Repele Andrea
Department of Biology, University of North Dakota, Grand Forks, ND 58202, USA.
Methods Protoc. 2019 Jul 25;2(3):62. doi: 10.3390/mps2030062.
Transient Luciferase reporter assays are widely used in the study of gene regulation and intracellular cell signaling. In order to control for sample-to-sample variation in luminescence arising from variability in transfection efficiency and other sources, an internal control reporter is co-transfected with the experimental reporter. The luminescence of the experimental reporter is normalized against the control by taking the ratio of the two. Here we show that this method of normalization, "ratiometric", performs poorly when the transfection efficiency is low and leads to biased estimates of relative activity. We propose an alternative methodology based on linear regression that is much better suited for the normalization of reporter data, especially when transfection efficiency is low. We compare the ratiometric method against three regression methods on both simulated and empirical data. Our results suggest that robust errors-in-variables (REIV) regression performs the best in normalizing Luciferase reporter data. We have made the R code for Luciferase data normalization using REIV available on GitHub.
瞬时荧光素酶报告基因检测在基因调控和细胞内信号传导研究中被广泛应用。为了控制因转染效率和其他来源的差异而导致的样本间发光差异,将一个内参报告基因与实验报告基因共转染。通过计算两者的比值,将实验报告基因的发光值相对于内参进行归一化处理。我们在此表明,这种“比例法”归一化方法在转染效率较低时表现不佳,并会导致相对活性的估计出现偏差。我们提出了一种基于线性回归的替代方法,该方法更适合用于报告基因数据的归一化,尤其是在转染效率较低时。我们在模拟数据和实证数据上,将比例法与三种回归方法进行了比较。我们的结果表明,稳健变量误差(REIV)回归在归一化荧光素酶报告基因数据方面表现最佳。我们已将使用REIV进行荧光素酶数据归一化的R代码发布在GitHub上。