2022
DOI: 10.1111/age.13258
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Identification of a missense variant in the porcine AGPAT gene family associated with intramuscular fat content through whole‐genome sequencing

Abstract: 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

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Cited by 6 publications
(3 citation statements)
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“…AGPAT2 has been shown to play an important role in lipid metabolism in chickens [ 46 ]. AGPAT5 , on the other hand, is considered a potential genetic marker for excellent pork quality [ 48 ]. In a study conducted on cattle, AGPAT5 was found to be significantly correlated with pre-slaughter weight, carcass weight, and meat weight [ 49 ].…”
Section: Discussionmentioning
confidence: 99%
“…AGPAT2 has been shown to play an important role in lipid metabolism in chickens [ 46 ]. AGPAT5 , on the other hand, is considered a potential genetic marker for excellent pork quality [ 48 ]. In a study conducted on cattle, AGPAT5 was found to be significantly correlated with pre-slaughter weight, carcass weight, and meat weight [ 49 ].…”
Section: Discussionmentioning
confidence: 99%
“…The DNA samples were submitted to the Centre Nacional d’Anàlisi Genòmica (CNAG-CRG, Barcelona, Spain) for whole-genome sequencing on a NovaSeq 6000 instrument (Illumina, San Diego, CA, USA) in paired-end mode, as described by Molinero et al . (2022).…”
Section: Methodsmentioning
confidence: 99%
“…DNA extraction was carried out following a conventional phenol: chloroform protocol (Green & Sambrook, 2017) and used for single nucleotide polymorphism (SNP) genotyping with either the PorcineSNP60 v2 Genotyping BeadChip ( n = 138; Illumina, San Diego, CA, USA), the GGP Porcine HD Array ( n = 256; Illumina) porcine arrays or whole‐genome sequencing ( n = 262, of which 130 were also genotyped using a SNP array) on a NovaSeq 6000 instrument (Illumina) in paired‐end mode, as described by Molinero et al. (2022). SNPs from the SNP arrays that mapped to sex chromosomes or with minor allele frequency <0.05 were discarded from further analyses.…”
Section: Figurementioning
confidence: 99%