plasmid ColE1 site-specific recombination, is identical to pepA, encoding aminopeptidase A, a protein with substantial similarity to bovine lens leucine aminopeptidase.

Authors:  C J Stirling; S D Colloms; J F Collins; G Szatmari; D J Sherratt
Journal:  EMBO J       Date:  1989-05       Impact factor: 11.598

10.  Derivatives of ColE1 cer show altered topological specificity in site-specific recombination.

Authors:  D K Summers
Journal:  EMBO J       Date:  1989-01       Impact factor: 11.598

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  8 in total

1.  All major regions of FtsK are required for resolution of chromosome dimers.

Authors:  D S Boyle; D Grant; G C Draper; W D Donachie
Journal:  J Bacteriol       Date:  2000-07       Impact factor: 3.490

2.  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

3.  Isolation of SOS constitutive mutants of Escherichia coli.

Authors:  Erin K O'Reilly; Kenneth N Kreuzer
Journal:  J Bacteriol       Date:  2004-11       Impact factor: 3.490

Review 4.  Linkage map of Escherichia coli K-12, edition 10: the traditional map.

Authors:  M K Berlyn
Journal:  Microbiol Mol Biol Rev       Date:  1998-09       Impact factor: 11.056

5.  oriC region and replication termination site, dif, of the Xanthomonas campestris pv. campestris 17 chromosome.

Authors:  Ming-Ren Yen; Nien-Tsung Lin; Chih-Hsin Hung; Ka-Tim Choy; Shu-Fen Weng; Yi-Hsiung Tseng
Journal:  Appl Environ Microbiol       Date:  2002-06       Impact factor: 4.792

6.  Osmoregulation of dimer resolution at the plasmid pJHCMW1 mwr locus by Escherichia coli XerCD recombination.

Authors:  Huong Pham; Ken J Dery; David J Sherratt; Marcelo E Tolmasky
Journal:  J Bacteriol       Date:  2002-03       Impact factor: 3.490

7.  Characterization of the Chromosome Dimer Resolution Site in Caulobacter crescentus.

Authors:  Ali Farrokhi; Hua Liu; George Szatmari
Journal:  J Bacteriol       Date:  2019-11-20       Impact factor: 3.490

8.  Construction of consecutive deletions of the Escherichia coli chromosome.

Authors:  Jun-ichi Kato; Masayuki Hashimoto
Journal:  Mol Syst Biol       Date:  2007-08-14       Impact factor: 11.429

  8 in total

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