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大鼠NAD(P)H:醌还原酶基因的转录调控。平面芳香化合物和酚类抗氧化剂对控制基础水平表达和诱导性表达的调控元件的鉴定。

Transcriptional regulation of the rat NAD(P)H:quinone reductase gene. Identification of regulatory elements controlling basal level expression and inducible expression by planar aromatic compounds and phenolic antioxidants.

作者信息

Favreau L V, Pickett C B

机构信息

Merck Frosst Centre for Therapeutic Research, Pointe-Claire-Dorval, Quebec, Canada.

出版信息

J Biol Chem. 1991 Mar 5;266(7):4556-61.

PMID:1900296
Abstract

We have identified two regions in the 5'-flanking sequence of the rat quinone reductase gene that contain xenobiotic responsive elements. The DNA sequence of the first region spans nucleotides -393 to -352 of the 5'-flanking region and shares sequence identity with the xenobiotic responsive element (XRE) described for the cytochrome P-450 CYPIA1 gene. The DNA sequence of the second region spans nucleotides -434 to -404 of the 5'-flanking region of the quinone reductase structural gene. When a synthetic oligonucleotide corresponding to nucleotides -434 to -404 was inserted in front of a heterologous promoter linked to the chloramphenicol acetyltransferase structural gene, an increase in basal level expression as well as responsiveness to beta-naphthoflavone and t-butylhydroquinone, but not 2,3,7,8-tetrachlorodibenzo-p-dioxin, was observed. The sequence, -434 to -404, did not have any sequence identity with the XRE but shared a large degree of identity with the antioxidant responsive element recently described for the rat glutathione S-transferase Ya subunit gene (Rushmore, T. H., King, R. G., Paulson, K. E., and Pickett, C. B. (1990) Proc. Natl. Acad. Sci. U. S. A. 87, 3826-3830; Rushmore, T. H., and Pickett, C. B. (1990) J. Biol. Chem. 265, 14648-14653). These results indicate that the antioxidant responsive element can be distinguished functionally from the classical XRE and is also involved in the regulation of the quinone reductase gene by planar aromatic compounds and phenolic antioxidants.

摘要

我们已在大鼠醌还原酶基因的5'侧翼序列中鉴定出两个含有外源性应答元件的区域。第一个区域的DNA序列跨越5'侧翼区域的核苷酸-393至-352,与细胞色素P-450 CYPIA1基因所描述的外源性应答元件(XRE)具有序列同源性。第二个区域的DNA序列跨越醌还原酶结构基因5'侧翼区域的核苷酸-434至-404。当将对应于核苷酸-434至-404的合成寡核苷酸插入与氯霉素乙酰转移酶结构基因相连的异源启动子之前时,观察到基础水平表达增加以及对β-萘黄酮和叔丁基对苯二酚有反应,但对2,3,7,8-四氯二苯并对二恶英无反应。序列-434至-404与XRE没有任何序列同源性,但与最近描述的大鼠谷胱甘肽S-转移酶Ya亚基基因的抗氧化剂应答元件有很大程度的同源性(拉什莫尔,T.H.,金,R.G.,保尔森,K.E.,和皮克特,C.B.(1990年)美国国家科学院院刊87,3826 - 3830;拉什莫尔,T.H.,和皮克特,C.B.(1990年)生物化学杂志265,14648 - 14653)。这些结果表明,抗氧化剂应答元件在功能上可与经典的XRE区分开来,并且也参与平面芳香化合物和酚类抗氧化剂对醌还原酶基因的调控。

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