Aug 2026· International Journal of Veterinary Medicine· 0 citations· 21 references
Abstract
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
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· Legal regulation in veterina...· 0 citations
The study aimed to detect the genotype of the FABP gene T>A: 3499 in a sample of 41 buffaloes to investigate the relation between this genotype and several productive traits. The study was conducted from October 1st, 2024, to January 30th, 2025, at the Ruminant Research Station in Abu Ghraib. By detecting the genotype of the FABP gene at the T>A: 3499 site, two genotypes, TT and TA, were identified. Their distribution ratios were 80.49% and 19.51%, respectively (P≤0.01). The allelic frequencies for the T and A alleles were 0.90 and 0.10, respectively. Significant differences (P≤0.01) were found in body length, Heart girth, and body temperature during the 2nd month of the study. Regarding milk production and composition, the first month was represented by milk density, the 2nd month by the daily milk yield (DMY), and the 3rd by DMY and density. The TA genotype showed superiority over the TT genotype for heart girth, milk density in the first month, DMY in the 3rd month. In conclusion, the study of genetic structures in the FABP gene: T>A: 3499, the resulting changes can be used in the process of genetic improvement of Iraqi buffaloes performance.
S. K. Kazem, N. N. Al-Anbari, S. N. Alwaeli· IRAQI JOURNAL OF AGRICULTURA...· 0 citations
Objectives: To determine the association of polymorphism rs10741657 in the CYP2R1 gene with vitamin D deficiency in apparently healthy subjects.
Method: The prospective, case-control study was conducted from June 2023 to January 2024 at the CREAM Lab of Army Medical College, Rawalpindi, and comprised vitamin D-deficient cases in group A and healthy controls in group B. Genotyping of rs10741657 polymorphism in the CYP2R1 gene was performed using allele-specific polymerase chain reaction (AS-PCR). Genotypic and allelic frequencies, Hardy–Weinberg equilibrium, and genetic inheritance models were analysed using SNPStats, a web-based statistical software for genetic association studies.
Results: Of the 300 subjects with a mean age of 43.56 ± 15.26 years, 150 (50%) were in group A, comprising 91 (61%) females and 59 (39%) males, with a mean age of 44.49 ± 15.12 years. There were 150 (50%) controls in group B, including 83 (55%) males and 67 (45%) females, with a mean age of 42.63 ± 15.40 years. The genotypic frequencies in group A were A/A 45(30%), A/C 101(67.34%), C/C 4(2.66%). The corresponding values in group B were 39(26%), 110(73.34%) and 1(0.66%). The allele frequency of A was 191 (64%) in vitamin D-deficient cases and 188 (63%) in healthy controls (p = 0.8775), while the C allele frequency was 109 (36%) in cases and 112 (37%) in controls (p = 0.8401). The genotype frequencies in cases were A/A 45 (30%), A/C 101 (67%), and C/C 4 (2.67%), compared to A/A 39 (26%), A/C 110 (73%), and C/C 1 (0.67%) in controls, with no statistically significant difference observed between the groups (p > 0.05). The inheritance genetic models suggested no association with vitamin D deficiency (p>0.05); codominant model – A/C odds ratio 0.70 (95% confidence interval: 0.45-1.23), C/C odds ratio 4.00 (95% confidence interval: 0.45-36.96); dominant model odds ratio 0.80 (95% confidence interval: 0.49-1.35); recessive model odds ratio 4.00 (95% confidence interval: 0.45-36.96); and overdominant model odds ratio 0.70 (95% confidence interval: 0.45-1.23).
Conclusion: The A allele was found to be the most common variant of rs10741657 in both the groups. The rs10741657 polymorphism was not a risk for the susceptibility to vitamin D deficiency. No correlation of genotype with serum vitamin D levels was noted.
Key Words: Allele-specific polymerase chain reaction, Single nucleotide polymorphism, Calcitriol, 25 Hydroxylase, Vitamin D binding protein.
