Human glutamate cysteine ligase gene regulation through the electrophile response element

被引:169
作者
Dickinson, DA
Levonen, AL
Moellering, DR
Arnold, EK
Zhang, HQ
Darley-Usmar, VM
Forman, HJ
机构
[1] Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Environm Hlth Sci, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Mol & Cellular Div, Birmingham, AL 35294 USA
[4] Univ Alabama Birmingham, Ctr Free Rad Biol, Birmingham, AL 35294 USA
[5] Univ Alabama Birmingham, Dept Nutr Sci, Birmingham, AL 35294 USA
[6] Univ Kuopio, AI Virtanen Inst Mol Sci, FIN-70211 Kuopio, Finland
[7] Univ Calif Merced, Sch Nat Sci, Merced, CA 95344 USA
关键词
antioxidant defense; glutamate-cysteine ligase; GCS; Nrf2; redox cell signalling; thiol modification; free radicals;
D O I
10.1016/j.freeradbiomed.2004.06.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glutathione (GSH) is the primary nonprotein thiol in the cell. It has many important roles in cell function, including regulating redox-dependent signal transduction pathways. The content of GSH within the cell varies with stress. In many cases, a process involving GSH synthesis results in adaptation to subsequent stressors. Sustained increases in GSH content are controlled primarily through induction of two genes, Gclc and Gclm, leading to the synthesis of the rate: limiting enzyme for GSH synthesis, glutamate cysteine ligase. Each of these genes in humans has a number of putative enhancer elements in their promoters. Overall, the most important element in both Gclc and Gclm expression is the electrophile response element. We review the evidence that has led to this conclusion and the implications for the redox-dependent regulation of this critical intracellular antioxidant. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1152 / 1159
页数:8
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