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Analysis of Induction Mechanisms of an Insulin-lnducible Transcription Factor SHARP-2 Gene by (-)-Epigallocatechin-3-gallate

机译:(-)-Epigallocatechin-3-gallate诱导胰岛素诱导的转录因子SHARP-2基因的诱导机制分析

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The rat enhancer of split- and hairy-related protein-2 (SHARP-2) is an insulin-inducible transcription factor. In this study, we examined the mechanism(s) involved in the regulation of the rat SHARP-2 gene expression by (-)-epigallocatechin-3-gallate (EGCG). The induction of SHARP-2 mRNA by EGCG was repressed by pretreatments with inhibitors for either phosphoinositide 3-kinase (PI3K.) or RNA polymerase II. Then, we examined a biological relationship between EGCG and transcription factor NF-kB interfering with the insulin action. The protein levels of the NF-kB were rapidly decreased by an EGCG treatment. Finally, the mechanism(s) of transcriptional activation of the rat SHARP-2 gene by both NF-kB and EGCG was analyzed. While overexpression of the NF-/cB p65 protein decreased the promoter activity of the SHARP-2 gene, EGCG did not affect it. Thus, we conclude that EGCG induces the expression of the rat SHARP-2 gene via both the PI3K pathway and degradation of the NF-kB p65 protein.
机译:大鼠与毛发相关蛋白2(SHARP-2)的增强子是胰岛素诱导的转录因子。在这项研究中,我们研究了通过(-)-epigallocatechin-3-gallate(EGCG)调控大鼠SHARP-2基因表达的机制。通过用磷酸肌醇3-激酶(PI3K。)或RNA聚合酶II的抑制剂预处理抑制了EGCG对SHARP-2 mRNA的诱导。然后,我们检查了EGCG和转录因子NF-kB干扰胰岛素作用之间的生物学关系。通过EGCG处理,NF-kB的蛋白质水平迅速降低。最后,分析了NF-kB和EGCG对大鼠SHARP-2基因转录激活的机制。 NF- / cB p65蛋白的过表达降低了SHARP-2基因的启动子活性,而EGCG却没有影响它。因此,我们得出结论,EGCG通过PI3K途径和NF-kB p65蛋白的降解诱导了大鼠SHARP-2基因的表达。

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