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      Elephant shark genome provides unique insights into gnathostome evolution

      research-article
      1 , 2 , , 1 , 1 , 3 , 1 , 4 , 5 ,   5 , 6 , 6 , 7 , 7 , 8 , 9 , 10 , 10 , 1 , 1 , 1 , 7 , 7 , 11 , 12 , 11 , 12 , 11 , 12 , 13 , 3 , 1 , 14 , 14 , 4 , 14 , 1 , 14 ,
      Nature
      Nature Publishing Group UK
      Molecular evolution, Cellular immunity, Comparative genomics, Development

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          Abstract

          The emergence of jawed vertebrates (gnathostomes) from jawless vertebrates was accompanied by major morphological and physiological innovations, such as hinged jaws, paired fins and immunoglobulin-based adaptive immunity. Gnathostomes subsequently diverged into two groups, the cartilaginous fishes and the bony vertebrates. Here we report the whole-genome analysis of a cartilaginous fish, the elephant shark ( Callorhinchus milii). We find that the C. milii genome is the slowest evolving of all known vertebrates, including the ‘living fossil’ coelacanth, and features extensive synteny conservation with tetrapod genomes, making it a good model for comparative analyses of gnathostome genomes. Our functional studies suggest that the lack of genes encoding secreted calcium-binding phosphoproteins in cartilaginous fishes explains the absence of bone in their endoskeleton. Furthermore, the adaptive immune system of cartilaginous fishes is unusual: it lacks the canonical CD4 co-receptor and most transcription factors, cytokines and cytokine receptors related to the CD4 lineage, despite the presence of polymorphic major histocompatibility complex class II molecules. It thus presents a new model for understanding the origin of adaptive immunity.

          Supplementary information

          The online version of this article (doi:10.1038/nature12826) contains supplementary material, which is available to authorized users.

          Abstract

          Whole-genome analysis of the elephant shark, a cartilaginous fish, shows that it is the slowest evolving of all known vertebrates, lacks critical bone formation genes and has an unusual adaptive immune system.

          Supplementary information

          The online version of this article (doi:10.1038/nature12826) contains supplementary material, which is available to authorized users.

          First genome of a cartilaginous fish

          The elephant shark ( Callorhinchus milii) is a cartilaginous fish native to the temperate waters off southern Australia and New Zealand, living at depths of 200 to 500 metres and migrating into shallow waters during spring for breeding. The genome sequence is published in this issue of Nature. Comparison with other vertebrate genomes shows that it is the slowest evolving genome of all known vertebrates — coelacanth included. Genome analysis points to an unusual adaptive immune system lacking the CD4 receptor and some associated cytokines, indicating that cartilaginous fishes possess a primordial gnathostome adaptive immune system. Also absent are genes encoding secreted calcium-binding phosphoproteins, in line with the absence of bone in cartilaginous fish.

          Supplementary information

          The online version of this article (doi:10.1038/nature12826) contains supplementary material, which is available to authorized users.

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          Most cited references36

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          Projection of an immunological self shadow within the thymus by the aire protein.

          Humans expressing a defective form of the transcription factor AIRE (autoimmune regulator) develop multiorgan autoimmune disease. We used aire- deficient mice to test the hypothesis that this transcription factor regulates autoimmunity by promoting the ectopic expression of peripheral tissue- restricted antigens in medullary epithelial cells of the thymus. This hypothesis proved correct. The mutant animals exhibited a defined profile of autoimmune diseases that depended on the absence of aire in stromal cells of the thymus. Aire-deficient thymic medullary epithelial cells showed a specific reduction in ectopic transcription of genes encoding peripheral antigens. These findings highlight the importance of thymically imposed "central" tolerance in controlling autoimmunity.
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            Ensembl 2012

            The Ensembl project (http://www.ensembl.org) provides genome resources for chordate genomes with a particular focus on human genome data as well as data for key model organisms such as mouse, rat and zebrafish. Five additional species were added in the last year including gibbon (Nomascus leucogenys) and Tasmanian devil (Sarcophilus harrisii) bringing the total number of supported species to 61 as of Ensembl release 64 (September 2011). Of these, 55 species appear on the main Ensembl website and six species are provided on the Ensembl preview site (Pre!Ensembl; http://pre.ensembl.org) with preliminary support. The past year has also seen improvements across the project.
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              The genome sequence of Atlantic cod reveals a unique immune system.

