Literature DB >> 1729222

New minC mutations suggest different interactions of the same region of division inhibitor MinC with proteins specific for minD and dicB coinhibition pathways.

E Mulder1, C L Woldringh, F Tétart, J P Bouché.   

Abstract

Proper positioning of division sites in Escherichia coli requires balanced expression of minC, minD, and minE gene products. Previous genetic analysis has shown that either MinD or an apparently unrelated protein, DicB, cooperates with MinC to inhibit division. We have isolated and sequenced minC mutations that suppress division inhibition caused by overproduction of either DicB or MinD proteins. Most missense mutations were located in the amino acid 160 to 200 region of MinC (231 amino acids). Some mutations exhibited preferential resistance to one or the other coinhibitor, suggesting that two distinct proteins, possibly MinD and DicB themselves, interact in slightly different manners with the same region of MinC to promote division inhibition.

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Year:  1992        PMID: 1729222      PMCID: PMC205673          DOI: 10.1128/jb.174.1.35-39.1992

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


  14 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.  Isolation and mapping of Escherichia coli mutations conferring resistance to division inhibition protein DicB.

Authors:  C Labie; F Bouché; J P Bouché
Journal:  J Bacteriol       Date:  1989-08       Impact factor: 3.490

3.  Central role for the Escherichia coli minC gene product in two different cell division-inhibition systems.

Authors:  P A de Boer; R E Crossley; L I Rothfield
Journal:  Proc Natl Acad Sci U S A       Date:  1990-02       Impact factor: 11.205

Review 4.  Role of the nucleoid in the toporegulation of division.

Authors:  C L Woldringh; E Mulder; J A Valkenburg; F B Wientjes; A Zaritsky; N Nanninga
Journal:  Res Microbiol       Date:  1990-01       Impact factor: 3.992

5.  Division behavior and shape changes in isogenic ftsZ, ftsQ, ftsA, pbpB, and ftsE cell division mutants of Escherichia coli during temperature shift experiments.

Authors:  P E Taschner; P G Huls; E Pas; C L Woldringh
Journal:  J Bacteriol       Date:  1988-04       Impact factor: 3.490

6.  Isolation and properties of minB, a complex genetic locus involved in correct placement of the division site in Escherichia coli.

Authors:  P A de Boer; R E Crossley; L I Rothfield
Journal:  J Bacteriol       Date:  1988-05       Impact factor: 3.490

7.  Interaction between the min locus and ftsZ.

Authors:  E Bi; J Lutkenhaus
Journal:  J Bacteriol       Date:  1990-10       Impact factor: 3.490

8.  Actively replicating nucleoids influence positioning of division sites in Escherichia coli filaments forming cells lacking DNA.

Authors:  E Mulder; C L Woldringh
Journal:  J Bacteriol       Date:  1989-08       Impact factor: 3.490

9.  A pSC101-derived plasmid which shows no sequence homology to other commonly used cloning vectors.

Authors:  G Churchward; D Belin; Y Nagamine
Journal:  Gene       Date:  1984-11       Impact factor: 3.688

10.  A technique for integrating any DNA fragment into the chromosome of Escherichia coli.

Authors:  O Raibaud; M Mock; M Schwartz
Journal:  Gene       Date:  1984 Jul-Aug       Impact factor: 3.688

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  17 in total

1.  Analysis of MinC reveals two independent domains involved in interaction with MinD and FtsZ.

Authors:  Z Hu; J Lutkenhaus
Journal:  J Bacteriol       Date:  2000-07       Impact factor: 3.490

2.  Targeting of (D)MinC/MinD and (D)MinC/DicB complexes to septal rings in Escherichia coli suggests a multistep mechanism for MinC-mediated destruction of nascent FtsZ rings.

Authors:  Jay E Johnson; Laura L Lackner; Piet A J de Boer
Journal:  J Bacteriol       Date:  2002-06       Impact factor: 3.490

3.  Polar localization of the MinD protein of Bacillus subtilis and its role in selection of the mid-cell division site.

Authors:  A L Marston; H B Thomaides; D H Edwards; M E Sharpe; J Errington
Journal:  Genes Dev       Date:  1998-11-01       Impact factor: 11.361

4.  Interaction between FtsZ and inhibitors of cell division.

Authors:  J Huang; C Cao; J Lutkenhaus
Journal:  J Bacteriol       Date:  1996-09       Impact factor: 3.490

5.  Stability of the Escherichia coli division inhibitor protein MinC requires determinants in the carboxy-terminal region of the protein.

Authors:  M Sen; L I Rothfield
Journal:  J Bacteriol       Date:  1998-01       Impact factor: 3.490

6.  The Escherichia coli histone-like protein HU affects DNA initiation, chromosome partitioning via MukB, and cell division via MinCDE.

Authors:  A Jaffe; D Vinella; R D'Ari
Journal:  J Bacteriol       Date:  1997-06       Impact factor: 3.490

7.  MinCD-independent inhibition of cell division by a protein that fuses MalE to the topological specificity factor MinE.

Authors:  S Pichoff; B Vollrath; J P Bouché
Journal:  J Bacteriol       Date:  1997-07       Impact factor: 3.490

8.  MinC and FtsZ mutant analysis provides insight into MinC/MinD-mediated Z ring disassembly.

Authors:  Kyung-Tae Park; Alex Dajkovic; Mark Wissel; Shishen Du; Joe Lutkenhaus
Journal:  J Biol Chem       Date:  2018-02-02       Impact factor: 5.157

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

Authors:  A W Varley; G C Stewart
Journal:  J Bacteriol       Date:  1992-11       Impact factor: 3.490

10.  Identification of Bacillus subtilis genes for septum placement and shape determination.

Authors:  P A Levin; P S Margolis; P Setlow; R Losick; D Sun
Journal:  J Bacteriol       Date:  1992-11       Impact factor: 3.490

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