Identification of Single Nucleotide Polymorphism (SNP) in Early Exon 10 of Follicle Stimulating Hormone Receptor (FSHR) Gene in Pesisir Cattle

T. Afriani, E. Purwati, J. Hellyward, Jaswandi Jaswandi, M. Mundana, A. Farhana, A. Rastosari
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引用次数: 1

Abstract

The purpose of this study was to identify genetic diversity in the early exon 10 of the FSHR gene or follicle stimulating hormone receptor in Pesisir cattle. The blood samples used were 70 blood samples from female Pesisir cattle aged 2-5 years which were obtained from BPTU-HPT Padang Mengatas, West Sumatera. The isolated DNA was then amplified using a pair of primers L and R with PCR technique which produced a fragment with a length of 847 bp. The services of 1st Base Singapore are used for sequencing the amplified product. The results of the research on the identification of the early exon 10 FSHR gene in Pesisir cattle were found that there were 5 SNPs at positions --53T>C, +17A>G, +650C>T, +706A>C and +707 ins>A in some introns 9 to exon 10 first part. The results showed that the genotypic frequency of the Pesisir cattle population was in Hardy-Weinberg imbalance and polymorphisms were found in the early exon 10 FSHR gene diversity.
Pessir牛卵泡刺激激素受体(FSHR)基因早期外显子10单核苷酸多态性的鉴定
本研究的目的是鉴定Pessir牛FSHR基因或卵泡刺激激素受体早期外显子10的遗传多样性。所用血液样本为70份2-5岁的雌性Pessir牛的血液样本,这些样本取自西苏门答腊省的BPTU-HPT Padang Mengatas。然后使用一对引物L和R用PCR技术扩增分离的DNA,产生长度为847bp的片段。新加坡第一基地的服务用于扩增产物的测序。Pessir牛早期第10外显子FSHR基因的鉴定研究发现,在第9至第10外隐子第一部分的一些内含子中,有5个SNPs位于53T>C、+17A>G、+650C>T、+706A>C和+707ins>A位置。结果表明,Pessir牛群体的基因型频率处于Hardy-Weinberg不平衡状态,早期外显子10 FSHR基因多样性存在多态性。
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