Role of Nrf1 in antioxidant response element-mediated gene expression and beyond

被引:169
作者
Biswas, Madhurima [1 ]
Chan, Jefferson Y. [1 ]
机构
[1] Univ Calif Irvine, Dept Pathol & Lab Med, Irvine, CA 92697 USA
关键词
Oxidative stress; bZIP factor; Nrf1; Nrf2; Antioxidant; BZIP TRANSCRIPTION FACTOR; ENDOPLASMIC-RETICULUM; EMBRYONIC LETHALITY; NEGATIVE REGULATION; MOLECULAR-CLONING; OXIDATIVE STRESS; FACTOR TCF11; FAMILY; ACTIVATION; SELECTION;
D O I
10.1016/j.taap.2009.07.034
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Oxidative stress plays an important part in the pathogenesis of a variety of diseases. The ability to mount an efficient response against the continuous threat posed by exogenous and endogenous oxidants is essential for cellular homeostasis and survival. Oxidative stress activates transcription of a variety of antioxidant genes through cis-acting sequence known as antioxidant response element (ARE). Members of the Cap-N-Collar family of transcription factors, including Nrf1 and Nrf2, that bind ARE have been identified. Nrf1 and Nrf2 are expressed in a wide range of tissues and cell types, and both bind the ARE as heterodimers with small Maf proteins. Numerous studies indicate a pivotal role of Nrf2 in ARE function. Herein, we review data derived from cell-based studies and knockout mice in an attempt to define the role and regulation of Nrf1 in oxidative stress response and other functions. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:16 / 20
页数:5
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