Abstract #M75
Section: Animal Health (posters)
Session: Animal Health II
Format: Poster
Day/Time: Monday 7:30 AM–9:30 AM
Location: Exhibit Hall A
Session: Animal Health II
Format: Poster
Day/Time: Monday 7:30 AM–9:30 AM
Location: Exhibit Hall A
# M75
Genome-wide variation for visceral fat deposition in Holstein dairy cows.
Pedro Melendez*1, Scott Poock1, Pablo Pinedo2, Diego Manriquez2, Stephen Moore3, Matt Lucy3, Patrick Pithua1, Jessica Neal3, Jeremy Taylor3, 1College of Veterinary Medicine, University of Missouri, Columbia, MO, 2Department of Animal Sciences, Colorado State University, Fort Collins, CO, 3Division of Animal Sciences, University of Missouri, Columbia, MO.
Key Words: visceral fat, subcutaneous fat, genome-wide association study (GWAS)
Genome-wide variation for visceral fat deposition in Holstein dairy cows.
Pedro Melendez*1, Scott Poock1, Pablo Pinedo2, Diego Manriquez2, Stephen Moore3, Matt Lucy3, Patrick Pithua1, Jessica Neal3, Jeremy Taylor3, 1College of Veterinary Medicine, University of Missouri, Columbia, MO, 2Department of Animal Sciences, Colorado State University, Fort Collins, CO, 3Division of Animal Sciences, University of Missouri, Columbia, MO.
The objective of this study was to assess genetic variation in visceral adiposity in US Holstein cows. The study included adult Holstein cows sampled from a slaughterhouse (Green Bay, WI) during September 2016. Only animals with a body condition score (BCS) between 2.75 and 3.25 were considered. The extent of omental fat at the level of the insertion of the lesser omentum over the pylorus area was assessed. A group of 100 Holstein cows with an omental fold <5 mm in thickness, and a second group of 100 cows with an omental fold ≥20 mm in thickness were sampled. A piece of muscle from the neck was collected from each cow into a sterile container for DNA extraction. Samples were submitted to a commercial laboratory for interrogation of genome-wide genomic variation using the Illumina BovineHD BeadChip. A genome-wide association analysis was performed to test potential associations between fat deposition and genomic variation. A univariate mixed linear model analysis was performed using GEMMA to identify SNP significantly associated with variation in visceral fat deposition. The chip heritability was 0.686 and the estimated additive genetic and residual variance components were 0.427 and 0.074, respectively. Eleven SNP defining 4 QTL regions were found to be significantly associated with visceral fat deposition (P < 0.00001). Two of the QTL were detected with 4 and 5 significantly associated SNP, respectively, while the QTL detected on BTA12 and BTA19 were each detected with only 1 significantly associated SNP. No enriched gene ontology terms were found within the gene networks harboring these genes when supplied to DAVID using either the Bos taurus or human gene ontology databases. We conclude that excessive omental fat in Holstein cows with similar BCS is not caused by a single Mendelian locus and that the trait appears to be at least moderately heritable; consequently, selection to reduce excessive omental fat is possible but would require the generation of predicted transmitting abilities from larger and random samples of Holstein cattle.
Key Words: visceral fat, subcutaneous fat, genome-wide association study (GWAS)