              Atlantic cod (Gadus morhua) is a large, cold-adapted teleost that sustains long-standing commercial fisheries and incipient aquaculture. Here we present the genome sequence of Atlantic cod, showing evidence for complex thermal adaptations in its haemoglobin gene cluster and an unusual immune architecture compared to other sequenced vertebrates. The genome assembly was obtained exclusively by 454 sequencing of shotgun and paired-end libraries, and automated annotation identified 22,154 genes. The major histocompatibility complex (MHC) II is a conserved feature of the adaptive immune system of jawed vertebrates, but we show that Atlantic cod has lost the genes for MHC II, CD4 and invariant chain (Ii) that are essential for the function of this pathway. Nevertheless, Atlantic cod is not exceptionally susceptible to disease under natural conditions. We find a highly expanded number of MHC I genes and a unique composition of its Toll-like receptor (TLR) families. This indicates how the Atlantic cod immune system has evolved compensatory mechanisms in both adaptive and innate immunity in the absence of MHC II. These observations affect fundamental assumptions about the evolution of the adaptive immune system and its components in vertebrates.
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                Author and article information

                Contributors
                mcbbv@imcb.a-star.edu.sg
                wwarren@genome.wustl.edu
                Journal
                Nature
                Nature
                Nature
                Nature Publishing Group UK (London )
                0028-0836
                1476-4687
                8 January 2014
                8 January 2014
                2014
                : 505
                : 7482
                : 174-179
                Affiliations
                [1 ]GRID grid.418812.6, ISNI 0000 0004 0620 9243, Comparative Genomics Laboratory, Institute of Molecular and Cell Biology, A*STAR, Biopolis, Singapore 138673, ; ,
                [2 ]GRID grid.4280.e, ISNI 0000 0001 2180 6431, Department of Paediatrics, , Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, ; ,
                [3 ]GRID grid.418812.6, ISNI 0000 0004 0620 9243, Developmental and Biomedical Genetics Laboratory, Institute of Molecular and Cell Biology, A*STAR, Biopolis, Singapore 138673, ; ,
                [4 ]GRID grid.429509.3, ISNI 0000 0004 0491 4256, Department of Developmental Immunology, , Max-Planck-Institute of Immunobiology and Epigenetics, Stuebeweg 51, 79108 Freiburg, Germany, ; ,
                [5 ]GRID grid.411024.2, ISNI 0000 0001 2175 4264, Department of Microbiology and Immunology, , University of Maryland, ; Baltimore, 21201 Maryland USA
                [6 ]GRID grid.39158.36, ISNI 0000 0001 2173 7691, Department of Pathology, , Hokkaido University Graduate School of Medicine, Sapporo 060-8638, Japan, ; ,
                [7 ]GRID grid.185448.4, ISNI 0000 0004 0637 0221, Molecular Engineering Laboratory, Biomedical Sciences Institutes, A*STAR, Biopolis, Singapore 138673, ; ,
                [8 ]GRID grid.263091.f, ISNI 0000000106792318, Department of Biology, , San Francisco State University, ; San Francisco, 94132 California USA
                [9 ]GRID grid.17063.33, ISNI 0000 0001 2157 2938, Banting and Best Department of Medical Research and Donnelly Centre, , University of Toronto, Toronto, Ontario M5S 3E1, Canada, ; ,
                [10 ]GRID grid.418812.6, ISNI 0000 0004 0620 9243, Fish Developmental Biology Laboratory, Institute of Molecular and Cell Biology, A*STAR, Biopolis, Singapore 138673, ; ,
                [11 ]GRID grid.5612.0, ISNI 0000 0001 2172 2676, Institut de Biologia Evolutiva (UPF-CSIC), PRBB, 08003 Barcelona, Spain, ; ,
                [12 ]GRID grid.425902.8, ISNI 0000 0000 9601 989X, Institució Catalana de Recerca i Estudis Avançats (ICREA), 08010 Barcelona, Catalonia, Spain, ; ,
                [13 ]GRID grid.205975.c, ISNI 0000 0001 0740 6917, Center for Biomolecular Science and Engineering, School of Engineering, University of California Santa Cruz, ; Santa Cruz, 95064 California USA
                [14 ]GRID grid.4367.6, ISNI 0000 0001 2355 7002, The Genome Institute at Washington University, ; St Louis, 63108 Missouri USA
                Article
                BFnature12826
                10.1038/nature12826
                3964593
                24402279
                6342b260-3e66-4653-b6e2-1f0e4c00521f
                © The Author(s) 2014

                This work is licensed under a Creative Commons Attribution-Non-Commercial-ShareAlike 3.0 Unported licence. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-sa/3.0/.

                History
                : 22 May 2013
                : 1 November 2013
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                © Springer Nature Limited 2014

                Uncategorized
                molecular evolution,cellular immunity,comparative genomics,development
                Uncategorized
                molecular evolution, cellular immunity, comparative genomics, development

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