Proceedings of the National Academy of Sciences · 2017 · 61 citations · 27 references
Life SciencesCell BiologyMolecular BiologyCarcinogenesisCell SignalingSignal TransductionCancer Cell SignalingCancer Stem Cell MaintenanceCancer Stem CellsOncogenic Signaling PathwaysSignal Transduction In CancerWnt SignalingApc InactivationBeta-catenin RegulationDestruction ComplexIntestinal Stem CellsRegulation By E3 Ubiquitin LigasesWnt Signaling DisruptionWnt Signaling In Stem Cell MaintenanceWnt Target Gene Regulation
) gene, whose product is an important component of the destruction complex that regulates β-catenin levels. Stabilization and nuclear localization of β-catenin result in the expression of a panel of Wnt target genes. We previously showed that Mule/Huwe1/Arf-BP1 (Mule) controls murine intestinal stem and progenitor cell proliferation by modulating the Wnt pathway via c-Myc. Here we extend our investigation of Mule's influence on oncogenesis by showing that Mule interacts directly with β-catenin and targets it for degradation under conditions of hyperactive Wnt signaling. Our findings suggest that Mule uses various mechanisms to fine-tune the Wnt pathway and provides multiple safeguards against tumorigenesis.
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