Literature DB >> 31548274

Characterization of the Chromosome Dimer Resolution Site in Caulobacter crescentus.

Ali Farrokhi1, Hua Liu2, George Szatmari1.   

Abstract

Chromosome dimers occur in bacterial cells as a result of the recombinational repair of DNA. In most bacteria, chromosome dimers are resolved by XerCD site-specific recombination at the dif (deletion-induced filamentation) site located in the terminus region of the chromosome. Caulobacter crescentus, a Gram-negative oligotrophic bacterium, also possesses Xer recombinases, called CcXerC and CcXerD, which have been shown to interact with the Escherichia coli dif site in vitro Previous studies on Caulobacter have suggested the presence of a dif site (referred to in this paper as dif1CC ), but no in vitro data have shown any association with this site and the CcXer proteins. Using recursive hidden Markov modeling, another group has proposed a second dif site, which we call dif2CC , which shows more similarity to the dif consensus sequence. Here, by using a combination of in vitro experiments, we compare the affinities and the cleavage abilities of CcXerCD recombinases for both dif sites. Our results show that dif2CC displays a higher affinity for CcXerC and CcXerD and is bound cooperatively by these proteins, which is not the case for the original dif1CC site. Furthermore, dif2CC nicked substrates are more efficiently cleaved by CcXerCD, and deletion of the site results in about 5 to 10% of cells showing an altered cellular morphology.IMPORTANCE Bacteria utilize site-specific recombination for a variety of purposes, including the control of gene expression, acquisition of genetic elements, and the resolution of dimeric chromosomes. Failure to resolve dimeric chromosomes can lead to cell division defects in a percentage of the cell population. The work presented here shows the existence of a chromosomal resolution system in C. crescentus Defects in this resolution system result in the formation of chains of cells. Further understanding of how these cells remain linked together will help in the understanding of how chromosome segregation and cell division are linked in C. crescentus.
Copyright © 2019 American Society for Microbiology.

Entities:  

Keywords:  Caulobacter crescentus; Xer; cell division; chromosome dimers; chromosome segregation; dif site; protein-DNA interactions; site-specific recombination

Mesh:

Substances:

Year:  2019        PMID: 31548274      PMCID: PMC6872196          DOI: 10.1128/JB.00391-19

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  41 in total

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Authors:  Nora Ausmees; Jeffrey R Kuhn; Christine Jacobs-Wagner
Journal:  Cell       Date:  2003-12-12       Impact factor: 41.582

2.  XerCD-mediated site-specific recombination leads to loss of the 57-kilobase gonococcal genetic island.

Authors:  Nadia M Domínguez; Kathleen T Hackett; Joseph P Dillard
Journal:  J Bacteriol       Date:  2010-11-12       Impact factor: 3.490

3.  Mutations in the Lipopolysaccharide biosynthesis pathway interfere with crescentin-mediated cell curvature in Caulobacter crescentus.

Authors:  Matthew T Cabeen; Michelle A Murolo; Ariane Briegel; N Khai Bui; Waldemar Vollmer; Nora Ausmees; Grant J Jensen; Christine Jacobs-Wagner
Journal:  J Bacteriol       Date:  2010-04-30       Impact factor: 3.490

4.  Identification and characterization of the dif Site from Bacillus subtilis.

Authors:  S A Sciochetti; P J Piggot; G W Blakely
Journal:  J Bacteriol       Date:  2001-02       Impact factor: 3.490

5.  Chromosome methylation and measurement of faithful, once and only once per cell cycle chromosome replication in Caulobacter crescentus.

Authors:  G T Marczynski
Journal:  J Bacteriol       Date:  1999-04       Impact factor: 3.490

6.  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

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

Authors:  M Tecklenburg; A Naumer; O Nagappan; P Kuempel
Journal:  Proc Natl Acad Sci U S A       Date:  1995-02-28       Impact factor: 11.205

8.  The bifunctional FtsK protein mediates chromosome partitioning and cell division in Caulobacter.

Authors:  Sherry C E Wang; Lisandra West; Lucy Shapiro
Journal:  J Bacteriol       Date:  2006-02       Impact factor: 3.490

9.  Inhibition of FtsZ polymerization by SulA, an inhibitor of septation in Escherichia coli.

Authors:  A Mukherjee; C Cao; J Lutkenhaus
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-17       Impact factor: 11.205

10.  SeqA structures behind Escherichia coli replication forks affect replication elongation and restart mechanisms.

Authors:  Ida Benedikte Pedersen; Emily Helgesen; Ingvild Flåtten; Solveig Fossum-Raunehaug; Kirsten Skarstad
Journal:  Nucleic Acids Res       Date:  2017-06-20       Impact factor: 16.971

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Journal:  Microorganisms       Date:  2019-12-03

2.  Riboswitch theo/metE as a Transcription Regulation Tool for Xanthomonas citri subsp. citri.

Authors:  Danilo Bueno; Danielle B Pedrolli; Paula M M Martins; Daniela A Bocchini; Karen C M Moraes; Agda P Facincani; Jesus A Ferro; Alessandro M Varani; Michelle M Pena; Henrique Ferreira
Journal:  Microorganisms       Date:  2021-02-06
  2 in total

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