Abstract

In order to study the genetic diversity among 16 genotypes of Hippophae salicifolia D. Don of Uttarakhand region, random amplified polymorphic DNA (RAPD)–PCR analysis along with protein profiling of seed storage proteins was carried out for selection of superior genotype having high economic importance. A total of 21 RAPD primers were assayed for their specificity in detecting genetic variability in H. salicifolia genotypes, of which 11 RAPD primers were highly reproducible and were found suitable for use in PCR analysis. A total of 198 bands were scored corresponding to an average of 10.8 bands per primer with 138 bands showing polymorphism (73.2 %) with similarity coefficient ranging from 0.011 to 0.999. A dendrogram constructed based on the UPGMA clustering method revealed two major clusters. Cluster-I comprises of 13 cultivars, while cluster-II includes the remaining three cultivars. The cultivar ST-4, ST-5 and ST-16 were quite unique from the remaining cultivars as evident from the dendrogram. The analysis of total seed storage protein (quantitative) and protein profiling (qualitative) among 16 genotypes of H. salicifolia was performed to indentify novel proteins of important functional attributes. SDS-PAGE based generated profiles of seed proteins showed major differences in banding patterns among these genotypes with respect to altitude besides differences in seed protein contents. This study helps in the selection of superior genotype of H. salicifolia having higher economic importance by using developed molecular and protein based markers in Uttarakhand regions.

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