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      Highly dense linkage maps from 31 full-sibling families of turbot ( Scophthalmus maximus) provide insights into recombination patterns and chromosome rearrangements throughout a newly refined genome assembly

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          Abstract

          Highly dense linkage maps enable positioning thousands of landmarks useful for anchoring the whole genome and for analysing genome properties. Turbot is the most important cultured flatfish worldwide and breeding programs in the fifth generation of selection are targeted to improve growth rate, obtain disease resistant broodstock and understand sex determination to control sex ratio. Using a Restriction-site Associated DNA approach, we genotyped 18,214 single nucleotide polymorphism in 1,268 turbot individuals from 31 full-sibling families. Individual linkage maps were combined to obtain a male, female and species consensus maps. The turbot consensus map contained 11,845 markers distributed across 22 linkage groups representing a total normalised length of 3,753.9 cM. The turbot genome was anchored to this map, and scaffolds representing 96% of the assembly were ordered and oriented to obtain the expected 22 megascaffolds according to its karyotype. Recombination rate was lower in males, especially around centromeres, and pairwise comparison of 44 individual maps suggested chromosome polymorphism at specific genomic regions. Genome comparison across flatfish provided new evidence on karyotype reorganisations occurring across the evolution of this fish group.

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          The genomic basis of adaptive evolution in threespine sticklebacks

          Summary Marine stickleback fish have colonized and adapted to innumerable streams and lakes formed since the last ice age, providing an exceptional opportunity to characterize genomic mechanisms underlying repeated ecological adaptation in nature. Here we develop a high quality reference genome assembly for threespine sticklebacks. By sequencing the genomes of 20 additional individuals from a global set of marine and freshwater populations, we identify a genome-wide set of loci that are consistently associated with marine-freshwater divergence. Our results suggest that reuse of globally-shared standing genetic variation, including chromosomal inversions, plays an important role in repeated evolution of distinct marine and freshwater sticklebacks, and in the maintenance of divergent ecotypes during early stages of reproductive isolation. Both coding and regulatory changes occur in the set of loci underlying marine-freshwater evolution, with regulatory changes likely predominating in this classic example of repeated adaptive evolution in nature.
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            The impact of next-generation sequencing technology on genetics.

            If one accepts that the fundamental pursuit of genetics is to determine the genotypes that explain phenotypes, the meteoric increase of DNA sequence information applied toward that pursuit has nowhere to go but up. The recent introduction of instruments capable of producing millions of DNA sequence reads in a single run is rapidly changing the landscape of genetics, providing the ability to answer questions with heretofore unimaginable speed. These technologies will provide an inexpensive, genome-wide sequence readout as an endpoint to applications ranging from chromatin immunoprecipitation, mutation mapping and polymorphism discovery to noncoding RNA discovery. Here I survey next-generation sequencing technologies and consider how they can provide a more complete picture of how the genome shapes the organism.
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              From 2R to 3R: evidence for a fish-specific genome duplication (FSGD).

              An important mechanism for the evolution of phenotypic complexity, diversity and innovation, and the origin of novel gene functions is the duplication of genes and entire genomes. Recent phylogenomic studies suggest that, during the evolution of vertebrates, the entire genome was duplicated in two rounds (2R) of duplication. Later, approximately 350 mya, in the stem lineage of ray-finned (actinopterygian) fishes, but not in that of the land vertebrates, a third genome duplication occurred-the fish-specific genome duplication (FSGD or 3R), leading, at least initially, to up to eight copies of the ancestral deuterostome genome. Therefore, the sarcopterygian (lobe-finned fishes and tetrapods) genome possessed originally only half as many genes compared to the derived fishes, just like the most-basal and species-poor lineages of extant fishes that diverged from the fish stem lineage before the 3R duplication. Most duplicated genes were secondarily lost, yet some evolved new functions. The genomic complexity of the teleosts might be the reason for their evolutionary success and astounding biological diversity.
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                Author and article information

                Journal
                DNA Res
                DNA Res
                dnares
                DNA Research: An International Journal for Rapid Publication of Reports on Genes and Genomes
                Oxford University Press
                1340-2838
                1756-1663
                August 2018
                11 June 2018
                11 June 2018
                : 25
                : 4
                : 439-450
                Affiliations
                [1 ]GENEAQUA S.L, 2007 Lugo, Spain
                [2 ]Departamento de Zoología, Genética y Antropología Física, Facultad de Veterinaria, Universidade de Santiago de Compostela, Lugo, Spain
                [3 ]Departamento de Mejora Genética Animal, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Madrid, Spain
                [4 ]Department of Comparative Biomedicine and Food Science, University of Padova, Legnaro, Padova, Italy
                [5 ]Cluster de Acuicultura de Galicia (Punta do Couso), Aguiño-Ribeira, Spain
                Author notes
                To whom correspondence should be addressed. Tel. +34 982 822423. Email: francesco.maroso@ 123456gmail.com (F.M.); Tel. +34982822425. Fax. +982822001. Email: paulino.martinez@ 123456usc.es (P.M.)

                Edited by Dr. Toshihiko Shiroishi

                Author information
                http://orcid.org/0000-0003-3524-5916
                Article
                dsy015
                10.1093/dnares/dsy015
                6105115
                29897548
                e15e1866-043f-4058-b90b-90609bda19e7
                © The Author(s) 2018. Published by Oxford University Press on behalf of Kazusa DNA Research Institute.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 15 February 2018
                : 05 May 2018
                Page count
                Pages: 12
                Funding
                Funded by: FISHBOOST
                Award ID: 613611
                Funded by: European Community's Seventh Framework Programme
                Award ID: FP7/2007-2013
                Funded by: Consellería de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia 10.13039/501100008425
                Award ID: GRC2014/010
                Funded by: Centro de Supercomputaciòn de Galicia
                Funded by: CESGA
                Categories
                Full Papers

                Genetics
                scophthalmus maximus,2b-rad sequencing,linkage mapping,genome assembly,chromosome reorganisations

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