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大鼠肝脏NAD(P)H:醌还原酶。平面芳香化合物对醌还原酶基因表达的调控及醌还原酶结构基因外显子结构的确定。

Rat liver NAD(P)H: Quinone reductase. Regulation of quinone reductase gene expression by planar aromatic compounds and determination of the exon structure of the quinone reductase structural gene.

作者信息

Bayney R M, Morton M R, Favreau L V, Pickett C B

机构信息

Department of Molecular Pharmacology and Biochemistry, Merck Sharp & Dohme Research Laboratories, Rahway, New Jersey 07065.

出版信息

J Biol Chem. 1989 Dec 25;264(36):21793-7.

PMID:2480957
Abstract

We have determined the effect of beta-naphthoflavone and the azo dye, sudan III, on the level of quinone reductase mRNA in a responsive rat hepatoma cell line. Our data indicate that both of these planar aromatic compounds produce a 4-5-fold elevation in quinone reductase mRNA. The induction of quinone reductase mRNA can be blocked by cycloheximide, suggesting a requirement for ongoing protein synthesis in the induction process. We have determined the exon structure of the quinone reductase structural gene. The gene is separated into six exons by five introns. A "TATA" box is located 29 base pairs upstream from the transcription initiation site. A "CCAAT" sequence is found at position -129, and an inverted "GC" box is located at position -78. Quinone reductase promoter-chlor-amphenicol acetyltransferase fusion genes containing different lengths of the 5'-flanking region were transfected into rat and human hepatoma cells. Treatment of the transfected cells with beta-naphthoflavone or sudan III resulted in a 4-5-fold elevation in chloramphenicol acetyltransferase activity. These data suggest the presence of a cis-acting regulatory element(s) in the 5'-flanking region of the quinone reductase structural gene which regulates inducible expression.

摘要

我们已经确定了β-萘黄酮和偶氮染料苏丹III对一种反应性大鼠肝癌细胞系中醌还原酶mRNA水平的影响。我们的数据表明,这两种平面芳香族化合物均可使醌还原酶mRNA升高4至5倍。醌还原酶mRNA的诱导可被环己酰亚胺阻断,这表明诱导过程中需要持续的蛋白质合成。我们已经确定了醌还原酶结构基因的外显子结构。该基因被5个内含子分隔为6个外显子。一个“TATA”框位于转录起始位点上游29个碱基对处。在-129位置发现一个“CCAAT”序列,在-78位置有一个反向的“GC”框。将含有不同长度5'-侧翼区的醌还原酶启动子-氯霉素乙酰转移酶融合基因转染到大鼠和人肝癌细胞中。用β-萘黄酮或苏丹III处理转染细胞后,氯霉素乙酰转移酶活性升高4至5倍。这些数据表明,醌还原酶结构基因的5'-侧翼区存在一个顺式作用调节元件,可调节诱导性表达。

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