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The Groundnut Improvement Network for Africa (GINA) Germplasm collection: a unique genetic resource for breeding and gene discovery.

Soukeye CondeJean-François RamiDavid K OkelloAissatou SambouAmade MuitiaRichard Oteng-FrimpongLutangu MakwetiDramane SakoIssa FayeJustus ChintuAdama M CoulibalyAmos MiningouJames Y AsibuoMoumouni KonateEssohouna M BanlaMaguette SeyeYvette R DjibouneHodo-Abalo TossimSamba N SyllaDavid HoisingtonJosh P ClevengerYe ChuShyam TalluryPeggy Ozias-AkinsDaniel Fonceka
Published in: G3 (Bethesda, Md.) (2023)
Cultivated peanut or groundnut (Arachis hypogaea L.) is a grain legume grown in many developing countries by smallholder farmers for food, feed and/or income. The speciation of the cultivated species, that involved polyploidization followed by domestication, greatly reduced its variability at the DNA level. Mobilizing peanut diversity is a pre-requisite for any breeding program for overcoming the main constraints that plague production and for increasing yield in farmer fields. In this study, the Groundnut Improvement Network for Africa (GINA) assembled a collection of 1049 peanut breeding lines, varieties and landraces from nine countries in Africa. The collection was genotyped with the Axiom_Arachis2 48 K SNP array and 8229 polymorphic single nucleotide polymorphism (SNP) markers were used to analyze the genetic structure of this collection and quantify the level of genetic diversity in each breeding program. A supervised model was developed using dapc to unambiguously assign 542, 35, and 172 genotypes to the Spanish, Valencia and Virginia market types, respectively. Distance based clustering of the collection showed a clear grouping structure according to subspecies and market types, with 73% of the genotypes classified as fastigiata and 27% as hypogaea subspecies. Using STRUCTURE, the global structuration was confirmed and showed that, at a minimum membership of 0.8, 76% of the varieties that were not assigned by dapc were actually admixed. This was particularly the case of most of the genotype of the Valencia subgroup that exhibited admixed genetic heritage. The results also showed that the geographic origin (i.e. East, Southern and West Africa) did not strongly explain the genetic structure. The gene diversity managed by each breeding program, measured by the expected heterozygosity, ranged from 0.25 to 0.39, with the Niger breeding program having the lowest diversity mainly because only lines that belong to the fastigiata subspecies are used in this program. Finally, we developed a core collection composed of 300 accessions based on breeding traits and genetic diversity. This collection, which is composed of 205 genotypes of fastigiata subspecies (158 Spanish and 47 Valencia) and 95 genotypes of hypogaea subspecies (all Virginia), improves the genetic diversity of each individual breeding program and is therefore a unique resource for allele mining and breeding.
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