Research Article
BibTex RIS Cite

Year 2025, Volume: 44 Issue: 2, 133 - 145, 31.12.2025
https://doi.org/10.30782/jrvm.1798308

Abstract

References

  • Utrera ÁR, Van Vleck LD. Heritability estimates for carcass traits of cattle: a review. Genetics and Molecular Research, 2004; 3(3), 380-394.
  • Casas E, White SN, Riley DG, et al. Assessment of single nucleotide polymorphisms in genes residing on bovine chromosome 5: associations with beef carcass traits. Journal of Animal Science, 2000; 78(5), 1224-1230.
  • Schenkel FS, Miller SP, Jiang Z, et al. Association of a single nucleotide polymorphism in the calpastatin gene with carcass and meat quality traits of beef cattle. Journal of Animal Science, 2006; 84(2), 291-299.
  • Ardicli S, Dincel D, Samli H, et al. Effects of polymorphisms at LEP, CAST, CAPN1, GHR, FABP4 and DGAT1 genes on fattening performance and carcass traits in Simmental bulls. Archives Animal Breeding, 2017a; 60(2), 61-70.
  • Liefers SC, Te Pas MFW, Veerkamp RF, et al. Associations between leptin gene polymorphisms and production, live weight, energy balance, feed intake, and fertility in Holstein heifers. Journal of Dairy Science, 2002; 85(6), 1633-1638.
  • Liefers SC, Veerkamp RF, Te Pas MFW, et al. Leptin promoter mutations affect leptin levels and performance traits in dairy cows 1. Animal Genetics, 2005; 36(2), 111-118.
  • Kumar S, Dahiya S, Magotra A, et al. Study of Polymorphism in exon 3 region of leptin Gene in Harnali sheep. The Pharma Innovation Journal, 2020; 9(2), 360-363.
  • Salgado Pardo JI, Delgado Bermejo JV, González Ariza A, et al. Candidate genes and their expressions involved in the regulation of milk and meat production and quality in goats (Capra hircus). Animals, 2022; 12(8), 988.
  • Banos G, Woolliams JA, Woodward BW, et al. Impact of single nucleotide polymorphisms in leptin, leptin receptor, growth hormone receptor, and diacylglycerol acyltransferase (DGAT1) gene loci on milk production, feed, and body energy traits of UK dairy cows. Journal of Dairy Science, 2008; 91(8), 3190-3200.
  • Oztabak K, Toker NY, Un C, et al. Leptin gene polymorphisms in native Turkish cattle breeds. Kafkas Üniversitesi Veteriner Fakültesi Dergisi, 2010; 16(6).
  • De Matteis G, Scatà MC, Grandoni F, et al. Association analyses of single-nucleotide polymorphisms in the leptin and leptin receptor genes on milk and morphological traits in Holstein cows. Open Journal of Animal Sciences, 2012; 2(3), 174-182.
  • Kawaguchi F, Okura K, Oyama K, et al. Identification of leptin gene polymorphisms associated with carcass traits and fatty acid composition in Japanese Black cattle. Animal Science Journal, 2017; 88(3), 433-438.
  • Ardicli S, Samli H, Vatansever B, et al. Comprehensive assessment of candidate genes associated with fattening performance in Holstein–Friesian bulls. Archives Animal Breeding, 2019a; 62(1), 9-32.
  • Prihandini PW, Hariyono DNH, Sari APZNL, et al. Association between GH, PRL, LEP, and PIT-1 gene polymorphisms and growth traits in Indonesian Rambon indigenous cattle. Tropical Animal Health and Production, 2025; 57(2), 56.
  • Singh SK, Rout PK, Agarwal R, et al. Characterization of exon 2 and intron 2 of leptin gene in Indian goats. Animal Biotechnology, 2009; 20(2), 80-85.
  • Korkmaz-Agaoglu O, Elmaz O, Akyuz B, et al. Identifying polymorphism in some genes and their effects on growth performance in Honamli and hair goat breeds. Genetika, 2019; 51(3), 995-1008.
  • Senturk N, Selvi TN, Demir M, et al. The impact of LEP gene polymorphisms located at exon 2 (LEP-HinfI) and intron 2 (LEP-Sau3AI) on growth and reproductive traits in Saanen goats. Archives Animal Breeding, 2024; 67(4), 523-531.
  • Stone RT, Kappes SM, Beattie CW. The bovine homolog of the obese gene maps to chromosome 4. Mammalian Genome, 1996; 7,399–400.
  • Nkrumah JD, Keisler DH, Crews Jr DH, et al. Genetic and phenotypic relationships of serum leptin concentration with performance, efficiency of gain, and carcass merit of feedlot cattle. Journal of Animal Science, 2007; 85(9), 2147-2155.
  • Giblin L, Butler ST, Kearney BM, et al. Association of bovine leptin polymorphisms with energy output and energy storage traits in progeny tested Holstein-Friesian dairy cattle sires. BMC Genetics, 2010; 11(1), 73.
  • Friedman JM, Halaas JL. Leptin and the regulation of body weight in mammals. Nature, 1998; 395(6704), 763-770.
  • Yazdani H, Rahmani HR, Edris MA, et al. Association between A59V polymorphism in exon 3 of leptin gene and reproduction traits in cows of Iranian Holstein. African Journal of Biotechnology, 2010; 9(36).
  • Ardicli S, Samli H, Dincel D, et al. Individual and combined effects of CAPN1, CAST, LEP and GHR gene polymorphisms on carcass characteristics and meat quality in Holstein bulls. Archives Animal Breeding, 2017b; 60(3), 303-313.
  • Ge W, Davis ME, Hines HC, et al. Association of a genetic marker with blood serum insulin-like growth factor-I concentration and growth traits in Angus cattle. Journal of Animal Science, 2001; 79(7), 1757-1762.
  • Bishop MD., Tavakkol A, Threadgill DW, et al. Somatic cell mapping and restriction fragment length polymorphism analysis of bovine insulin-like growth factor I. Journal of Animal Science, 1991; 69(11), 4306-4311.
  • Miller JR, Thomsen PD, Dixon SC, et al. Synteny mapping of the bovine IGHG2, CRC and IGF1 genes. Animal Genetics,1992; 23, 51-58.
  • Li C, Basarab J, Snelling WM, et al. Assessment of positional candidate genes myf 5 and igf 1 for growth on bovine chromosome 5 in commercial lines of Bos taurus. Journal of Animal Science, 2004; 82(1), 1-7.
