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      Population genomics shed light on the demographic and adaptive histories of European invasion in the Pacific oyster, Crassostrea gigas

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          Abstract

          Crassostrea gigas originated from the Pacific coast of Asia, but was introduced into several European countries in the early 1970s. Natural populations have now spread across the length of the western seaboard of Europe. To elucidate the demographic and selective processes at play during this rapid expansion, genome-scan analysis was performed on different populations. High diversities and low differentiation were observed overall, but significant genetic differentiation was found among newly established populations and between the newly established northern group and a nearly panmictic group composed of southern European populations and a population from Japan. Loss of genetic diversity was also seen in the north, likely caused by founder events during colonization. The few strongly supported outlier loci revealed a genetic structure uncorrelated with the north/south differentiation, but grouping two samples from the Danish fjords (northern group) and one from the Dutch Scheldt estuary (southern group) with the one from Japan. These findings might reflect the following: (i) parallel adaptation to similar environmental pressures (fjord-like environment) within each of the two groups or (ii) a footprint of a secondary introduction of an alternative genomic background maintained by multifarious isolation factors. Our results call for a closer examination of adaptive genetic structure in the area of origin.

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          R: A language and environment for statistical computing

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            Estimation of average heterozygosity and genetic distance from a small number of individuals.

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            The magnitudes of the systematic biases involved in sample heterozygosity and sample genetic distances are evaluated, and formulae for obtaining unbiased estimates of average heterozygosity and genetic distance are developed. It is also shown that the number of individuals to be used for estimating average heterozygosity can be very small if a large number of loci are studied and the average heterozygosity is low. The number of individuals to be used for estimating genetic distance can also be very small if the genetic distance is large and the average heterozygosity of the two species compared is low.
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              AFLP: a new technique for DNA fingerprinting.

              A novel DNA fingerprinting technique called AFLP is described. The AFLP technique is based on the selective PCR amplification of restriction fragments from a total digest of genomic DNA. The technique involves three steps: (i) restriction of the DNA and ligation of oligonucleotide adapters, (ii) selective amplification of sets of restriction fragments, and (iii) gel analysis of the amplified fragments. PCR amplification of restriction fragments is achieved by using the adapter and restriction site sequence as target sites for primer annealing. The selective amplification is achieved by the use of primers that extend into the restriction fragments, amplifying only those fragments in which the primer extensions match the nucleotides flanking the restriction sites. Using this method, sets of restriction fragments may be visualized by PCR without knowledge of nucleotide sequence. The method allows the specific co-amplification of high numbers of restriction fragments. The number of fragments that can be analyzed simultaneously, however, is dependent on the resolution of the detection system. Typically 50-100 restriction fragments are amplified and detected on denaturing polyacrylamide gels. The AFLP technique provides a novel and very powerful DNA fingerprinting technique for DNAs of any origin or complexity.
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                Author and article information

                Journal
                Evol Appl
                Evol Appl
                eva
                Evolutionary Applications
                Blackwell Publishing Ltd
                1752-4571
                1752-4571
                November 2013
                24 July 2013
                : 6
                : 7
                : 1064-1078
                Affiliations
                [1 ]Ifremer, Laboratoire de génétique et pathologie des mollusques marins La Tremblade, France
                [2 ]Département Biologie Intégrative, ISEM Sète, France
                [3 ]Ifremer, Laboratoire des Sciences de l'Environnement Marin Plouzané, France
                Author notes
                Sylvie Lapègue, Ifremer, SG2M-LGPMM, Laboratoire de Génétique et Pathologie des Mollusques Marins, avenue de Mus de Loup 17390 La Tremblade, France. Tel.: 33 5 46 76 26 31; fax: 33 5 46 76 26 11; e-mail: Sylvie.Lapegue@ 123456ifremer.fr
                Article
                10.1111/eva.12086
                3804239
                24187588
                8672868f-2250-4ab5-bf4c-b8482e37c219
                Copyright © 2013 Wiley Periodicals, Inc.

                Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.

                History
                : 31 October 2012
                : 27 May 2013
                Categories
                Original Articles

                Evolutionary Biology
                aflps,crassostrea gigas,genome scan,invasive species,microsatellites,snps
                Evolutionary Biology
                aflps, crassostrea gigas, genome scan, invasive species, microsatellites, snps

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