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The Impact of Non-additive Effects on the Genetic Correlation Between Populations

Average effects of alleles can show considerable differences between populations. The magnitude of these differences can be measured by the additive genetic correlation between populations ([Formula: see text]). This [Formula: see text] can be lower than one due to the presence of non-additive genet...

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Autores principales: Duenk, Pascal, Bijma, Piter, Calus, Mario P. L., Wientjes, Yvonne C. J., van der Werf, Julius H. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003072/
https://www.ncbi.nlm.nih.gov/pubmed/31857332
http://dx.doi.org/10.1534/g3.119.400663
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author Duenk, Pascal
Bijma, Piter
Calus, Mario P. L.
Wientjes, Yvonne C. J.
van der Werf, Julius H. J.
author_facet Duenk, Pascal
Bijma, Piter
Calus, Mario P. L.
Wientjes, Yvonne C. J.
van der Werf, Julius H. J.
author_sort Duenk, Pascal
collection PubMed
description Average effects of alleles can show considerable differences between populations. The magnitude of these differences can be measured by the additive genetic correlation between populations ([Formula: see text]). This [Formula: see text] can be lower than one due to the presence of non-additive genetic effects together with differences in allele frequencies between populations. However, the relationship between the nature of non-additive effects, differences in allele frequencies, and the value of [Formula: see text] remains unclear, and was therefore the focus of this study. We simulated genotype data of two populations that have diverged under drift only, or under drift and selection, and we simulated traits where the genetic model and magnitude of non-additive effects were varied. Results showed that larger differences in allele frequencies and larger non-additive effects resulted in lower values of [Formula: see text]. In addition, we found that with epistasis, [Formula: see text] decreases with an increase of the number of interactions per locus. For both dominance and epistasis, we found that, when non-additive effects became extremely large, [Formula: see text] had a lower bound that was determined by the type of inter-allelic interaction, and the difference in allele frequencies between populations. Given that dominance variance is usually small, our results show that it is unlikely that true [Formula: see text] values lower than 0.80 are due to dominance effects alone. With realistic levels of epistasis, [Formula: see text] dropped as low as 0.45. These results may contribute to the understanding of differences in genetic expression of complex traits between populations, and may help in explaining the inefficiency of genomic trait prediction across populations.
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spelling pubmed-70030722020-02-14 The Impact of Non-additive Effects on the Genetic Correlation Between Populations Duenk, Pascal Bijma, Piter Calus, Mario P. L. Wientjes, Yvonne C. J. van der Werf, Julius H. J. G3 (Bethesda) Investigations Average effects of alleles can show considerable differences between populations. The magnitude of these differences can be measured by the additive genetic correlation between populations ([Formula: see text]). This [Formula: see text] can be lower than one due to the presence of non-additive genetic effects together with differences in allele frequencies between populations. However, the relationship between the nature of non-additive effects, differences in allele frequencies, and the value of [Formula: see text] remains unclear, and was therefore the focus of this study. We simulated genotype data of two populations that have diverged under drift only, or under drift and selection, and we simulated traits where the genetic model and magnitude of non-additive effects were varied. Results showed that larger differences in allele frequencies and larger non-additive effects resulted in lower values of [Formula: see text]. In addition, we found that with epistasis, [Formula: see text] decreases with an increase of the number of interactions per locus. For both dominance and epistasis, we found that, when non-additive effects became extremely large, [Formula: see text] had a lower bound that was determined by the type of inter-allelic interaction, and the difference in allele frequencies between populations. Given that dominance variance is usually small, our results show that it is unlikely that true [Formula: see text] values lower than 0.80 are due to dominance effects alone. With realistic levels of epistasis, [Formula: see text] dropped as low as 0.45. These results may contribute to the understanding of differences in genetic expression of complex traits between populations, and may help in explaining the inefficiency of genomic trait prediction across populations. Genetics Society of America 2019-12-19 /pmc/articles/PMC7003072/ /pubmed/31857332 http://dx.doi.org/10.1534/g3.119.400663 Text en Copyright © 2020 Duenk et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Duenk, Pascal
Bijma, Piter
Calus, Mario P. L.
Wientjes, Yvonne C. J.
van der Werf, Julius H. J.
The Impact of Non-additive Effects on the Genetic Correlation Between Populations
title The Impact of Non-additive Effects on the Genetic Correlation Between Populations
title_full The Impact of Non-additive Effects on the Genetic Correlation Between Populations
title_fullStr The Impact of Non-additive Effects on the Genetic Correlation Between Populations
title_full_unstemmed The Impact of Non-additive Effects on the Genetic Correlation Between Populations
title_short The Impact of Non-additive Effects on the Genetic Correlation Between Populations
title_sort impact of non-additive effects on the genetic correlation between populations
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003072/
https://www.ncbi.nlm.nih.gov/pubmed/31857332
http://dx.doi.org/10.1534/g3.119.400663
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