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      Mesodermal Gene Expression in the Acoel Isodiametra pulchra Indicates a Low Number of Mesodermal Cell Types and the Endomesodermal Origin of the Gonads

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          Abstract

          Acoelomorphs are bilaterally symmetric small marine worms that lack a coelom and possess a digestive system with a single opening. Two alternative phylogenetic positions of this group within the animal tree are currently debated. In one view, Acoelomorpha is the sister group to all remaining Bilateria and as such, is a morphologically simple stepping stone in bilaterian evolution. In the other, the group is a lineage within the Deuterostomia, and therefore, has derived a simple morphology from a more complex ancestor. Acoels and the closely related Nemertodermatida and Xenoturbellida, which together form the Acoelomorpha, possess a very limited number of cell types. To further investigate the diversity and origin of mesodermal cell types we describe the expression pattern of 12 orthologs of bilaterian mesodermal markers including Six1/2, Twist, FoxC, GATA4/5/6, in the acoel Isodiametra pulchra. All the genes are expressed in stem cells (neoblasts), gonads, and at least subsets of the acoel musculature. Most are expressed in endomesodermal compartments of I. pulchra developing embryos similar to what has been described in cnidarians. Our molecular evidence indicates a very limited number of mesodermal cell types and suggests an endomesodermal origin of the gonads and the stem cell system. We discuss our results in light of the two prevailing phylogenetic positions of Acoelomorpha.

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          Mechanisms of germ cell specification across the metazoans: epigenesis and preformation.

          Germ cells play a unique role in gamete production, heredity and evolution. Therefore, to understand the mechanisms that specify germ cells is a central challenge in developmental and evolutionary biology. Data from model organisms show that germ cells can be specified either by maternally inherited determinants (preformation) or by inductive signals (epigenesis). Here we review existing data on 28 metazoan phyla, which indicate that although preformation is seen in most model organisms, it is actually the less prevalent mode of germ cell specification, and that epigenetic germ cell specification may be ancestral to the Metazoa.
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            SMEDWI-2 is a PIWI-like protein that regulates planarian stem cells.

            We have identified two genes, smedwi-1 and smedwi-2, expressed in the dividing adult stem cells (neoblasts) of the planarian Schmidtea mediterranea. Both genes encode proteins that belong to the Argonaute/PIWI protein family and that share highest homology with those proteins defined by Drosophila PIWI. RNA interference (RNAi) of smedwi-2 blocks regeneration, even though neoblasts are present, irradiation-sensitive, and capable of proliferating in response to wounding; smedwi-2(RNAi) neoblast progeny migrate to sites of cell turnover but, unlike normal cells, fail at replacing aged tissue. We suggest that SMEDWI-2 functions within dividing neoblasts to support the generation of cells that promote regeneration and homeostasis.
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              Acoelomorph flatworms are deuterostomes related to Xenoturbella.

              Xenoturbellida and Acoelomorpha are marine worms with contentious ancestry. Both were originally associated with the flatworms (Platyhelminthes), but molecular data have revised their phylogenetic positions, generally linking Xenoturbellida to the deuterostomes and positioning the Acoelomorpha as the most basally branching bilaterian group(s). Recent phylogenomic data suggested that Xenoturbellida and Acoelomorpha are sister taxa and together constitute an early branch of Bilateria. Here we assemble three independent data sets-mitochondrial genes, a phylogenomic data set of 38,330 amino-acid positions and new microRNA (miRNA) complements-and show that the position of Acoelomorpha is strongly affected by a long-branch attraction (LBA) artefact. When we minimize LBA we find consistent support for a position of both acoelomorphs and Xenoturbella within the deuterostomes. The most likely phylogeny links Xenoturbella and Acoelomorpha in a clade we call Xenacoelomorpha. The Xenacoelomorpha is the sister group of the Ambulacraria (hemichordates and echinoderms). We show that analyses of miRNA complements have been affected by character loss in the acoels and that both groups possess one miRNA and the gene Rsb66 otherwise specific to deuterostomes. In addition, Xenoturbella shares one miRNA with the ambulacrarians, and two with the acoels. This phylogeny makes sense of the shared characteristics of Xenoturbellida and Acoelomorpha, such as ciliary ultrastructure and diffuse nervous system, and implies the loss of various deuterostome characters in the Xenacoelomorpha including coelomic cavities, through gut and gill slits.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2013
                6 February 2013
                : 8
                : 2
                : e55499
                Affiliations
                [1 ]Departament de Genètica, Universitat de Barcelona, Barcelona, Spain
                [2 ]Sars International Centre for Marine Molecular Biology, University of Bergen, Bergen, Norway
                [3 ]Institute of Zoology and Center for Molecular Biosciences, University of Innsbruck, Innsbruck, Austria
                [4 ]Hubrecht Institute, Utrecht, The Netherlands
                [5 ]Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona, Spain
                Ecole Normale Supérieure de Lyon, France
                Author notes

                Competing Interests: The authors have read the journal's policy and have the following conflicts: AH is an Academic Editor of PLOS ONE. This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials.

                Conceived and designed the experiments: AH MC PL PM. Performed the experiments: AB AH MC. Analyzed the data: AH MC PL PM. Contributed reagents/materials/analysis tools: EB PL. Wrote the paper: AH MC.

                Article
                PONE-D-12-29959
                10.1371/journal.pone.0055499
                3566195
                23405161
                6e2f5bfa-37ea-4015-9008-f4e2bb539839
                Copyright @ 2013

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 30 September 2012
                : 23 December 2012
                Page count
                Pages: 15
                Funding
                The work was supported by the following funding agencies: FP7 Marie Curie International Re-integration Grant (IRG) “Mesoderm Evolution” (246450) to AH ( http://tinyurl.com/9covbsz); the Spanish Ministry of Science and Innovation to MC and PM (BFU2006-00898/BMC) ( http://www.idi.mineco.gob.es); Austrian Science Fund (FWF) ( http://www.fwf.ac.at) 18099 to PL. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology
                Developmental Biology
                Morphogenesis
                Body Plan Organization
                Regeneration
                Organism Development
                Organogenesis
                Pattern Formation
                Regeneration
                Stem Cells
                Adult Stem Cells
                Mesenchymal Stem Cells
                Cell Differentiation
                Cell Fate Determination
                Embryology
                Evolutionary Developmental Biology
                Evolutionary Biology
                Evolutionary Systematics
                Molecular Systematics
                Phylogenetics
                Organismal Evolution
                Animal Evolution
                Evolutionary Developmental Biology
                Zoology
                Animal Phylogenetics
                Comparative Anatomy

                Uncategorized
                Uncategorized

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