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Pleiotropy or linkage? Their relative contributions to the genetic correlation of quantitative traits and detection by multi-trait GWA studiesuse asterix (*) to get italics
Jobran Chebib and Frédéric GuillaumePlease use the format "First name initials family name" as in "Marie S. Curie, Niels H. D. Bohr, Albert Einstein, John R. R. Tolkien, Donna T. Strickland"
2019
<p>Genetic correlations between traits may cause correlated responses to selection depending on the source of those genetic dependencies. Previous models described the conditions under which genetic correlations were expected to be maintained. Selection, mutation and migration are all proposed to have similar effects on genetic correlation, regardless of whether the underlying genetic architecture consists of pleiotropic or tightly-linked loci affecting the traits. Here, we investigate the conditions under which pleiotropy and linkage have differential effects on the genetic correlations between traits by explicitly modeling multiple genetic architectures to look at the effects of selection strength, degree of correlational selection, mutation rate, mutational variance, recombination rate, and migration rate. We show that at mutation-selection(-migration) balance, mutation rates differentially affect the equilibrium levels of genetic correlation when architectures are composed of pairs of physically linked loci compared to architectures of pleiotropic loci. Even when there is perfect linkage (no recombination within pairs of linked loci), a lower genetic correlation is maintained than with pleiotropy, with a lower mutation rate leading to a larger decrease. These results imply that the detection of causal loci in multi-trait association studies will be affected by the type of underlying architectures, whereby pleiotropic variants are more likely to be underlying multiple detected associations. We also confirm that tighter linkage between non-pleiotropic causal loci maintains higher genetic correlations at the traits and leads to a greater proportion of false positives in association analyses.</p>
https://zenodo.org/record/3370185#collapseTwoYou should fill this box only if you chose 'All or part of the results presented in this preprint are based on data'. URL must start with http:// or https://
You should fill this box only if you chose 'Scripts were used to obtain or analyze the results'. URL must start with http:// or https://
https://sourceforge.net/projects/nemo2/files/Publications-Code/ChebibGuillaume-PleiotropyOrLinkage-2019You should fill this box only if you chose 'Codes have been used in this study'. URL must start with http:// or https://
pleiotropy, linkage, mutation, GWAS, genotype-phenotype map, genetics, quantitative traits
NonePlease indicate the methods that may require specialised expertise during the peer review process (use a comma to separate various required expertises).
Bioinformatics & Computational Biology, Evolutionary Applications, Evolutionary Dynamics, Evolutionary Theory, Genome Evolution, Genotype-Phenotype, Molecular Evolution, Population Genetics / Genomics, Quantitative Genetics
e.g. John Doe john@doe.com
No need for them to be recommenders of PCIEvolBiol. Please do not suggest reviewers for whom there might be a conflict of interest. Reviewers are not allowed to review preprints written by close colleagues (with whom they have published in the last four years, with whom they have received joint funding in the last four years, or with whom they are currently writing a manuscript, or submitting a grant proposal), or by family members, friends, or anyone for whom bias might affect the nature of the review - see the code of conduct
e.g. John Doe john@doe.com
2019-06-05 13:51:43
Kathleen Lotterhos