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1.
Genetics ; 212(1): 317-332, 2019 05.
Article in English | MEDLINE | ID: mdl-30885982

ABSTRACT

Deconvolution of the genetic architecture underlying yield is critical for understanding bases of genetic gain in species of agronomic importance. To dissect the genetic components of yield in potato, we adopted a reference-based recombination map composed of four segregating alleles from an interspecific pseudotestcross F1 potato population (n = 90). Approximately 1.5 million short nucleotide variants were utilized during map construction, resulting in unprecedented resolution for an F1 population, estimated by a median bin length of 146 kb and 11 genes per bin. Regression models uncovered 14 quantitative trait loci (QTL) underpinning yield, average tuber weight, and tubers produced per plant in a population exhibiting a striking 332% average midparent-value heterosis. Nearly 80% of yield-associated QTL were epistatic, and contained between 0 and 44 annotated genes. We found that approximately one-half of epistatic QTL overlap regions of residual heterozygosity identified in the inbred parental parent (M6). Genomic regions recalcitrant to inbreeding were associated with an increased density of genes, many of which demonstrated signatures of selection and floral tissue specificity. Dissection of the genome-wide additive and dominance values for yield and yield components indicated a widespread prevalence of dominance contributions in this population, enriched at QTL and regions of residual heterozygosity. Finally, the effects of short nucleotide variants and patterns of gene expression were determined for all genes underlying yield-associated QTL, exposing several promising candidate genes for future investigation.


Subject(s)
Diploidy , Epistasis, Genetic , Heterozygote , Quantitative Trait Loci , Solanum tuberosum/genetics , Genes, Plant , Haplotypes , Hybrid Vigor , Inbreeding , Polymorphism, Genetic
2.
Genome Biol ; 18(1): 203, 2017 10 30.
Article in English | MEDLINE | ID: mdl-29084572

ABSTRACT

BACKGROUND: Meiotic recombination is the foundation for genetic variation in natural and artificial populations of eukaryotes. Although genetic maps have been developed for numerous plant species since the late 1980s, few of these maps have provided the necessary resolution needed to investigate the genomic and epigenomic features underlying meiotic crossovers. RESULTS: Using a whole genome sequencing-based approach, we developed two high-density reference-based haplotype maps using diploid potato clones as parents. The vast majority (81%) of meiotic crossovers were mapped to less than 5 kb. The fine-scale accuracy of crossover detection was validated by Sanger sequencing for a subset of ten crossover events. We demonstrate that crossovers reside in genomic regions of "open chromatin", which were identified based on hypersensitivity to DNase I digestion and association with H3K4me3-modified nucleosomes. The genomic regions spanning crossovers were significantly enriched with the Stowaway family of miniature inverted-repeat transposable elements (MITEs). The occupancy of Stowaway elements in gene promoters is concomitant with an increase in recombination rate. A generalized linear model identified the presence of Stowaway elements as the third most important genomic or chromatin feature behind genes and open chromatin for predicting crossover formation over 10-kb windows. CONCLUSIONS: Collectively, our results suggest that meiotic crossovers in potato are largely determined by the local chromatin status, marked by accessible chromatin, H3K4me3-modified nucleosomes, and the presence of Stowaway transposons.


Subject(s)
Chromatin/chemistry , Crossing Over, Genetic , DNA Transposable Elements , Meiosis/genetics , Solanum tuberosum/genetics , Chromosome Mapping , Chromosomes, Plant , Genomics , Haplotypes
3.
Plant Physiol ; 154(2): 939-48, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20736383

ABSTRACT

Potato (Solanum tuberosum) is the third most important food crop in the world. Potato tubers must be stored at cold temperatures to prevent sprouting, minimize disease losses, and supply consumers and the processing industry with high-quality tubers throughout the year. Unfortunately, cold storage triggers an accumulation of reducing sugars in tubers. High-temperature processing of these tubers results in dark-colored, bitter-tasting products. Such products also have elevated amounts of acrylamide, a neurotoxin and potential carcinogen. We demonstrate that silencing the potato vacuolar acid invertase gene VInv prevents reducing sugar accumulation in cold-stored tubers. Potato chips processed from VInv silencing lines showed a 15-fold acrylamide reduction and were light in color even when tubers were stored at 4°C. Comparable, low levels of VInv gene expression were observed in cold-stored tubers from wild potato germplasm stocks that are resistant to cold-induced sweetening. Thus, both processing quality and acrylamide problems in potato can be controlled effectively by suppression of the VInv gene through biotechnology or targeted breeding.


Subject(s)
Carbohydrates/biosynthesis , Cold Temperature , Plant Proteins/metabolism , Plant Tubers/enzymology , Solanum tuberosum/genetics , beta-Fructofuranosidase/metabolism , Acrylamide/analysis , Food Handling , Gene Expression Regulation, Plant , Genes, Plant , Plant Proteins/genetics , Plant Tubers/chemistry , Plant Tubers/genetics , Plants, Genetically Modified/enzymology , Plants, Genetically Modified/genetics , RNA Interference , Solanum tuberosum/enzymology , Vacuoles/metabolism , beta-Fructofuranosidase/genetics
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