Abstract
Gene regulatory networks control the complex programs that drive development. Deciphering the connections between transcription factors (TFs) and target genes is challenging, in part because TFs bind to thousands of places in the genome but control expression through a subset of these binding events. We hypothesize that we can combine natural variation of expression levels and predictions of TF binding sites to identify TF targets. We gather RNA-seq data from 71 genetically distinct F1 Drosophila melanogaster embryos and calculate the correlations between TF and potential target genes' expression levels, which we call “regulatory strength.” To separate direct and indirect TF targets, we hypothesize that direct TF targets will have a preponderance of binding sites in their upstream regions. Using 14 TFs active during embryogenesis, we find that 12 TFs showed a significant correlation between their binding strength and regulatory strength on downstream targets, and 10 TFs showed a significant correlation between the number of binding sites and the regulatory effect on target genes. The general roles, e.g. bicoid’s role as an activator, and the particular interactions we observed between our TFs, e.g. twist’s role as a repressor of sloppy paired and odd paired, generally coincide with the literature.
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Osman, N.M., Kitapci, T.H., Vlaho, S. et al. Inference of Transcription Factor Regulation Patterns Using Gene Expression Covariation in Natural Populations of Drosophila melanogaster. BIOPHYSICS 63, 43–51 (2018). https://doi.org/10.1134/S0006350918010128
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DOI: https://doi.org/10.1134/S0006350918010128