Literature DB >> 11591668

Gonococcal MinD affects cell division in Neisseria gonorrhoeae and Escherichia coli and exhibits a novel self-interaction.

J Szeto1, S Ramirez-Arcos, C Raymond, L D Hicks, C M Kay, J A Dillon.   

Abstract

The Min proteins are involved in determining cell division sites in bacteria and have been studied extensively in rod-shaped bacteria. We have recently shown that the gram-negative coccus Neisseria gonorrhoeae contains a min operon, and the present study investigates the role of minD from this operon. A gonococcal minD insertional mutant, CJSD1, was constructed and exhibited both grossly abnormal cell division and morphology as well as altered cell viability. Western blot analysis verified the absence of MinD from N. gonorrhoeae (MinD(Ng)) in this mutant. Hence, MinD(Ng) is required for maintaining proper cell division and growth in N. gonorrhoeae. Immunoblotting of soluble and insoluble gonococcal cell fractions revealed that MinD(Ng) is both cytosolic and associated with the insoluble membrane fraction. The joint overexpression of MinC(Ng) and MinD(Ng) from a shuttle vector resulted in a significant enlargement of gonococcal cells, while cells transformed with plasmids encoding either MinC(Ng) or MinD(Ng) alone did not display noticeable morphological changes. These studies suggest that MinD(Ng) is involved in inhibiting gonococcal cell division, likely in conjunction with MinC(Ng). The alignment of MinD sequences from various bacteria showed that the proteins are highly conserved and share several regions of identity, including a conserved ATP-binding cassette. The overexpression of MinD(Ng) in wild-type Escherichia coli led to cell filamentation, while overexpression in an E. coli minD mutant restored a wild-type morphology to the majority of cells; therefore, gonococcal MinD is functional across species. Yeast two-hybrid studies and gel-filtration and sedimentation equilibrium analyses of purified His-tagged MinD(Ng) revealed a novel MinD(Ng) self-interaction. We have also shown by yeast two-hybrid analysis that MinD from E. coli interacts with itself and with MinD(Ng). These results indicate that MinD(Ng) is required for maintaining proper cell division and growth in N. gonorrhoeae and suggests that the self-interaction of MinD may be important for cell division site selection across species.

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Year:  2001        PMID: 11591668      PMCID: PMC100108          DOI: 10.1128/JB.183.21.6253-6264.2001

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


  38 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.  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

3.  Crystal structure of the bacterial cell division regulator MinD.

Authors:  S C Cordell; J Löwe
Journal:  FEBS Lett       Date:  2001-03-09       Impact factor: 4.124

Review 4.  Genetic systems in pathogenic Neisseriae.

Authors:  H S Seifert; M So
Journal:  Methods Enzymol       Date:  1991       Impact factor: 1.600

5.  Localization of the Escherichia coli cell division protein Ftsl (PBP3) to the division site and cell pole.

Authors:  D S Weiss; K Pogliano; M Carson; L M Guzman; C Fraipont; M Nguyen-Distèche; R Losick; J Beckwith
Journal:  Mol Microbiol       Date:  1997-08       Impact factor: 3.501

Review 6.  Morphogenesis of Escherichia coli.

Authors:  N Nanninga
Journal:  Microbiol Mol Biol Rev       Date:  1998-03       Impact factor: 11.056

7.  Deletion of the cell-division inhibitor MinC results in lysis of Neisseria gonorrhoeae.

Authors:  S Ramirez-Arcos; J Szeto; T Beveridge; C Victor; F Francis; J Dillon
Journal:  Microbiology       Date:  2001-01       Impact factor: 2.777

8.  NEISSERIA GONORRHOEAE. I. VIRULENCE GENETICALLY LINKED TO CLONAL VARIATION.

Authors:  D S KELLOGG; W L PEACOCK; W E DEACON; L BROWN; D I PIRKLE
Journal:  J Bacteriol       Date:  1963-06       Impact factor: 3.490

9.  The MinD protein is a membrane ATPase required for the correct placement of the Escherichia coli division site.

Authors:  P A de Boer; R E Crossley; A R Hand; L I Rothfield
Journal:  EMBO J       Date:  1991-12       Impact factor: 11.598

10.  Distantly related sequences in the alpha- and beta-subunits of ATP synthase, myosin, kinases and other ATP-requiring enzymes and a common nucleotide binding fold.

Authors:  J E Walker; M Saraste; M J Runswick; N J Gay
Journal:  EMBO J       Date:  1982       Impact factor: 11.598

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  26 in total

1.  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

2.  Dynamic assembly of MinD on phospholipid vesicles regulated by ATP and MinE.

Authors:  Zonglin Hu; Edward P Gogol; Joe Lutkenhaus
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-30       Impact factor: 11.205

3.  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

4.  Recruitment of MinC, an inhibitor of Z-ring formation, to the membrane in Escherichia coli: role of MinD and MinE.

Authors:  Zonglin Hu; Cristian Saez; Joe Lutkenhaus
Journal:  J Bacteriol       Date:  2003-01       Impact factor: 3.490

Review 5.  Prokaryotic development: emerging insights.

Authors:  Lee Kroos; Janine R Maddock
Journal:  J Bacteriol       Date:  2003-02       Impact factor: 3.490

6.  The switch I and II regions of MinD are required for binding and activating MinC.

Authors:  Huaijin Zhou; Joe Lutkenhaus
Journal:  J Bacteriol       Date:  2004-03       Impact factor: 3.490

Review 7.  FtsZ and the division of prokaryotic cells and organelles.

Authors:  William Margolin
Journal:  Nat Rev Mol Cell Biol       Date:  2005-11       Impact factor: 94.444

8.  Identification of ZipA, a signal recognition particle-dependent protein from Neisseria gonorrhoeae.

Authors:  Ying Du; Cindy Grove Arvidson
Journal:  J Bacteriol       Date:  2003-04       Impact factor: 3.490

9.  The N terminus of MinD contains determinants which affect its dynamic localization and enzymatic activity.

Authors:  Jason Szeto; Sudeep Acharya; Nelson F Eng; Jo-Anne R Dillon
Journal:  J Bacteriol       Date:  2004-11       Impact factor: 3.490

10.  Bacillus subtilis MinC destabilizes FtsZ-rings at new cell poles and contributes to the timing of cell division.

Authors:  James A Gregory; Eric C Becker; Kit Pogliano
Journal:  Genes Dev       Date:  2008-12-15       Impact factor: 11.361

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