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Inferring Quantitative Trait Pathways Associated with Bull Fertility from a Genome-Wide Association Study
Whole-genome association studies typically focus on genetic markers with the strongest evidence of association. However, single markers often explain only a small component of the genetic variance and hence offer a limited understanding of the trait under study. As such, the objective of this study...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542705/ https://www.ncbi.nlm.nih.gov/pubmed/23335935 http://dx.doi.org/10.3389/fgene.2012.00307 |
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author | Peñagaricano, Francisco Weigel, Kent A. Rosa, Guilherme J. M. Khatib, Hasan |
author_facet | Peñagaricano, Francisco Weigel, Kent A. Rosa, Guilherme J. M. Khatib, Hasan |
author_sort | Peñagaricano, Francisco |
collection | PubMed |
description | Whole-genome association studies typically focus on genetic markers with the strongest evidence of association. However, single markers often explain only a small component of the genetic variance and hence offer a limited understanding of the trait under study. As such, the objective of this study was to perform a pathway-based association analysis in Holstein dairy cattle in order to identify relevant pathways involved in bull fertility. The results of a single-marker association analysis, using 1,755 bulls with sire conception rate data and genotypes for 38,650 single nucleotide polymorphisms (SNPs), were used in this study. A total of 16,819 annotated genes, including 2,767 significantly associated with bull fertility, were used to interrogate a total of 662 Gene Ontology (GO) terms and 248 InterPro (IP) entries using a test of proportions based on the cumulative hypergeometric distribution. After multiple-testing correction, 20 GO categories and one IP entry showed significant overrepresentation of genes statistically associated with bull fertility. Several of these functional categories such as small GTPases mediated signal transduction, neurogenesis, calcium ion binding, and cytoskeleton are known to be involved in biological processes closely related to male fertility. These results could provide insight into the genetic architecture of this complex trait in dairy cattle. In addition, this study shows that quantitative trait pathways inferred from single-marker analyses could enhance our interpretations of the results of genome-wide association studies. |
format | Online Article Text |
id | pubmed-3542705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-35427052013-01-18 Inferring Quantitative Trait Pathways Associated with Bull Fertility from a Genome-Wide Association Study Peñagaricano, Francisco Weigel, Kent A. Rosa, Guilherme J. M. Khatib, Hasan Front Genet Genetics Whole-genome association studies typically focus on genetic markers with the strongest evidence of association. However, single markers often explain only a small component of the genetic variance and hence offer a limited understanding of the trait under study. As such, the objective of this study was to perform a pathway-based association analysis in Holstein dairy cattle in order to identify relevant pathways involved in bull fertility. The results of a single-marker association analysis, using 1,755 bulls with sire conception rate data and genotypes for 38,650 single nucleotide polymorphisms (SNPs), were used in this study. A total of 16,819 annotated genes, including 2,767 significantly associated with bull fertility, were used to interrogate a total of 662 Gene Ontology (GO) terms and 248 InterPro (IP) entries using a test of proportions based on the cumulative hypergeometric distribution. After multiple-testing correction, 20 GO categories and one IP entry showed significant overrepresentation of genes statistically associated with bull fertility. Several of these functional categories such as small GTPases mediated signal transduction, neurogenesis, calcium ion binding, and cytoskeleton are known to be involved in biological processes closely related to male fertility. These results could provide insight into the genetic architecture of this complex trait in dairy cattle. In addition, this study shows that quantitative trait pathways inferred from single-marker analyses could enhance our interpretations of the results of genome-wide association studies. Frontiers Media S.A. 2013-01-11 /pmc/articles/PMC3542705/ /pubmed/23335935 http://dx.doi.org/10.3389/fgene.2012.00307 Text en Copyright © 2013 Peñagaricano, Weigel, Rosa and Khatib. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Genetics Peñagaricano, Francisco Weigel, Kent A. Rosa, Guilherme J. M. Khatib, Hasan Inferring Quantitative Trait Pathways Associated with Bull Fertility from a Genome-Wide Association Study |
title | Inferring Quantitative Trait Pathways Associated with Bull Fertility from a Genome-Wide Association Study |
title_full | Inferring Quantitative Trait Pathways Associated with Bull Fertility from a Genome-Wide Association Study |
title_fullStr | Inferring Quantitative Trait Pathways Associated with Bull Fertility from a Genome-Wide Association Study |
title_full_unstemmed | Inferring Quantitative Trait Pathways Associated with Bull Fertility from a Genome-Wide Association Study |
title_short | Inferring Quantitative Trait Pathways Associated with Bull Fertility from a Genome-Wide Association Study |
title_sort | inferring quantitative trait pathways associated with bull fertility from a genome-wide association study |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542705/ https://www.ncbi.nlm.nih.gov/pubmed/23335935 http://dx.doi.org/10.3389/fgene.2012.00307 |
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