Kahyo Tomoaki, Sugimura Haruhiko
Department of Tumor Pathology, Hamamatsu University School of Medicine;
Department of Tumor Pathology, Hamamatsu University School of Medicine.
J Vis Exp. 2018 Aug 20(138):58199. doi: 10.3791/58199.
The quantitative analysis of human genetic variation is crucial for understanding the molecular characteristics of serious medical conditions, such as tumors. Because digital polymerase chain reactions (PCR) enable the precise quantification of DNA copy number variants, they are becoming an essential tool for detecting rare genetic variations, such as drug-resistant mutations. It is expected that molecular diagnoses using digital PCR (dPCR) will be available in clinical practice in the near future; thus, how to efficiently conduct dPCR with human genetic material is a hot topic. Here, we introduce a method to detect Adenomatous polyposis coli (APC) somatic mosaicism using dPCR with the chip-in-a-tube format, which allows eight dPCR reactions to be simultaneously conducted. Care should be taken when filling and sealing the reaction mixture on the chips. This article demonstrates how to avoid the over- and underestimation of positive partitions. Furthermore, we present a simple procedure for collecting the dPCR product from the partitions on the chips, which can then be used to confirm the specific amplification. We hope that this methods report will help promote the dPCR with the chip-in-a-tube method in genetic research.
人类遗传变异的定量分析对于理解严重医疗状况(如肿瘤)的分子特征至关重要。由于数字聚合酶链反应(PCR)能够精确量化DNA拷贝数变异,因此它正成为检测罕见遗传变异(如耐药突变)的重要工具。预计在不久的将来,使用数字PCR(dPCR)的分子诊断将在临床实践中得以应用;因此,如何有效地利用人类遗传物质进行dPCR是一个热门话题。在此,我们介绍一种使用芯片管格式的dPCR检测腺瘤性息肉病(APC)体细胞嵌合体的方法,该方法可同时进行8个dPCR反应。在芯片上填充和密封反应混合物时应小心谨慎。本文展示了如何避免阳性分区的高估和低估。此外,我们还介绍了一种从芯片上的分区收集dPCR产物的简单程序,该产物随后可用于确认特异性扩增。我们希望本方法报告将有助于推动芯片管法dPCR在基因研究中的应用。