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    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • Iranian Journal of Applied Animal Science
    • Volume 9, Issue 4
    • مشاهده مورد
    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • Iranian Journal of Applied Animal Science
    • Volume 9, Issue 4
    • مشاهده مورد
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    Allelic and Genotypic Distribution in Single Nucleotide Polymorphism (SNP) G.676A > G of Melanocortin-1 Receptor (<i>MC1R</i>) Gene in Indonesian Goat Breeds

    (ندگان)پدیدآور
    Maharani, D.Elieser, S.Budisatria, I.G.S.Batubara, A.Hariyono, D.N.H.Sari, A.P.Z.N.L.
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    نوع مدرک
    Text
    Research Articles
    زبان مدرک
    English
    نمایش کامل رکورد
    چکیده
    The melanocortin-1 receptor (MC1R) gene has been investigated by many studies regarding the pigmentation variation in various species. In order to determine its allelic and genotypic distribution, we sequenced the goat MC1R gene from 78 individuals in ten populations (Gembrong, Senduro, Ettawa Grade, Boerawa, Boerka, Kosta, Samosir, Muara, Boer and Kacang). Direct sequencing method was performed to detect the single nucleotide polymorphisms (SNPs). Three SNPs (g.676A>G, g.748G>T and g.801C>G) were identified in the gene target. The SNP g.676 A > G was used to genotype the investigated animals by using polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) method with G, g.748G>T and g.801C>G) were identified in the gene target. The SNP g.676 A > G was used to genotype the investigated animals by using polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) method with T and g.801C>G) were identified in the gene target. The SNP g.676 A > G was used to genotype the investigated animals by using polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) method with G) were identified in the gene target. The SNP g.676 A > G was used to genotype the investigated animals by using polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) method with G was used to genotype the investigated animals by using polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) method with EarI restriction enzyme. In all studied populations, the A allele had the highest frequency (83%) and the G allele had the lowest frequency (17%). The frequency of homozygous AA genotype was the highest (90%) in Kacang goats, while that of heterozygous AG genotype was fixed in Senduro and Boer goats. Analysis of observed heterozygosity, expected heterozygosity, Nei's (1973) expected heterozygosity, and Shannon index were found to be 0.3425, 0.2858, 0.2838 and 0.4578, respectively.The distribution of MC1R gene in overall breeds confirmed with Hardy-Weinberg equilibrium (P>0.05).
    کلید واژگان
    allele distribution
    local goat
    <i>MC1R</i> gene

    شماره نشریه
    4
    تاریخ نشر
    2019-12-01
    1398-09-10
    ناشر
    Islamic Azad University - Rasht Branch
    Islamic Azad University - Rasht Branch
    سازمان پدید آورنده
    Department of Animal Breeding and Reproduction, Faculty of Animal Science, Universitas Gadjah Mada, Jl. Fauna 3, Bulaksumur, Yogyakarta 55281, Indonesia
    Indonesian Goat Research Institute Sei Putih, Galang 20585, North Sumatera, Indonesia
    Department of Animal Breeding and Reproduction, Faculty of Animal Science, Universitas Gadjah Mada, Jl. Fauna 3, Bulaksumur, Yogyakarta 55281, Indonesia
    Indonesian Goat Research Institute Sei Putih, Galang 20585, North Sumatera, Indonesia
    Department of Animal Breeding and Reproduction, Faculty of Animal Science, Universitas Gadjah Mada, Jl. Fauna 3, Bulaksumur, Yogyakarta 55281, Indonesia
    Department of Animal Breeding and Reproduction, Faculty of Animal Science, Universitas Gadjah Mada, Jl. Fauna 3, Bulaksumur, Yogyakarta 55281, Indonesia

    شاپا
    2251-628X
    2251-631X
    URI
    http://ijas.iaurasht.ac.ir/article_669379.html
    https://iranjournals.nlai.ir/handle/123456789/344764

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