TIF1{gamma} Regulates Epithelial Mesenchymal Transition by Operating as a SUMO E3 Ligase for theTranscriptional Regulator SnoN1 [Signal Transduction]

July 24th, 2014 by Ikeuchi, Y., Dadakhujaev, S., Chandhoke, A. S., Huynh, M. A., Oldenborg, A., Ikeuchi, M., Deng, L., Bennett, E. J., Harper, J. W., Bonni, A., Bonni, S.

Epithelial mesenchymal transition (EMT) is a fundamental cellular process that contributes to epithelial tissue morphogenesis during normal development and in tumor invasiveness and metastasis. The transcriptional regulator SnoN robustly influences EMT in response to the cytokine TGFβ, but the mechanisms that regulate the fundamental role of SnoN in TGFβ-induced EMT remain incompletely understood. Here, we employ interaction proteomics to uncover the signaling protein TIF1γ as a specific interactor of SnoN1 but not the closely related isoform SnoN2. A 16 amino acid peptide within a unique region of SnoN1 mediates the interaction of SnoN1 with TIF1γ. Strikingly, although TIF1γ is thought to act as a ubiquitin E3 ligase, we find that TIF1γ operates as a SUMO E3 ligase that promotes the sumoylation of SnoN1 at distinct lysine residues. Importantly, TIF1γ-induced sumoylation is required for the ability of SnoN1 to suppress TGFβ-induced EMT as assayed by the disruption of the morphogenesis of acini in a physiologically relevant three-dimensional model of NMuMG mammary epithelial cells. Collectively, our findings define a novel TIF1γ-SnoN1 sumoylation pathway that plays a critical role in EMT, with important implications for our understanding of TGFβ signaling and diverse biological processes in normal development and cancer biology.
  • Posted in Journal of Biological Chemistry, Publications
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