Regulatory mechanisms of cellular response to oxidative stress

被引:335
作者
Itoh, K
Ishii, T
Wakabayashi, N
Yamamoto, M
机构
[1] Univ Tsukuba, Ctr TARA, Tsukuba, Ibaraki 3058577, Japan
[2] Univ Tsukuba, Inst Basic Med Sci, Tsukuba, Ibaraki 3058577, Japan
关键词
ARE; EpRE; Nrf2; phase II enzyme;
D O I
10.1080/10715769900300881
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
An antioxidant responsive element (ARE) or electrophile responsive element (EpRE) mediates the transcriptional activation of genes encoding phase II drug metabolizing enzymes. The ARE consensus sequence shows high similarity to an erythroid gene regulatory element, and based on the observation, we have recently found that transcription factor Nrf2 is essential for the coordinate induction of phase II detoxifying enzymes. The expression of anti-oxidative stress enzyme genes is also regulated by Nrf2. Detailed analysis of the regulatory mechanisms of Nrf2 activity has ultimately led us to the identification of a new protein, which we have named Keap1, that suppresses Nrf2 activity by specific binding to its evolutionarily-conserved N-terminal Neh2 regulatory domain.
引用
收藏
页码:319 / 324
页数:6
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