Associations Between Polymorphisms of the Csn1s1, Csn1s2, Csn2 and Csn3 Genes and Milk Composition Traits in Holstein Cattle

dc.contributor.author Demirel, Ahmet Fatih
dc.contributor.author Cak, Bahattin
dc.date.accessioned 2025-05-10T17:29:46Z
dc.date.available 2025-05-10T17:29:46Z
dc.date.issued 2025
dc.description.abstract Background Caseins are the major proteins found in cow's milk. There are four known casein fractions: alpha S1-casein, alpha S2-casein, beta-casein and kappa-casein, encoded by the CSN1S1, CSN1S2, CSN2 and CSN3 genes located on the sixth chromosome of cattle. These genes are considered candidate genes in marker-assisted selection. Therefore, it is essential to determine the relationship between these genes and quantitative characters. Objectives This study aimed to identify genotypes of CSN1S1, CSN1S2, CSN2 and CSN3 genes and investigate their effect on milk components with the PCR-RFLP method in Holstein cattle. Methods The material of the study consisted of 519 Holstein cows that managed under intensive systems in Konya (n:189), Manisa (n:195) and Diyarbak & imath;r (n:135) provinces in T & uuml;rkiye. Blood and milk samples from these cows were used in the study. The genetic structures of bovine CSN1S1, CSN1S2, CSN2 and CSN3 genes were examined by PCR-RFLP in three Holstein cattle populations. A general linear model (GLM) was applied to analyse the effect of genotypic variants on phenotypic characters. Results Results indicated that milk solids-non-fat (SNF) (p < 0.01), protein (p < 0.05) and lactose (p < 0.01) percentages were significantly affected by the genetic variants of the CSN2 gene of cow in general population. CSN2 A2A2 genotype led to a significant increase in SNF, protein and lactose percentages by 0.14, 0.05 and 0.08 in comparison to other genotypes, respectively. Moreover, significant effect of the CSN1S1 BC (p < 0.05) and CSN3 AA (p < 0.01) genotypes on fat percentage were found in Konya province. Furthermore, a statistically significant genotype-by-environment interaction was identified in both the CSN1S1 (p < 0.05) and CSN3 (p < 0.01) genes in relation to milk fat content. Conclusions As a result, after increasing the number of studies that investigated the relationship between casein genes and milk traits and determined the genetic variation of CSN1S1, CSN2 and CSN3 genes of the Holstein cattle, these genes can be a strong genetic marker as marker-assisted selection programme in early selection. en_US
dc.description.sponsorship Van Yuzuncu Yimath;l University Scientific Research Projects Coordination Unit [TDK-2018-6796] en_US
dc.description.sponsorship This study was supported by Van Yuzuncu Y & imath;l University Scientific Research Projects Coordination Unit via project TDK-2018-6796. en_US
dc.identifier.doi 10.1002/vms3.70334
dc.identifier.issn 2053-1095
dc.identifier.scopus 2-s2.0-105002068725
dc.identifier.uri https://doi.org/10.1002/vms3.70334
dc.identifier.uri https://hdl.handle.net/20.500.14720/12455
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Csn2 en_US
dc.subject Csn3 en_US
dc.subject Holstein Cattle en_US
dc.subject Pcr-Rflp en_US
dc.title Associations Between Polymorphisms of the Csn1s1, Csn1s2, Csn2 and Csn3 Genes and Milk Composition Traits in Holstein Cattle en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.scopusid 57194699004
gdc.author.scopusid 14033719700
gdc.author.wosid Çak, Bahattin/Aam-2319-2020
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Demirel, Ahmet Fatih; Cak, Bahattin] Van Yuzuncu Yil Univ, Fac Vet Med, Dept Anim Husb, Van, Turkiye en_US
gdc.description.issue 3 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.volume 11 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q2
gdc.identifier.pmid 40184159
gdc.identifier.wos WOS:001459522400001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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