  • Curi RA, De Oliveira HN, Silveira AC, et al. Effects of polymorphic microsatellites in the regulatory region of IGF1 and GHR on growth and carcass traits in beef cattle. Animal Genetics, 2005; 36(1), 58-62.
  • Siadkowska E, Zwierzchowski L, Oprzadek J, et al. Effect of polymorphism in IGF-1 gene on production traits in Polish Holstein-Friesian cattle. Animal Science Papers and Reports, 2006; 24(3), 225-37.
  • Ardicli S, Samli H, Dincel D, et al. Relationship of the bovine IGF1, TG, DGAT1 and MYF5 genes to meat colour, tenderness and cooking loss. Journal of the Hellenic Veterinary Medical Society, 2018; 69(3), 1077-1087.
  • Weintraub H, Davis R, Tapscott S, et al. The myoD gene family: nodal point during specification of the muscle cell lineage. Science, 1991;251(4995):761–766.
  • Ujan J, Zan L, Ujan S, et al. Back fat thickness and meat tenderness are associated with a 526 T/A mutation in the exon 1 promoter region of the MyF-5 gene in Chinese Bos taurus. Genetics and Molecular Research, 2011;10(4):3070–3079.
  • Zhao C, Raza SHA, Khan R, et al. Genetic variants in MYF5 affected growth traits and beef quality traits in Chinese Qinchuan cattle. Genomics, 2020;112(4): 2804–2812.
  • Bhuiyan MSA, Kim NK, Cho YM, et al. Identification of SNPs in MYOD gene family and their associations with carcass traits in cattle. Livestock Science, 2009; 126(1-3), 292-297.
  • Kisacova J, Kubek A, Melus V, et al. Genetic polymorphism of Myf-5 and myostatin in Charolais breed. Journal of Agrobiology, 2009; 26: 7-11.
  • Sagsoz Y, Coban O., Lacin E, et al. Esmer ve Şarole x Esmer danaların besi performansı ve karkas özellikleri. Atatürk Üniversitesi Ziraat Fakültesi Dergisi, 2005; 36(2), 163-169.
  • Ekiz B, Yilmaz A, Ozcan M, et al. Carcass measurements and meat quality of Turkish Merino, Ramlic, Kivircik, Chios and Imroz lambs raised under an intensive production system. Meat Science, 2009; 82(1), 64-70.
  • Ekiz B, Ekiz EE, Kocak O, et al. Effect of pre-slaughter management regarding transportation and time in lairage on certain stress parameters, carcass and meat quality characteristics in Kivircik lambs. Meat Science, 2012; 90(4), 967-976.
  • Beriain MJ, Horcada A, Purroy A, et al. Characteristics of Lacha and Rasa Aragonesa lambs slaughtered at three live weights. Journal of Animal Science, 2000; 78(12), 3070-3077. 40. Falconer DS, Mackay TFC. Introduction to Quantitative Genetics, Harlow, Pearson Education Ltd., ISBN 0582243025,1996.
  • Nei M, Roychoudhury, A. Sampling variances of heterozygosity and genetic distance, Genetics, 1974; 76, 379–390.
  • Botstein D, White RL, Skolnick M, et al. Construction of a genetic linkage map in man using restriction fragment length polymorphisms. American Journal of Human Genetics, 1980; 32(3), 314.
  • Lacorte GA, Machado MA, Martinez ML, et al. DGAT1 K232A polymorphism in Brazilian cattle breeds. Genetics and Molecular Research, 2006; 5(3), 475-482.
  • Houseknecht K, Baile CA, Matteri RL, et al. The biology of leptin: a review. Journal of Animal Science, 1998; 76(5), 1405-1420.
  • Florini JR, Ewton DZ, Coolican SA. Growth hormone and the insulin-like growth factor system in myogenesis. Endocrine Reviews, 1996; 17(5), 481-517.
  • Trujillo AI, Casal A, Penagaricano F, et al. Association of SNP of neuropeptide Y, leptin, and IGF-1 genes with residual feed intake in confinement and under grazing condition in Angus cattle. Journal of Animal Science, 2013; 91(9), 4235-4244.
  • Dar MR, Singh M, Thakur S, et al. Exploring the relationship between polymorphisms of leptin and IGF-1 genes with milk yield in indicine and taurine crossbred cows. Tropical Animal Health and Production, 2021; 53(4), 413.
  • Montelli NLLL, Alvarenga TIRC, Almeida AK., et al. Associations of feed efficiency with circulating IGF-1 and leptin, carcass traits and meat quality of lambs. Meat Science, 2021; 173, 108379.
  • Darwish AM, Abdelhafez MA, Abdel-Hamid ZG, et al. Correlation analysis between polymorphism of leptin and IGFI genes and body measurements in Barki and Farafra sheep. Beni-Suef University Journal of Basic and Applied Sciences, 2023; 12(1), 119.
  • Morissette MR, Cook SA, Buranasombati C, et al. Myostatin inhibits IGF-I-induced myotube hypertrophy through Akt. American Journal of Physiology-Cell Physiology, 2009; 297, C1124–C1132.
  • Ardicli S, Dincel D, Samli H, et al. Association of polymorphisms in lipid and energy metabolism-related genes with fattening performance in Simmental cattle. Animal Biotechnology, 2023; 34(8), 3428-3440.
  • Bongiorni S, Mancini G, Chillemi G, et al. Identification of a short region on chromosome 6 affecting direct calving ease in Piedmontese cattle breed. PLoS One, 2012; 7(12), e50137.
  • Carvalho TDD, Siqueira F, Torres Júnior RADA, et al. Association of polymorphisms in the leptin and thyroglobulin genes with meat quality and carcass traits in beef cattle. Revista Brasileira de Zootecnia, 2012; 41, 2162-2168.
  • Woronuk GN, Marquess FL, James ST, et al. Association of leptin genotypes with beef cattle characteristics. Animal Genetics, 2012; 43(5), 608-610.
  • Sedykh TA, Kalashnikova LA, Gizatullin RS et al. Effects of leptin gene polymorphism on beef cattle performance. Russian Agricultural Sciences, 2020; 46(6), 614-618.
  • Matsumoto H, Kimura S, Nagai Y, et al. Leptin gene contributes to beef marbling standard, meat brightness, meat firmness, and beef fat standard of the Kumamoto sub‐breed of Japanese Brown cattle. Animal Science Journal, 2022; 93(1), e13698.
