Abstract

Polymorphisms that affect complex traits or quantitative trait loci (QTL) often affect multiple traits. We describe two novel methods (1) for finding single nucleotide polymorphisms (SNPs) significantly associated with one or more traits using a multi-trait, meta-analysis, and (2) for distinguishing between a single pleiotropic QTL and multiple linked QTL. The meta-analysis uses the effect of each SNP on each of n traits, estimated in single trait genome wide association studies (GWAS). These effects are expressed as a vector of signed t-values (t) and the error covariance matrix of these t values is approximated by the correlation matrix of t-values among the traits calculated across the SNP (V). Consequently, t'V−1t is approximately distributed as a chi-squared with n degrees of freedom. An attractive feature of the meta-analysis is that it uses estimated effects of SNPs from single trait GWAS, so it can be applied to published data where individual records are not available. We demonstrate that the multi-trait method can be used to increase the power (numbers of SNPs validated in an independent population) of GWAS in a beef cattle data set including 10,191 animals genotyped for 729,068 SNPs with 32 traits recorded, including growth and reproduction traits. We can distinguish between a single pleiotropic QTL and multiple linked QTL because multiple SNPs tagging the same QTL show the same pattern of effects across traits. We confirm this finding by demonstrating that when one SNP is included in the statistical model the other SNPs have a non-significant effect. In the beef cattle data set, cluster analysis yielded four groups of QTL with similar patterns of effects across traits within a group. A linear index was used to validate SNPs having effects on multiple traits and to identify additional SNPs belonging to these four groups.

Highlights

  • Polymorphisms that affect complex traits may affect multiple traits

  • We describe novel methods for finding significant associations between a genome wide panel of SNPs and multiple complex traits, and further for distinguishing between genes with effects on multiple traits and multiple linked genes affecting different traits

  • The method uses a meta-analysis based on estimates of SNP effects from independent single trait genome wide association studies (GWAS)

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Summary

Introduction

Polymorphisms that affect complex traits (quantitative trait loci or QTL) may affect multiple traits. This pleiotropy is the main cause of the genetic correlations between traits, another possible cause of genetic correlation is linkage disequilibrium (LD) between the QTL for different traits. Genome wide association studies (GWAS) are usually performed one trait at a time, it is not uncommon to find that two traits are associated with SNPs in the same region of a chromosome. This has been described as cross phenotype association [1]. Resolving whether cross phenotype associations are due to one QTL with pleiotropic effects or two linked QTL [1] has proved challenging, given the large number of loci that appear to cause variation in complex traits [2,3,4,5]

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