Literature DB >> 9720867

Assembly of the FtsZ ring at the central division site in the absence of the chromosome.

Q Sun1, X C Yu, W Margolin.   

Abstract

The FtsZ ring assembles between segregated daughter chromosomes in prokaryotic cells and is essential for cell division. To understand better how the FtsZ ring is influenced by chromosome positioning and structure in Escherichia coli, we investigated its localization in parC and mukB mutants that are defective for chromosome segregation. Cells of both mutants at non-permissive temperatures were either filamentous with unsegregated nucleoids or short and anucleate. In parC filaments, FtsZ rings tended to localize only to either side of the central unsegregated nucleoid and rarely to the cell midpoint; however, medial rings reappeared soon after switching back to the permissive temperature. Filamentous mukB cells were usually longer and lacked many potential rings. At temperatures permissive for mukB viability, medial FtsZ rings assembled despite the presence of apparently unsegregated nucleoids. However, a significant proportion of these FtsZ rings were mislocalized or structurally abnormal. The most surprising result of this study was revealed upon further examination of FtsZ ring positioning in anucleate cells generated by the parC and mukB mutants: many of these cells, despite having no chromosome, possessed FtsZ rings at their midpoints. This discovery strongly suggests that the chromosome itself is not required for the proper positioning and development of the medial division site.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9720867     DOI: 10.1046/j.1365-2958.1998.00942.x

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


  44 in total

1.  MinDE-dependent pole-to-pole oscillation of division inhibitor MinC in Escherichia coli.

Authors:  D M Raskin; P A de Boer
Journal:  J Bacteriol       Date:  1999-10       Impact factor: 3.490

2.  Timing of FtsZ assembly in Escherichia coli.

Authors:  T Den Blaauwen; N Buddelmeijer; M E Aarsman; C M Hameete; N Nanninga
Journal:  J Bacteriol       Date:  1999-09       Impact factor: 3.490

3.  Suppression of chromosome segregation defects of Escherichia coli muk mutants by mutations in topoisomerase I.

Authors:  J A Sawitzke; S Austin
Journal:  Proc Natl Acad Sci U S A       Date:  2000-02-15       Impact factor: 11.205

4.  Exploring intracellular space: function of the Min system in round-shaped Escherichia coli.

Authors:  Brian D Corbin; Xuan-Chuan Yu; William Margolin
Journal:  EMBO J       Date:  2002-04-15       Impact factor: 11.598

5.  Deletion of the min operon results in increased thermosensitivity of an ftsZ84 mutant and abnormal FtsZ ring assembly, placement, and disassembly.

Authors:  X C Yu; W Margolin
Journal:  J Bacteriol       Date:  2000-11       Impact factor: 3.490

6.  Evidence for polar positional information independent of cell division and nucleoid occlusion.

Authors:  Anuradha Janakiraman; Marcia B Goldberg
Journal:  Proc Natl Acad Sci U S A       Date:  2004-01-08       Impact factor: 11.205

7.  A widely conserved bacterial cell division protein that promotes assembly of the tubulin-like protein FtsZ.

Authors:  Frederico J Gueiros-Filho; Richard Losick
Journal:  Genes Dev       Date:  2002-10-01       Impact factor: 11.361

Review 8.  The bacterial divisome: ready for its close-up.

Authors:  Veronica W Rowlett; William Margolin
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2015-10-05       Impact factor: 6.237

9.  Detection of uracil within DNA using a sensitive labeling method for in vitro and cellular applications.

Authors:  Gergely Róna; Ildikó Scheer; Kinga Nagy; Hajnalka L Pálinkás; Gergely Tihanyi; Máté Borsos; Angéla Békési; Beáta G Vértessy
Journal:  Nucleic Acids Res       Date:  2015-10-01       Impact factor: 16.971

10.  Cell shape dynamics in Escherichia coli.

Authors:  Galina Reshes; Sharon Vanounou; Itzhak Fishov; Mario Feingold
Journal:  Biophys J       Date:  2007-08-31       Impact factor: 4.033

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.