  • Couto CE, Livramento KGD, Paiva LV, et al. DGAT and LEP gene polymorphisms and their association with carcass characteristics and the lipid profile of meat from Nellore cattle. Revista Brasileira de Saúde e Produção Animal, 2023; 24, 20220012.
  • Valencia CPL, Franco LÁÁ, Herrera DH. Association of single nucleotide polymorphisms in the CAPN, CAST, LEP, GH, and IGF-1 genes with growth parameters and ultrasound characteristics of the Longissimus dorsi muscle in Colombian hair sheep. Tropical Animal Health and Production, 2022; 54(1), 82.
  • Liu Y, Kong L, Li S, et al. Correlation and regression analysis of GH and IGF-1 genes in Liaoning cashmere goats with body size and other production performance. Journal of Genetic Engineering and Biotechnology, 2024; 22(4), 100440.
  • Kader Esen V, Esen S. Association of the IGF1 5′ UTR polymorphism in meat-type sheep breeds considering growth, body size, slaughter, and meat quality traits in Turkey. Veterinary Sciences, 2023; 10(4), 270.
  • Meira AN, Montenegro H, Coutinho L., et al. Single nucleotide polymorphisms in the growth hormone and IGF type-1 (IGF1) genes associated with carcass traits in Santa Ines sheep. Animal, 2019; 13(3), 460-468.
  • Islam KK, Vinsky M, Crews RE, et al. Association analyses of a SNP in the promoter of IGF1 with fat deposition and carcass merit traits in hybrid, Angus and Charolais beef cattle. Animal Genetics, 2009; 40, 766–769.
  • Pereira AGT, Utsunomiya YT, Milanesi M, et al. Pleiotropic genes affecting carcass traits in Bos indicus (Nellore) cattle are modulators of growth. PLoS One, 2016; 11(7), e0158165.
  • Cobanoglu O, Ardicli S.Genetic variation at the OLR1, ANXA9, MYF5, LTF, IGF1, LGB, CSN3, PIT1, MBL1, CACNA2D1, and ABCG2 loci in Turkish Grey Steppe, Anatolian Black, and East Anatolian Red cattle. Turkish Journal of Veterinary & Animal Sciences, 2022; 46(3), 494-504.
  • Gerasimov NP, Dzhulamanov KM, Lebedev SV, et al. Effect of IGF-1 C472T, GH C2141G, and GHR T914A polymorphisms on growth performance and feed efficiency in young Kazakh white-headed cattle. Veterinary World, 2023; 16(8), 1584.
  • Saleh AA, Hassan TG, El-Hedainy DK, et al. IGF-I and GH Genes polymorphism and their association with milk yields, composition and reproductive performance in Holstein–Friesian dairy cattle. BMC Veterinary Research, 2023; 20(1), 341.
  • Sen U, Gokcek, D, Yılmaz OF, et al. Relationships among growth, carcass characteristics, and Myf5, Myf6, MyoD, and MyoG genes expression level in Saanen male kids with varying slaughter weights. Animals, 2024; 15(1), 16.
  • Daldaban F, Arslan K, Aksel EG, et al. Polymorphism of the STAT5A and MYF-5 genes in Anatolian water buffalo. Turkish Journal of Veterinary & Animal Sciences, 2020; 44(2), 284-289.
  • Zayed MA, El-Kholy AF, Shehata MF, et al. Genetic contribution of myogenic factor 5 and growth hormone genes for live body measurements, carcass traits and meat quality of dromedary camel. Journal of Animal and Poultry Production, 2022; 13(10), 153-156.
  • Fadhil M, Zülkadir U. Association between polymorphisms of Myf5, MSTN and CAST genes and fattening performance in Brown Swiss and Holstein cattle breeds. Animal Biotechnology, 2021; 32(1), 121-129.
  • Ardicli S, Ustuner H, Arslan O, et al. Variability of CAPN1 g. 5709 C> G and MYF5 g. 1911 A> G Polymorphisms in Beef Cattle Imported from Brazil to Turkey. Lalahan Hayvancılık Araştırma Enstitüsü Dergisi, 2019b; 59(2), 72-78.
  • MacNeil MD, Nkrumah JD, Woodward BW, et al. Genetic evaluation of Angus cattle for carcass marbling using ultrasound and genomic indicators. Journal of Animal Science, 2010; 88(2), 517-522.
  • Ardicli S. Genetik ve postmortem mekanizmaların sığır eti renk özellikleri üzerine etkisi. Uludağ Üniversitesi Veteriner Fakültesi Dergisi, 2018; 37(1), 49-59. https://doi.org/10.30782/uluvfd.398947
  • Ustuner H, Ardicli S, Arslan O, Brav FC. Fattening performance and carcass traits of imported Simmental bulls at different initial fattening age. Large Animal Review, 2020; 26: 161-165.
  • Ustuner H, Ardicli S, Arslan O. Determination of the alterations in quality parameters and consumer preference of dry-aged beef based on different periods of ageing using a purposive incubator. Journal of the Hellenic Veterinary Medical Society, 2021; 72(1): 2669-2676. https://doi.org/10.12681/jhvms.26749
  • Ardicli S, Ardicli O, Ustuner H. Unraveling the Complexities of Beef Marination: Effect of Marinating Time, Marination Treatments, and Breed. Foods, 2024, 13(18): 2979. https://doi.org/10.3390/foods13182979
  • Ardicli, S. Analysis of IGF1 C472T and TG C422T polymorphisms in Turkish Grey Steppe and Holstein crossbred bulls. 2018. Uludağ Üniversitesi Veteriner Fakültesi Dergisi, 37(1), 21-28.
  • Ardicli, S., Aldevir, O., Aksu, E., & Gumen, A. The variation in the beta-casein genotypes and its effect on milk yield and genomic values in Holstein-Friesian cows. 2023. Animal Biotechnology, 34(8), 4116-4125.
  • Ardicli, S., Aldevir, Ö., Aksu, E., Kucuk, K., & Gümen, A. Associations of bovine beta-casein and kappa-casein genotypes with genomic merit in Holstein Friesian cattle. 2024. Archives Animal Breeding, 67(1), 61-71.
  • Ardicli, S., Senturk, N., Bozkurt, B., Babayev, H., Selvi, T., Skolnick, S., ... & Cobanoglu, O. The impact of genetic variants related to the fatty acid metabolic process pathway on milk production traits in Jersey cows. 2024. Animal Biotechnology, 35(1), 2396421.
  • Saleh, A.A., Hassan, T.G.M., EL-Hedainy, D.K.A. et al. IGF-I and GH Genes polymorphism and their association with milk yields, composition and reproductive performance in Holstein–Friesian dairy cattle. BMC Vet Res 20, 341 (2024). https://doi.org/10.1186/s12917-024-04188-4.

