首页> 外文期刊>FEBS Letters >Phenobarbital induces cytochrome P4501A2 hnRNA, mRNA and protein in the liver of C57BL/6J wild type and aryl hydrocarbon receptor knock‐out mice
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Phenobarbital induces cytochrome P4501A2 hnRNA, mRNA and protein in the liver of C57BL/6J wild type and aryl hydrocarbon receptor knock‐out mice

机译:苯巴比妥诱导C57BL / 6J野生型和芳烃受体敲除小鼠肝脏中的细胞色素P4501A2 hnRNA,mRNA和蛋白质

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摘要

>The aryl hydrocarbon receptor mediates the transcriptional response to a variety of hydrocarbons of members of the aryl hydrocarbon gene battery. Phenobarbital does not bind the aryl hydrocarbon receptor with high affinity but induces, in liver cells, expression of cytochrome P4501A. Using both wild type and aryl hydrocarbon receptor knock out C57BL/6J mice, we demonstrate that phenobarbital induced hnRNA, mRNA and protein for the cytochrome P-4501A2 gene in the presence or absence of the aryl hydrocarbon receptor. Using the DNA binding site for the aryl hydrocarbon receptor as a probe, gel retardation analyses showed that phenobarbital treatment induced protein binding, regardless of the presence of the aryl hydrocarbon receptor.
机译:芳基烃受体介导对芳基烃基因电池成员的多种烃的转录反应。苯巴比妥不以高亲和力结合芳基烃受体,而是在肝细胞中诱导细胞色素P4501A的表达。使用野生型和芳基烃受体敲除C57BL / 6J小鼠,我们证明了在存在或不存在芳基烃受体的情况下苯巴比妥诱导的hnRNA,mRNA和细胞色素P-4501A2基因的蛋白。使用芳基烃受体的DNA结合位点作为探针,凝胶阻滞分析表明,无论芳基烃受体的存在如何,苯巴比妥治疗均可诱导蛋白结合。

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