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Functional and physical interaction between the selenium-binding protein 1 (SBP1) and the glutathione peroxidase 1 selenoprotein

机译:硒结合蛋白1(SBP1)和谷胱甘肽过氧化物酶1硒蛋白之间的功能和物理相互作用

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摘要

Selenium-binding protein (SBP) 1 is present in reduced levels in several cancer types as compared with normal tissues, and lower levels are associated with poor clinical prognosis. Another selenium-containing protein, glutathione peroxidase 1 (GPX1), has been associated with cancer risk and development. The interaction between these representatives of different classes of selenoproteins was investigated. Increasing SBP1 levels in either human colorectal or breast cancer cells by transfection of an expression construct resulted in the reduction of GPX1 enzyme activity. Increased expression of GPX1 in the same cell types resulted in the transcriptional and translational repression of SBP1, as evidenced by the reduction of SBP1 messenger RNA and protein and the inhibition of transcription measured using an SBP1 reporter construct. The opposing effects of SBP1 and GPX1 on each other were also observed when GPX1 was increased by supplementing the media of these tissue culture cells with selenium, and the effect of selenium on SBP1 was shown to be GPX1 dependent. Decreasing or increasing GPX1 levels in colonic epithelial cells of mice fed a selenium-deficient, -adequate or -supplemented diet resulted in the opposing effect on SBP1 levels. These data are explained in part by the demonstration that SBP1 and GPX1 form a physical association, as determined by coimmunoprecipitation and fluorescence resonance energy transfer assay. The results presented establish an interaction between two distinct selenium-containing proteins that may enhance the understanding of the mechanisms by which selenium and selenoproteins affect carcinogenesis in humans.
机译:与正常组织相比,硒结合蛋白(SBP)1在几种癌症类型中的含量降低,而较低的含量与不良的临床预后相关。另一个含硒的蛋白谷胱甘肽过氧化物酶1(GPX1)与癌症的风险和发展有关。研究了不同类别的硒蛋白的这些代表之间的相互作用。通过转染表达构建体而在人结肠直肠或乳腺癌细胞中增加SBP1水平会导致GPX1酶活性降低。 GPX1在相同细胞类型中表达的增加导致SBP1的转录和翻译受阻,如SBP1信使RNA和蛋白质的减少以及使用SBP1报告基因构建物检测到的转录抑制所证明的。当通过向这些组织培养细胞的培养基中添加硒来增加GPX1时,也观察到SBP1和GPX1彼此相反的作用,并且硒对SBP1的作用被证明是GPX1依赖性的。饲喂缺乏硒,充足或补充饮食的小鼠结肠上皮细胞中GPX1水平的降低或增加导致对SBP1水平的相反作用。这些数据部分通过证明SBP1和GPX1形成了物理缔合来解释,如通过免疫共沉淀和荧光共振能量转移测定所确定的。提出的结果建立了两种不同的含硒蛋白之间的相互作用,可以增强对硒和硒蛋白影响人类致癌作用机理的理解。

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