1993
DOI: 10.1007/bf00222076
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Repetitive DNA of grapevine: classes present and sequences suitable for cultivar identification

Abstract: Repetitive DNA sequences present in the grapevine genome were investigated as probes for distinguishing species and cultivars. Microsatellite sequences, minisatellite sequences, tandemly arrayed genes and highly repetitive grapevine sequences were studied. The relative abundance of microsatellite and minisatellite DNA in the genome varied with the repeat sequence and determined their usefulness in detecting RFLPs. Cloned Vitis ribosomal repeat units were characterised and showed length heterogeneity (9.14-12.1… Show more

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Cited by 213 publications
(115 citation statements)
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“…The studied varieties, the viticultural areas in which their cultivation is recommended or allowed according to the Greek legislation, and the areas from where the samples were collected are presented in detail in Table 1 The AFLP molecular analysis was conducted as reported by Vos et al (1995), following the AFLP Plant Mapping Protocol by Applied Biosystems (2007), with several modifications . Grapevine DNA was extracted from young and fully expanded leaves according to Thomas et al (1993), with minor modifications. A total of seven primer combinations with three selective nucleotides and fluorescent dye (in the form of EcoRI[Primer-Axx-Dye] and MseI[PrimerCxx]) were used to amplify genomic DNA through the Polymerase Chain Reaction in order to identify and discriminate the selected cultivars (Table 2).…”
Section: Plant Materialsmentioning
confidence: 99%
“…The studied varieties, the viticultural areas in which their cultivation is recommended or allowed according to the Greek legislation, and the areas from where the samples were collected are presented in detail in Table 1 The AFLP molecular analysis was conducted as reported by Vos et al (1995), following the AFLP Plant Mapping Protocol by Applied Biosystems (2007), with several modifications . Grapevine DNA was extracted from young and fully expanded leaves according to Thomas et al (1993), with minor modifications. A total of seven primer combinations with three selective nucleotides and fluorescent dye (in the form of EcoRI[Primer-Axx-Dye] and MseI[PrimerCxx]) were used to amplify genomic DNA through the Polymerase Chain Reaction in order to identify and discriminate the selected cultivars (Table 2).…”
Section: Plant Materialsmentioning
confidence: 99%
“…DNA was extracted from grapevine plantlets grown in vitro using the method of Thomas et al (1993). PCR amplification was performed using specific primer pairs for transgenic VvPIP2;4N (Supplemental Table S2) and nptII (Gambino et al, 2010) genes.…”
Section: Grapevine Transformation and Selectionmentioning
confidence: 99%
“…Different morphological characteristics were the methodology used for selecting wild vines in the field. DNA from all samples was extracted, following the protocol of Thomas et al (1993). Primer sequences and DNA analysis were carried out, following the protocols described by Almadanim et al (2007) and Cunha et al (2009).…”
Section: S54mentioning
confidence: 99%