iScience · 2020 · 33 citations · 25 references
Life SciencesCell BiologyMolecular BiologyCell SignalingSignal TransductionTranscriptional RegulationCancer Cell SignalingCell Signaling NetworksOncogenic Signaling PathwaysPromoter ArchitectureProtein Kinase CascadesSignal Transduction ComplexesCis-acting Regulatory ElementsErk SignalingNegative FeedbackNegative Feedback MechanismsNegative Feedback SignalingNuclear-cytoplasmic InteractionsOncogenic Fusion ProteinsTranscriptional Activator Recruitment
-regulatory elements (CREs) in DUSP6 promoter. p90RSK, a downstream target of ERK1/2, phosphorylates CIC at S173 and S301 sites, which creates a 14-3-3 recognition motif, resulting in 14-3-3-mediated nuclear export of CIC and derepression of DUSP6. Finally, we demonstrate that the oncogenic CIC-DUX4 fusion protein acts as a transcriptional activator of DUSP6 and its nuclear/cytoplasmic distribution remains regulated by ERK1/2 signaling. These results complete an ERK1/2/p90RSK/CIC/DUSP6 negative feedback circuit and elucidate the molecular mechanism of how RTK/MAPK signaling harnesses the transcriptional repressor activity of CIC in mammalian cells.
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