28
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      MreB polymers and curvature localization are enhanced by RodZ and predict E. coli's cylindrical uniformity

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The actin-like protein MreB has been proposed to coordinate the synthesis of the cell wall to determine cell shape in bacteria. MreB is preferentially localized to areas of the cell with specific curved geometries, avoiding the cell poles. It remains unclear whether MreB’s curvature preference is regulated by additional factors, and which specific features of MreB promote specific features of rod shape growth. Here, we show that the transmembrane protein RodZ modulates MreB curvature preference and polymer number in E. coli, properties which are regulated independently. An unbiased machine learning analysis shows that MreB polymer number, the total length of MreB polymers, and MreB curvature preference are key correlates of cylindrical uniformity, the variability in radius within a single cell. Changes in the values of these parameters are highly predictive of the resulting changes in cell shape ( r 2 = 0.93). Our data thus suggest RodZ promotes the assembly of geometrically-localized MreB polymers that lead to the growth of uniform cylinders.

          Abstract

          The actin-like protein MreB coordinates the synthesis of the cell wall, which determines cell shape in bacteria. Here, Bratton et al. show that the transmembrane protein RodZ modulates MreB polymer number and curvature preference, contributing to the cylindrical uniform shape of E. coli cells.

          Related collections

          Most cited references28

          • Record: found
          • Abstract: found
          • Article: not found

          Tightly regulated tac promoter vectors useful for the expression of unfused and fused proteins in Escherichia coli.

          A series of new plasmid expression vectors (the pTrc series) has been constructed for the regulated expression of genes in Escherichia coli. Based on pKK233-2 [Amann and Brosius, Gene 40 (1985) 183-190], the vectors carry a strong hybrid trp/lac promoter, the lacZ ribosome-binding site (RBS), the multiple cloning site of pUC18 and the rrnB transcription terminators. With the aid of synthetic oligodeoxynucleotides, the multiple cloning site has been inserted behind an NcoI site in three reading frames. Thus, the vectors are equally useful for the expression of proteins in their authentic, non-fused form (by using the NcoI site) and for the expression of fusion proteins (by choosing any of the cloning sites in the correct translational frame). To ensure complete repression of the hybrid trp/lac promoter during construction and growth in any host strain, the lacIq allele of the lac repressor gene was added to some of the vectors. The complete vector nucleotide sequence and examples of heterologous gene expression (human coagulation factor XIIIa and human placental anticoagulant protein PP4) with the new vectors are presented.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Transduction of linked genetic characters of the host by bacteriophage P1.

            E. Lennox (1955)
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              RodZ (YfgA) is required for proper assembly of the MreB actin cytoskeleton and cell shape in E. coli.

              The bacterial MreB actin cytoskeleton is required for cell shape maintenance in most non-spherical organisms. In rod-shaped cells such as Escherichia coli, it typically assembles along the long axis in a spiral-like configuration just underneath the cytoplasmic membrane. How this configuration is controlled and how it helps dictate cell shape is unclear. In a new genetic screen for cell shape mutants, we identified RodZ (YfgA) as an important transmembrane component of the cytoskeleton. Loss of RodZ leads to misassembly of MreB into non-spiral structures, and a consequent loss of cell shape. A juxta-membrane domain of RodZ is essential to maintain rod shape, whereas other domains on either side of the membrane have critical, but partially redundant, functions. Though one of these domains resembles a DNA-binding motif, our evidence indicates that it is primarily responsible for association of RodZ with the cytoskeleton.
                Bookmark

                Author and article information

                Contributors
                zgitai@princeton.edu
                randy.morgenstein@okstate.edu
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                18 July 2018
                18 July 2018
                2018
                : 9
                : 2797
                Affiliations
                [1 ]ISNI 0000 0001 2097 5006, GRID grid.16750.35, Department of Molecular Biology, , Princeton University, ; Princeton, NJ 08544 USA
                [2 ]ISNI 0000 0001 2097 5006, GRID grid.16750.35, Department of Physics and Lewis-Sigler Institute for Integrative Genomics, , Princeton University, ; Princeton, NJ 08544 USA
                [3 ]ISNI 0000 0001 0721 7331, GRID grid.65519.3e, Department of Microbiology and Molecular Genetics, , Oklahoma State University, ; Stillwater, OK 74078 USA
                Author information
                http://orcid.org/0000-0003-1128-2560
                http://orcid.org/0000-0002-3280-6178
                http://orcid.org/0000-0003-0749-6830
                Article
                5186
                10.1038/s41467-018-05186-5
                6052060
                30022070
                2e621023-bcbd-4b6a-9a27-8e8c6ff81f04
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 15 December 2017
                : 20 June 2018
                Funding
                Funded by: FundRef https://doi.org/10.13039/100000057, U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS);
                Award ID: R01GM107384
                Award ID: R01GM107384
                Award ID: F32GM103290
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100000166, NSF | Directorate for Mathematical & Physical Sciences | Division of Physics (PHY);
                Award ID: PHY1734030
                Award ID: PHY1734030
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100000060, U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID);
                Award ID: R21AI121828
                Award ID: R21AI121828
                Award ID: R21AI121828
                Award Recipient :
                Funded by: Glenn Centers for Aging Research
                Categories
                Article
                Custom metadata
                © The Author(s) 2018

                Uncategorized
                Uncategorized

                Comments

                Comment on this article