PSI-B-27 Association of multiple SNP in the LRP4 gene with features of the cattle elemental status

Abstract

Abstract Bovine syndactyly is an autosomal monogenic recessive trait associated with multiple mutations in the LRP4 gene encoding low-density lipoprotein receptor-related protein 4. This protein is a specific facilitator of sclerostin-mediated inhibition of both Wnt1/ β-catenin signaling and osteocyte-secreted bone formation. It is assumed that sclerostin induces a decrease in extracellular pH and promotes the release of calcium ions from mineralized substrates. Therefore, mutations in the LRP4 gene might be associated with changes in the elemental status. The aim of this research was to evaluate the elemental composition of serum in cattle carrying multiple SNP in the LRP4 gene (16 trial animals) compared to animals without such mutations (62 control animals). DNA samples from 78 Black Pied cattle were sequenced with a TruSeq Bovine Parentage Sequencing Panel (Illumina, USA) on a MiSeq Illumina platform following by SNP analysis. The elemental composition of the serum was determined using ICP-AES and ICP-MS. The levels of Ca and P, crucial bone elements, were higher in trial cattle than in control group by 12.9% (P = 0.004) and 22.5% (P = 0.008), respectively. The level of V affecting the uniform distribution of calcium salts in bones, was higher in trial group than in control one by 34.5% (P = 0.001). The concentrations of Mn and Mg were higher in trial group than in control one by 23.6% (P = 0.026) and 10.0% (P = 0.044), respectively. The Sr level in trial cattle was higher by 18.8% (P = 0.04) that may indicate the rickets-like state. A similar trend was observed for toxic metals As and Li. This study demonstrates the association of the LRP4 multiple SNP and the changes in cattle elemental status. Moreover, such heterozygous animals have a higher risk of mineral metabolism disorders. This research was supported by The Ministry of Science and Higher Education of the Russian Federation (Project No. 0526-2019-0001).