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Identification of a missense variant in the porcine AGPAT gene family associated with intramuscular fat content through whole‐genome sequencing

The 1‐acylglycerol‐3‐phosphate O‐acyltransferases (AGPATs) are enzymes that catalyze the conversion of lysophosphatidic acid to phosphatidic acid, which is a precursor of triacylglycerol, the main fat reservoir in mammals. We used whole‐genome sequencing of 205 pigs to identify 6639 genetic variants...

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Autores principales: Molinero, Eduard, Pena, Ramona N., Estany, Joan, Ros‐Freixedes, Roger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826064/
https://www.ncbi.nlm.nih.gov/pubmed/36108237
http://dx.doi.org/10.1111/age.13258
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author Molinero, Eduard
Pena, Ramona N.
Estany, Joan
Ros‐Freixedes, Roger
author_facet Molinero, Eduard
Pena, Ramona N.
Estany, Joan
Ros‐Freixedes, Roger
author_sort Molinero, Eduard
collection PubMed
description The 1‐acylglycerol‐3‐phosphate O‐acyltransferases (AGPATs) are enzymes that catalyze the conversion of lysophosphatidic acid to phosphatidic acid, which is a precursor of triacylglycerol, the main fat reservoir in mammals. We used whole‐genome sequencing of 205 pigs to identify 6639 genetic variants in the porcine AGPAT gene family. Of these, 166 common variants in the AGPAT5 gene had significant associations with fat content and composition traits. We preselected a missense single nucleotide polymorphism in exon 6 of AGPAT5 (rs196952262, A>G) for validation of its associations in 1034 pigs from the same Duroc line. The A allele showed a positive additive effect for intramuscular fat content (+1.12% ± 0.21, p < 0.001, for gluteus medius and +0.89% ± 0.33, p < 0.01, for longissimus). We also observed significant associations with fatty acid composition that were, at least in part, independent of the increased intramuscular fat. The A allele resulted in more monounsaturated fatty acids (+0.34% ± 0.15, p < 0.05, for longissimus) and a greater monounsaturated/polyunsaturated fatty acids ratio (+0.11 ± 0.04, p < 0.01, for gluteus medius and +0.13 ± 0.05, p < 0.05, for longissimus). The effect of the AGPAT5 variant on intramuscular fat was more noticeable in fatter pigs, and AGPAT5 interacts with other genes that affect overall fatness such as LEPR. AGPAT5 was the most expressed gene of the AGPAT family in pig skeletal muscle. This variant can be used as a marker in assisted selection for modulating pig fat deposition and fatty acid content.
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spelling pubmed-98260642023-01-09 Identification of a missense variant in the porcine AGPAT gene family associated with intramuscular fat content through whole‐genome sequencing Molinero, Eduard Pena, Ramona N. Estany, Joan Ros‐Freixedes, Roger Anim Genet Research Articles The 1‐acylglycerol‐3‐phosphate O‐acyltransferases (AGPATs) are enzymes that catalyze the conversion of lysophosphatidic acid to phosphatidic acid, which is a precursor of triacylglycerol, the main fat reservoir in mammals. We used whole‐genome sequencing of 205 pigs to identify 6639 genetic variants in the porcine AGPAT gene family. Of these, 166 common variants in the AGPAT5 gene had significant associations with fat content and composition traits. We preselected a missense single nucleotide polymorphism in exon 6 of AGPAT5 (rs196952262, A>G) for validation of its associations in 1034 pigs from the same Duroc line. The A allele showed a positive additive effect for intramuscular fat content (+1.12% ± 0.21, p < 0.001, for gluteus medius and +0.89% ± 0.33, p < 0.01, for longissimus). We also observed significant associations with fatty acid composition that were, at least in part, independent of the increased intramuscular fat. The A allele resulted in more monounsaturated fatty acids (+0.34% ± 0.15, p < 0.05, for longissimus) and a greater monounsaturated/polyunsaturated fatty acids ratio (+0.11 ± 0.04, p < 0.01, for gluteus medius and +0.13 ± 0.05, p < 0.05, for longissimus). The effect of the AGPAT5 variant on intramuscular fat was more noticeable in fatter pigs, and AGPAT5 interacts with other genes that affect overall fatness such as LEPR. AGPAT5 was the most expressed gene of the AGPAT family in pig skeletal muscle. This variant can be used as a marker in assisted selection for modulating pig fat deposition and fatty acid content. John Wiley and Sons Inc. 2022-09-15 2022-12 /pmc/articles/PMC9826064/ /pubmed/36108237 http://dx.doi.org/10.1111/age.13258 Text en © 2022 The Authors. Animal Genetics published by John Wiley & Sons Ltd on behalf of Stichting International Foundation for Animal Genetics. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Molinero, Eduard
Pena, Ramona N.
Estany, Joan
Ros‐Freixedes, Roger
Identification of a missense variant in the porcine AGPAT gene family associated with intramuscular fat content through whole‐genome sequencing
title Identification of a missense variant in the porcine AGPAT gene family associated with intramuscular fat content through whole‐genome sequencing
title_full Identification of a missense variant in the porcine AGPAT gene family associated with intramuscular fat content through whole‐genome sequencing
title_fullStr Identification of a missense variant in the porcine AGPAT gene family associated with intramuscular fat content through whole‐genome sequencing
title_full_unstemmed Identification of a missense variant in the porcine AGPAT gene family associated with intramuscular fat content through whole‐genome sequencing
title_short Identification of a missense variant in the porcine AGPAT gene family associated with intramuscular fat content through whole‐genome sequencing
title_sort identification of a missense variant in the porcine agpat gene family associated with intramuscular fat content through whole‐genome sequencing
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826064/
https://www.ncbi.nlm.nih.gov/pubmed/36108237
http://dx.doi.org/10.1111/age.13258
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