Extensive impact of low-frequency variants on the phenotypic landscape at population-scale
Year: 2019
Type: article
Abstract: Genome-wide association studies (GWAS) allows to dissect the genetic basis of complex traits at the population level 1 . However, despite the extensive number of trait-associated loci found, they often fail to explain a large part of the observed phenotypic variance 2–4 . One potential source of this discrepancy could be the preponderance of undetected low-frequency genetic variants in natural populations 5,6 . To increase the allele frequency of those variants and assess their phenotypic effects at the population level, we generated a diallel panel consisting of 3,025 hybrids, derived from pairwise crosses between a subset of natural isolates from a completely sequenced 1,011 Saccharomyces cerevisiae population. We examined each hybrid across a large number of growth traits, resulting in a total of 148,225 cross/trait combinations. Parental versus hybrid regression analysis showed that while most phenotypic variance is explained by additivity, a significant proportion (29%) is governed by non-additive effects. This is confirmed by the fact that a majority of complete dominance is observed in 25% of the traits. By performing GWAS on the diallel panel, we detected 1,723 significantly associated genetic variants, with 16.3% of them being low-frequency variants in the initial population. These variants, which would not be detected using classical GWAS, explain 21% of the phenotypic variance on average. Altogether, our results demonstrate that low-frequency variants should be accounted for as they contribute to a large part of the phenotypic variation observed in a population.
Source: eLife
DOI: 10.7554/elife.49258
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,415
Funders: Agence Nationale de la Recherche, Fondation pour la Recherche Médicale, Université de Strasbourg, Ministère de l'Enseignement Supérieur et de la Recherche, Institut Universitaire de France, National Institutes of Health, European Research Council, National Institute of General Medical Sciences
OpenAlex ID: W2982084346