Epistatic Interaction Between LEP and MYF5 Is Associated with Carcass Traits in Holstein–Friesian Bulls

Year 2025, Volume: 44 Issue: 2, 133 - 145, 31.12.2025
https://doi.org/10.30782/jrvm.1798308

Abstract

This study aims to investigate the relationship between carcass and meat quality traits and Insulin-like growth factor 1 (IGF1), myogenic factor 5 (MYF5) and leptin (LEP) genes in Holstein-Friesian bulls. One hundred three cattle were genotyped using the PCR-RFLP method. Afterwards, the relationship of IGF1, MYF5 and LEP genes with live weight, hot carcass weight, chilled carcass weight, dressing percentage, musculus longissimus dorsi, Warner-Bratzler shear force, cooking loss, chilling loss, water holding capacity, carcass length, chest width, and meat color parameters (L*, a*, b*) were examined. Trade-offs between carcass and meat quality were assessed using a Pareto front approach, where non-dominated genotype combinations were identified as the best attainable balance between yield and quality. No significant association was observed between IGF1, MYF5, and LEP genes individually and traits (P>0.05). However, LEP × MYF5 interaction was observed in association with live weight, hot carcass weight, and chilled carcass weight traits (P<0.05). This genotypic interaction revealed an epistatic pattern that may significantly affect the live weight, hot carcass weight, and chilled carcass weight of Holstein-Friesian cattle. To our knowledge, although the individual associations of LEP and MYF5 with carcass traits in Holstein–Friesian cattle have been reported, the joint (epistatic) effect of these loci has not been systematically evaluated. The present study provides the first evidence that the LEP × MYF5 interaction is associated with carcass performance, whereas no corresponding interaction was detected for standard meat-quality endpoints. These findings support incorporating epistatic marker combinations, rather than single-locus effects alone, into selection indices and mating plans to improve carcass yield. More broadly, the results motivate validation in independent populations and further investigation of gene–gene and gene–environment interactions underlying carcass and meat-quality traits.

Ethical Statement

This study did not involve any invasive procedures in animals by the authors. Therefore, no specific ethics statement was required, as the blood samples were collected from the natural flow of exsanguination during routine slaughterhouse procedures.

Thanks

The authors gratefully acknowledge the support of Tabiat Agriculture Farm/Özdilek (Bursa).

