Abstract

The phenotypic outcome of a mutation cannot be simply mapped onto the underlying DNA variant. Instead, the phenotype is a function of the allele, the genetic background in which it occurs and the environment where the mutational effects are expressed. While the influence of genetic background on the expressivity of individual mutations is recognized, its consequences on the interactions between genes, or the genetic network they form, is largely unknown. The description of genetic networks is essential for much of biology; yet if, and how, the topologies of such networks are influenced by background is unknown. Furthermore, a comprehensive examination of the background dependent nature of genetic interactions may lead to identification of novel modifiers of biological processes. Previous work in Drosophila melanogaster demonstrated that wild-type genetic background influences the effects of an allele of scalloped (sd), with respect to both its principal consequence on wing development and its interactions with a mutation in optomotor blind. In this study we address whether the background dependence of mutational interactions is a general property of genetic systems by performing a genome wide dominant modifier screen of the sdE3 allele in two wild-type genetic backgrounds using molecularly defined deletions. We demonstrate that ∼74% of all modifiers of the sdE3 phenotype are background-dependent due in part to differential sensitivity to genetic perturbation. These background dependent interactions include some with qualitative differences in the phenotypic outcome, as well as instances of sign epistasis. This suggests that genetic interactions are often contingent on genetic background, with flexibility in genetic networks due to segregating variation in populations. Such background dependent effects can substantially alter conclusions about how genes influence biological processes, the potential for genetic screens in alternative wild-type backgrounds identifying new loci that contribute to trait expression, and the inferences of the topology of genetic networks.

Highlights

  • Fundamental to the logic of genetic analysis is that the observed variation in a phenotype for a genetically mediated trait is causally linked to one or more DNA lesions/variants

  • We have previously shown that the phenotypic effects of an allele of the scalloped gene in Drosophila melanogaster is Examining the consequences of how one mutation behaves when in the presence of a second mutation forms the basis of our understanding of genetic interactions, and is part of the fundamental toolbox of genetic analysis

  • We previously demonstrated that the genetic interaction between mutations in two genes, sd and omb, is dependent on genetic background [36]

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Summary

Introduction

Fundamental to the logic of genetic analysis is that the observed variation in a phenotype for a genetically mediated trait is causally linked to one or more DNA lesions/variants. Genetic background has long been known to influence observed phenotypic expression across traits, organisms, and a range of allelic effects, including hypomorphs, amorphs/nulls and neomorphs [1,2,3,4,5,6,7,8,9]. These results make it clear that the phenotypic effects of a mutation (i.e. penetrance and expressivity) are themselves ‘‘complex traits’’, subject to environmental and polygenic influences [1]. We have previously shown that the phenotypic effects of an allele of the scalloped gene (sdE3) in Drosophila melanogaster is Author Summary

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