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Detection of multiple quantitative trait loci and their pleiotropic effects in outbred pig populations

BACKGROUND: Simultaneous detection of multiple QTLs (quantitative trait loci) may allow more accurate estimation of genetic effects. We have analyzed outbred commercial pig populations with different single and multiple models to clarify their genetic properties and in addition, we have investigated...

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Autores principales: Nagamine, Yoshitaka, Pong-Wong, Ricardo, Visscher, Peter M, Haley, Chris S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2762464/
https://www.ncbi.nlm.nih.gov/pubmed/19807906
http://dx.doi.org/10.1186/1297-9686-41-44
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author Nagamine, Yoshitaka
Pong-Wong, Ricardo
Visscher, Peter M
Haley, Chris S
author_facet Nagamine, Yoshitaka
Pong-Wong, Ricardo
Visscher, Peter M
Haley, Chris S
author_sort Nagamine, Yoshitaka
collection PubMed
description BACKGROUND: Simultaneous detection of multiple QTLs (quantitative trait loci) may allow more accurate estimation of genetic effects. We have analyzed outbred commercial pig populations with different single and multiple models to clarify their genetic properties and in addition, we have investigated pleiotropy among growth and obesity traits based on allelic correlation within a gamete. METHODS: Three closed populations, (A) 427 individuals from a Yorkshire and Large White synthetic breed, (B) 547 Large White individuals and (C) 531 Large White individuals, were analyzed using a variance component method with one-QTL and two-QTL models. Six markers on chromosome 4 and five to seven markers on chromosome 7 were used. RESULTS: Population A displayed a high test statistic for the fat trait when applying the two-QTL model with two positions on two chromosomes. The estimated heritabilities for polygenic effects and for the first and second QTL were 19%, 17% and 21%, respectively. The high correlation of the estimated allelic effect on the same gamete and QTL test statistics suggested that the two separate QTL which were detected on different chromosomes both have pleiotropic effects on the two fat traits. Analysis of population B using the one-QTL model for three fat traits found a similar peak position on chromosome 7. Allelic effects of three fat traits from the same gamete were highly correlated suggesting the presence of a pleiotropic QTL. In population C, three growth traits also displayed similar peak positions on chromosome 7 and allelic effects from the same gamete were correlated. CONCLUSION: Detection of the second QTL in a model reduced the polygenic heritability and should improve accuracy of estimated heritabilities for both QTLs.
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spelling pubmed-27624642009-10-16 Detection of multiple quantitative trait loci and their pleiotropic effects in outbred pig populations Nagamine, Yoshitaka Pong-Wong, Ricardo Visscher, Peter M Haley, Chris S Genet Sel Evol Research BACKGROUND: Simultaneous detection of multiple QTLs (quantitative trait loci) may allow more accurate estimation of genetic effects. We have analyzed outbred commercial pig populations with different single and multiple models to clarify their genetic properties and in addition, we have investigated pleiotropy among growth and obesity traits based on allelic correlation within a gamete. METHODS: Three closed populations, (A) 427 individuals from a Yorkshire and Large White synthetic breed, (B) 547 Large White individuals and (C) 531 Large White individuals, were analyzed using a variance component method with one-QTL and two-QTL models. Six markers on chromosome 4 and five to seven markers on chromosome 7 were used. RESULTS: Population A displayed a high test statistic for the fat trait when applying the two-QTL model with two positions on two chromosomes. The estimated heritabilities for polygenic effects and for the first and second QTL were 19%, 17% and 21%, respectively. The high correlation of the estimated allelic effect on the same gamete and QTL test statistics suggested that the two separate QTL which were detected on different chromosomes both have pleiotropic effects on the two fat traits. Analysis of population B using the one-QTL model for three fat traits found a similar peak position on chromosome 7. Allelic effects of three fat traits from the same gamete were highly correlated suggesting the presence of a pleiotropic QTL. In population C, three growth traits also displayed similar peak positions on chromosome 7 and allelic effects from the same gamete were correlated. CONCLUSION: Detection of the second QTL in a model reduced the polygenic heritability and should improve accuracy of estimated heritabilities for both QTLs. BioMed Central 2009-10-06 /pmc/articles/PMC2762464/ /pubmed/19807906 http://dx.doi.org/10.1186/1297-9686-41-44 Text en Copyright ©2009 Nagamine et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Nagamine, Yoshitaka
Pong-Wong, Ricardo
Visscher, Peter M
Haley, Chris S
Detection of multiple quantitative trait loci and their pleiotropic effects in outbred pig populations
title Detection of multiple quantitative trait loci and their pleiotropic effects in outbred pig populations
title_full Detection of multiple quantitative trait loci and their pleiotropic effects in outbred pig populations
title_fullStr Detection of multiple quantitative trait loci and their pleiotropic effects in outbred pig populations
title_full_unstemmed Detection of multiple quantitative trait loci and their pleiotropic effects in outbred pig populations
title_short Detection of multiple quantitative trait loci and their pleiotropic effects in outbred pig populations
title_sort detection of multiple quantitative trait loci and their pleiotropic effects in outbred pig populations
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2762464/
https://www.ncbi.nlm.nih.gov/pubmed/19807906
http://dx.doi.org/10.1186/1297-9686-41-44
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