Genomic sequence of human glyoxalase-I: analysis of promoter activity and its regulation

被引:63
作者
Ranganathan, S [1 ]
Ciaccio, PJ [1 ]
Walsh, ES [1 ]
Tew, KD [1 ]
机构
[1] Fox Chase Canc Ctr, Dept Pharmacol, Philadelphia, PA 19111 USA
关键词
diabetes; glutathione-binding; insulin; methylglyoxal; zinc-binding;
D O I
10.1016/S0378-1119(99)00420-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Glyoxalase-I is a glutathione-binding protein involved in the detoxification of methylglyoxal, a by-product of glycolysis. Aberrations in the expression of human glyoxalase in cancer and diabetes have been reported. To gain a better understanding of the glyoxalase-I regulation under normal physiological conditions and in disease processes, we have cloned 12 kb of genomic sequence, comprising five exons, separated by four introns. A fragment comprising 982 bp of 5' flanking region was used in the pSEAP reporter system to identify the minimal promoter and to locate any cis-acting functional elements. This region contained a minimal promoter between -20 and -160 bp. Cells transfected with a construct containing the 5' flanking sequence exhibited a 45-fold higher activity over vector transfected cells. A twofold reproducible increase in reporter activity was seen with insulin and ZnCl2 treatments, indicating a functionally operative insulin response element (IRE) and metal response element (MRE). Knowledge regarding the regulation of glyoxalase-I may provide insights into the importance of this enzyme in human diseases. (C) 1999 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:149 / 155
页数:7
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