Title: Gene co-regulation and co-expression in the aryl hydrocarbon receptor-mediated transcriptional regulatory network in the mouse liver.

Authors: Josyula, Navya; Andersen, Melvin E; Kaminski, Norbert E; Dere, Edward; Zacharewski, Timothy R; Bhattacharya, Sudin

Published In Arch Toxicol, (2020 01)

Abstract: Four decades after its discovery, the aryl hydrocarbon receptor (AHR), a ligand-inducible transcription factor (TF) activated by the persistent environmental contaminant 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD), remains an enigmatic molecule with a controversial endogenous role. Here, we have assembled a global map of the AHR gene regulatory network in female C57BL/6 mice orally gavaged with 30 µg/kg of TCDD from a combination of previously published gene expression and genome-wide TF-binding data sets. Using Kohonen self-organizing maps and subspace clustering, we show that genes co-regulated by common upstream TFs in the AHR network exhibit a pattern of co-expression. Directly bound, indirectly bound, and non-genomic AHR target genes exhibit distinct expression patterns, with the directly bound targets associated with highest median expression. Interestingly, among the directly bound AHR target genes, the expression level increases with the number of AHR-binding sites in the proximal promoter regions. Finally, we show that co-regulated genes in the AHR network activate distinct groups of downstream biological processes. Although the specific findings described here are restricted to hepatic effects under short-term TCDD exposure, this work describes a generalizable approach to the reconstruction and analysis of transcriptional regulatory cascades underlying cellular stress response, revealing network hierarchy and the nature of information flow from the initial signaling events to phenotypic outcomes. Such reconstructed networks can form the basis of a new generation of quantitative adverse outcome pathways.

PubMed ID: 31728591

MeSH Terms: Animals; Basic Helix-Loop-Helix Transcription Factors/genetics*; Basic Helix-Loop-Helix Transcription Factors/metabolism; Chromatin Immunoprecipitation Sequencing; Female; Gene Regulatory Networks/drug effects*; Liver/drug effects*; Liver/physiology; Mice, Inbred C57BL; Multigene Family; Polychlorinated Dibenzodioxins/toxicity*; Receptors, Aryl Hydrocarbon/genetics*; Receptors, Aryl Hydrocarbon/metabolism