4.6 Article

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

期刊

TOXICOLOGY AND APPLIED PHARMACOLOGY
卷 244, 期 1, 页码 16-20

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.taap.2009.07.034

关键词

Oxidative stress; bZIP factor; Nrf1; Nrf2; Antioxidant

资金

  1. NCI NIH HHS [R01 CA091907, R01 CA091907-05] Funding Source: Medline
  2. NIDDK NIH HHS [K08 DK002603-01, R03 DK063757-01] Funding Source: Medline

向作者/读者索取更多资源

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.

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