Microsatellite polymorphism analysis on 25 different “Sangiovese” accessions was carried out at eight microsatellite loci (VVS2, VVS4, VVS29, VVMD3, VVMD6, VVMD7, VVMD17 and VVMD21). In order to evaluate variability within the “Sangiovese” variety and to confirm variety identification, genotype analysis, allele distribution and pedigree information were processed with a DNA-automated sequencer running AlleleLinks software. DNA typing revealed three cases of genetic dissimilarity compared to registered “Sangiovese” clones and the divergent accessions thought to be different clones of the same variety. The divergent accessions were different from “Sangiovese” at four microsatellite loci (VVS2, VVS4, VVMD7 and VVMD21). An innovative nonradioactive modification of AFLP genome profiling confirmed the data obtained by microsatellite amplification test. These results underline the importance of biotechnological testing, such as the PCRbased DNA tests together with traditional ampelography, in Vitis vinifera L. clone and variety selection programmes to avoid misnaming and erroneous identification and to evaluate genetic relatedness and variability within populations.

Genomic variability in Vitis vinifera L. “Sangiovese” assessed bymicrosatellite and non-radioactive AFLP test / R.Vignani; M.Scali; E.Masi; M.Cresti. - In: ELECTRONIC JOURNAL OF BIOTECHNOLOGY. - ISSN 0717-3458. - STAMPA. - 5:(2002), pp. 1-11.

Genomic variability in Vitis vinifera L. “Sangiovese” assessed bymicrosatellite and non-radioactive AFLP test

MASI, ELISA;
2002

Abstract

Microsatellite polymorphism analysis on 25 different “Sangiovese” accessions was carried out at eight microsatellite loci (VVS2, VVS4, VVS29, VVMD3, VVMD6, VVMD7, VVMD17 and VVMD21). In order to evaluate variability within the “Sangiovese” variety and to confirm variety identification, genotype analysis, allele distribution and pedigree information were processed with a DNA-automated sequencer running AlleleLinks software. DNA typing revealed three cases of genetic dissimilarity compared to registered “Sangiovese” clones and the divergent accessions thought to be different clones of the same variety. The divergent accessions were different from “Sangiovese” at four microsatellite loci (VVS2, VVS4, VVMD7 and VVMD21). An innovative nonradioactive modification of AFLP genome profiling confirmed the data obtained by microsatellite amplification test. These results underline the importance of biotechnological testing, such as the PCRbased DNA tests together with traditional ampelography, in Vitis vinifera L. clone and variety selection programmes to avoid misnaming and erroneous identification and to evaluate genetic relatedness and variability within populations.
2002
5
1
11
R.Vignani; M.Scali; E.Masi; M.Cresti
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/647520
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