Literature DB >> 16702547

The positioning of cytoplasmic protein clusters in bacteria.

Stephen R Thompson1, George H Wadhams, Judith P Armitage.   

Abstract

Cell division is a carefully orchestrated procedure. Bacterial cells have intricate mechanisms to ensure that genetic material is copied, proofread, and accurately partitioned into daughter cells. Partitioning now appears to also occur for some cytoplasmic proteins. Previously, using chromosomal fluorescent protein fusions, we demonstrated that a subset of Rhodobacter sphaeroides chemotaxis proteins colocalize to a discrete region within the bacterial cytoplasm. Using TlpT-yellow fluorescent protein as a marker for the position of the cytoplasmic protein clusters, we show most cells contain either one cluster localized at mid-cell or two clusters at the one-fourth and three-fourths positions of cell length. The number and positioning of these protein clusters depend on a previously unrecognized bacterial protein positioning factor, PpfA, which has homology to bacterial type I DNA partitioning factors. These data suggest that there is a mechanism involved in partitioning some cytoplasmic proteins upon cell division that is analogous to a mechanism seen for plasmid and chromosomal DNA.

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Year:  2006        PMID: 16702547      PMCID: PMC1472454          DOI: 10.1073/pnas.0600919103

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  35 in total

1.  A requirement for sodium in the growth of Rhodopseudomonas spheroides.

Authors:  W R SISTROM
Journal:  J Gen Microbiol       Date:  1960-06

2.  Bacterial mitosis: partitioning protein ParA oscillates in spiral-shaped structures and positions plasmids at mid-cell.

Authors:  Gitte Ebersbach; Kenn Gerdes
Journal:  Mol Microbiol       Date:  2004-04       Impact factor: 3.501

Review 3.  Making sense of it all: bacterial chemotaxis.

Authors:  George H Wadhams; Judith P Armitage
Journal:  Nat Rev Mol Cell Biol       Date:  2004-12       Impact factor: 94.444

4.  Robustness in bacterial chemotaxis.

Authors:  U Alon; M G Surette; N Barkai; S Leibler
Journal:  Nature       Date:  1999-01-14       Impact factor: 49.962

5.  Structure of CheA, a signal-transducing histidine kinase.

Authors:  A M Bilwes; L A Alex; B R Crane; M I Simon
Journal:  Cell       Date:  1999-01-08       Impact factor: 41.582

6.  Chromosome and low copy plasmid segregation in E. coli: visual evidence for distinct mechanisms.

Authors:  G S Gordon; D Sitnikov; C D Webb; A Teleman; A Straight; R Losick; A W Murray; A Wright
Journal:  Cell       Date:  1997-09-19       Impact factor: 41.582

7.  Active site interference and asymmetric activation in the chemotaxis protein histidine kinase CheA.

Authors:  M Levit; Y Liu; M Surette; J Stock
Journal:  J Biol Chem       Date:  1996-12-13       Impact factor: 5.157

8.  Phosphorylation of three proteins in the signaling pathway of bacterial chemotaxis.

Authors:  J F Hess; K Oosawa; N Kaplan; M I Simon
Journal:  Cell       Date:  1988-04-08       Impact factor: 41.582

9.  A superfamily of ATPases with diverse functions containing either classical or deviant ATP-binding motif.

Authors:  E V Koonin
Journal:  J Mol Biol       Date:  1993-02-20       Impact factor: 5.469

10.  Localization of MreB in Rhodobacter sphaeroides under conditions causing changes in cell shape and membrane structure.

Authors:  Peter M Slovak; George H Wadhams; Judith P Armitage
Journal:  J Bacteriol       Date:  2005-01       Impact factor: 3.490

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  46 in total

1.  ParA-like protein uses nonspecific chromosomal DNA binding to partition protein complexes.

Authors:  Mark A J Roberts; George H Wadhams; Katie A Hadfield; Susan Tickner; Judith P Armitage
Journal:  Proc Natl Acad Sci U S A       Date:  2012-04-10       Impact factor: 11.205

Review 2.  Spatial organization in bacterial chemotaxis.

Authors:  Victor Sourjik; Judith P Armitage
Journal:  EMBO J       Date:  2010-08-18       Impact factor: 11.598

Review 3.  Protein subcellular localization in bacteria.

Authors:  David Z Rudner; Richard Losick
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-03-03       Impact factor: 10.005

Review 4.  Poles apart: prokaryotic polar organelles and their spatial regulation.

Authors:  Clare L Kirkpatrick; Patrick H Viollier
Journal:  Cold Spring Harb Perspect Biol       Date:  2011-03-01       Impact factor: 10.005

5.  Transcriptome analysis of Pseudomonas putida KT2440 harboring the completely sequenced IncP-7 plasmid pCAR1.

Authors:  Masatoshi Miyakoshi; Masaki Shintani; Tsuguno Terabayashi; Satoshi Kai; Hisakazu Yamane; Hideaki Nojiri
Journal:  J Bacteriol       Date:  2007-08-03       Impact factor: 3.490

6.  Bacterial signaling and motility: sure bets.

Authors:  Robert Belas; Igor B Zhulin; Zhaomin Yang
Journal:  J Bacteriol       Date:  2008-01-18       Impact factor: 3.490

7.  Localization of a bacterial cytoplasmic receptor is dynamic and changes with cell-cell contacts.

Authors:  Emilia M F Mauriello; David P Astling; Oleksii Sliusarenko; David R Zusman
Journal:  Proc Natl Acad Sci U S A       Date:  2009-03-09       Impact factor: 11.205

8.  Polar chemoreceptor clustering by coupled trimers of dimers.

Authors:  Robert G Endres
Journal:  Biophys J       Date:  2009-01       Impact factor: 4.033

9.  ParP prevents dissociation of CheA from chemotactic signaling arrays and tethers them to a polar anchor.

Authors:  Simon Ringgaard; Martha Zepeda-Rivera; Xiaoji Wu; Kathrin Schirner; Brigid M Davis; Matthew K Waldor
Journal:  Proc Natl Acad Sci U S A       Date:  2013-12-30       Impact factor: 11.205

10.  A minimal model for metabolism-dependent chemotaxis in Rhodobacter sphaeroides (†).

Authors:  Sisi Fan; Robert G Endres
Journal:  Interface Focus       Date:  2014-12-06       Impact factor: 3.906

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