References

  • Utrera ÁR, Van Vleck LD. Heritability estimates for carcass traits of cattle: a review. Genetics and Molecular Research, 2004; 3(3), 380-394.
  • Casas E, White SN, Riley DG, et al. Assessment of single nucleotide polymorphisms in genes residing on bovine chromosome 5: associations with beef carcass traits. Journal of Animal Science, 2000; 78(5), 1224-1230.
  • Schenkel FS, Miller SP, Jiang Z, et al. Association of a single nucleotide polymorphism in the calpastatin gene with carcass and meat quality traits of beef cattle. Journal of Animal Science, 2006; 84(2), 291-299.
  • Ardicli S, Dincel D, Samli H, et al. Effects of polymorphisms at LEP, CAST, CAPN1, GHR, FABP4 and DGAT1 genes on fattening performance and carcass traits in Simmental bulls. Archives Animal Breeding, 2017a; 60(2), 61-70.
  • Liefers SC, Te Pas MFW, Veerkamp RF, et al. Associations between leptin gene polymorphisms and production, live weight, energy balance, feed intake, and fertility in Holstein heifers. Journal of Dairy Science, 2002; 85(6), 1633-1638.
  • Liefers SC, Veerkamp RF, Te Pas MFW, et al. Leptin promoter mutations affect leptin levels and performance traits in dairy cows 1. Animal Genetics, 2005; 36(2), 111-118.
  • Kumar S, Dahiya S, Magotra A, et al. Study of Polymorphism in exon 3 region of leptin Gene in Harnali sheep. The Pharma Innovation Journal, 2020; 9(2), 360-363.
  • Salgado Pardo JI, Delgado Bermejo JV, González Ariza A, et al. Candidate genes and their expressions involved in the regulation of milk and meat production and quality in goats (Capra hircus). Animals, 2022; 12(8), 988.
  • Banos G, Woolliams JA, Woodward BW, et al. Impact of single nucleotide polymorphisms in leptin, leptin receptor, growth hormone receptor, and diacylglycerol acyltransferase (DGAT1) gene loci on milk production, feed, and body energy traits of UK dairy cows. Journal of Dairy Science, 2008; 91(8), 3190-3200.
  • Oztabak K, Toker NY, Un C, et al. Leptin gene polymorphisms in native Turkish cattle breeds. Kafkas Üniversitesi Veteriner Fakültesi Dergisi, 2010; 16(6).
  • De Matteis G, Scatà MC, Grandoni F, et al. Association analyses of single-nucleotide polymorphisms in the leptin and leptin receptor genes on milk and morphological traits in Holstein cows. Open Journal of Animal Sciences, 2012; 2(3), 174-182.
  • Kawaguchi F, Okura K, Oyama K, et al. Identification of leptin gene polymorphisms associated with carcass traits and fatty acid composition in Japanese Black cattle. Animal Science Journal, 2017; 88(3), 433-438.
  • Ardicli S, Samli H, Vatansever B, et al. Comprehensive assessment of candidate genes associated with fattening performance in Holstein–Friesian bulls. Archives Animal Breeding, 2019a; 62(1), 9-32.
  • Prihandini PW, Hariyono DNH, Sari APZNL, et al. Association between GH, PRL, LEP, and PIT-1 gene polymorphisms and growth traits in Indonesian Rambon indigenous cattle. Tropical Animal Health and Production, 2025; 57(2), 56.
  • Singh SK, Rout PK, Agarwal R, et al. Characterization of exon 2 and intron 2 of leptin gene in Indian goats. Animal Biotechnology, 2009; 20(2), 80-85.
  • Korkmaz-Agaoglu O, Elmaz O, Akyuz B, et al. Identifying polymorphism in some genes and their effects on growth performance in Honamli and hair goat breeds. Genetika, 2019; 51(3), 995-1008.
  • Senturk N, Selvi TN, Demir M, et al. The impact of LEP gene polymorphisms located at exon 2 (LEP-HinfI) and intron 2 (LEP-Sau3AI) on growth and reproductive traits in Saanen goats. Archives Animal Breeding, 2024; 67(4), 523-531.
  • Stone RT, Kappes SM, Beattie CW. The bovine homolog of the obese gene maps to chromosome 4. Mammalian Genome, 1996; 7,399–400.
  • Nkrumah JD, Keisler DH, Crews Jr DH, et al. Genetic and phenotypic relationships of serum leptin concentration with performance, efficiency of gain, and carcass merit of feedlot cattle. Journal of Animal Science, 2007; 85(9), 2147-2155.
  • Giblin L, Butler ST, Kearney BM, et al. Association of bovine leptin polymorphisms with energy output and energy storage traits in progeny tested Holstein-Friesian dairy cattle sires. BMC Genetics, 2010; 11(1), 73.
  • Friedman JM, Halaas JL. Leptin and the regulation of body weight in mammals. Nature, 1998; 395(6704), 763-770.
  • Yazdani H, Rahmani HR, Edris MA, et al. Association between A59V polymorphism in exon 3 of leptin gene and reproduction traits in cows of Iranian Holstein. African Journal of Biotechnology, 2010; 9(36).
  • Ardicli S, Samli H, Dincel D, et al. Individual and combined effects of CAPN1, CAST, LEP and GHR gene polymorphisms on carcass characteristics and meat quality in Holstein bulls. Archives Animal Breeding, 2017b; 60(3), 303-313.
  • Ge W, Davis ME, Hines HC, et al. Association of a genetic marker with blood serum insulin-like growth factor-I concentration and growth traits in Angus cattle. Journal of Animal Science, 2001; 79(7), 1757-1762.
  • Bishop MD., Tavakkol A, Threadgill DW, et al. Somatic cell mapping and restriction fragment length polymorphism analysis of bovine insulin-like growth factor I. Journal of Animal Science, 1991; 69(11), 4306-4311.
  • Miller JR, Thomsen PD, Dixon SC, et al. Synteny mapping of the bovine IGHG2, CRC and IGF1 genes. Animal Genetics,1992; 23, 51-58.
  • Li C, Basarab J, Snelling WM, et al. Assessment of positional candidate genes myf 5 and igf 1 for growth on bovine chromosome 5 in commercial lines of Bos taurus. Journal of Animal Science, 2004; 82(1), 1-7.
  • Curi RA, De Oliveira HN, Silveira AC, et al. Effects of polymorphic microsatellites in the regulatory region of IGF1 and GHR on growth and carcass traits in beef cattle. Animal Genetics, 2005; 36(1), 58-62.
