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A panel of single nucleotide polymorphism (SNP) markers identifies potential duplicates in cassava (Manihot esculenta Crantz) varieties from Cote dIvoire

Mutuku, J. M.; YEO, E.; AMOAKON, W.; PITA, J.; NZUE, B.; KOUASSI, M.; YAO, N.; OTRON, D.; SHAH, T.; VANIE-LEABO, L.; KPAHE, K.; SIE, R.; SORHO, F.; KONE, D.; NGUETTA, S.-P.; FERGUSON, M.

2021-05-24 plant biology
10.1101/2021.05.24.445412 bioRxiv
Show abstract

Accurate identification of varieties is paramount to optimizing efficiencies in the management and conservation of genetic resources. A relatively inexpensive, rapid methodology is required to identify putative duplicates from any collection, when morphological traits give insufficient discrimination. Here we select a panel of 36 SNPs, visualized using the Kompetitive Allele-specific PCR (KASP) system. We used a panel of 95 cassava genotypes from Cote dIvoire to identify varieties that are not duplicates and few potential duplicates which could be put forward for further verification. The genetic variability and population structure of the germplasm is also described. 36 SNPs were polymorphic across the panel of 95 varieties with polymorphic information contents ranging from 0.23 to 0.37. Using these SNPs, we were able to identify 66 unique genotypes from the panel of 95 genotypes, discriminate three sets of known duplicates and identify 11 sets of unknown putative duplicates which can be subjected to further verification using higher density genotyping. As expected in an outcrossing species, both expected heterozygosity (0.46) and observed heterozygosity (0.48) were high with an analysis of molecular variance (AMOVA) indicating that the majority of variation was within individuals. Three statistical approaches i.e., hierarchical ascending clustering, Bayesian analysis and discriminant analysis of principal components were used and all revealed low genetic differentiation between sub-populations, a conclusion that was supported by the low value of the fixation index (0.05). This panel of SNPs can be used to enhance cost-effectiveness and efficiency of germplasm conservation and enhance quality control at various stages in the breeding process through varietal tracking.

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