4.7 Article

Genetic variance of metabolomic features and their relationship with body weight and body weight gain in Holstein cattle

Journal

JOURNAL OF ANIMAL SCIENCE
Volume 97, Issue 9, Pages 3832-3844

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/jas/skz228

Keywords

cattle; correlation; genetic variance; heritability; metabolomic features; quantitative traits

Funding

  1. Danish Strategic Research Council (GenSAP: Centre for Genomic Selection in Animals and Plants) [12-132452]

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In recent years, metabolomics has been used to clarify the biology underlying biological samples. In the field of animal breeding, investigating the magnitude of genetic control on the metabolomic profiles of animals and their relationships with quantitative traits adds valuable information to animal improvement schemes. In this study, we analyzed metabolomic features (MFs) extracted from the metabolomic profiles of 843 male Holstein calves. The metabolomic profiles were obtained using nuclear magnetic resonance (NMR) spectroscopy. We investigated 2 alternative methods to control for peak shifts in the NMR spectra, binning and aligning, to determine which approach was the most efficient for assessing genetic variance. Series of univariate analyses were implemented to elucidate the heritability of each ME Furthermore, records on BW and ADG from 154 to 294 d of age (ADG(154-294)), 294 to 336 d of age (ADG(294-336)), and 154 to 336 d of age (ADG(154-339)) were used in a series of bivariate analyses to establish the genetic and phenotypic correlations with MFs. Bivariate analyses were only performed for MFs that had a heritability significantly different from zero. The heritabilities obtained in the univariate analyses for the MFs in the binned data set were low (<0.2). In contrast, in the aligned data set, we obtained moderate heritability (0.2 to 0.5) for 3.5% of MFs and high heritability (more than 0.5) for 1% of MFs. The bivariate analyses showed that similar to 12%, similar to 3%, similar to 9%, and similar to 9% of MFs had significant additive genetic correlations with BW, ADG(154-294) ADG(294-336), and ADG(154-336), respectively. In all of the bivariate analyses, the percentage of significant additive genetic correlations was higher than the percentage of significant phenotypic correlations of the corresponding trait. Our results provided insights into the influence of the underlying genetic mechanisms on MFs. Further investigations in this field are needed for better understanding of the genetic relationship among the MFs and quantitative traits.

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