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      Size-independent symmetric division in extraordinarily long cells

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          Abstract

          Two long-standing paradigms in biology are that cells belonging to the same population exhibit little deviation from their average size and that symmetric cell division is size limited. Here, ultrastructural, morphometric and immunocytochemical analyses reveal that two Gammaproteobacteria attached to the cuticle of the marine nematodes Eubostrichus fertilis and E. dianeae reproduce by constricting a single FtsZ ring at midcell despite being 45 μm and 120 μm long, respectively. In the crescent-shaped bacteria coating E. fertilis, symmetric FtsZ-based fission occurs in cells with lengths spanning one order of magnitude. In the E. dianeae symbiont, formation of a single functional FtsZ ring makes this the longest unicellular organism in which symmetric division has ever been observed. In conclusion, the reproduction modes of two extraordinarily long bacterial cells indicate that size is not the primary trigger of division and that yet unknown mechanisms time the localization of both DNA and the septum.

          Abstract

          Known mechanisms that determine symmetric division-plane positioning during cell division are unlikely to operate effectively over very long distances. Pende et al. show that extraordinarily long Gammaproteobacteria divide symmetrically despite reaching 120 microns in length

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          Most cited references38

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          NIH Image to ImageJ: 25 years of image analysis.

          For the past 25 years NIH Image and ImageJ software have been pioneers as open tools for the analysis of scientific images. We discuss the origins, challenges and solutions of these two programs, and how their history can serve to advise and inform other software projects.
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            The discovery of novel small-molecule antibacterial drugs has been stalled for many years. The purpose of this review is to underscore and illustrate those scientific problems unique to the discovery and optimization of novel antibacterial agents that have adversely affected the output of the effort. The major challenges fall into two areas: (i) proper target selection, particularly the necessity of pursuing molecular targets that are not prone to rapid resistance development, and (ii) improvement of chemical libraries to overcome limitations of diversity, especially that which is necessary to overcome barriers to bacterial entry and proclivity to be effluxed, especially in Gram-negative organisms. Failure to address these problems has led to a great deal of misdirected effort.
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              Bacterial cell division: assembly, maintenance and disassembly of the Z ring.

              Bacterial cell division is orchestrated by a tubulin homologue, FtsZ, which polymerizes to form a ring-like structure that is both a scaffold for the assembly of the bacterial cytokinetic machinery and, at least in part, a source of the energy for constriction. FtsZ assembly is tightly regulated, and a diverse repertoire of accessory proteins contributes to the formation of a functional division machine that is responsive to cell cycle status and environmental stress. In this Review, we describe the interaction of these proteins with FtsZ and discuss recent advances in our understanding of Z ring assembly.
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                Author and article information

                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Pub. Group
                2041-1723
                15 September 2014
                : 5
                : 4803
                Affiliations
                [1 ]Department of Ecogenomics and Systems Biology, University of Vienna , Althanstrasse 14, 1090 Vienna, Austria
                [2 ]Department of Symbiosis, Max Planck Institute for Marine Microbiology , Celsiusstrasse 1, D-28359 Bremen, Germany
                [3 ]Department of Limnology and Biooceanography, University of Vienna , Althanstrasse 14, 1090 Vienna, Austria
                [4 ]Department of Bacterial Cell Biology, Swammerdam Institute of Life Sciences, Faculty of Science, University of Amsterdam , Science Park 904, 1098 XH Amsterdam, the Netherlands
                [5 ]Center for Anatomy and Cell Biology, Medical University of Vienna , Währingerstrasse 10, 1090 Vienna, Austria
                [6 ]These authors contributed equally to this work
                Author notes
                Article
                ncomms5803
                10.1038/ncomms5803
                4175584
                25221974
                02618355-37a6-4f9e-836a-537b66f3bf74
                Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 12 June 2014
                : 24 July 2014
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