FB2026_02 , released June 18, 2026
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Citation
Huang, W., Richards, S., Carbone, M.A., Zhu, D., Anholt, R.R., Ayroles, J.F., Duncan, L., Jordan, K.W., Lawrence, F., Magwire, M.M., Warner, C.B., Blankenburg, K., Han, Y., Javaid, M., Jayaseelan, J., Jhangiani, S.N., Muzny, D., Ongeri, F., Perales, L., Wu, Y.Q., Zhang, Y., Zou, X., Stone, E.A., Gibbs, R.A., Mackay, T.F. (2012). Epistasis dominates the genetic architecture of Drosophila quantitative traits.  Proc. Natl. Acad. Sci. U.S.A. 109(39): 15553--15559.
FlyBase ID
FBrf0219551
Publication Type
Research paper
Abstract
Epistasis-nonlinear genetic interactions between polymorphic loci-is the genetic basis of canalization and speciation, and epistatic interactions can be used to infer genetic networks affecting quantitative traits. However, the role that epistasis plays in the genetic architecture of quantitative traits is controversial. Here, we compared the genetic architecture of three Drosophila life history traits in the sequenced inbred lines of the Drosophila melanogaster Genetic Reference Panel (DGRP) and a large outbred, advanced intercross population derived from 40 DGRP lines (Flyland). We assessed allele frequency changes between pools of individuals at the extremes of the distribution for each trait in the Flyland population by deep DNA sequencing. The genetic architecture of all traits was highly polygenic in both analyses. Surprisingly, none of the SNPs associated with the traits in Flyland replicated in the DGRP and vice versa. However, the majority of these SNPs participated in at least one epistatic interaction in the DGRP. Despite apparent additive effects at largely distinct loci in the two populations, the epistatic interactions perturbed common, biologically plausible, and highly connected genetic networks. Our analysis underscores the importance of epistasis as a principal factor that determines variation for quantitative traits and provides a means to uncover genetic networks affecting these traits. Knowledge of epistatic networks will contribute to our understanding of the genetic basis of evolutionarily and clinically important traits and enhance predictive ability at an individualized level in medicine and agriculture.
PubMed ID
PubMed Central ID
PMC3465439 (PMC) (EuropePMC)
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    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Proc. Natl. Acad. Sci. U.S.A.
    Title
    Proceedings of the National Academy of Sciences of the United States of America
    Publication Year
    1915-
    ISBN/ISSN
    0027-8424
    Data From Reference