Abstract

Causal mutations and their intra- and inter-locus interactions play a critical role in complex trait variation. It is often not easy to detect epistatic quantitative trait loci (QTL) due to complicated population structure requirements for detecting epistatic effects in linkage analysis studies and due to main effects often being hidden by interaction effects. Mapping their positions is even harder when they are closely linked. The data structure requirement may be overcome when information on linkage disequilibrium is used. We present an approach using a mixed linear model nested in an empirical Bayesian approach, which simultaneously takes into account additive, dominance and epistatic effects due to multiple QTL. The covariance structure used in the mixed linear model is based on combined linkage disequilibrium and linkage information. In a simulation study where there are complex epistatic interactions between QTL, it is possible to simultaneously map interacting QTL into a small region using the proposed approach. The estimated variance components are accurate and less biased with the proposed approach compared with traditional models.

Highlights

  • Phenotypic variation in complex traits may involve the action of many causal genes and their intra- and inter-locus interaction, in addition to environmental factors

  • Multiple interacting QTL may play a critical role in quantitative trait variation and epistatic interaction can exist between closely linked quantitative trait loci [5, 11, 15, 28, 33]

  • The results show that the QTL density profiles of the model including dominance and epistasis are the same with the additive model when dominance and epistasis are absent

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Summary

Introduction

Phenotypic variation in complex traits may involve the action of many causal genes and their intra- (dominance) and inter-locus interaction (epistasis), in addition to environmental factors. Multiple interacting QTL may play a critical role in quantitative trait variation and epistatic interaction can exist between closely linked quantitative trait loci [5, 11, 15, 28, 33]. Ignoring such non-additive effects due to gene interaction may result in biased estimation. S.H. Lee and J.H.J. van der Werf of QTL position and effects. Interacting QTL showing negligible main effects may not be detected. If the interacting QTL are closely linked, it might be even harder to distinguish their positions

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