Analysis of Polymorphism of Callipyge Gene in Lori Sheep by PCR-RFLP Method

Shahram Nanekarani, Majid Goodarzi, Morteza Mahdavi
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引用次数: 5

Abstract

The callipyge locus has been localized in the telomeric region on ovine chromosome 18, within a cluster of imprinted genes. In this study were collected blood samples from 124 Lori sheep. Genomic DNA was extracted from blood sample. Gel monitoring and spectrophotometer methods were used to determination quality and quantity of DNA. FaqI enzyme was used for restricting of PCR products. Digested products were separated by electrophoresis on 2% agarose gel and visualized after staining with ethidium bromide on UV transillumination. The PCR product (426 bp) was digested by restriction endonucleases FaqI. The FaqI digestion of the PCR products produced digestion fragments of 395, 278, 117 and 31 bp. Data analysis was done using PopGen32 software. There was no difference between digestion patterns and all sampled animals displayed AA genotype. As such, three 278, 117 and 31 bp amplified fragments from enzyme digestion were observed for all animals, indicating that the total population of sheep was monomorphic for CLPG gene.

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PCR-RFLP法分析洛瑞羊Callipyge基因多态性
callipyge基因座定位于羊18号染色体的端粒区,在一组印迹基因中。本研究采集了124只洛里羊的血液样本。从血样中提取基因组DNA。采用凝胶监测和分光光度计法测定DNA的质量和数量。采用FaqI酶对PCR产物进行限制性反应。消化产物经2%琼脂糖凝胶电泳分离,溴化乙啶紫外透照染色。PCR产物(426 bp)用限制性内切酶FaqI酶切。PCR产物经FaqI酶切得到395、278、117和31 bp的酶切片段。数据分析采用PopGen32软件。消化模式之间没有差异,所有取样动物均为AA基因型。结果表明,在所有动物中均有278、117和31 bp的酶切扩增片段,表明CLPG基因在绵羊群体中为单态。
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