Journal of Cell Science · 2010 · 86 citations · 30 references
Life SciencesCell BiologyMolecular BiologyCarcinogenesisCell SignalingMolecular OncologyCytokine Receptor SignalingProtein Complex AnalysisCoiled-coil DomainsCoiled-coil MotifsJak-stat Signaling PathwayRing Finger DomainsStat3 SignalingTripartite StructureUbiquitin-proteasome ProteolysisUbiquitin-proteasome Signaling
TRIM8 is a member of the protein family defined by the presence of a common domain structure composed of a tripartite motif: a RING-finger, one or two B-box domains and a coiled-coil motif. Here, we show that TRIM8 interacts with protein inhibitor of activated STAT3 (PIAS3), which inhibits IL-6-dependent activation of STAT3. Ectopic expression of TRIM8 cancels the negative effect of PIAS3 on STAT3, either by degradation of PIAS3 through the ubiquitin-proteasome pathway or exclusion of PIAS3 from the nucleus. Furthermore, expression of TRIM8 in NIH3T3 cells enhances Src-dependent tumorigenesis. These findings indicate that TRIM8 enhances the STAT3-dependent signal pathway by inhibiting the function of PIAS3.
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The tripartite motif family identifies cell compartments
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