Design of grapevine (Vitis vinifera L.) cultivar-specific SCAR primers for PCR fingerprinting

• Published in: Theoretical and applied genetics 2000-12, Vol.101 (8), p.1194-1201
• Main Authors: VIDAL, J. R, DELAVAULT, P, COARER, M, DEFONTAINE, A
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Classical genetics, quantitative genetics, hybrids; Cloning; Cultivars; Fundamental and applied biological sciences. Psychology; Genetics of eukaryotes. Biological and molecular evolution; Genotype & phenotype; Identification; Polymorphism; Pteridophyta, spermatophyta; Vegetals; Vitis vinifera
• ISSN: 0040-5752; 1432-2242
• DOI: 10.1007/s001220051597

Among 34 grapevine cultivars (Vitis vinifera L.), eight putative genotype-specific RAPD markers, from 'Albariño', 'Caíño blanco', 'Chardonnay', 'Folle blanche', 'Grenache blanc', 'Malvasía Sitges', 'Torrontés' and 'Treixadura' respectively, were selected to transform into SCAR markers. Of these, seven markers were cloned and then five which showed a positive specific hybridization signal were sequenced. For these five markers, 30 sequence-specific primers ranging from 14 to 29 bases were designed to amplify genomic DNA from 64 grapevine cultivars under more-stringent PCR conditions. Only, two primer pairs, OpA11^sub 1175^p17R/ p17F and OpD10^sub 800^p14R/p14F, still produced a specific SCAR marker, the 'Folle blanche' ScA11^sub 1175^and the 'Malvasía Sitges' ScD10^sub 800^ respectively. Moreover, the ScA11^sub 1175^marker was amplified only in 'Folle blanche' among the 64 cultivars tested with a large annealing temperature range using either two different Taq DNA polymerases or two separate thermocyclers. In addition, we discuss the initial polymorphism originated by the RAPD technique and suggest a new design of SCAR primers to obtain reliable cultivar-specific SCAR markers from single PCR-based bands for identification purposes.[PUBLICATION ABSTRACT]