Publication | Open Access
The aryl hydrocarbon receptor regulates nucleolar activity and protein synthesis in MYC-expressing cells
43
Citations
28
References
2018
Year
Molecular RegulationMolecular BiologyCancer BiologyCellular PhysiologyTumor BiologyMyc-driven TumorsProtein SynthesisTranscriptional RegulationSignaling PathwayCell RegulationMyc-expressing CellsCancer Cell BiologyCell SignalingMyc-induced Protein TranslationMolecular PathwayAryl Hydrocarbon ReceptorReceptor (Biochemistry)Gene ExpressionCell BiologySignal TransductionNatural SciencesCellular BiochemistryMedicine
MYC enhances protein synthesis by regulating genes involved in ribosome biogenesis and protein translation. Here, we show that MYC-induced protein translation is mediated by the transcription factor aryl hydrocarbon receptor (AHR), which is induced by MYC in colonic cells. AHR promotes protein synthesis by activating the transcription of genes required for ribosome biogenesis and protein translation, including OGFOD1 and NOLC1. Using surface sensing of translation (SUnSET) to measure global protein translation, we found that silencing AHR or its targets diminishes protein synthesis. Therefore, targeting AHR or its downstream pathways could provide a novel approach to limit biomass production in MYC-driven tumors.
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