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Genome-wide association analyses reveal significant loci and strong candidate genes for growth and fatness traits in two pig populations

BACKGROUND: Recently, genome-wide association studies (GWAS) have been reported on various pig traits. We performed a GWAS to analyze 22 traits related to growth and fatness on two pig populations: a White Duroc × Erhualian F(2) intercross population and a Chinese Sutai half-sib population. RESULTS:...

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Autores principales: Qiao, Ruimin, Gao, Jun, Zhang, Zhiyan, Li, Lin, Xie, Xianhua, Fan, Yin, Cui, Leilei, Ma, Junwu, Ai, Huashui, Ren, Jun, Huang, Lusheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358731/
https://www.ncbi.nlm.nih.gov/pubmed/25885760
http://dx.doi.org/10.1186/s12711-015-0089-5
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author Qiao, Ruimin
Gao, Jun
Zhang, Zhiyan
Li, Lin
Xie, Xianhua
Fan, Yin
Cui, Leilei
Ma, Junwu
Ai, Huashui
Ren, Jun
Huang, Lusheng
author_facet Qiao, Ruimin
Gao, Jun
Zhang, Zhiyan
Li, Lin
Xie, Xianhua
Fan, Yin
Cui, Leilei
Ma, Junwu
Ai, Huashui
Ren, Jun
Huang, Lusheng
author_sort Qiao, Ruimin
collection PubMed
description BACKGROUND: Recently, genome-wide association studies (GWAS) have been reported on various pig traits. We performed a GWAS to analyze 22 traits related to growth and fatness on two pig populations: a White Duroc × Erhualian F(2) intercross population and a Chinese Sutai half-sib population. RESULTS: We identified 14 and 39 loci that displayed significant associations with growth and fatness traits at the genome-wide level and chromosome-wide level, respectively. The strongest association was between a 750 kb region on SSC7 (SSC for Sus scrofa) and backfat thickness at the first rib. This region had pleiotropic effects on both fatness and growth traits in F(2) animals and contained a promising candidate gene HMGA1 (high mobility group AT-hook 1). Unexpectedly, population genetic analysis revealed that the allele at this locus that reduces fatness and increases growth is derived from Chinese indigenous pigs and segregates in multiple Chinese breeds. The second strongest association was between the region around 82.85 Mb on SSC4 and average backfat thickness. PLAG1 (pleiomorphic adenoma gene 1), a gene under strong selection in European domestic pigs, is proximal to the top SNP and stands out as a strong candidate gene. On SSC2, a locus that significantly affects fatness traits mapped to the region around the IGF2 (insulin-like growth factor 2) gene but its non-imprinting inheritance excluded IGF2 as a candidate gene. A significant locus was also detected within a recombination cold spot that spans more than 30 Mb on SSCX, which hampered the identification of plausible candidate genes. Notably, no genome-wide significant locus was shared by the two experimental populations; different loci were observed that had both constant and time-specific effects on growth traits at different stages, which illustrates the complex genetic architecture of these traits. CONCLUSIONS: We confirm several previously reported QTL and provide a list of novel loci for porcine growth and fatness traits in two experimental populations with Chinese Taihu and Western pigs as common founders. We showed that distinct loci exist for these traits in the two populations and identified HMGA1 and PLAG1 as strong candidate genes on SSC7 and SSC4, respectively. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12711-015-0089-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-43587312015-03-14 Genome-wide association analyses reveal significant loci and strong candidate genes for growth and fatness traits in two pig populations Qiao, Ruimin Gao, Jun Zhang, Zhiyan Li, Lin Xie, Xianhua Fan, Yin Cui, Leilei Ma, Junwu Ai, Huashui Ren, Jun Huang, Lusheng Genet Sel Evol Research BACKGROUND: Recently, genome-wide association studies (GWAS) have been reported on various pig traits. We performed a GWAS to analyze 22 traits related to growth and fatness on two pig populations: a White Duroc × Erhualian F(2) intercross population and a Chinese Sutai half-sib population. RESULTS: We identified 14 and 39 loci that displayed significant associations with growth and fatness traits at the genome-wide level and chromosome-wide level, respectively. The strongest association was between a 750 kb region on SSC7 (SSC for Sus scrofa) and backfat thickness at the first rib. This region had pleiotropic effects on both fatness and growth traits in F(2) animals and contained a promising candidate gene HMGA1 (high mobility group AT-hook 1). Unexpectedly, population genetic analysis revealed that the allele at this locus that reduces fatness and increases growth is derived from Chinese indigenous pigs and segregates in multiple Chinese breeds. The second strongest association was between the region around 82.85 Mb on SSC4 and average backfat thickness. PLAG1 (pleiomorphic adenoma gene 1), a gene under strong selection in European domestic pigs, is proximal to the top SNP and stands out as a strong candidate gene. On SSC2, a locus that significantly affects fatness traits mapped to the region around the IGF2 (insulin-like growth factor 2) gene but its non-imprinting inheritance excluded IGF2 as a candidate gene. A significant locus was also detected within a recombination cold spot that spans more than 30 Mb on SSCX, which hampered the identification of plausible candidate genes. Notably, no genome-wide significant locus was shared by the two experimental populations; different loci were observed that had both constant and time-specific effects on growth traits at different stages, which illustrates the complex genetic architecture of these traits. CONCLUSIONS: We confirm several previously reported QTL and provide a list of novel loci for porcine growth and fatness traits in two experimental populations with Chinese Taihu and Western pigs as common founders. We showed that distinct loci exist for these traits in the two populations and identified HMGA1 and PLAG1 as strong candidate genes on SSC7 and SSC4, respectively. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12711-015-0089-5) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-14 /pmc/articles/PMC4358731/ /pubmed/25885760 http://dx.doi.org/10.1186/s12711-015-0089-5 Text en © Qiao et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Qiao, Ruimin
Gao, Jun
Zhang, Zhiyan
Li, Lin
Xie, Xianhua
Fan, Yin
Cui, Leilei
Ma, Junwu
Ai, Huashui
Ren, Jun
Huang, Lusheng
Genome-wide association analyses reveal significant loci and strong candidate genes for growth and fatness traits in two pig populations
title Genome-wide association analyses reveal significant loci and strong candidate genes for growth and fatness traits in two pig populations
title_full Genome-wide association analyses reveal significant loci and strong candidate genes for growth and fatness traits in two pig populations
title_fullStr Genome-wide association analyses reveal significant loci and strong candidate genes for growth and fatness traits in two pig populations
title_full_unstemmed Genome-wide association analyses reveal significant loci and strong candidate genes for growth and fatness traits in two pig populations
title_short Genome-wide association analyses reveal significant loci and strong candidate genes for growth and fatness traits in two pig populations
title_sort genome-wide association analyses reveal significant loci and strong candidate genes for growth and fatness traits in two pig populations
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358731/
https://www.ncbi.nlm.nih.gov/pubmed/25885760
http://dx.doi.org/10.1186/s12711-015-0089-5
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