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Microsatellites for cultivar identification in Pelargonium
Authors:S A Becher  K Steinmetz  K Weising  S Boury  D Peltier  J-P Renou  G Kahl  K Wolff
Institution:(1) School of Evolutionary and Environmental Biology, Sir Harold Mitchell Building, University of St. Andrews, KY16 9TH, Scotland, UK, Present address: K. Wolff, University of Newcastle, Department of Agriculture and Environmental Science, Newcastle-upon-Tyne, NE1 7RU, UK, GB;(2) Plant Molecular Biology, Biozentrum, N200, University of Frankfurt, Marie-Curie-Str. 9, D-60439, Frankfurt am Main, Germany, DE;(3) Bretagne Biotechnologie Végétale, Penn Ar Prat, F-29250, St Pol de Léon, France, FR;(4) Université d’Angers, UFR Sciences, Laboratoire de Génétique, 2 bd Lavoisier, F-49045 Angers Cedex, France, FR;(5) INRA d’Angers, Rue Georges Morel, F-49054 Beaucouzé, France, FR
Abstract:We have isolated and characterised microsatellite loci from Pelargonium sp. to explore the potential of these markers for cultivar identification. Small-insert libraries from a zonal (Pelargonium x hortorum cv. Isabell) and an ivy-leaved variety (P. peltatum cv. Guenievre gergue) were enriched for d(AG), d(AC), d(CAA), d(GAA) and d(GATA) repeats. Of 141 positive clones sequenced, 133 contained a microsatellite. Primers for PCR amplification were designed to the flanking regions of 57 microsatellites, resulting in interpretable amplification products of the expected size for 29 loci. Seventeen primer pairs amplifying 18 loci were used to fingerprint 44 di- and tetra-ploid Pelargonium accessions representative of commercially available varieties. Multilocus genotypes obtained at 3 loci distinguished among all accessions, except for three known flower colour sports and a fourth, phenotypically very similar, variety. Allelic composition was also identical within two other sport ’families’ typed at the same 18 loci. UPGMA and principal co-ordinate analysis of pairwise distance matrices derived from PCR amplification patterns revealed four distinct assemblages. The first group consisted of tetraploid P. x hortorum varieties; a second group contained diploid P. x hortorum, a third, tetraploid P. peltatum accessions, while a fourth, very distinct, group consisted solely of diploid P. peltatum varieties. Polymorphism in P. peltatum was equal or greater than in P. x hortorum at 17 of the 18 loci, indicating that the analysed P. peltatum varieties form a genetically more variable array. Received: 5 November 1999 / Accepted: 12 January 2000
Keywords:  Cultivar identification  Geranium  Pelargonium  Simple sequence repeats  Protected varieties
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