  • Siadkowska E, Zwierzchowski L, Oprzadek J, et al. Effect of polymorphism in IGF-1 gene on production traits in Polish Holstein-Friesian cattle. Animal Science Papers and Reports, 2006; 24(3), 225-37.
  • Ardicli S, Samli H, Dincel D, et al. Relationship of the bovine IGF1, TG, DGAT1 and MYF5 genes to meat colour, tenderness and cooking loss. Journal of the Hellenic Veterinary Medical Society, 2018; 69(3), 1077-1087.
  • Weintraub H, Davis R, Tapscott S, et al. The myoD gene family: nodal point during specification of the muscle cell lineage. Science, 1991;251(4995):761–766.
  • Ujan J, Zan L, Ujan S, et al. Back fat thickness and meat tenderness are associated with a 526 T/A mutation in the exon 1 promoter region of the MyF-5 gene in Chinese Bos taurus. Genetics and Molecular Research, 2011;10(4):3070–3079.
  • Zhao C, Raza SHA, Khan R, et al. Genetic variants in MYF5 affected growth traits and beef quality traits in Chinese Qinchuan cattle. Genomics, 2020;112(4): 2804–2812.
  • Bhuiyan MSA, Kim NK, Cho YM, et al. Identification of SNPs in MYOD gene family and their associations with carcass traits in cattle. Livestock Science, 2009; 126(1-3), 292-297.
  • Kisacova J, Kubek A, Melus V, et al. Genetic polymorphism of Myf-5 and myostatin in Charolais breed. Journal of Agrobiology, 2009; 26: 7-11.
  • Sagsoz Y, Coban O., Lacin E, et al. Esmer ve Şarole x Esmer danaların besi performansı ve karkas özellikleri. Atatürk Üniversitesi Ziraat Fakültesi Dergisi, 2005; 36(2), 163-169.
  • Ekiz B, Yilmaz A, Ozcan M, et al. Carcass measurements and meat quality of Turkish Merino, Ramlic, Kivircik, Chios and Imroz lambs raised under an intensive production system. Meat Science, 2009; 82(1), 64-70.
  • Ekiz B, Ekiz EE, Kocak O, et al. Effect of pre-slaughter management regarding transportation and time in lairage on certain stress parameters, carcass and meat quality characteristics in Kivircik lambs. Meat Science, 2012; 90(4), 967-976.
  • Beriain MJ, Horcada A, Purroy A, et al. Characteristics of Lacha and Rasa Aragonesa lambs slaughtered at three live weights. Journal of Animal Science, 2000; 78(12), 3070-3077. 40. Falconer DS, Mackay TFC. Introduction to Quantitative Genetics, Harlow, Pearson Education Ltd., ISBN 0582243025,1996.
  • Nei M, Roychoudhury, A. Sampling variances of heterozygosity and genetic distance, Genetics, 1974; 76, 379–390.
  • Botstein D, White RL, Skolnick M, et al. Construction of a genetic linkage map in man using restriction fragment length polymorphisms. American Journal of Human Genetics, 1980; 32(3), 314.
  • Lacorte GA, Machado MA, Martinez ML, et al. DGAT1 K232A polymorphism in Brazilian cattle breeds. Genetics and Molecular Research, 2006; 5(3), 475-482.
  • Houseknecht K, Baile CA, Matteri RL, et al. The biology of leptin: a review. Journal of Animal Science, 1998; 76(5), 1405-1420.
  • Florini JR, Ewton DZ, Coolican SA. Growth hormone and the insulin-like growth factor system in myogenesis. Endocrine Reviews, 1996; 17(5), 481-517.
  • Trujillo AI, Casal A, Penagaricano F, et al. Association of SNP of neuropeptide Y, leptin, and IGF-1 genes with residual feed intake in confinement and under grazing condition in Angus cattle. Journal of Animal Science, 2013; 91(9), 4235-4244.
  • Dar MR, Singh M, Thakur S, et al. Exploring the relationship between polymorphisms of leptin and IGF-1 genes with milk yield in indicine and taurine crossbred cows. Tropical Animal Health and Production, 2021; 53(4), 413.
  • Montelli NLLL, Alvarenga TIRC, Almeida AK., et al. Associations of feed efficiency with circulating IGF-1 and leptin, carcass traits and meat quality of lambs. Meat Science, 2021; 173, 108379.
  • Darwish AM, Abdelhafez MA, Abdel-Hamid ZG, et al. Correlation analysis between polymorphism of leptin and IGFI genes and body measurements in Barki and Farafra sheep. Beni-Suef University Journal of Basic and Applied Sciences, 2023; 12(1), 119.
  • Morissette MR, Cook SA, Buranasombati C, et al. Myostatin inhibits IGF-I-induced myotube hypertrophy through Akt. American Journal of Physiology-Cell Physiology, 2009; 297, C1124–C1132.
  • Ardicli S, Dincel D, Samli H, et al. Association of polymorphisms in lipid and energy metabolism-related genes with fattening performance in Simmental cattle. Animal Biotechnology, 2023; 34(8), 3428-3440.
  • Bongiorni S, Mancini G, Chillemi G, et al. Identification of a short region on chromosome 6 affecting direct calving ease in Piedmontese cattle breed. PLoS One, 2012; 7(12), e50137.
  • Carvalho TDD, Siqueira F, Torres Júnior RADA, et al. Association of polymorphisms in the leptin and thyroglobulin genes with meat quality and carcass traits in beef cattle. Revista Brasileira de Zootecnia, 2012; 41, 2162-2168.
  • Woronuk GN, Marquess FL, James ST, et al. Association of leptin genotypes with beef cattle characteristics. Animal Genetics, 2012; 43(5), 608-610.
  • Sedykh TA, Kalashnikova LA, Gizatullin RS et al. Effects of leptin gene polymorphism on beef cattle performance. Russian Agricultural Sciences, 2020; 46(6), 614-618.
  • Matsumoto H, Kimura S, Nagai Y, et al. Leptin gene contributes to beef marbling standard, meat brightness, meat firmness, and beef fat standard of the Kumamoto sub‐breed of Japanese Brown cattle. Animal Science Journal, 2022; 93(1), e13698.
  • Couto CE, Livramento KGD, Paiva LV, et al. DGAT and LEP gene polymorphisms and their association with carcass characteristics and the lipid profile of meat from Nellore cattle. Revista Brasileira de Saúde e Produção Animal, 2023; 24, 20220012.
