Literature DB >> 1400225

The divIVB region of the Bacillus subtilis chromosome encodes homologs of Escherichia coli septum placement (minCD) and cell shape (mreBCD) determinants.

A W Varley1, G C Stewart.   

Abstract

Mutation of the divIVB locus in Bacillus subtilis causes frequent misplacement of the division septum, resulting in circular minicells, short rods, and filaments of various sizes. The divIVB1 mutant allele maps to a region of the chromosome also known to encode sporulation (spo0B, spoIVF, spoIIB) and cell shape (rodB) determinants. This study reports the cloning and sequence analysis of 4.4 kb of the B. subtilis chromosome encompassing the divIVB locus. This region contains five open reading frames (ORFs) arranged in two functionally distinct gene clusters (mre and min) and transcribed colinearly with the direction of replication. Although sequence analysis reveals potential promoters preceding each gene cluster, studies with integrational plasmids suggest that all five ORFs are part of a single transcription unit. The first gene cluster contains three ORFs (mreBCD) homologous to the mre genes of Escherichia coli. We show that rodB1 is allelic to mreD and identify the rodB1 mutation. The second gene cluster contains two ORFs (minCD) homologous to minC and minD of E. coli but lacks a minE homolog. We show that divIVB1 is allelic to minD and identify two mutations in the divIVB1 allele. Insertional inactivation of either minC or minD or the presence of the divIVB region on plasmids produces a severe minicell phenotype in wild-type cells. Moreover, E. coli cells carrying the divIVB region on a low-copy-number plasmid produce minicells, suggesting that a product of this locus may retain some function across species boundaries.

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Year:  1992        PMID: 1400225      PMCID: PMC207348          DOI: 10.1128/jb.174.21.6729-6742.1992

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


  36 in total

1.  Minicell-forming mutants of Escherichia coli: suppression of both DicB- and MinD-dependent division inhibition by inactivation of the minC gene product.

Authors:  C Labie; F Bouché; J P Bouché
Journal:  J Bacteriol       Date:  1990-10       Impact factor: 3.490

2.  Low copy number plasmids for regulated low-level expression of cloned genes in Escherichia coli with blue/white insert screening capability.

Authors:  C G Lerner; M Inouye
Journal:  Nucleic Acids Res       Date:  1990-08-11       Impact factor: 16.971

Review 3.  Bacterial cell division.

Authors:  P A de Boer; W R Cook; L I Rothfield
Journal:  Annu Rev Genet       Date:  1990       Impact factor: 16.830

4.  New mre genes mreC and mreD, responsible for formation of the rod shape of Escherichia coli cells.

Authors:  M Wachi; M Doi; Y Okada; M Matsuhashi
Journal:  J Bacteriol       Date:  1989-12       Impact factor: 3.490

5.  A division inhibitor and a topological specificity factor coded for by the minicell locus determine proper placement of the division septum in E. coli.

Authors:  P A de Boer; R E Crossley; L I Rothfield
Journal:  Cell       Date:  1989-02-24       Impact factor: 41.582

6.  Negative control of cell division by mreB, a gene that functions in determining the rod shape of Escherichia coli cells.

Authors:  M Wachi; M Matsuhashi
Journal:  J Bacteriol       Date:  1989-06       Impact factor: 3.490

7.  FtsZ ring structure associated with division in Escherichia coli.

Authors:  E F Bi; J Lutkenhaus
Journal:  Nature       Date:  1991-11-14       Impact factor: 49.962

8.  Regulation of cell division in E. coli.

Authors:  J Lutkenhaus
Journal:  Trends Genet       Date:  1990-01       Impact factor: 11.639

9.  The nucleotide sequence of the rodC operon of Bacillus subtilis.

Authors:  A L Honeyman; G C Stewart
Journal:  Mol Microbiol       Date:  1989-09       Impact factor: 3.501

10.  Analysis of cell division gene ftsZ (sulB) from gram-negative and gram-positive bacteria.

Authors:  J C Corton; J E Ward; J Lutkenhaus
Journal:  J Bacteriol       Date:  1987-01       Impact factor: 3.490

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  54 in total

1.  Rapid pole-to-pole oscillation of a protein required for directing division to the middle of Escherichia coli.

Authors:  D M Raskin; P A de Boer
Journal:  Proc Natl Acad Sci U S A       Date:  1999-04-27       Impact factor: 11.205

Review 2.  Bacterial cell division: a moveable feast.

Authors:  C Jacobs; L Shapiro
Journal:  Proc Natl Acad Sci U S A       Date:  1999-05-25       Impact factor: 11.205

3.  Role of SpoVG in asymmetric septation in Bacillus subtilis.

Authors:  K Matsuno; A L Sonenshein
Journal:  J Bacteriol       Date:  1999-06       Impact factor: 3.490

4.  MinCD-dependent regulation of the polarity of SpoIIIE assembly and DNA transfer.

Authors:  Marc D Sharp; Kit Pogliano
Journal:  EMBO J       Date:  2002-11-15       Impact factor: 11.598

5.  Promiscuous targeting of Bacillus subtilis cell division protein DivIVA to division sites in Escherichia coli and fission yeast.

Authors:  D H Edwards; H B Thomaides; J Errington
Journal:  EMBO J       Date:  2000-06-01       Impact factor: 11.598

6.  Localization of the vegetative cell wall hydrolases LytC, LytE, and LytF on the Bacillus subtilis cell surface and stability of these enzymes to cell wall-bound or extracellular proteases.

Authors:  Hiroki Yamamoto; Shin-ichirou Kurosawa; Junichi Sekiguchi
Journal:  J Bacteriol       Date:  2003-11       Impact factor: 3.490

Review 7.  Compartmentalization of gene expression during Bacillus subtilis spore formation.

Authors:  David W Hilbert; Patrick J Piggot
Journal:  Microbiol Mol Biol Rev       Date:  2004-06       Impact factor: 11.056

8.  The nucleotide sequence of a linear plasmid of Borrelia burgdorferi reveals similarities to those of circular plasmids of other prokaryotes.

Authors:  A G Barbour; C J Carter; V Bundoc; J Hinnebusch
Journal:  J Bacteriol       Date:  1996-11       Impact factor: 3.490

9.  Changes in wall teichoic acid during the rod-sphere transition of Bacillus subtilis 168.

Authors:  J H Pollack; F C Neuhaus
Journal:  J Bacteriol       Date:  1994-12       Impact factor: 3.490

10.  Bacterial motility complexes require the actin-like protein, MreB and the Ras homologue, MglA.

Authors:  Emilia M F Mauriello; Fabrice Mouhamar; Beiyan Nan; Adrien Ducret; David Dai; David R Zusman; Tâm Mignot
Journal:  EMBO J       Date:  2009-12-03       Impact factor: 11.598

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