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Including Phenotypic Causal Networks in Genome-Wide Association Studies Using Mixed Effects Structural Equation Models

Network based statistical models accounting for putative causal relationships among multiple phenotypes can be used to infer single-nucleotide polymorphism (SNP) effect which transmitting through a given causal path in genome-wide association studies (GWAS). In GWAS with multiple phenotypes, reconst...

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Autores principales: Momen, Mehdi, Ayatollahi Mehrgardi, Ahmad, Amiri Roudbar, Mahmoud, Kranis, Andreas, Mercuri Pinto, Renan, Valente, Bruno D., Morota, Gota, Rosa, Guilherme J. M., Gianola, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189326/
https://www.ncbi.nlm.nih.gov/pubmed/30356716
http://dx.doi.org/10.3389/fgene.2018.00455
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author Momen, Mehdi
Ayatollahi Mehrgardi, Ahmad
Amiri Roudbar, Mahmoud
Kranis, Andreas
Mercuri Pinto, Renan
Valente, Bruno D.
Morota, Gota
Rosa, Guilherme J. M.
Gianola, Daniel
author_facet Momen, Mehdi
Ayatollahi Mehrgardi, Ahmad
Amiri Roudbar, Mahmoud
Kranis, Andreas
Mercuri Pinto, Renan
Valente, Bruno D.
Morota, Gota
Rosa, Guilherme J. M.
Gianola, Daniel
author_sort Momen, Mehdi
collection PubMed
description Network based statistical models accounting for putative causal relationships among multiple phenotypes can be used to infer single-nucleotide polymorphism (SNP) effect which transmitting through a given causal path in genome-wide association studies (GWAS). In GWAS with multiple phenotypes, reconstructing underlying causal structures among traits and SNPs using a single statistical framework is essential for understanding the entirety of genotype-phenotype maps. A structural equation model (SEM) can be used for such purposes. We applied SEM to GWAS (SEM-GWAS) in chickens, taking into account putative causal relationships among breast meat (BM), body weight (BW), hen-house production (HHP), and SNPs. We assessed the performance of SEM-GWAS by comparing the model results with those obtained from traditional multi-trait association analyses (MTM-GWAS). Three different putative causal path diagrams were inferred from highest posterior density (HPD) intervals of 0.75, 0.85, and 0.95 using the inductive causation algorithm. A positive path coefficient was estimated for BM → BW, and negative values were obtained for BM → HHP and BW → HHP in all implemented scenarios. Further, the application of SEM-GWAS enabled the decomposition of SNP effects into direct, indirect, and total effects, identifying whether a SNP effect is acting directly or indirectly on a given trait. In contrast, MTM-GWAS only captured overall genetic effects on traits, which is equivalent to combining the direct and indirect SNP effects from SEM-GWAS. Although MTM-GWAS and SEM-GWAS use the similar probabilistic models, we provide evidence that SEM-GWAS captures complex relationships in terms of causal meaning and mediation and delivers a more comprehensive understanding of SNP effects compared to MTM-GWAS. Our results showed that SEM-GWAS provides important insight regarding the mechanism by which identified SNPs control traits by partitioning them into direct, indirect, and total SNP effects.
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spelling pubmed-61893262018-10-23 Including Phenotypic Causal Networks in Genome-Wide Association Studies Using Mixed Effects Structural Equation Models Momen, Mehdi Ayatollahi Mehrgardi, Ahmad Amiri Roudbar, Mahmoud Kranis, Andreas Mercuri Pinto, Renan Valente, Bruno D. Morota, Gota Rosa, Guilherme J. M. Gianola, Daniel Front Genet Genetics Network based statistical models accounting for putative causal relationships among multiple phenotypes can be used to infer single-nucleotide polymorphism (SNP) effect which transmitting through a given causal path in genome-wide association studies (GWAS). In GWAS with multiple phenotypes, reconstructing underlying causal structures among traits and SNPs using a single statistical framework is essential for understanding the entirety of genotype-phenotype maps. A structural equation model (SEM) can be used for such purposes. We applied SEM to GWAS (SEM-GWAS) in chickens, taking into account putative causal relationships among breast meat (BM), body weight (BW), hen-house production (HHP), and SNPs. We assessed the performance of SEM-GWAS by comparing the model results with those obtained from traditional multi-trait association analyses (MTM-GWAS). Three different putative causal path diagrams were inferred from highest posterior density (HPD) intervals of 0.75, 0.85, and 0.95 using the inductive causation algorithm. A positive path coefficient was estimated for BM → BW, and negative values were obtained for BM → HHP and BW → HHP in all implemented scenarios. Further, the application of SEM-GWAS enabled the decomposition of SNP effects into direct, indirect, and total effects, identifying whether a SNP effect is acting directly or indirectly on a given trait. In contrast, MTM-GWAS only captured overall genetic effects on traits, which is equivalent to combining the direct and indirect SNP effects from SEM-GWAS. Although MTM-GWAS and SEM-GWAS use the similar probabilistic models, we provide evidence that SEM-GWAS captures complex relationships in terms of causal meaning and mediation and delivers a more comprehensive understanding of SNP effects compared to MTM-GWAS. Our results showed that SEM-GWAS provides important insight regarding the mechanism by which identified SNPs control traits by partitioning them into direct, indirect, and total SNP effects. Frontiers Media S.A. 2018-10-09 /pmc/articles/PMC6189326/ /pubmed/30356716 http://dx.doi.org/10.3389/fgene.2018.00455 Text en Copyright © 2018 Momen, Ayatollahi Mehrgardi, Amiri Roudbar, Kranis, Mercuri Pinto, Valente, Morota, Rosa and Gianola. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Momen, Mehdi
Ayatollahi Mehrgardi, Ahmad
Amiri Roudbar, Mahmoud
Kranis, Andreas
Mercuri Pinto, Renan
Valente, Bruno D.
Morota, Gota
Rosa, Guilherme J. M.
Gianola, Daniel
Including Phenotypic Causal Networks in Genome-Wide Association Studies Using Mixed Effects Structural Equation Models
title Including Phenotypic Causal Networks in Genome-Wide Association Studies Using Mixed Effects Structural Equation Models
title_full Including Phenotypic Causal Networks in Genome-Wide Association Studies Using Mixed Effects Structural Equation Models
title_fullStr Including Phenotypic Causal Networks in Genome-Wide Association Studies Using Mixed Effects Structural Equation Models
title_full_unstemmed Including Phenotypic Causal Networks in Genome-Wide Association Studies Using Mixed Effects Structural Equation Models
title_short Including Phenotypic Causal Networks in Genome-Wide Association Studies Using Mixed Effects Structural Equation Models
title_sort including phenotypic causal networks in genome-wide association studies using mixed effects structural equation models
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189326/
https://www.ncbi.nlm.nih.gov/pubmed/30356716
http://dx.doi.org/10.3389/fgene.2018.00455
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