11
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Early evolution of radial glial cells in Bilateria

      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

          Bilaterians usually possess a central nervous system, composed of neurons and supportive cells called glial cells. Whereas neuronal cells are highly comparable in all these animals, glial cells apparently differ, and in deuterostomes, radial glial cells are found. These particular secretory glial cells may represent the archetype of all (macro) glial cells and have not been reported from protostomes so far. This has caused controversial discussions of whether glial cells represent a homologous bilaterian characteristic or whether they (and thus, centralized nervous systems) evolved convergently in the two main clades of bilaterians. By using histology, transmission electron microscopy, immunolabelling and whole-mount in situ hybridization, we show here that protostomes also possess radial glia-like cells, which are very likely to be homologous to those of deuterostomes. Moreover, our antibody staining indicates that the secretory character of radial glial cells is maintained throughout their various evolutionary adaptations. This implies an early evolution of radial glial cells in the last common ancestor of Protostomia and Deuterostomia. Furthermore, it suggests that an intraepidermal nervous system—composed of sensory cells, neurons and radial glial cells—was probably the plesiomorphic condition in the bilaterian ancestor.

          Related collections

          Most cited references50

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          SMART: recent updates, new developments and status in 2015

          SMART (Simple Modular Architecture Research Tool) is a web resource (http://smart.embl.de/) providing simple identification and extensive annotation of protein domains and the exploration of protein domain architectures. In the current version, SMART contains manually curated models for more than 1200 protein domains, with ∼200 new models since our last update article. The underlying protein databases were synchronized with UniProt, Ensembl and STRING, bringing the total number of annotated domains and other protein features above 100 million. SMART's ‘Genomic’ mode, which annotates proteins from completely sequenced genomes was greatly expanded and now includes 2031 species, compared to 1133 in the previous release. SMART analysis results pages have been completely redesigned and include links to several new information sources. A new, vector-based display engine has been developed for protein schematics in SMART, which can also be exported as high-resolution bitmap images for easy inclusion into other documents. Taxonomic tree displays in SMART have been significantly improved, and can be easily navigated using the integrated search engine.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            SMART, a simple modular architecture research tool: identification of signaling domains.

            Accurate multiple alignments of 86 domains that occur in signaling proteins have been constructed and used to provide a Web-based tool (SMART: simple modular architecture research tool) that allows rapid identification and annotation of signaling domain sequences. The majority of signaling proteins are multidomain in character with a considerable variety of domain combinations known. Comparison with established databases showed that 25% of our domain set could not be deduced from SwissProt and 41% could not be annotated by Pfam. SMART is able to determine the modular architectures of single sequences or genomes; application to the entire yeast genome revealed that at least 6.7% of its genes contain one or more signaling domains, approximately 350 greater than previously annotated. The process of constructing SMART predicted (i) novel domain homologues in unexpected locations such as band 4.1-homologous domains in focal adhesion kinases; (ii) previously unknown domain families, including a citron-homology domain; (iii) putative functions of domain families after identification of additional family members, for example, a ubiquitin-binding role for ubiquitin-associated domains (UBA); (iv) cellular roles for proteins, such predicted DEATH domains in netrin receptors further implicating these molecules in axonal guidance; (v) signaling domains in known disease genes such as SPRY domains in both marenostrin/pyrin and Midline 1; (vi) domains in unexpected phylogenetic contexts such as diacylglycerol kinase homologues in yeast and bacteria; and (vii) likely protein misclassifications exemplified by a predicted pleckstrin homology domain in a Candida albicans protein, previously described as an integrin.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              The cell biology of neurogenesis.

              During the development of the mammalian central nervous system, neural stem cells and their derivative progenitor cells generate neurons by asymmetric and symmetric divisions. The proliferation versus differentiation of these cells and the type of division are closely linked to their epithelial characteristics, notably, their apical-basal polarity and cell-cycle length. Here, we discuss how these features change during development from neuroepithelial to radial glial cells, and how this transition affects cell fate and neurogenesis.
                Bookmark

                Author and article information

                Journal
                Proc Biol Sci
                Proc. Biol. Sci
                RSPB
                royprsb
                Proceedings of the Royal Society B: Biological Sciences
                The Royal Society
                0962-8452
                1471-2954
                26 July 2017
                19 July 2017
                19 July 2017
                : 284
                : 1859
                : 20170743
                Affiliations
                [1 ]Sars International Center for Marine Molecular Biology, University of Bergen , 5008 Bergen, Norway
                [2 ]Paul-Flechsig-Institute for Brain Research, University of Leipzig , 04103 Leipzig, Germany
                [3 ]Translational Center for Regenerative Medicine, University of Leipzig , 04103 Leipzig, Germany
                [4 ]Carl-Ludwig-Institute for Physiology, University of Leipzig , 04103 Leipzig, Germany
                [5 ]Institute of Evolutionary Biology and Ecology, University of Bonn , 53121 Bonn, Germany
                [6 ]Department of Integrative Biology, University of Vienna , 1090 Vienna, Austria
                [7 ]Biotechnology Center, Technische Universität Dresden , 01307 Dresden, Germany
                [8 ]Museo Nacional de Ciencias Naturales, Spanish National Research Council (CSIC) , 28006 Madrid, Spain
                Author notes
                [†]

                These authors contributed equally to this study.

                Electronic supplementary material is available online at https://dx.doi.org/10.6084/m9.figshare.c.3811681.

                Author information
                http://orcid.org/0000-0002-0308-8402
                http://orcid.org/0000-0001-5662-7919
                Article
                rspb20170743
                10.1098/rspb.2017.0743
                5543218
                28724733
                41315d9a-ef16-4ae2-9086-6824622b6ad1
                © 2017 The Authors.

                Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.

                History
                : 6 April 2017
                : 13 June 2017
                Funding
                Funded by: Bundesministerium für Bildung und Forschung, http://dx.doi.org/10.13039/501100002347;
                Award ID: BMBF 1315883
                Funded by: Deutsche Forschungsgemeinschaft, http://dx.doi.org/10.13039/501100001659;
                Award ID: HE 7224/1-1
                Award ID: SPP 175/
                Funded by: Austrian Science Fund, http://dx.doi.org/10.13039/501100002428;
                Award ID: M 1485-B19
                Funded by: Ministerio de Economía y Competitividad, http://dx.doi.org/10.13039/501100003329;
                Award ID: RYC-2014-15615
                Categories
                1001
                33
                70
                133
                Neuroscience and Cognition
                Research Article
                Custom metadata
                July 26, 2017

                Life sciences
                deuterostomia,glia,nervous system,reissner's fibre
                Life sciences
                deuterostomia, glia, nervous system, reissner's fibre

                Comments

                Comment on this article