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Nganga, M. L.

Publications and source records attributed to Nganga, M. L..

2 recordsLinked to original sources

A K-mer based Bulked Segregant Analysis approach to map seed traits in unphased heterozygous potato genomes

High-throughput sequencing-based methods for bulked segregant analysis (BSA) allow for the rapid identification of genetic markers associated with traits of interest. BSA studies have successfully identified qualitative (binary) and quantitative trait loci using QTL mapping. However, most traditional QTL mapping approaches require a reference genome. Here, we combine high throughput short read sequencing with bulk segregant analysis of k-mers (BSA-k-mer). This method can be applied to any organism and is particularly useful for species with genomes too different from the closest sequenced genome. It is also instrumental when dealing with highly heterozygous and polyploid genomes without phased haplotype assemblies and for which a single haplotype can control a trait. Finally, it is flexible in terms of population structure. Here, we present the application of the BSA-k-mer method for the rapid identification of candidate regions related to seed spot and seed size in diploid potato. While conventional QTL mapping of parental genotypes did not generate any signal, candidate loci were identified for each trait using the BSA-k-mer approach. The seed spot loci match with previously identified loci associated with pigmentation in potato. The loci associated with seed size are novel. Both sets of loci are potentially instrumental in future breeding towards true seeds in potato. Article SummaryIdentifying genes linked to agronomic traits in potatoes is challenging because potato genomes are complex and variable. We are investigating the genetic basis of seed size and color. Seeds were categorized as large or small, or spotted or not, based on simple visual observation. Next, DNA sequences from each individual were mined for association between random short sequences (k-mers) and those two traits. This more flexible method allowed us to identify regions of the potato genome associated with both traits.

plant biology↗

Rare instances of haploid inducer DNA in potato dihaploids and ploidy-dependent genome instability

In cultivated tetraploid potato, reduction to diploidy (dihaploidy) allows hybridization to diploid germplasm, introgression breeding, and may facilitate the production of inbreds. Pollination with haploid inducers yields maternal dihaploids, as well as triploid and tetraploid hybrids. It is not known if dihaploids result from parthenogenesis, entailing development of embryos from unfertilized eggs, or genome elimination, entailing missegregation and loss of paternal chromosomes. A sign of genome elimination is the occasional persistence of haploid inducer DNA in some of the dihaploids. We characterized the genomes of 1,001 putative dihaploids and 134 hybrids produced by pollinating tetraploid clones with three haploid inducers, IVP35, IVP101, and PL4. We detected inheritance of full or partial chromosomes from the haploid inducer parent in 0.87% of the overall dihaploid progeny, irrespective of the combination of parental genotypes. Chromosomal breaks commonly affected the paternal genome in the dihaploid and tetraploid progeny, but not in the triploid progeny. Residual haploid inducer DNA is consistent with genome elimination as the mechanism of haploid induction. Further, the fact that paternal chromosome breaks are specific to dihaploids and tetraploid progeny suggests that they may be specific to 2x sperms, and supports the hypothesis that 2x sperms facilitate genome elimination.

plant biology↗