Staurosporine通过CRE依赖方式刺激胰岛素基因表达。

Yoriko Shinozuka, Masayuki Okada, Nobuyuki Yasuda, Kazunari K Yokoyama
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引用次数: 1

摘要

我们检测了各种化合物来刺激大鼠胰岛素I启动子- plap报告基因稳定转染的胰腺HIT-T15细胞启动子-报告结构的转录,发现纳米剂量的斯陶菌素显著增强胰岛素启动子活性。Northern blotting分析和ELISA(酶联免疫吸附试验)结果显示,胰岛素基因启动子活性与HIT-T15内源性胰岛素mRNA和蛋白水平有良好的相关性,表明staurosporine在转录和翻译水平上刺激了胰岛素的生物合成。胰岛素基因启动子区cAMP反应元件(CRE)的缺失和点突变导致报告基因启动子活性丧失。这些结果表明,staurosporine刺激的胰岛素启动子活性是cre依赖性的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Staurosporine stimulates insulin gene expression via CRE dependent manner.

We examined various compounds to stimulate the transcription of promoter-reporter construct in pancreatic HIT-T15 cells, that had been stably transfected with the rat insulin I promoter-PLAP reporter gene, and found staurosporine at dose of nanomole enhanced insulin promoter activity significantly. Northern blotting analysis and ELISA (enzyme linked immunosorbent assay) showed that the promoter activity of insulin gene was well correlated with the endogenous level of insulin mRNA and protein in HIT-T15, indicating that staurosporine stimulated the biosynthesis of insulin at levels of transcription and translation. The deletion and point mutation of cAMP response element (CRE) in the promoter region of insulin gene lost the promoter activity of reporter gene induced by staurosporine. These results suggested that insulin promoter activity stimulated by staurosporine is CRE-dependent.

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