Literature DB >> 17704222

Changes in nucleoid morphology and origin localization upon inhibition or alteration of the actin homolog, MreB, of Vibrio cholerae.

Preeti Srivastava1, Gäelle Demarre, Tatiana S Karpova, James McNally, Dhruba K Chattoraj.   

Abstract

MreB is an actin homolog required for the morphogenesis of most rod-shaped bacteria and for other functions, including chromosome segregation. In Caulobacter crescentus and Escherichia coli, the protein seems to play a role in the segregation of sister origins, but its role in Bacillus subtilis chromosome segregation is less clear. To help clarify its role in segregation, we have here studied the protein in Vibrio cholerae, whose chromosome I segregates like the one in C. crescentus and whose chromosome II like the one in E. coli or B. subtilis. The properties of Vibrio MreB were similar to those of its homologs in other bacteria in that it formed dynamic helical filaments, was essential for viability, and was inhibited by the drug A22. Wild-type (WT) cells exposed to A22 became spherical and larger. The nucleoids enlarged correspondingly, and the origin positions for both the chromosomes no longer followed any fixed pattern. However, the sister origins separated, unlike the situation in other bacteria. In mutants isolated as A22 resistant, the nucleoids in some cases appeared compacted even when the cell shape was nearly normal. In these cells, the origins of chromosome I were at the distal edges of the nucleoid but not all the way to the poles where they normally reside. The sister origins of chromosome II also separated less. Thus, it appears that the inhibition or alteration of Vibrio MreB can affect both the nucleoid morphology and origin localization.

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Year:  2007        PMID: 17704222      PMCID: PMC2168437          DOI: 10.1128/JB.00362-07

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


  55 in total

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Authors:  L J Jones; R Carballido-López; J Errington
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Review 2.  Chromosome segregation during the prokaryotic cell division cycle.

Authors:  R B Jensen; L Shapiro
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4.  Polar targeting of Shigella virulence factor IcsA in Enterobacteriacae and Vibrio.

Authors:  M Charles; M Pérez; J H Kobil; M B Goldberg
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-31       Impact factor: 11.205

5.  Prokaryotic origin of the actin cytoskeleton.

Authors:  F van den Ent; L A Amos; J Löwe
Journal:  Nature       Date:  2001-09-06       Impact factor: 49.962

6.  The segregation of the Escherichia coli origin and terminus of replication.

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Journal:  Mol Microbiol       Date:  2002-11       Impact factor: 3.501

7.  Pairing of P1 plasmid partition sites by ParB.

Authors:  R Edgar; D K Chattoraj; M Yarmolinsky
Journal:  Mol Microbiol       Date:  2001-12       Impact factor: 3.501

8.  Distinct replication requirements for the two Vibrio cholerae chromosomes.

Authors:  Elizabeth S Egan; Matthew K Waldor
Journal:  Cell       Date:  2003-08-22       Impact factor: 41.582

9.  Prokaryotic DNA segregation by an actin-like filament.

Authors:  Jakob Møller-Jensen; Rasmus Bugge Jensen; Jan Löwe; Kenn Gerdes
Journal:  EMBO J       Date:  2002-06-17       Impact factor: 11.598

10.  Fine-scale time-lapse analysis of the biphasic, dynamic behaviour of the two Vibrio cholerae chromosomes.

Authors:  Aretha Fiebig; Kinneret Keren; Julie A Theriot
Journal:  Mol Microbiol       Date:  2006-06       Impact factor: 3.501

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  23 in total

Review 1.  The structure and function of bacterial actin homologs.

Authors:  Joshua W Shaevitz; Zemer Gitai
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2.  A Periplasmic Polymer Curves Vibrio cholerae and Promotes Pathogenesis.

Authors:  Thomas M Bartlett; Benjamin P Bratton; Amit Duvshani; Amanda Miguel; Ying Sheng; Nicholas R Martin; Jeffrey P Nguyen; Alexandre Persat; Samantha M Desmarais; Michael S VanNieuwenhze; Kerwyn Casey Huang; Jun Zhu; Joshua W Shaevitz; Zemer Gitai
Journal:  Cell       Date:  2017-01-12       Impact factor: 41.582

3.  Growth conditions regulate the requirements for Caulobacter chromosome segregation.

Authors:  Conrad W Shebelut; Rasmus B Jensen; Zemer Gitai
Journal:  J Bacteriol       Date:  2008-11-21       Impact factor: 3.490

4.  The cell wall regulator {sigma}I specifically suppresses the lethal phenotype of mbl mutants in Bacillus subtilis.

Authors:  Kathrin Schirner; Jeff Errington
Journal:  J Bacteriol       Date:  2008-12-29       Impact factor: 3.490

5.  Mechanical control of bacterial cell shape.

Authors:  Hongyuan Jiang; Fangwei Si; William Margolin; Sean X Sun
Journal:  Biophys J       Date:  2011-07-20       Impact factor: 4.033

6.  The helical MreB cytoskeleton in Escherichia coli MC1000/pLE7 is an artifact of the N-Terminal yellow fluorescent protein tag.

Authors:  Matthew T Swulius; Grant J Jensen
Journal:  J Bacteriol       Date:  2012-08-17       Impact factor: 3.490

Review 7.  Multidimensional view of the bacterial cytoskeleton.

Authors:  Katherine Celler; Roman I Koning; Abraham J Koster; Gilles P van Wezel
Journal:  J Bacteriol       Date:  2013-02-15       Impact factor: 3.490

8.  Rhodoccoccus erythropolis Is Different from Other Members of Actinobacteria: Monoploidy, Overlapping Replication Cycle, and Unique Segregation Pattern.

Authors:  Divya Singhi; Aashima Goyal; Gunjan Gupta; Aniruddh Yadav; Preeti Srivastava
Journal:  J Bacteriol       Date:  2019-11-20       Impact factor: 3.490

9.  RodZ (YfgA) is required for proper assembly of the MreB actin cytoskeleton and cell shape in E. coli.

Authors:  Felipe O Bendezú; Cynthia A Hale; Thomas G Bernhardt; Piet A J de Boer
Journal:  EMBO J       Date:  2008-12-11       Impact factor: 11.598

10.  A22 disrupts the bacterial actin cytoskeleton by directly binding and inducing a low-affinity state in MreB.

Authors:  G J Bean; S T Flickinger; W M Westler; M E McCully; D Sept; D B Weibel; K J Amann
Journal:  Biochemistry       Date:  2009-06-09       Impact factor: 3.162

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