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细胞对氧化应激反应的调控机制。

Regulatory mechanisms of cellular response to oxidative stress.

作者信息

Itoh K, Ishii T, Wakabayashi N, Yamamoto M

机构信息

Center for TARA and Institute for Basic Medical Sciences, University of Tsukuba, Japan.

出版信息

Free Radic Res. 1999 Oct;31(4):319-24. doi: 10.1080/10715769900300881.

Abstract

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.

摘要

抗氧化反应元件(ARE)或亲电反应元件(EpRE)介导编码II相药物代谢酶的基因的转录激活。ARE共有序列与一种红系基因调控元件高度相似,基于这一观察结果,我们最近发现转录因子Nrf2对于II相解毒酶的协同诱导至关重要。抗氧化应激酶基因的表达也受Nrf2调控。对Nrf2活性调控机制的详细分析最终使我们鉴定出一种新蛋白,我们将其命名为Keap1,它通过与Nrf2进化保守的N端Neh2调控域特异性结合来抑制Nrf2活性。

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