Genetic variability of CSN1S1 gene in goat populations raised in southeastern region of Turkey
Bu çalışmanın amacı güneydoğu anadolu bölgesinde yetiştirilen keçilerde alfa-s1-kazeini kodlayan CSN1S1 genindeki çeşitliliğin araştırılmasıdır. Türkiye’nin Kilis (n=60) Şanlıurfa (n=56) ve Siirt (n=55) illerinde yetiştirilen keçilerden kan örnekleri toplanmıştır. Kan örneklerinden fenol-kloroform yöntemi ile DNA izolasyonu yapılmıştır. Keçilerin genotipleri polimeraz zincir reaksiyonu (PCR), allel spesifik PCR ve kesim bölgesi polimorfizmi yöntemleri ile belirlenmiştir. Kilis ve Şanlıurfa populasyonlarında A*, B*, F ve N allelleri gözlenirken Siirt populasyonunda sadece A* ve B* allelleri bulunmuştur. A*, B*, F and N allellerinin frekansları sırasıyla Kilis keçilerinde 0.375, 0.367, 0.017 ve 0.242, Şanlıurfa populasyonunda 0.632, 0.208, 0.009 ve 0.151, Siirt populasyonunda ise 0.782, 0.218, 0.000 ve 0.000, rolarak hesaplanmıştır. İncelenen populasyonlarda CSN1S1 E ve 01 allelleri gözlenmemiştir. Beklenen ve gözlenen genotip frekansları arasında önemli bir farklılık bulunmamıştır (P>0.05). Çalışma sonucunda özellikle Kilis ve Şanlıurfa populasyonlarında değişik yetiştirme hedefleri açısından seleksiyon yapılabilecek düzeyde genetik çeşitliliğin bulunduğu kanaatine varılmıştır.
Güneydoğu anadolu bölgesi’nde yetiştirilen keçilerde alfa-s1-kazein (CSN1S1) genindeki genetik çeşitlilik
The objective of this study was to investigate genetic variability of CSN1S1 gene coding for alpha-s1-casein in goat populations raised in Southeastern Region of Turkey. Blood samples were collected from goats raised in Kilis(n=60), Sanliurfa (n=56), and Siirt (n=55) provinces of Turkey. From the blood samples DNA was isolated by using phenol-chloroform extraction. Genotypes of animals were determined by using polymerase chain reaction (PCR), allele specific PCR or PCR and restriction fragment length polymorphism methods. In Kilis and Sanliurfa populations CSN1S1 A*, B*, F and N alleles were observed, while in Siirt population only A* and B* alleles were found. Frequencies of A*, B*, F and N alleles were 0.375, 0.367, 0.017 and 0.242 in Kilis, 0.632, 0.208, 0.009 and 0.151in Sanliurfa and 0.782, 0.218, 0.000 and 0.000 in Siirt populations, respectively. CSN1S1 E and 01 alleles were not observed among the populations studied. Observed and expected genotype frequencies did not differ significantly (P>0.05). The results of this study suggested that there were sufficient genetic variability of CSN1S1 gene especially in Sanliurfa and Kilis populations in order to select individuals for different breeding purposes.
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