Garcia-Bardon Andreas, Thal Serge C
Department of Anesthesiology, Medical Center of the Johannes Gutenberg University, Mainz, Germany.
PLoS One. 2016 Nov 29;11(11):e0167209. doi: 10.1371/journal.pone.0167209. eCollection 2016.
Real-time reverse transcription polymerase chain reaction (PCR) is the gold standard for expression analysis. Designed to improve reproducibility and sensitivity, commercial kits are commonly used for the critical step of cDNA synthesis. The present study was designed to determine the impact of these kits. mRNA from mouse brains were pooled to create serial dilutions ranging from 0.0625 μg to 2 μg, which were transcribed into cDNA using four different commercial reverse-transcription kits. Next, we transcribed mRNA from brain tissue after acute brain injury and naïve mice into cDNA for qPCR. Depending on tested genes, some kits failed to show linear results in dilution series and revealed strong variations in cDNA yield. Absolute expression data in naïve and trauma settings varied substantially between these kits. Normalization with a housekeeping gene failed to reduce kit-dependent variations, whereas normalization eliminated differences when naïve samples from the same region were used. The study shows strong evidence that choice of commercial cDNA synthesis kit has a major impact on PCR results and, consequently, on comparability between studies. Additionally, it provides a solution to overcome this limitation by normalization with data from naïve samples. This simple step helps to compare mRNA expression data between different studies and groups.
实时逆转录聚合酶链反应(PCR)是表达分析的金标准。为提高重现性和灵敏度而设计的商业试剂盒通常用于cDNA合成这一关键步骤。本研究旨在确定这些试剂盒的影响。将来自小鼠大脑的mRNA汇集起来,制成浓度范围从0.0625μg到2μg的系列稀释液,使用四种不同的商业逆转录试剂盒将其转录为cDNA。接下来,我们将急性脑损伤后小鼠脑组织和未受伤小鼠的mRNA转录为cDNA用于定量PCR。根据所检测的基因,一些试剂盒在稀释系列中未显示出线性结果,并且在cDNA产量上表现出很大差异。在未受伤和创伤情况下,这些试剂盒之间的绝对表达数据差异很大。用管家基因进行标准化未能减少试剂盒依赖性差异,而当使用来自同一区域的未受伤样本进行标准化时,则消除了差异。该研究有力地证明,商业cDNA合成试剂盒的选择对PCR结果有重大影响,因此也对不同研究之间的可比性有重大影响。此外,它提供了一种通过用未受伤样本的数据进行标准化来克服这一局限性的解决方案。这一简单步骤有助于比较不同研究和组之间的mRNA表达数据。