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Detection of the rs10250202 polymorphism in protection of telomeres 1 gene through introducing a new restriction enzyme site for PCR–RFLP assay

机译:通过引入新的限制酶切位点进行PCR-RFLP检测来检测端粒1基因保护中的rs10250202多态性

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摘要

Human protection of telomeres 1 (POT1) gene is a single stranded telomere binding proteins with a critical role in ensuring chromosome stability. There have been variants of POT1 gene, and the polymorphisms of POT1 gene were associated with some diseases. Polymerase chain reaction–restriction fragment length polymorphism (PCR–RFLP) is a traditional method to detect the single nucleotide polymorphism (SNP), and it can be used to detect the polymorphism of rs10250202. But the restriction enzymes required for the detection of the polymorphism of rs10250202 are expensive. So we designed a novel PCR–RFLP assay for genotyping the POT1 rs10250202 SNP. In the study, a new restriction enzyme cutting site was created by created restriction site PCR (CRS-PCR), and the restriction enzyme BclI for CRS-PCR was cheaper than other enzymes. After detecting Han Chinese workers, Allele frequencies were found to be 51.54 % for allele A and 48.46 % for allele C respectively. The PCR results were confirmed by DNA sequencing. CRS-PCR provides a simple, low-cost, practical, and reproducible method.
机译:端粒1(POT1)基因的人类保护是一种单链端粒结合蛋白,在确保染色体稳定性方面起着关键作用。 POT1基因已经有变异,POT1基因的多态性与某些疾病有关。聚合酶链反应-限制性片段长度多态性(PCR-RFLP)是检测单核苷酸多态性(SNP)的传统方法,可用于检测rs10250202的多态性。但是检测rs10250202的多态性所需的限制酶很昂贵。因此,我们设计了一种新颖的PCR-RFLP测定法,对POT1 rs10250202 SNP进行基因分型。在这项研究中,通过创建限制性酶切位点PCR(CRS-PCR)创建了一个新的限制性酶切位点,用于CRS-PCR的限制性酶BclI比其他酶便宜。在检测到汉族工人后,发现等位基因A的等位基因频率分别为51.54%和C等位基因的48.46%。 PCR结果通过DNA测序证实。 CRS-PCR提供了一种简单,低成本,实用且可重现的方法。

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