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Genome-Wide Association Study Reveals Constant and Specific Loci for Hematological Traits at Three Time Stages in a White Duroc × Erhualian F(2) Resource Population

Hematological traits are important indicators of immune function and have been commonly examined as biomarkers of disease and disease severity in humans. Pig is an ideal biomedical model for human diseases due to its high degree of similarity with human physiological characteristics. Here, we conduc...

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Autores principales: Zhang, Zhiyan, Hong, Yuan, Gao, Jun, Xiao, Shijun, Ma, Junwu, Zhang, Wanchang, Ren, Jun, Huang, Lusheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656948/
https://www.ncbi.nlm.nih.gov/pubmed/23691082
http://dx.doi.org/10.1371/journal.pone.0063665
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author Zhang, Zhiyan
Hong, Yuan
Gao, Jun
Xiao, Shijun
Ma, Junwu
Zhang, Wanchang
Ren, Jun
Huang, Lusheng
author_facet Zhang, Zhiyan
Hong, Yuan
Gao, Jun
Xiao, Shijun
Ma, Junwu
Zhang, Wanchang
Ren, Jun
Huang, Lusheng
author_sort Zhang, Zhiyan
collection PubMed
description Hematological traits are important indicators of immune function and have been commonly examined as biomarkers of disease and disease severity in humans. Pig is an ideal biomedical model for human diseases due to its high degree of similarity with human physiological characteristics. Here, we conducted genome-wide association studies (GWAS) for 18 hematological traits at three growth stages (days 18, 46 and 240) in a White Duroc × Erhualian F(2) intercross. In total, we identified 38 genome-wide significant regions containing 185 genome-wide significant SNPs by single-marker GWAS or LONG-GWAS. The significant regions are distributed on pig chromosomes (SSC) 1, 4, 5, 7, 8, 10, 11, 12, 13, 17 and 18, and most of significant SNPs reside on SSC7 and SSC8. Of the 38 significant regions, 7 show constant effects on hematological traits across the whole life stages, and 6 regions have time-specific effects on the measured traits at early or late stages. The most prominent locus is the genomic region between 32.36 and 84.49 Mb on SSC8 that is associated with multiple erythroid traits. The KIT gene in this region appears to be a promising candidate gene. The findings improve our understanding of the genetic architecture of hematological traits in pigs. Further investigations are warranted to characterize the responsible gene(s) and causal variant(s) especially for the major loci on SSC7 and SSC8.
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spelling pubmed-36569482013-05-20 Genome-Wide Association Study Reveals Constant and Specific Loci for Hematological Traits at Three Time Stages in a White Duroc × Erhualian F(2) Resource Population Zhang, Zhiyan Hong, Yuan Gao, Jun Xiao, Shijun Ma, Junwu Zhang, Wanchang Ren, Jun Huang, Lusheng PLoS One Research Article Hematological traits are important indicators of immune function and have been commonly examined as biomarkers of disease and disease severity in humans. Pig is an ideal biomedical model for human diseases due to its high degree of similarity with human physiological characteristics. Here, we conducted genome-wide association studies (GWAS) for 18 hematological traits at three growth stages (days 18, 46 and 240) in a White Duroc × Erhualian F(2) intercross. In total, we identified 38 genome-wide significant regions containing 185 genome-wide significant SNPs by single-marker GWAS or LONG-GWAS. The significant regions are distributed on pig chromosomes (SSC) 1, 4, 5, 7, 8, 10, 11, 12, 13, 17 and 18, and most of significant SNPs reside on SSC7 and SSC8. Of the 38 significant regions, 7 show constant effects on hematological traits across the whole life stages, and 6 regions have time-specific effects on the measured traits at early or late stages. The most prominent locus is the genomic region between 32.36 and 84.49 Mb on SSC8 that is associated with multiple erythroid traits. The KIT gene in this region appears to be a promising candidate gene. The findings improve our understanding of the genetic architecture of hematological traits in pigs. Further investigations are warranted to characterize the responsible gene(s) and causal variant(s) especially for the major loci on SSC7 and SSC8. Public Library of Science 2013-05-17 /pmc/articles/PMC3656948/ /pubmed/23691082 http://dx.doi.org/10.1371/journal.pone.0063665 Text en © 2013 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhang, Zhiyan
Hong, Yuan
Gao, Jun
Xiao, Shijun
Ma, Junwu
Zhang, Wanchang
Ren, Jun
Huang, Lusheng
Genome-Wide Association Study Reveals Constant and Specific Loci for Hematological Traits at Three Time Stages in a White Duroc × Erhualian F(2) Resource Population
title Genome-Wide Association Study Reveals Constant and Specific Loci for Hematological Traits at Three Time Stages in a White Duroc × Erhualian F(2) Resource Population
title_full Genome-Wide Association Study Reveals Constant and Specific Loci for Hematological Traits at Three Time Stages in a White Duroc × Erhualian F(2) Resource Population
title_fullStr Genome-Wide Association Study Reveals Constant and Specific Loci for Hematological Traits at Three Time Stages in a White Duroc × Erhualian F(2) Resource Population
title_full_unstemmed Genome-Wide Association Study Reveals Constant and Specific Loci for Hematological Traits at Three Time Stages in a White Duroc × Erhualian F(2) Resource Population
title_short Genome-Wide Association Study Reveals Constant and Specific Loci for Hematological Traits at Three Time Stages in a White Duroc × Erhualian F(2) Resource Population
title_sort genome-wide association study reveals constant and specific loci for hematological traits at three time stages in a white duroc × erhualian f(2) resource population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656948/
https://www.ncbi.nlm.nih.gov/pubmed/23691082
http://dx.doi.org/10.1371/journal.pone.0063665
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