  • Valencia CPL, Franco LÁÁ, Herrera DH. Association of single nucleotide polymorphisms in the CAPN, CAST, LEP, GH, and IGF-1 genes with growth parameters and ultrasound characteristics of the Longissimus dorsi muscle in Colombian hair sheep. Tropical Animal Health and Production, 2022; 54(1), 82.
  • Liu Y, Kong L, Li S, et al. Correlation and regression analysis of GH and IGF-1 genes in Liaoning cashmere goats with body size and other production performance. Journal of Genetic Engineering and Biotechnology, 2024; 22(4), 100440.
  • Kader Esen V, Esen S. Association of the IGF1 5′ UTR polymorphism in meat-type sheep breeds considering growth, body size, slaughter, and meat quality traits in Turkey. Veterinary Sciences, 2023; 10(4), 270.
  • Meira AN, Montenegro H, Coutinho L., et al. Single nucleotide polymorphisms in the growth hormone and IGF type-1 (IGF1) genes associated with carcass traits in Santa Ines sheep. Animal, 2019; 13(3), 460-468.
  • Islam KK, Vinsky M, Crews RE, et al. Association analyses of a SNP in the promoter of IGF1 with fat deposition and carcass merit traits in hybrid, Angus and Charolais beef cattle. Animal Genetics, 2009; 40, 766–769.
  • Pereira AGT, Utsunomiya YT, Milanesi M, et al. Pleiotropic genes affecting carcass traits in Bos indicus (Nellore) cattle are modulators of growth. PLoS One, 2016; 11(7), e0158165.
  • Cobanoglu O, Ardicli S.Genetic variation at the OLR1, ANXA9, MYF5, LTF, IGF1, LGB, CSN3, PIT1, MBL1, CACNA2D1, and ABCG2 loci in Turkish Grey Steppe, Anatolian Black, and East Anatolian Red cattle. Turkish Journal of Veterinary & Animal Sciences, 2022; 46(3), 494-504.
  • Gerasimov NP, Dzhulamanov KM, Lebedev SV, et al. Effect of IGF-1 C472T, GH C2141G, and GHR T914A polymorphisms on growth performance and feed efficiency in young Kazakh white-headed cattle. Veterinary World, 2023; 16(8), 1584.
  • Saleh AA, Hassan TG, El-Hedainy DK, et al. IGF-I and GH Genes polymorphism and their association with milk yields, composition and reproductive performance in Holstein–Friesian dairy cattle. BMC Veterinary Research, 2023; 20(1), 341.
  • Sen U, Gokcek, D, Yılmaz OF, et al. Relationships among growth, carcass characteristics, and Myf5, Myf6, MyoD, and MyoG genes expression level in Saanen male kids with varying slaughter weights. Animals, 2024; 15(1), 16.
  • Daldaban F, Arslan K, Aksel EG, et al. Polymorphism of the STAT5A and MYF-5 genes in Anatolian water buffalo. Turkish Journal of Veterinary & Animal Sciences, 2020; 44(2), 284-289.
  • Zayed MA, El-Kholy AF, Shehata MF, et al. Genetic contribution of myogenic factor 5 and growth hormone genes for live body measurements, carcass traits and meat quality of dromedary camel. Journal of Animal and Poultry Production, 2022; 13(10), 153-156.
  • Fadhil M, Zülkadir U. Association between polymorphisms of Myf5, MSTN and CAST genes and fattening performance in Brown Swiss and Holstein cattle breeds. Animal Biotechnology, 2021; 32(1), 121-129.
  • Ardicli S, Ustuner H, Arslan O, et al. Variability of CAPN1 g. 5709 C> G and MYF5 g. 1911 A> G Polymorphisms in Beef Cattle Imported from Brazil to Turkey. Lalahan Hayvancılık Araştırma Enstitüsü Dergisi, 2019b; 59(2), 72-78.
  • MacNeil MD, Nkrumah JD, Woodward BW, et al. Genetic evaluation of Angus cattle for carcass marbling using ultrasound and genomic indicators. Journal of Animal Science, 2010; 88(2), 517-522.
  • Ardicli S. Genetik ve postmortem mekanizmaların sığır eti renk özellikleri üzerine etkisi. Uludağ Üniversitesi Veteriner Fakültesi Dergisi, 2018; 37(1), 49-59. https://doi.org/10.30782/uluvfd.398947
  • Ustuner H, Ardicli S, Arslan O, Brav FC. Fattening performance and carcass traits of imported Simmental bulls at different initial fattening age. Large Animal Review, 2020; 26: 161-165.
  • Ustuner H, Ardicli S, Arslan O. Determination of the alterations in quality parameters and consumer preference of dry-aged beef based on different periods of ageing using a purposive incubator. Journal of the Hellenic Veterinary Medical Society, 2021; 72(1): 2669-2676. https://doi.org/10.12681/jhvms.26749
  • Ardicli S, Ardicli O, Ustuner H. Unraveling the Complexities of Beef Marination: Effect of Marinating Time, Marination Treatments, and Breed. Foods, 2024, 13(18): 2979. https://doi.org/10.3390/foods13182979
  • Ardicli, S. Analysis of IGF1 C472T and TG C422T polymorphisms in Turkish Grey Steppe and Holstein crossbred bulls. 2018. Uludağ Üniversitesi Veteriner Fakültesi Dergisi, 37(1), 21-28.
  • Ardicli, S., Aldevir, O., Aksu, E., & Gumen, A. The variation in the beta-casein genotypes and its effect on milk yield and genomic values in Holstein-Friesian cows. 2023. Animal Biotechnology, 34(8), 4116-4125.
  • Ardicli, S., Aldevir, Ö., Aksu, E., Kucuk, K., & Gümen, A. Associations of bovine beta-casein and kappa-casein genotypes with genomic merit in Holstein Friesian cattle. 2024. Archives Animal Breeding, 67(1), 61-71.
  • Ardicli, S., Senturk, N., Bozkurt, B., Babayev, H., Selvi, T., Skolnick, S., ... & Cobanoglu, O. The impact of genetic variants related to the fatty acid metabolic process pathway on milk production traits in Jersey cows. 2024. Animal Biotechnology, 35(1), 2396421.
  • Saleh, A.A., Hassan, T.G.M., EL-Hedainy, D.K.A. et al. IGF-I and GH Genes polymorphism and their association with milk yields, composition and reproductive performance in Holstein–Friesian dairy cattle. BMC Vet Res 20, 341 (2024). https://doi.org/10.1186/s12917-024-04188-4.
There are 80 citations in total.

