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Design of FRET Probes for SNP RS1006737, Related to Mood Disorder

机译:与情绪障碍相关的SNP RS1006737 FRET探针的设计

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Background: Several studies have shown that the Single Nucleotide Polymorphism (SNP) in the CACAN1C gene, rs1006737, is related to different mood disorder illnesses, such as bipolar disorder and schizophrenia. Current day molecular procedures for allele detection of this gene can be very expensive and time consuming. Hence, a sensitive and specific molecular procedure for detecting these mutations in a large number of subjects is desirable, especially for research groups who have no complex laboratory equipment. Objective: The possibility of using a Fluorescence Resonance Energy Transfer (FRET) probe was evaluated by means of bioinformatic tools, designed for forecasting the molecular behavior of DNA probes used in the research field or for laboratory analysis methods. Method: In this study we used the DINAMelt Web Server to predict the T ms of FRET oligo in the presence of the A and/or G allele in rs1006737. The PCR primers were designed by using oligo 4 and oligo 6 primer analysis software, Results: The molecular probe described in this study detected a T m difference of 5-6°C between alleles A and G in rs1006737, which also showed good discrimination for a heterozygous profile for this genomic region. Conclusion: Although in silico studies represent a relatively new avenue of inquiry, they have now started to be used to predict how a molecular probe interacts with its biological target, reducing the time and costs of molecular test tuning. The results of this study seem promising for further laboratory tests on allele detection in rs1006737 region.
机译:背景:多项研究表明,CACAN1C基因rs1006737中的单核苷酸多态性(SNP)与不同的情绪障碍疾病有关,例如躁郁症和精神分裂症。目前,用于等位基因检测该基因的分子程序可能非常昂贵且耗时。因此,需要一种灵敏而特异的分子程序来检测大量受试者中的这些突变,特别是对于没有复杂实验室设备的研究小组。目的:通过生物信息学工具评估了使用荧光共振能量转移(FRET)探针的可能性,该工具旨在预测研究领域或实验室分析方法中使用的DNA探针的分子行为。方法:在这项研究中,我们使用DINAMelt Web服务器预测rs1006737中存在A和/或G等位基因的FRET寡核苷酸的T ms。使用oligo 4和oligo 6引物分析软件设计了PCR引物,结果:本研究中描述的分子探针检测到rs1006737的等位基因A和G之间的T m差异为5-6°C,这也显示了对该基因组区域的杂合谱。结论:尽管计算机研究代表了一个相对较新的研究途径,但现在它们已开始用于预测分子探针如何与其生物学靶标相互作用,从而减少了分子测试调谐的时间和成本。这项研究的结果对于在rs1006737地区进行等位基因检测进行进一步的实验室测试似乎很有希望。

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