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  • Abbreviations: BPA: N-benzyl-9-[2-tetrahydro-pyranyl]-adenine; PCR: polymerase chain reaction; RAPD: random amplified polymorphic DNA; RFLP: restriction fragment length polymorphism; TAE buffer: 40 mM Tris acetate, 20 mM sodium acetate, 1 mM EDTA, pH 7.8  (1)
  • Actinidia  (1)
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  • 1
    ISSN: 1432-203X
    Keywords: Abbreviations: BPA: N-benzyl-9-[2-tetrahydro-pyranyl]-adenine; PCR: polymerase chain reaction; RAPD: random amplified polymorphic DNA; RFLP: restriction fragment length polymorphism; TAE buffer: 40 mM Tris acetate, 20 mM sodium acetate, 1 mM EDTA, pH 7.8 ; Keywords:Achillea– Simple repetitive sequences – Oligonucleotide fingerprinting – RAPD analysis – Clone identification
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. Two different DNA fingerprinting techniques were applied to a set of Achillea samples (Asteraceae), comprising ten taxa of the medicinally important A. millefolium group and six related species. Field-grown as well as in vitro-micropropagated plants were indivually screened for abundance and polymorphism of target sequences recognized by oligonucleotide fingerprinting with 13 different microsatellite-complementary probes. While most probes revealed a high level of intra- and interspecific variability, fingerprints proved to be somatically stable, in vegetatively propagated plant material. Analysis of the same samples by polymerase chain reaction with arbitrary 10-mer primers yielded less polymorphic patterns. Because of its higher discriminatory ability, olignonucleotide fingerprinting offers itself as the method of choice for the identification and discrimination of A. asplenifolia and A. roseoalba clones, as well as for monitoring their stability during micropropagation.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-9788
    Keywords: Actinidia ; dinucleotide repeats ; genetic markers ; kiwifruit ; simple sequence repeats polyploidy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract We have identified a set of informative microsatellite markers for genome analysis in kiwifruit and related Actinidia species. A small-insert genomic library was constructed from Actinidia chinensis DNA, and screened for microsatellites. About 1.2% of the total colonies hybridised to a (GA)8 probe, 0.4% to (GT)8, and 0.1% to a mixture of three different trinucleotide repeat probes, (CAA)5, (GAA)5 and (CTA)5. From the DNA sequences of 35 hybridising clones, 18 primer pairs were designed, and used to amplify genomic DNA from 38 individual plants, representing 30 different accessions of ten Actinidia species. The banding patterns for most of the dinucleotide repeats showed a high degree of polymorphism in the diploid and tetraploid A. chinensis, and in the hexaploid A. deliciosa (kiwifruit). Heterozygosity levels of up to 100% were found among eight diploid accessions of A. chinensis examined, and the number of different-sized bands among all the species varied from 3 to 36 for each microsatellite. One simple CT microsatellite gave 21 bands with sizes suggesting that the number of repeats ranged from 9 to 37. The highest number of bands (36) and the largest size variation (〉100 bp) were observed with a complex microsatellite harbouring four different repeat motifs. The majority of primer pairs amplified bands from most of the ten Actinidia species tested. The most polymorphic primer pairs were used successfully to fingerprint a range of closely related varieties of kiwifruit (A. deliciosa).
    Type of Medium: Electronic Resource
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