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Detection of two major cytochrome b lineages in pike-perch, Sander lucioperca, and first data on their distribution in European populations

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Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Despite of the growing interest in pike-perch for aquaculture and its economic importance in fisheries, knowledge on the population structure and phylogeography of the species is still limited. We report the discovery of two major cytochrome b lineages and describe a simple method for their detection based on PCR amplification followed by restriction digestion with Alw26I. Screening of 708 individuals showed that haplotype A was fixed or dominating in Central and East European countries, whereas haplotype B was mainly found in several French populations and Tunisian pike-perch introduced from Europe. Sequencing the complete cytochrome b cds of 17 representative individuals revealed that haplotypes A and B differed by five substitutions but also showed further differentiation of both haplotypes due to an additional substitution in a single haplotype A and B individual from France, respectively. Five partial pike-perch cytochrome b cds available from NCBI GenBank could also clearly be assigned to one or the other of the two major lineages. Therefore, this new mtDNA marker might be considered as suitable not only for studies on population structure and phylogeography of pikeperch but also to trace its introduction history and to assess the genetic composition of aquaculture brood stocks.
Rocznik
Strony
1--5
Opis fizyczny
Bibliogr. 15 poz., rys., tab.
Twórcy
autor
  • Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Department of Ecophysiology and Aquaculture, Müggelseedamm 310, 12587 Berlin, Germany, Phone: 0049-30-64 181 634; Fax: 0049-30-64 181 663
autor
  • Unité de Recherche de Biologie Intégrative et Écologie Evolutive et Fonctionnelle des Milieux Aquatiques, Faculté des Sciences de Tunis, 2092 El Manar, Tunisie
autor
  • Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Department of Ecophysiology and Aquaculture, Müggelseedamm 310, 12587 Berlin, Germany
  • Unité de Recherche de Biologie Intégrative et Écologie Evolutive et Fonctionnelle des Milieux Aquatiques, Faculté des Sciences de Tunis, 2092 El Manar, Tunisie
autor
  • French National Agency for Water and Aquatic Environment (ONEMA), “Le Nadar” Hall C5, square Félix Nadar, 94300 Vincennes, France
  • Unité de Recherche de Biologie Intégrative et Écologie Evolutive et Fonctionnelle des Milieux Aquatiques, Faculté des Sciences de Tunis, 2092 El Manar, Tunisie
Bibliografia
  • Björklund, M., T. Aho, L.C. Larsson. 2007. Genetic differentiation in pikeperch (Sander lucioperca): the relative importance of gene flow, drift and common history. Journal of Fish Biology 71 (supplement B): 264-278.
  • Borer, S.O., L.M. Miller, A.R. Kapuscinski. 1999. Microsatellites in walleye Stizostedion vitreum. Molecular Ecology 8: 335-346.
  • Kahilainen, K.K., A.G.F. Teacher, K. Kähkönen, M. Vinni, H. Lehtonen, J. Merilä. 2011. First record of natural hybridization and introgression between pikeperch (Sander lucioperca) and perch (Perca fluviatilis). Annales Zoologici Fennici 48: 39-44.
  • Kalous, L., V. Šlechtová, M. Petryl, J. Kohout, M. Cech. 2010. Do small fish mean no voucher? Using a flatbed desktop scanner to document larval and small specimens before destructive analyses. Journal of Applied Ichthyology 26: 614-617.
  • Khurshut, E., K. Kohlmann. 2009. Application of nine species-specific microsatellite loci to characterize three pike-perch (Sander lucioperca) populations from the Aral Sea basin in Uzbekistan. Environmental Biotechnology 5: 3-10.
  • Kohlmann, K., P. Kersten. 2008. Isolation and characterization of nine microsatellite loci from the pike-perch, Sander lucioperca (Linnaeus, 1758). Molecular Ecology Resources 8: 1085-1087.
  • Kottelat, M., J. Freyhof. 2007. Handbook of European Freshwater Fishes. Publications Kottelat, Cornol, Switzerland. 646 p.
  • Kumar, S., K. Tamura, M. Nei. 2004. MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment. Briefings in Bioinformatics 5: 150-163.
  • Leclerc, D., T. Wirth, L. Bernatchez. 2000. Isolation and characterization of microsatellite loci in the yellow perch (Perca flavescens), and cross-species amplification within the family Percidae. Molecular Ecology 9: 995-997.
  • Matschiner, M., R. Hanel, W. Salzburger. 2011. On the origin and trigger of the Notothenioid adaptive radiation. PLoS ONE 6 (4), e18911.
  • Poulet, N., P. Balaresque, T. Aho, M. Björklund. 2009. Genetic structure and dynamics of a small introduced population: the pikeperch, Sander lucioperca, in the Rhône delta. Genetica 135: 77-86.
  • Säisä, M., M. Salminen, M.-L. Koljonen, J. Ruuhijärvi. 2010. Coastal and freshwater pikeperch (Sander lucioperca) populations differ genetically in the Baltic Sea basin. Hereditas 147: 205-214.
  • Sloss, L.B., N. Billington, B.M. Burr. 2004. A molecular phylogeny of the Percidae (Teleostei, Perciformes) based on mitochondrial DNA sequence. Molecular Phylogenetics and Evolution 32: 545-562.
  • Song, C.B., T.J. Near, L.M. Page. 1998. Phylogenetic relations among percid fishes as inferred from mitochondrial cytochrome b DNA sequence data. Molecular Phylogenetics and Evolution 10: 343-353.
  • Wirth, T., R. Saint-Laurent, L. Bernatchez. 1999. Isolation and characterization of microsatellite loci in the walleye (Stizostedion vitreum), and cross-species amplification within the family Percidae. Molecular Ecology 8: 1960-1962.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-f592f8a1-3349-4b6a-b55d-52ce47775447
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