Determination of Genetic Mutation Profile of drpr Gene in Drosophila melanogaster using High-Resolution Melting Analysis

Ahmad Mu’arif, Rudi Arfiansyah, Tri Puspita Roska, H. Rante, F. Nainu
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Abstract

Genotype determination of experimental animals is generally conducted using sequencing methods that require expensive cost as well as experience and special equipment. This study aimed to determine the presence of drpr gene mutation in Drosophila melanogaster using coupled real time PCR-High Resolution Melting (real time PCR-HRM) as an alternative method. Two types of fly samples, w1118 and drprΔ5 were used as wildtype control and mutant genotype, respectively. The DNA from twenty of each w1118 and mutant drprΔ5 flies were isolated and amplified using real time PCR. The generated amplicons were then further processed by HRM method at the temperature of 60-95°C. This study demonstrated that the real time PCR-HRM method could distinguish wildtype control w1118 and mutant drprΔ5 based on the HRM data with the confidence level was more than 90%. Therefore, this study provides an evidence that real time PCR-HRM method might be beneficial to screen the mutant genotype from its wildtype counterpart based on differences in the melting temperatures due to changes at nucleotide base level
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用高分辨率熔融分析法测定黑腹果蝇drpr基因突变谱
实验动物的基因型测定一般采用测序方法,这需要昂贵的成本、经验和专用设备。本研究旨在利用实时荧光定量pcr -高分辨率熔融(real time PCR-HRM)作为替代方法,检测黑胃果蝇中drpr基因突变的存在。以w1118和drprΔ5两种蝇类分别作为野生型对照和突变型。从w1118和突变体drprΔ5各20只蝇中分离DNA,采用实时PCR扩增。生成的扩增子在60-95℃的温度下用HRM法进一步处理。本研究表明,基于HRM数据,实时PCR-HRM方法可以区分野生型对照w1118和突变体drprΔ5,置信度在90%以上。因此,本研究提供了一个证据,即实时PCR-HRM方法可能有助于根据核苷酸碱基水平变化导致的熔化温度差异从野生型中筛选突变基因型
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