Details

Primary Language English
Subjects Veterinary Sciences (Other)
Journal Section Research Article
Authors

Nursen Şentürk 0000-0003-1975-0103

Tuğçe Necla Selvi 0000-0003-3425-3201

Huseyn Babayev 0000-0001-6985-9436

Hakan Üstüner 0000-0002-4341-5842

Sena Ardıclı 0000-0003-2758-5945

Submission Date October 6, 2025
Acceptance Date December 11, 2025
Publication Date December 31, 2025
Published in Issue Year 2025 Volume: 44 Issue: 2

Cite

APA Şentürk, N., Selvi, T. N., Babayev, H., … Üstüner, H. (2025). Epistatic Interaction Between LEP and MYF5 Is Associated with Carcass Traits in Holstein–Friesian Bulls. Journal of Research in Veterinary Medicine, 44(2), 133-145. https://doi.org/10.30782/jrvm.1798308
AMA Şentürk N, Selvi TN, Babayev H, Üstüner H, Ardıclı S. Epistatic Interaction Between LEP and MYF5 Is Associated with Carcass Traits in Holstein–Friesian Bulls. J Res Vet Med. December 2025;44(2):133-145. doi:10.30782/jrvm.1798308
Chicago Şentürk, Nursen, Tuğçe Necla Selvi, Huseyn Babayev, Hakan Üstüner, and Sena Ardıclı. “Epistatic Interaction Between LEP and MYF5 Is Associated With Carcass Traits in Holstein–Friesian Bulls”. Journal of Research in Veterinary Medicine 44, no. 2 (December 2025): 133-45. https://doi.org/10.30782/jrvm.1798308.
EndNote Şentürk N, Selvi TN, Babayev H, Üstüner H, Ardıclı S (December 1, 2025) Epistatic Interaction Between LEP and MYF5 Is Associated with Carcass Traits in Holstein–Friesian Bulls. Journal of Research in Veterinary Medicine 44 2 133–145.
IEEE N. Şentürk, T. N. Selvi, H. Babayev, H. Üstüner, and S. Ardıclı, “Epistatic Interaction Between LEP and MYF5 Is Associated with Carcass Traits in Holstein–Friesian Bulls”, J Res Vet Med, vol. 44, no. 2, pp. 133–145, 2025, doi: 10.30782/jrvm.1798308.
ISNAD Şentürk, Nursen et al. “Epistatic Interaction Between LEP and MYF5 Is Associated With Carcass Traits in Holstein–Friesian Bulls”. Journal of Research in Veterinary Medicine 44/2 (December2025), 133-145. https://doi.org/10.30782/jrvm.1798308.
JAMA Şentürk N, Selvi TN, Babayev H, Üstüner H, Ardıclı S. Epistatic Interaction Between LEP and MYF5 Is Associated with Carcass Traits in Holstein–Friesian Bulls. J Res Vet Med. 2025;44:133–145.
MLA Şentürk, Nursen et al. “Epistatic Interaction Between LEP and MYF5 Is Associated With Carcass Traits in Holstein–Friesian Bulls”. Journal of Research in Veterinary Medicine, vol. 44, no. 2, 2025, pp. 133-45, doi:10.30782/jrvm.1798308.
Vancouver Şentürk N, Selvi TN, Babayev H, Üstüner H, Ardıclı S. Epistatic Interaction Between LEP and MYF5 Is Associated with Carcass Traits in Holstein–Friesian Bulls. J Res Vet Med. 2025;44(2):133-45.