EFFECTS OF BOVINE PPARGC1A AND LTF GENE VARIANTS ON MILK YIELD AND COMPOSITION TRAITS IN HOLSTEIN-FRIESIAN AND JERSEY COWS

Main Article Content

Ozden Cobanoğlu
Sena Ardicli

Abstract

In this study, the association of bovine PPARGC1A and LTF gene polymorphisms with milk production and composition was investigated in dairy cattle. A total of 200 Holstein and Jersey cows, 100 from each breed, were used in the study. Total milk yield, 305-day, and test-day milk yield records were recorded. Milk fat/protein yield and percentage were calculated. Lactation rank, calving season, and service period were also taken into account in the analyses. Genomic DNA was extracted from whole blood samples by the phenol-chloroform-isoamyl alcohol method. Genotyping was carried out by the PCR-RFLP method. In this context, two polymorphisms at PPARGC1A and LTF genes located in intron 9 and 6, respectively, were evaluated. Genotypic/allelic frequencies, compliance with Hardy-Weinberg Equilibrium, and population genetics parameters were calculated. The general linear model (GLM) procedure was used to reveal the individual or interaction effects of these genes on the studied traits. The LTF/EcoRI marker was significantly associated with the lactation milk yield, 305-d milk yield, and 305-d milk fat yield in Jersey cattle. Moreover, the PPARGC1A×LTF interaction affected the test-d milk yield, test-d protein yield, 305-d milk yield, and 305-d milk fat yield in Jersey cattle. The CCAA and TTAB genotypes were found to be desirable for milk yield and fat content in Jersey cattle. The PPARGC1A×LTF interaction was also significantly associated with the test-d protein yield in the entire study population. This study may provide important knowledge on the genetic markers affecting milk production and the selection strategies in dairy cattle.

Downloads

Download data is not yet available.

