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4 results for “large effect locus”
Fitness maps to a large-effect locus in introduced stickleback populations
<p>Mutations of small effect underlie most adaptation to new environments, but beneficial variants with large fitness effects are expected to contribute under certain conditions. Genes and genomic regions having large effects on phenotypic differences between populations are known from numerous taxa, but fitness effect sizes have rarely been estimated. We mapped fitness over a generation in an F2 intercross between a marine and a lake stickleback population introduced to a freshwater pond. A QTL map of the number of surviving offspring per F2 female detected a single, large-effect locus near <i>Ectodysplasin</i> (<i>Eda</i>), a gene having an ancient freshwater allele causing reduced bony armor and other changes. F2 females homozygous for the freshwater allele had twice the number of surviving offspring as homozygotes for the marine allele, producing a large selection coefficient, <i>s</i> = 0.50 ± 0.09 SE. Correspondingly, the frequency of the freshwater allele increased from 0.50 in F2 mothers to 0.58 in surviving offspring. We compare these results to observed allele frequency changes at the <i>Eda</i> gene in an Alaskan lake population colonized by marine stickleback in the 1980's. The frequency of the freshwater <i>Eda</i> allele rose steadily over multiple generations and reached 95% within 20 years, yielding a similar estimate of selection, <i>s</i> = 0.49 ± 0.05. These findings are consistent with other studies suggesting strong selection on this gene (and/or linked genes) in fresh water. Selection on ancient genetic variants carried by colonizing ancestors is likely to increase the prevalence of large-effect fitness variants in adaptive evolution.</p>
Fitness maps to a large-effect locus in introduced stickleback populations
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Data for: Refining the genomic location of single nucleotide polymorphism variation affecting Atlantic salmon maturation timing at a key large‐effect locus
<p><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span>Efforts to understand the genetic underpinnings of phenotypic variation are becoming more and more frequent in molecular ecology. Such efforts often lead to the identification of candidate regions showing signals of association and/or selection. These regions may contain multiple genes and therefore validation of which genes are actually responsible for the signal is required. In Atlantic salmon (</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span><em>Salmo salar</em><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span>), a large‐effect locus for maturation timing, an ecologically important trait, occurs in a genomic region including two genes, </span></span></span></span></span></span></span></span></span></span></span></span></span></span></span><em>vgll3</em><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span> and </span></span></span></span></span></span></span></span></span></span></span></span></span></span></span><em>akap11</em><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span>, but data for clearly determining which of the genes (or both) contribute to the association have been lacking. Here, we take advantage of natural recombination events detected between the two candidate genes in a salmon broodstock to reduce linkage disequilibrium at the locus, thus enabling delineation of the influence of variation at these two genes on early maturation. By rearing 5,895</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span>males to maturation age, of which 81% had recombinant </span></span></span></span></span></span></span></span></span></span></span></span></span></span></span><em>vgll3</em><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span>/</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span><em>akap11</em><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span> allelic combinations, we found that </span></span></span></span></span></span></span></span></span></span></span></span></span></span></span><em>vgll3</em> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span>single nucleotide polymorphism (SNP) variation was strongly associated with early maturation, whereas there was little or no association between </span></span></span></span></span></span></span></span></span></span></span></span></span></span></span><em>akap11</em><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span> SNP variation and early maturation. These findings provide strong evidence supporting </span></span></span></span></span></span></span></span></span></span></span></span></span></span></span><em>vgll3</em><span><span><span><span><span><span><span><span><span><span><span><span><span><span><span> as the primary candidate gene in the chromosome 25</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span> <span><span><span><span><span><span><span><span><span><span><span><span><span><span><span>locus for influencing early maturation. This will help guide future research for understanding the genetic processes controlling early maturation. This also exemplifies the utility of natural recombinants to more precisely map causal variation underlying ecologically important phenotypic diversity.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></p>
Data for: Refining the genomic location of single nucleotide polymorphism variation affecting Atlantic salmon maturation timing at a key large‐effect locus
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