首页> 外文期刊>Cancer genomics & proteomics >Identification and Quantification of Heterogeneously-methylated DNA Fragments Using Epiallele-sensitive Droplet Digital Polymerase Chain Reaction (EAST-ddPCR)
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Identification and Quantification of Heterogeneously-methylated DNA Fragments Using Epiallele-sensitive Droplet Digital Polymerase Chain Reaction (EAST-ddPCR)

机译:使用上等位基因敏感的液滴数字聚合酶链反应(EAST-ddPCR)鉴定和定量异甲基化的DNA片段

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Background/Aim: DNA methylation plays an important role in the initiation and propagation of carcinogenesis; however, the role of heterogeneously methylated epialleles is currently not well studied, also due to the lack of sensitive, unbiased and high throughput methods. Here, a newly developed droplet digital PCR (ddPCR)-based method was evaluated regarding its ability to quantify such heterogeneously methylated epialleles with sufficient analytical sensitivity and specificity. Materials and Methods: Genomic DNA from blood leukocytes and bone marrow aspirate of an 8-year old male with B-cell acute lymphoblastic leukemia (B-ALL) and from normal and malignant prostate cell lines were analysed using ddPCR. Results: By using these DNA samples, the specificity of an applied set of fluorescence-labeled probes was demonstrated as a proof of concept. Conclusion: All individual heterogeneously-methylated epialleles were quantifiable by a set of fluorescence-labeled probes with complementary sequences to epialleles in a closed-tube and high-throughput manner. The new method named epiallele-sensitive droplet digital PCR (EAST-ddPCR) may give new insights in the generation and regulation of epialleles and may help in finding new biomarkers for the diagnosis of benign und malignant diseases.
机译:背景/目的:DNA甲基化在致癌作用的起始和传播中起着重要作用。然而,由于缺乏灵敏,公正和高通量的方法,目前还没有很好地研究异质甲基化等位基因的作用。在这里,对一种新开发的基于液滴数字PCR(ddPCR)的方法进行了评估,该方法具有足够的分析灵敏度和特异性来量化这种异质甲基化的等位基因。材料和方法:使用ddPCR分析了8岁男性B细胞急性淋巴细胞白血病(B-ALL)的正常血液和恶性前列腺细胞系的血液白细胞和骨髓穿刺液的基因组DNA。结果:通过使用这些DNA样品,证明了一组应用的荧光标记探针的特异性是一种概念证明。结论:所有单个异质甲基化的等位基因都可以通过一组荧光标记的探针进行定量,这些探针具有与等位基因互补的序列,且采用封闭管高通量方式。名为表位等位基因敏感液滴数字PCR(EAST-ddPCR)的新方法可能为表位等位基因的产生和调控提供新的见解,并可能有助于寻找新的生物标志物,以诊断良性和恶性疾病。

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