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Participation of altered upstream stimulatory factor in the induction of rat heme oxygenase-1 by cadmium.

机译:改变的上游刺激因子参与镉诱导的大鼠血红素加氧酶-1。

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摘要

We have reported that an upstream stimulatory factor (USF) binding site is functional in transcription of the heme oxygenase-1 gene. In this study, we examined the role of USF in the induced state. By transient expression analyses with the chloramphenicol acetyl-transferase gene, we found that the USF binding site plays an important role in the induction of rat heme oxygenase-1 by cadmium, but not by hemin. To elucidate the role of USF, we prepared USF-rich nuclear extracts from control and cadmium-treated rat liver. On electrophoretic mobility shift assay using control nuclear proteins, one slowly migrating band was detected, whereas using nuclear proteins of cadmium-treated rat liver, two fast migrating bands were detected. The molecular masses of the two subunits of USF prepared from cadmium-treated rat liver were approximately 34 kDa as determined by UV cross-linking and subsequent SDS-PAGE, while the two subunits of native USF were 43 kDa and 44 kDa. DNase I footprinting analysis revealed that both the nuclear proteins bound to the same region including the USF binding site. We therefore suppose that cadmium causes some structural changes in the two proteins of USF and that the altered USF participates in the effective initiation of transcription of the rat heme oxygenase-1 gene.
机译:我们已经报道了上游刺激因子(USF)结合位点在血红素加氧酶-1基因的转录中起作用。在这项研究中,我们检查了USF在诱导状态中的作用。通过使用氯霉素乙酰转移酶基因的瞬时表达分析,我们发现USF结合位点在镉诱导大鼠血红素加氧酶-1中起重要作用,而在血红素中则没有。为了阐明USF的作用,我们从对照和镉处理的大鼠肝脏中制备了富含USF的核提取物。在使用对照核蛋白的电泳迁移率变动分析中,检测到一个缓慢迁移的条带,而使用镉处理的大鼠肝脏的核蛋白,检测到两个快速迁移的条带。通过UV交联和随后的SDS-PAGE测定,由镉处理过的大鼠肝脏制备的USF的两个亚基的分子量约为34 kDa,而天然USF的两个亚基的分子量为43 kDa和44 kDa。 DNase I足迹分析表明,两种核蛋白都结合到包括USF结合位点的同一区域。因此,我们假设镉在USF的两种蛋白质中引起一些结构变化,而改变后的USF参与了大鼠血红素加氧酶-1基因转录的有效启动。

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