Abstract

Data analysis methods for estimating promoter activity from gene reporter data frequently involve the reconstruction of the dynamics of unobserved species and numerical search algorithms for determining optimal model parameters. In contrast, we argue that posttranscriptional dynamics effectively behave like a singlestep stochastic process when gene expression variability is relatively low and, half-lives of the unobserved species are relatively small compared to characteristic observation time scales. In this case, by means of maximum likelihood estimators, for which analytical expressions exist, transcriptional activity of gene promoters can be estimated directly from observed gene reporter data without the need for numerical search algorithms and the reconstruction of unobserved variables. In addition, the model-based data analysis approach yields a single variable that measures the effective strength of the sources that give rise to gene expression variability. The approach is applied to conduct a model-based analysis of the inflammatory pathway under hypoxia condition and stimulation with tumor necrosis factor alpha in HEK293 cells.

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