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E. R. Gainutdinova

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Open access Aug 2026

Polymorphism of the CSN3 gene and its association with the blood biochemical profile in Holstein cattle

Molecular genetic markers, such as the polymorphism of the kappa-casein gene (CSN3), are a important tool for increasing the efficiency of dairy cattle breeding. The aim of this study was to investigate CSN3 polymorphism in a Holstein cattle population and to assess its associations with blood biochemical parameters reflecting the animals’ metabolic status. In the studied herd (146 animals), allele (A — 0,651, B — 0,349) and genotype frequencies were determined using the PCR-RFLP method: AB (47,9 %; 70 animals), AA (41,1 %; 60 animals), and BB (11,0 %; 16 animals). The results of the biochemical analysis for 12 blood serum parameters were statistically processed using t-test Student in the context of the identified genotypes. Significant associations of CSN3 polymorphism with the biochemical profile were revealed. Carriers of the B allele, especially those with the BB genotype, were characterized by a significantly higher level of protein metabolism indicators (total protein, albumin, urea, creatinine) and activity of enzymes from the classes of aminotransferases (AST, ALT) and hydrolases (alkaline phosphatase), as well as lower concentrations of bilirubin and glucose compared to animals with the AA genotype. The obtained data indicate more intensive metabolism and efficient liver function in cows with the B allele. The results confirm the pleiotropic effect of the CSN3 gene, linking the genetic variant not only to milk quality but also to the body’s metabolic profile. This substantiates the feasibility of using this gene as a marker for the comprehensive assessment and prediction of metabolic adaptation in Holstein cattle breeding programs. The work was carried out according to a state assignment, registration number 125031003428-9

N. Safina, E. Krupin, S. Shakirov et al. · 0 citations
Open access Aug 2026

Complex combination of polymorphic variants of the OPN and IGF-1 genes in a cattle population

The article presents the results of a study on the combined genotypes of OPN (c.8514C/T) and IGF-1 (512T/C) genes in a population of Holstein heifers (n=202). The experiment was conducted at the Lenin Breeding Farm (Atninsky District, Republic of Tatarstan), and laboratory analyses were carried out at the Tatar Research Institute of Agriculture, Kazan Scientific Center of the Russian Academy of Sciences. The relevance of the study is driven by the need to identify genetic markers associated with reproductive traits in cattle, as fertility indicators alongside milk productivity determine the economic efficiency of dairy farming. The OPN and IGF-1 genes are involved in the regulation of embryogenesis, implantation, folliculogenesis, and early embryonic development; however, their combined interaction remains insufficiently studied. Genotyping was performed using PCR-RFLP with restriction endonucleases BseI (for OPN ) and BstSNI (for IGF-1 ). The analysis revealed the presence of all nine possible combined genotype combinations, confirming the genetic heterogeneity of the studied population. The highest frequency was observed for the combined genotype CT/AB (29.7%), while the lowest frequencies were found for CC/BB (2.0%) and CC/AA (3.0%) by OPN / IGF-1 . A pattern of decreasing frequency of combined genotypes was established with an increasing number of homozygous loci. Comparison of the observed and theoretically expected distributions showed no statistically significant deviations (χ² = 4.67; p > 0.05), indicating independent allele combination of the studied genes and the absence of factors disrupting genetic equilibrium in the sample. The obtained data can be applied in breeding programs for marker-assisted selection of parental pairs, genetic passportization, and monitoring of the genetic structure of cattle populations.

N. Safina, E. Mukhanina, E. R. Gainutdinova · 0 citations