Abdur Rauf, Asifa Majeed· JOURNAL OF PAKISTAN MEDICAL...· 0 citations
The study was conducted to identify the genotypes of single-nucleotide polymorphisms (SNPs) in the GHRL, GAST, and SCTR genes for early performance assessment in Smena 9 poultry. The study was performed on 170 CM5/CM7 roosters and 750 final-hybrid CM5679 broiler chickens with individual feed intake monitoring at ages 36-42 days and 21-42 days, respectively. Groups were formed randomly. Polymorphisms were identified using genotyping using real-time PCR with fluorescently labelled probes. CM5 roosters homozygous for the T allele and heterozygous (TC) for the rs312295326 polymorphism demonstrated improved feed conversion in the 36-42-day period. The feed conversion ratio (FCR) for this period was 1.89 for birds with the TT genotype and 1.91 for TC. The CC genotype was associated with a 7.3-8.5% decrease in FCR (p<0.05). Statistically significant differences in feed conversion efficiency (FCR) were observed in broilers with polymorphic variants of the SCTR gene (rs314830059 and rs736374789). In birds of both sexes with the GG genotype of the rs314830059 polymorphic variant, a decrease in FCR by 8.6-16.9% was observed compared to the GT and TT genotypes from the 24th to the 33rd day (p<0.05). Females with the GG genotype of the rs736374789 polymorphism showed a lower FCR (2.18 to 2.48) compared to individuals with the GT genotype (2.41 to 2.89) on days 39, 40, and 42 (p < 0.05). The identified SNPs in the GHRL (rs312295326), SCTR (rs314830059), and SCTR (rs736374789) genes can be integrated into genomic selection programmes aimed at reducing FCR in meat-producing chickens.
L. G. Korshunova, E. I. Kulikov, D. M. Dmitrenko et al.· Achievements of Science and...· 0 citations
The aim of the study was to evaluate the effect of 12 complex GN and LEP genotypes on cow productivity in order to identify consistently effective allele combinations that account for genotype-environment interactions, and to develop personalized strategies for herd breeding and management. The conducted study revealed a significant association between complex genotypes of the somatotropin (GH, LV polymorphism) and leptin (LEP, R25C and A80V polymorphisms) genes and milk productivity in Holstein cows. A study of 120 animals (60 animals each from two agricultural organizations) showed a marked uneven distribution of the 12 analyzed genotypes in both herds, due to the farm breeding priorities. A key result was the identification of the GHLVR25CRRA80VAA genotype as the most promising for breeding for high lifetime milk productivity. Animals with this genotype consistently demonstrated maximum milk yields in the first and third lactations and lifetime productivity, demonstrating stability and high genetic potential. In parallel, genotypes associated with milk quality traits were identified. For example, in animals carrying the GHLVR25CCCA80VVV genotype at Organization "K," the lifetime fat and protein content was 3.92 and 3.27 %, respectively. Animals with the GHLVR25CCRA80VAA genotype in Organization "P" had a maximum fat content of 4.13 % while maintaining high milk yield. The study confirmed the critical influence of environmental factors (feeding, management) on the realization of genetic potential. The significantly higher milk yields in Organization "P" compared to Organization "K" highlight the need for a systematic approach combining genetic selection with improved livestock production technologies. The obtained data demonstrate that the complex GH and LEP genotypes serve as informative markers for predicting milk productivity and the adaptive potential of cows.
A. Yaryshkin, O. Shatalina, A. A. Zyryanova· Agricultural science Euro-No...· 0 citations
β-lactoglobulin (LGB) is a major whey protein in ruminant milk. Its genetic polymorphism is of great interest due to its influence on the qualitative and technological properties of milk. The experiment was con-ducted within a small Holstein-Friesian population reared at the Academic Technological Complex of Trakia University – Stara Zagora and aims to determine the gene and genotype frequency distribution of the two major alleles of the β-lactoglobulin locus – A and B. The molecular analyses of the LGB gene were completed using the Axiom Bovine Genotyping Array v3. The observed frequencies were compared to the expected val-ues according to the Hardy-Weinberg principle. The results obtained demonstrate that the frequency of allele A is 0.73, while allele B has a frequency of 0.27. The performed χ² test revealed the studied population is in a state of genetic equilibrium (χ² = 0.0189332, df=1, P>0.05).
Albena Bekyarova, T. Koynarski· Tradition and modernity in v...· 0 citations