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Identification and Dissection of Four Major QTL Affecting Milk Fat Content in the German Holstein-Friesian Population

Milk composition traits exhibit a complex genetic architecture with a small number of major quantitative trait loci (QTL) explaining a large fraction of the genetic variation and numerous QTL with minor effects. In order to identify QTL for milk fat percentage (FP) in the German Holstein-Friesian (H...

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Autores principales: Wang, Xiaolong, Wurmser, Christine, Pausch, Hubert, Jung, Simone, Reinhardt, Friedrich, Tetens, Jens, Thaller, Georg, Fries, Ruedi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394711/
https://www.ncbi.nlm.nih.gov/pubmed/22792397
http://dx.doi.org/10.1371/journal.pone.0040711
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author Wang, Xiaolong
Wurmser, Christine
Pausch, Hubert
Jung, Simone
Reinhardt, Friedrich
Tetens, Jens
Thaller, Georg
Fries, Ruedi
author_facet Wang, Xiaolong
Wurmser, Christine
Pausch, Hubert
Jung, Simone
Reinhardt, Friedrich
Tetens, Jens
Thaller, Georg
Fries, Ruedi
author_sort Wang, Xiaolong
collection PubMed
description Milk composition traits exhibit a complex genetic architecture with a small number of major quantitative trait loci (QTL) explaining a large fraction of the genetic variation and numerous QTL with minor effects. In order to identify QTL for milk fat percentage (FP) in the German Holstein-Friesian (HF) population, a genome-wide association study (GWAS) was performed. The study population consisted of 2327 progeny-tested bulls. Genotypes were available for 44,280 SNPs. Phenotypes in the form of estimated breeding values (EBVs) for FP were used as highly heritable traits. A variance components-based approach was used to account for population stratification. The GWAS identified four major QTL regions explaining 46.18% of the FP EBV variance. Besides two previously known FP QTL on BTA14 (P = 8.91×10−(198)) and BTA20 (P = 7.03×10(−12)) within DGAT1 and GHR, respectively, we uncovered two additional QTL regions on BTA5 (P = 2.00×10(−13)) and BTA27 (P = 9.83×10(−5)) encompassing EPS8 and GPAT4, respectively. EPS8 and GPAT4 are involved in lipid metabolism in mammals. Re-sequencing of EPS8 and GPAT4 revealed 50 polymorphisms. Genotypes for five of them were inferred for the entire study population. Two polymorphisms affecting potential transcription factor binding sites of EPS8 (P = 1.40×10(−12)) and GPAT4 (P = 5.18×10(−5)), respectively, were highly significantly associated with the FP EBV. Our results provide evidence that alteration of regulatory sites is an important aspect of genetic variation of complex traits in cattle.
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spelling pubmed-33947112012-07-12 Identification and Dissection of Four Major QTL Affecting Milk Fat Content in the German Holstein-Friesian Population Wang, Xiaolong Wurmser, Christine Pausch, Hubert Jung, Simone Reinhardt, Friedrich Tetens, Jens Thaller, Georg Fries, Ruedi PLoS One Research Article Milk composition traits exhibit a complex genetic architecture with a small number of major quantitative trait loci (QTL) explaining a large fraction of the genetic variation and numerous QTL with minor effects. In order to identify QTL for milk fat percentage (FP) in the German Holstein-Friesian (HF) population, a genome-wide association study (GWAS) was performed. The study population consisted of 2327 progeny-tested bulls. Genotypes were available for 44,280 SNPs. Phenotypes in the form of estimated breeding values (EBVs) for FP were used as highly heritable traits. A variance components-based approach was used to account for population stratification. The GWAS identified four major QTL regions explaining 46.18% of the FP EBV variance. Besides two previously known FP QTL on BTA14 (P = 8.91×10−(198)) and BTA20 (P = 7.03×10(−12)) within DGAT1 and GHR, respectively, we uncovered two additional QTL regions on BTA5 (P = 2.00×10(−13)) and BTA27 (P = 9.83×10(−5)) encompassing EPS8 and GPAT4, respectively. EPS8 and GPAT4 are involved in lipid metabolism in mammals. Re-sequencing of EPS8 and GPAT4 revealed 50 polymorphisms. Genotypes for five of them were inferred for the entire study population. Two polymorphisms affecting potential transcription factor binding sites of EPS8 (P = 1.40×10(−12)) and GPAT4 (P = 5.18×10(−5)), respectively, were highly significantly associated with the FP EBV. Our results provide evidence that alteration of regulatory sites is an important aspect of genetic variation of complex traits in cattle. Public Library of Science 2012-07-11 /pmc/articles/PMC3394711/ /pubmed/22792397 http://dx.doi.org/10.1371/journal.pone.0040711 Text en Wang 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
Wang, Xiaolong
Wurmser, Christine
Pausch, Hubert
Jung, Simone
Reinhardt, Friedrich
Tetens, Jens
Thaller, Georg
Fries, Ruedi
Identification and Dissection of Four Major QTL Affecting Milk Fat Content in the German Holstein-Friesian Population
title Identification and Dissection of Four Major QTL Affecting Milk Fat Content in the German Holstein-Friesian Population
title_full Identification and Dissection of Four Major QTL Affecting Milk Fat Content in the German Holstein-Friesian Population
title_fullStr Identification and Dissection of Four Major QTL Affecting Milk Fat Content in the German Holstein-Friesian Population
title_full_unstemmed Identification and Dissection of Four Major QTL Affecting Milk Fat Content in the German Holstein-Friesian Population
title_short Identification and Dissection of Four Major QTL Affecting Milk Fat Content in the German Holstein-Friesian Population
title_sort identification and dissection of four major qtl affecting milk fat content in the german holstein-friesian population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394711/
https://www.ncbi.nlm.nih.gov/pubmed/22792397
http://dx.doi.org/10.1371/journal.pone.0040711
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