Genetic and biochemical studies have led to the identification of the Stat3-Interacting Protein StIP1. The preferential association of StIP1 with inactive (i.e., unphosphorylated) Stat3 suggests that it may contribute to the regulation of Stat3 activation. Consistent with this possibility, StIP1 also exhibits an affinity for members of the Janus kinase family. Overexpression of the Stat3-binding domain of StIP1 blocks Stat3 activation, nuclear translocation, and Stat3-dependent induction of a reporter gene. These studies indicate that StIP1 regulates the ligand-dependent activation of Stat3, potentially by serving as a scaffold protein that promotes the interaction between Janus kinases and their Stat3 substrate. The ability of StIP1 to associate with several additional members of the signal transducer and activator of transcription family suggests that StIP1 may serve a broader role in cytokine-signaling events.
机构:
Oregon Hlth Sci Univ, Howard Hughes Med Inst L474, Vollum Inst, Portland, OR 97201 USAOregon Hlth Sci Univ, Howard Hughes Med Inst L474, Vollum Inst, Portland, OR 97201 USA
Schillace, RV
Scott, JD
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机构:
Oregon Hlth Sci Univ, Howard Hughes Med Inst L474, Vollum Inst, Portland, OR 97201 USAOregon Hlth Sci Univ, Howard Hughes Med Inst L474, Vollum Inst, Portland, OR 97201 USA
机构:
Oregon Hlth Sci Univ, Howard Hughes Med Inst L474, Vollum Inst, Portland, OR 97201 USAOregon Hlth Sci Univ, Howard Hughes Med Inst L474, Vollum Inst, Portland, OR 97201 USA
Schillace, RV
Scott, JD
论文数: 0引用数: 0
h-index: 0
机构:
Oregon Hlth Sci Univ, Howard Hughes Med Inst L474, Vollum Inst, Portland, OR 97201 USAOregon Hlth Sci Univ, Howard Hughes Med Inst L474, Vollum Inst, Portland, OR 97201 USA