Weak Epistasis Generally Stabilizes Phenotypes in a Mouse Intercross.

The extent and strength of epistasis is commonly unresolved in genetic studies, and observed epistasis is often difficult to interpret in terms of biological consequences or overall genetic architecture. We investigated the prevalence and consequences of epistasis by analyzing four body composition...

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Main Authors: Anna L Tyler, Leah Rae Donahue, Gary A Churchill, Gregory W Carter
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-02-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC4734753?pdf=render
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author Anna L Tyler
Leah Rae Donahue
Gary A Churchill
Gregory W Carter
author_facet Anna L Tyler
Leah Rae Donahue
Gary A Churchill
Gregory W Carter
author_sort Anna L Tyler
collection DOAJ
description The extent and strength of epistasis is commonly unresolved in genetic studies, and observed epistasis is often difficult to interpret in terms of biological consequences or overall genetic architecture. We investigated the prevalence and consequences of epistasis by analyzing four body composition phenotypes--body weight, body fat percentage, femoral density, and femoral circumference--in a large F2 intercross of B6-lit/lit and C3.B6-lit/lit mice. We used Combined Analysis of Pleiotropy and Epistasis (CAPE) to examine interactions for the four phenotypes simultaneously, which revealed an extensive directed network of genetic loci interacting with each other, circulating IGF1, and sex to influence these phenotypes. The majority of epistatic interactions had small effects relative to additive effects of individual loci, and tended to stabilize phenotypes towards the mean of the population rather than extremes. Interactive effects of two alleles inherited from one parental strain commonly resulted in phenotypes closer to the population mean than the additive effects from the two loci, and often much closer to the mean than either single-locus model. Alternatively, combinations of alleles inherited from different parent strains contribute to more extreme phenotypes not observed in either parental strain. This class of phenotype-stabilizing interactions has effects that are close to additive and are thus difficult to detect except in very large intercrosses. Nevertheless, we found these interactions to be useful in generating hypotheses for functional relationships between genetic loci. Our findings suggest that while epistasis is often weak and unlikely to account for a large proportion of heritable variance, even small-effect genetic interactions can facilitate hypotheses of underlying biology in well-powered studies.
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spelling doaj.art-ced243aa23cc4ba4a11d95f353b224502022-12-21T20:37:16ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042016-02-01122e100580510.1371/journal.pgen.1005805Weak Epistasis Generally Stabilizes Phenotypes in a Mouse Intercross.Anna L TylerLeah Rae DonahueGary A ChurchillGregory W CarterThe extent and strength of epistasis is commonly unresolved in genetic studies, and observed epistasis is often difficult to interpret in terms of biological consequences or overall genetic architecture. We investigated the prevalence and consequences of epistasis by analyzing four body composition phenotypes--body weight, body fat percentage, femoral density, and femoral circumference--in a large F2 intercross of B6-lit/lit and C3.B6-lit/lit mice. We used Combined Analysis of Pleiotropy and Epistasis (CAPE) to examine interactions for the four phenotypes simultaneously, which revealed an extensive directed network of genetic loci interacting with each other, circulating IGF1, and sex to influence these phenotypes. The majority of epistatic interactions had small effects relative to additive effects of individual loci, and tended to stabilize phenotypes towards the mean of the population rather than extremes. Interactive effects of two alleles inherited from one parental strain commonly resulted in phenotypes closer to the population mean than the additive effects from the two loci, and often much closer to the mean than either single-locus model. Alternatively, combinations of alleles inherited from different parent strains contribute to more extreme phenotypes not observed in either parental strain. This class of phenotype-stabilizing interactions has effects that are close to additive and are thus difficult to detect except in very large intercrosses. Nevertheless, we found these interactions to be useful in generating hypotheses for functional relationships between genetic loci. Our findings suggest that while epistasis is often weak and unlikely to account for a large proportion of heritable variance, even small-effect genetic interactions can facilitate hypotheses of underlying biology in well-powered studies.http://europepmc.org/articles/PMC4734753?pdf=render
spellingShingle Anna L Tyler
Leah Rae Donahue
Gary A Churchill
Gregory W Carter
Weak Epistasis Generally Stabilizes Phenotypes in a Mouse Intercross.
PLoS Genetics
title Weak Epistasis Generally Stabilizes Phenotypes in a Mouse Intercross.
title_full Weak Epistasis Generally Stabilizes Phenotypes in a Mouse Intercross.
title_fullStr Weak Epistasis Generally Stabilizes Phenotypes in a Mouse Intercross.
title_full_unstemmed Weak Epistasis Generally Stabilizes Phenotypes in a Mouse Intercross.
title_short Weak Epistasis Generally Stabilizes Phenotypes in a Mouse Intercross.
title_sort weak epistasis generally stabilizes phenotypes in a mouse intercross
url http://europepmc.org/articles/PMC4734753?pdf=render
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