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      The mid-developmental transition and the evolution of animal body plans

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          Abstract

          Animals are grouped into ~35 ‘phyla’ based upon the notion of distinct body plans 14 . Morphological and molecular analyses have revealed that a stage the middle of development—known as the phylotypic period—is conserved among species within some phyla 59 . While these analyses provide evidence for their existence, phyla have also been criticized as lacking an objective definition, and consequently based on arbitrary groupings of animals 10 . Here, we compare the developmental transcriptomes of ten species, each annotated to a different phylum, with a wide range of life histories and embryonic forms. We find that, in all ten species, development comprises the coupling of early and late phases of gene expression. These conserved phases are linked by a divergent ‘mid-developmental transition’ that deploys species-specific suites of signaling pathways and transcription factors. This mid-developmental transition overlaps with the phylotypic period that has been defined previously for three of the ten phyla, suggesting that transcriptional circuits and signaling mechanisms active during this transition are crucial for defining the phyletic body plan and that the mid-developmental transition may be used to define phylotypic periods in other phyla. Placing these observations alongside the reported conservation of mid-development within phyla, we propose that a phylum may be defined as a collection of species whose gene expression at the mid-developmental transition is both highly-conserved among them, yet divergent relative to species in other phyla.

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          The genome of the ctenophore Mnemiopsis leidyi and its implications for cell type evolution.

          An understanding of ctenophore biology is critical for reconstructing events that occurred early in animal evolution. Toward this goal, we have sequenced, assembled, and annotated the genome of the ctenophore Mnemiopsis leidyi. Our phylogenomic analyses of both amino acid positions and gene content suggest that ctenophores rather than sponges are the sister lineage to all other animals. Mnemiopsis lacks many of the genes found in bilaterian mesodermal cell types, suggesting that these cell types evolved independently. The set of neural genes in Mnemiopsis is similar to that of sponges, indicating that sponges may have lost a nervous system. These results present a newly supported view of early animal evolution that accounts for major losses and/or gains of sophisticated cell types, including nerve and muscle cells.
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            Assessing the root of bilaterian animals with scalable phylogenomic methods.

            A clear picture of animal relationships is a prerequisite to understand how the morphological and ecological diversity of animals evolved over time. Among others, the placement of the acoelomorph flatworms, Acoela and Nemertodermatida, has fundamental implications for the origin and evolution of various animal organ systems. Their position, however, has been inconsistent in phylogenetic studies using one or several genes. Furthermore, Acoela has been among the least stable taxa in recent animal phylogenomic analyses, which simultaneously examine many genes from many species, while Nemertodermatida has not been sampled in any phylogenomic study. New sequence data are presented here from organisms targeted for their instability or lack of representation in prior analyses, and are analysed in combination with other publicly available data. We also designed new automated explicit methods for identifying and selecting common genes across different species, and developed highly optimized supercomputing tools to reconstruct relationships from gene sequences. The results of the work corroborate several recently established findings about animal relationships and provide new support for the placement of other groups. These new data and methods strongly uphold previous suggestions that Acoelomorpha is sister clade to all other bilaterian animals, find diminishing evidence for the placement of the enigmatic Xenoturbella within Deuterostomia, and place Cycliophora with Entoprocta and Ectoprocta. The work highlights the implications that these arrangements have for metazoan evolution and permits a clearer picture of ancestral morphologies and life histories in the deep past.
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              The Shape of Life

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                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                Nature
                0028-0836
                1476-4687
                21 January 2016
                17 February 2016
                31 March 2016
                30 September 2016
                : 531
                : 7596
                : 637-641
                Affiliations
                [1 ]Department of Biology, Technion – Israel Institute of Technion, Haifa, Israel
                [2 ]School of Biological Sciences, University of Queensland, Brisbane, QLD, Australia
                [3 ]Whitney Laboratory for Marine Bioscience, University of Florida, 9505 N, Ocean Shore Blvd, St. Augustine, FL 32080-8610 USA
                [4 ]Developmental Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany
                [5 ]Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307 Dresden, Germany
                [6 ]Department of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel
                Author notes
                [& ]Correspondence and requests for materials should be addressed to I.Y. yanai@ 123456technion.ac.il
                [#]

                Present address: Laboratorio Nacional de Genómica para la Biodiversidad, Centro de Investigación y de Estudios Avanzados del IPN, Irapuato, Guanajuato, Mexico.

                [+]

                Present address: Center for Thrombosis and Hemostasis (CTH), University Medical Center Mainz, Mainz, Germany.

                [%]

                Present address: Whitney Laboratory for Marine Bioscience, University of Florida, 9505 N, Ocean Shore Blvd, St. Augustine, FL 32080-8610 USA.

                Article
                EMS66718
                10.1038/nature16994
                4817236
                26886793
                ddeef6ec-768d-4748-b752-f74354e21aa4

                Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms

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