Literature DB >> 16959967

The bacterial cytoskeleton.

Yu-Ling Shih1, Lawrence Rothfield.   

Abstract

In recent years it has been shown that bacteria contain a number of cytoskeletal structures. The bacterial cytoplasmic elements include homologs of the three major types of eukaryotic cytoskeletal proteins (actin, tubulin, and intermediate filament proteins) and a fourth group, the MinD-ParA group, that appears to be unique to bacteria. The cytoskeletal structures play important roles in cell division, cell polarity, cell shape regulation, plasmid partition, and other functions. The proteins self-assemble into filamentous structures in vitro and form intracellular ordered structures in vivo. In addition, there are a number of filamentous bacterial elements that may turn out to be cytoskeletal in nature. This review attempts to summarize and integrate the in vivo and in vitro aspects of these systems and to evaluate the probable future directions of this active research field.

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Year:  2006        PMID: 16959967      PMCID: PMC1594594          DOI: 10.1128/MMBR.00017-06

Source DB:  PubMed          Journal:  Microbiol Mol Biol Rev        ISSN: 1092-2172            Impact factor:   11.056


  221 in total

1.  Identification and characterization of a negative regulator of FtsZ ring formation in Bacillus subtilis.

Authors:  P A Levin; I G Kurtser; A D Grossman
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-17       Impact factor: 11.205

2.  Mapping the MinE site involved in interaction with the MinD division site selection protein of Escherichia coli.

Authors:  Lu-Yan Ma; Glenn King; Lawrence Rothfield
Journal:  J Bacteriol       Date:  2003-08       Impact factor: 3.490

Review 3.  Cytoplasmic intermediate filaments revealed as dynamic and multipurpose scaffolds.

Authors:  Pierre A Coulombe; Pauline Wong
Journal:  Nat Cell Biol       Date:  2004-08       Impact factor: 28.824

Review 4.  Tubulin and FtsZ form a distinct family of GTPases.

Authors:  E Nogales; K H Downing; L A Amos; J Löwe
Journal:  Nat Struct Biol       Date:  1998-06

Review 5.  Generating and exploiting polarity in bacteria.

Authors:  Lucy Shapiro; Harley H McAdams; Richard Losick
Journal:  Science       Date:  2002-12-06       Impact factor: 47.728

6.  spo0J is required for normal chromosome segregation as well as the initiation of sporulation in Bacillus subtilis.

Authors:  K Ireton; N W Gunther; A D Grossman
Journal:  J Bacteriol       Date:  1994-09       Impact factor: 3.490

7.  SlmA, a nucleoid-associated, FtsZ binding protein required for blocking septal ring assembly over Chromosomes in E. coli.

Authors:  Thomas G Bernhardt; Piet A J de Boer
Journal:  Mol Cell       Date:  2005-05-27       Impact factor: 17.970

8.  The minCD locus of Bacillus subtilis lacks the minE determinant that provides topological specificity to cell division.

Authors:  S Lee; C W Price
Journal:  Mol Microbiol       Date:  1993-02       Impact factor: 3.501

9.  The assembly of MreB, a prokaryotic homolog of actin.

Authors:  Osigwe Esue; Maria Cordero; Denis Wirtz; Yiider Tseng
Journal:  J Biol Chem       Date:  2004-11-16       Impact factor: 5.157

10.  A magnesium-dependent mreB null mutant: implications for the role of mreB in Bacillus subtilis.

Authors:  Alex Formstone; Jeffery Errington
Journal:  Mol Microbiol       Date:  2005-03       Impact factor: 3.501

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  92 in total

1.  Processivity of peptidoglycan synthesis provides a built-in mechanism for the robustness of straight-rod cell morphology.

Authors:  Oleksii Sliusarenko; Matthew T Cabeen; Charles W Wolgemuth; Christine Jacobs-Wagner; Thierry Emonet
Journal:  Proc Natl Acad Sci U S A       Date:  2010-05-17       Impact factor: 11.205

2.  Near-isotropic 3D optical nanoscopy with photon-limited chromophores.

Authors:  Jianyong Tang; Jasper Akerboom; Alipasha Vaziri; Loren L Looger; Charles V Shank
Journal:  Proc Natl Acad Sci U S A       Date:  2010-05-14       Impact factor: 11.205

3.  Plasmid segregation without partition.

Authors:  Catherine Guynet; Fernando de la Cruz
Journal:  Mob Genet Elements       Date:  2011-09-01

4.  Duplication and segregation of the actin (MreB) cytoskeleton during the prokaryotic cell cycle.

Authors:  Purva Vats; Lawrence Rothfield
Journal:  Proc Natl Acad Sci U S A       Date:  2007-10-31       Impact factor: 11.205

5.  Treadmilling of a prokaryotic tubulin-like protein, TubZ, required for plasmid stability in Bacillus thuringiensis.

Authors:  Rachel A Larsen; Christina Cusumano; Akina Fujioka; Grace Lim-Fong; Paula Patterson; Joe Pogliano
Journal:  Genes Dev       Date:  2007-05-17       Impact factor: 11.361

6.  Polymerization of the actin-like protein MamK, which is associated with magnetosomes.

Authors:  Azuma Taoka; Ryuji Asada; Long-Fei Wu; Yoshihiro Fukumori
Journal:  J Bacteriol       Date:  2007-09-28       Impact factor: 3.490

7.  RNaseE and RNA helicase B play central roles in the cytoskeletal organization of the RNA degradosome.

Authors:  Aziz Taghbalout; Lawrence Rothfield
Journal:  J Biol Chem       Date:  2008-03-12       Impact factor: 5.157

8.  FtsZ bacterial cytoskeletal polymers on curved surfaces: the importance of lateral interactions.

Authors:  Ines Hörger; Enrique Velasco; Germán Rivas; Marisela Vélez; Pedro Tarazona
Journal:  Biophys J       Date:  2008-03-21       Impact factor: 4.033

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.  Three-dimensional imaging of the highly bent architecture of Bdellovibrio bacteriovorus by using cryo-electron tomography.

Authors:  Mario J Borgnia; Sriram Subramaniam; Jacqueline L S Milne
Journal:  J Bacteriol       Date:  2008-01-18       Impact factor: 3.490

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