TAILIEUCHUNG - Evaluation of genetic diversity in Gloriosa superba L, an endangered medicinal plant using molecular marker

Genetic diversity evaluation among 16 Gloriosa accessions collected from different locations in Tamil Nadu was studied by using Inter-simple sequence repeat (ISSR) markers. Thirty six ISSR primers were used, among that 16 primers showed per cent polymorphism and produced 213 amplicons. This indicates that there is a high level of variation at the genetic level among these accessions. The primer UBC-807 showed the highest PIC value (), which represented the high efficiency of the individual primer. Gloriosa accessions GSU-6 and GSU-7 are highly similar with 68 per cent and GSU-7 and GSU-16 are distinctly similar with 39 per cent. Cluster analysis was done based on similarity coefficient value obtained from banding pattern of ISSR marker. The 16 Gloriosa accessions were grouped into two major clusters, of which one cluster contained all 15 accessions whereas as another cluster contained GSU-16 accession alone. This represents that the Gloriosa accession GSU-16 is genetically distinct from other accessions based on banding pattern. | Evaluation of genetic diversity in Gloriosa superba L, an endangered medicinal plant using molecular marker

• Sinh học
• Genetic diversity
• Intersimple sequence repeat
• Cluster analysis
• Endangered medicinal plant
• Molecular marker
• Evaluation of genetic diversity
• Genetic variability
• Similarity coefficient
• Soybean genotypes
• Genetic diversity analysis
• Molecular marker based genetic diversity
• Maize genetic diversity
• Very easy digestible
• Abiotic factor
• Genetic diversity in sunflower
• Sunflower (Helianthus annuus L )
• Inter varietal hybridization programme
• Assessment of genetic diversity
• Genetic diversity among fenugreek
• Fenugreek genotypes
• ISSR markers
• Genetic improvement
• Sequence related amplified polymorphism
• Simple sequence repeat
• Genetic diversity of watermelon
• Brassica compestris
• Genetic diversity analysis based
• Molecular level
• Onion genotypes through RAPD
• Genetic diversity remarkably
• Genetic diversity in Gangatiri cow
• Gangatiri cow
• Employing RAPD marker
• Threatened cycads (cycadaceae)
• Conservation of genetic diversity
• High propagules
• Levels of genetic diversity
• Inter Intra cluster distance
• Chickpea genotypes
• Genetic diversity in reference set
• Genetic advance
• Rainfed rice
• Rainfed rice genotypes
• Genetic diversity in rainfed rice genotypes
• Bottle gourd
• Genetic diversity in bottle gourd
• Yield improvement
• Diversity analysis
• Genetic diversity analysis in sunflower
• Parental lines
• RAPD markers
• Solanum lycopersicon L
• Genetic diversity studies
• Genetic diversity studies in tomato
• D2 statistics
• Genetic divergence
• Random amplified polymorphic DNA
• Polymerase chain reaction
• Genetic diversity analysis of citrus cultivars
• D2 analysis
• Landraces and salinity
• Saline stress condition
• Genetic diversity in traditional landraces
• Rice for yield
• Principal component analysis
• Principal component analysis approach
• Brinjal (Solanum melongena L
• Pinus kwangtungensis
• Pa Co pine (Pinus kwangtungensis Chun ex Tsiang)
• RAPD and ISSR markers
• Genetic diversity in Pa Co pine
• Thirty five genotypes
• Oilseed brassica species
• Gossypium hirsutum L
• Cotton germplasm
• Agro morphological characterization
• PIC and marker
• Genetic diversity in hybrids of tomato
• Tomato (Solanum lycopersicum L
• SSR markers
• Molecular characterization
• Soybean varieties
• Genetic diversity assessment
• Agarose gel electrophoresis
• ISSR primers
• Susceptible genotypes
• Genetic diversity in upland cotton
• Molecular markers
• Mungbean [Vigna radiata (L ) Wilczek]
• Screening and identification
• Identification of ssr markers
• Genetic diversity for mungbean
• Mahalanobis D2 statistics
• Genetic diversity in okra
• West Godavari district during kharif season
• Twenty nine hybrids