Article Details

Section
Articles

References

Arany, Z. (2008). PGC-1 coactivators and skeletal muscle adaptations in health and disease. Current opinion in genetics & development, 18, 426-434.
Ardicli, S., H. Samli, B. Soyudal, D. Dincel & F. Balci (2019a). Evaluation of candidate gene effects and environmental factors on reproductive performance of Holstein cows. South African Journal of Animal Science, 49, 379-374.
Ardicli, S., H. Samli, B. Vatansever, B. Soyudal, D. Dincel & F. Balci (2019b). Comprehensive assessment of candidate genes associated with fattening performance in Holstein–Friesian bulls. Archives Animal Breeding, 62, 9-32.
Asadollahpour Nanaei, H., S. Ansari Mahyari & M. Edriss (2016). Single nucleotide polymorphism of the lactoferrin gene and its association with milk production and reproduction traits in Iranian Holstein cattle. Journal of Livestock Science and Technologies, 4, 71-76.
Ateya, A., Y. El-Seady, S. Atwa, B. Merghani & N. Sayed (2016). Novel single nucleotide polymorphisms in lactoferrin gene and their association with mastitis susceptibility in Holstein cattle. Genetika, 48, 199-210.
Botstein, D., R. L. White, M. Skolnick & R. W. Davis (1980). Construction of a genetic linkage map in man using restriction fragment length polymorphisms. American journal of human genetics, 32, 314.
Eivers, S., B. McGivney, J. Gu, D. MacHugh, L. Katz & E. Hill (2012). PGC‐1α encoded by the PPARGC1A gene regulates oxidative energy metabolism in equine skeletal muscle during exercise. Animal genetics, 43, 153-162.
El‐Domany, W. B., H. A. Radwan, A. I. Ateya, H. H. Ramadan, B. H. Marghani & S. M. Nasr (2019). Genetic Polymorphisms in LTF/EcoRI and TLR4/AluI loci as candidates for milk and reproductive performance assessment in Holstein cattle. Reproduction in Domestic Animals, 54, 678-686.
Ensembl Genome Browser (2022). https://www.ensembl.org/index.html last access: 18.10.2022.
Falconer, D. S. & T. F. C. Mackay. (1996). Introduction to quantitative genetics. Harlow, England: Pearson Education Ltd.
Fleming, A., E. A. Abdalla, C. Maltecca & C. F. Baes (2018). Invited review: Reproductive and genomic technologies to optimize breeding strategies for genetic progress in dairy cattle. Archives Animal Breeding, 61, 43-57.
Green M & Sambrook, J. (2012). Isolation of high-molecular-weight DNA from mammalian cells using proteinase K and phenol. In Molecular Cloning: A Laboratory Manual, 47-48. Cold Spring Harbor, New York, USA: Cold Spring Harbor Laboratory Press.
Kaminski, S., K. Oleński, P. Brym, T. Malewski & A. Sazanov (2006). Single nucleotide polymorphism in the promoter region of the lactoferrin gene and its associations with milk performance traits in Polish Holstein-Friesian cows. Russian journal of genetics, 42, 924-927.
Khatkar, M. S., P. C. Thomson, I. Tammen & H. W. Raadsma (2004). Quantitative trait loci mapping in dairy cattle: review and meta-analysis. Genetics Selection Evolution, 36, 163-190.
Kowalewska-Łuczak, I., H. Kulig & M. Kmieć (2010) Associations between the bovine PPARGC1A gene and milk production traits. Czech Journal of Animal Science, 55, 195-199.
Lacorte, G., M. Machado, M. Martinez, A. Campos, R. Maciel, R. Verneque, R. Teodoro, M. Peixoto, M. Carvalho & C. Fonseca (2006). DGAT1 K232A polymorphism in Brazilian cattle breeds. Genetics and Molecular Research, 5, 475-482.
Le Hir, H., A. Nott & M. J. Moore (2003). How introns influence and enhance eukaryotic gene expression. Trends in biochemical sciences, 28, 215-220.
Lin, J., C. Handschin & B. M. Spiegelman (2005). Metabolic control through the PGC-1 family of transcription coactivators. Cell metabolism, 1, 361-370.
Maletić, M., S. Kanjac, N. Đelić, N. Lakić, M. Pavlović, S. Nedić & Z. Stanimirović (2013) Analysis of lactoferin gene polymophism and its association to milk quality and mammary gland health in Holstein-Friesian cows. Acta Veterinaria-Beograd, 63, 487-498.
NRC (2001). Nutrient Requirements of Dairy Cattle. Washington, DC., USA: Natl. Acad. Press.
O‘Halloran, F., B. Bahar, F. Buckley, O. O’Sullivan, T. Sweeney & L. Giblin (2009) Characterisation of single nucleotide polymorphisms identified in the bovine lactoferrin gene sequences across a range of dairy cow breeds. Biochimie, 91, 68-75.
Pasandideh, M., M. Mohammadabadi, A. Esmailizadeh & A. Tarang (2015). Association of bovine PPARGC1A and OPN genes with milk production and composition in Holstein cattle. Czech Journal of Animal Science, 60, 97-104.
Schennink, A., H. Bovenhuis, K. M. Léon‐Kloosterziel, J. A. Van Arendonk & M. H. Visker (2009). Effect of polymorphisms in the FASN, OLR1, PPARGC1A, PRL and STAT5A genes on bovine milk‐fat composition. Animal Genetics, 40, 909-916.
Schmid, M. & J. Bennewitz (2017). Invited review: Genome-wide association analysis for quantitative traits in livestock–a selective review of statistical models and experimental designs. Archives Animal Breeding, 60, 335-346.
Tambasco, D., C. Paz, M. Tambasco‐Studart, A. Pereira, M. Alencar, A. Freitas, L. Coutinho, I. Packer & L. d. A. Regitano (2003). Candidate genes for growth traits in beef cattle crosses Bos taurus× Bos indicus. Journal of Animal Breeding and Genetics, 120, 51-56.
Weikard, R., C. Kühn, T. Goldammer, G. Freyer & M. Schwerin (2005). The bovine PPARGC1A gene: molecular characterization and association of an SNP with variation of milk fat synthesis. Physiological Genomics, 21, 1-13.
Wojdak-Maksymiec, K., M. Kmiec & J. Ziemak (2006). Associations between bovine lactoferrin gene polymorphism and somatic cell count in milk. Veterinarni Medicina Praha, 51, 14.
Zhang, Y., K. Ma, P. Sadana, F. Chowdhury, S. Gaillard, F. Wang, D. P. McDonnell, T. G. Unterman, M. B. Elam & E. A. Park (2006). Estrogen-related receptors stimulate pyruvate dehydrogenase kinase isoform 4 gene expression. Journal of Biological Chemistry, 281, 39897-39906.
Zheng, J., J. L. Ather, T. S. Sonstegard & D. E. Kerr (2005). Characterization of the infection-responsive bovine lactoferrin promoter. Gene, 353, 107-117.