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Droplet digital PCR shows the D-Loop to be an error prone locus for mitochondrial DNA copy number determination

机译:液滴数字PCR显示D-Loop是线粒体DNA拷贝数确定的易错基因座

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摘要

Absolute quantification of mitochondrial DNA copy number (mCN) provides important insights in many fields of research including cancer, cardiovascular and reproductive health. Droplet digital PCR (ddPCR) natively reports absolute copy number, and we have developed a single-dye, multiplex assay to measure rat mCN that is accurate, precise and affordable. We demonstrate simple methods to optimize this assay and to determine nuclear reference pseudogene copy number to extend the range of mCN that can be measured with this assay. We evaluated two commonly used mitochondrial DNA reference loci to determine mCN, the ND1 gene and the D-Loop. Harnessing the absolute measures of ddPCR, we found that the D-Loop amplifies with a copy number of ~1.0–1.5 relative to other sites on the mitochondrial genome. This anomalous copy number varied significantly between rats and tissues (aorta, brain, heart, liver, soleus muscle). We advocate for avoiding the D-Loop as a mitochondrial reference in future studies of mCN. Further, we report a novel approach to quantifying immunolabelled mitochondrial DNA that provides single-cell estimates of mCN that closely agree with the population analyses by ddPCR. The combination of these assays represents a cost-effective and powerful suite of tools to study mCN.
机译:线粒体DNA拷贝数(mCN)的绝对定量提供了许多研究领域的重要见解,包括癌症,心血管疾病和生殖健康。液滴数字PCR(ddPCR)原生报告绝对拷贝数,并且我们开发了一种单染料,多重测定法来测量大鼠mCN,该方法准确,精确且负担得起。我们展示了简单的方法来优化此测定法,并确定核参照假基因拷贝数,以扩展可以用该测定法测量的mCN范围。我们评估了两个常用的线粒体DNA参考基因座,以确定mCN,ND1基因和D-Loop。利用ddPCR的绝对方法,我们发现D-Loop相对于线粒体基因组上的其他位点扩增了约1.0-1.5的拷贝数。在大鼠和组织(主动脉,大脑,心脏,肝脏,比目鱼肌)之间,此异常拷贝数差异很大。我们提倡在未来的mCN研究中避免使用D-Loop作为线粒体参考。此外,我们报告了一种新的量化免疫标记线粒体DNA的方法,该方法可提供与ddPCR的群体分析非常吻合的mCN单细胞估计。这些测定法的组合代表了一套经济高效且功能强大的研究mCN的工具。

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