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一种与细胞色素P-4501A1基因的外源性反应元件(XRE)结合的因子至少由两种螺旋-环-螺旋蛋白组成,即芳烃受体(Ah受体)和芳香烃受体核转运蛋白(Arnt)。

A factor binding to the xenobiotic responsive element (XRE) of P-4501A1 gene consists of at least two helix-loop-helix proteins, Ah receptor and Arnt.

作者信息

Matsushita N, Sogawa K, Ema M, Yoshida A, Fujii-Kuriyama Y

机构信息

Department of Chemistry, Faculty of Science, Tohoku University, Sendai, Japan.

出版信息

J Biol Chem. 1993 Oct 5;268(28):21002-6.

PMID:8407937
Abstract

Xenobiotic responsive element (XRE) is an inducible enhancer element that drives inducible expression of P-4501A1 gene in response to xenobiotic inducers. The XRE-binding factor appears in the nuclei of Hepa-1 cells treated with 3-methylcholanthrene (3-MC). Association of the Ah receptor and Arnt (Ah receptor nuclear translocator) in an XRE-binding complex was examined by anti-Ah receptor and Arnt antibodies. Both antibodies inhibited the sequence-specific XRE-binding activity of nuclear extracts from 3-MC-treated Hepa-1 cells and of the cytosolic fraction which was prepared from the nontreated cells and treated in vitro with 3-MC. These results indicate that Ah receptor and Arnt proteins are components of the XRE-binding factor and suggest that Arnt as well as the Ah receptor are localized in the cytosol of nontreated cells. The Ah receptor present in C4 cells, a mutant of Hepa-1 cells defective in the Arnt function, showed an inducer-dependent association with Arnt synthesized in an in vitro translation system. Co-transfection of the expression plasmids of the Ah receptor and Arnt exhibited synergistically more activated transcription from a reporter gene pMC6.3k consisting of the P-4501A1 gene promoter and enhancer than transfection with either of the two plasmids alone. These findings indicate that the Ah receptor and Arnt proteins form a complex that activates transcription in an inducer-dependent manner.

摘要

外源性物质反应元件(XRE)是一种可诱导的增强子元件,可驱动P-4501A1基因对外源性诱导剂产生可诱导性表达。在用3-甲基胆蒽(3-MC)处理的Hepa-1细胞的细胞核中出现了XRE结合因子。通过抗Ah受体和Arnt(Ah受体核转运蛋白)抗体检测了XRE结合复合物中Ah受体与Arnt的结合情况。两种抗体均抑制了来自3-MC处理的Hepa-1细胞的核提取物以及从未经处理的细胞制备并在体外经3-MC处理的胞质部分的序列特异性XRE结合活性。这些结果表明,Ah受体和Arnt蛋白是XRE结合因子的组成成分,并提示Arnt以及Ah受体定位于未经处理细胞的胞质溶胶中。存在于C4细胞(一种Arnt功能缺陷的Hepa-1细胞突变体)中的Ah受体,显示出与体外翻译系统中合成的Arnt存在诱导剂依赖性结合。Ah受体和Arnt的表达质粒共转染,与单独转染这两种质粒之一相比,由P-4501A1基因启动子和增强子组成的报告基因pMC6.3k的转录激活协同作用更强。这些发现表明,Ah受体和Arnt蛋白形成了一种复合物,该复合物以诱导剂依赖性方式激活转录。

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