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作 者:温进坤[1] 胡静[1] 魏素珍[1] 贾根深[1]
机构地区:[1]河北医学院基础医学研究所生化室
出 处:《生物化学杂志》1994年第6期733-736,共4页
摘 要:从对照和用DEHP处理的大鼠肝脏提取核蛋白,以含酰基CoA氧化酶(AOX)基因表达调控部位的DNA片段和该基因的不同蛋白结合位点的DNA片段作为核蛋白结合反应的探针,通过凝胶电泳迁移率改变实验和Southwestern印迹分析检查了DEHP对AOX基因反式作用因子的影响。结果表明,降血脂药物DEHP可显著增加AOX基因反式作用因子的含量和(或)与基因的结合活性,在转录水平上促进基因的表达。The liver nuclear proteins were extracted from the control and DEHP-treated wistar rats. Utilizing the radioactive DNA fragments containing upstream regulatory elements of AOX gene and protein-binding site A and B DNA fragments as probes, we have investigated the effect of hypolipidemic drug(DEHP) on the trans-acting factor(s) for AOX gene by electrophoretic band-shift experiment and Southwestern blot analysis. The results suggest that rat liver nuclear extracts contain a protein of 100kD which exhibits specific binding activity for the binding site B ,and that the 100kD protein was markedly increased in the liver of DEHP-treated rats. These data provide evidence for the presence of the trans-acting factor(s)that can be induced by DEHP in rat liver nuclei, which may be involved in the molecular events responsible for transcriptional regulation of AOX gene.
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