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亲电试剂加成的特定模式触发Keap1泛素化和Nrf2激活。

Specific patterns of electrophile adduction trigger Keap1 ubiquitination and Nrf2 activation.

作者信息

Hong Fei, Sekhar Konjeti R, Freeman Michael L, Liebler Daniel C

机构信息

Department of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson, Arizona 85721, USA.

出版信息

J Biol Chem. 2005 Sep 9;280(36):31768-75. doi: 10.1074/jbc.M503346200. Epub 2005 Jun 28.

Abstract

Activation of the transcription factor Nrf2 regulates expression of phase II enzymes and other adaptive responses to electrophile and oxidant stress. Nrf2 concentrations are regulated by the thiol-rich sensor protein Keap1, which is an adaptor protein for Cul3-dependent ubiquitination and degradation of Nrf2. However, the links between site specificity of Keap1 modification by electrophiles and mechanisms of Nrf2 activation are poorly understood. We studied the actions of the prototypical Nrf2 inducer tert-butylhydroquinone (tBHQ) and two biotin-tagged, thiol-reactive electrophiles, N-iodoacetyl-N-biotinylhexylenediamine (IAB) and 1-biotinamido-4-(4'-[maleimidoethyl-cyclohexane]-carboxamido)butane (BMCC). Both IAB and tBHQ induced antioxidant response element (ARE)-directed green fluorescent protein (GFP) expression in ARE/thymidine kinase GFP HepG2 cells, and both initiated nuclear Nrf2 accumulation and induction of heme oxygenase 1 in HEK293 cells. In contrast, BMCC produced none of these effects. Liquid chromatography tandem mass spectrometry (MS-MS) analysis of human Keap1 modified by IAB or BMCC in vitro indicated that IAB adduction occurred primarily in the central linker domain, whereas BMCC modified other Keap1 domains. Treatment of FLAG-Keap1-transfected HEK293 with the Nrf2-activating compounds IAB and tBHQ generated high molecular weight Keap1 forms, which were identified as K-48-linked polyubiquitin conjugates by immunoblotting and liquid chromatography MS-MS. Keap1 polyubiquitination coincided with Nrf2 stabilization and nuclear accumulation. In contrast, BMCC did not induce Keap1 polyubiquitination. Our results suggest that Nrf2 activation is regulated through the polyubiquitination of Keap1, which in turn is triggered by specific patterns of electrophile modification of the Keap1 central linker domain. These results suggest that Keap1 adduction triggers a switching of Cul3-dependent ubiquitination from Nrf2 to Keap1, leading to Nrf2 activation.

摘要

转录因子Nrf2的激活可调节II期酶的表达以及对亲电试剂和氧化应激的其他适应性反应。Nrf2的浓度受富含硫醇的传感蛋白Keap1调节,Keap1是一种衔接蛋白,参与Cul3依赖性的Nrf2泛素化和降解过程。然而,亲电试剂对Keap1修饰的位点特异性与Nrf2激活机制之间的联系仍知之甚少。我们研究了典型的Nrf2诱导剂叔丁基对苯二酚(tBHQ)以及两种生物素标记的、与硫醇反应的亲电试剂N-碘乙酰-N-生物素基己二胺(IAB)和1-生物素酰胺基-4-(4'-[马来酰亚胺基乙基-环己烷]-羧酰胺基)丁烷(BMCC)的作用。IAB和tBHQ均可在ARE/胸苷激酶绿色荧光蛋白(GFP)的HepG2细胞中诱导抗氧化反应元件(ARE)介导的绿色荧光蛋白(GFP)表达,并且二者均可在HEK293细胞中引发核Nrf2积累和血红素加氧酶1的诱导。相比之下,BMCC未产生上述任何效应。对体外经IAB或BMCC修饰的人Keap1进行液相色谱串联质谱(MS-MS)分析表明,IAB加合物主要出现在中央连接域,而BMCC修饰了Keap1的其他结构域。用Nrf2激活化合物IAB和tBHQ处理转染了FLAG-Keap1的HEK293细胞,产生了高分子量的Keap1形式,通过免疫印迹和液相色谱MS-MS鉴定为K-48连接的多聚泛素缀合物。Keap1多聚泛素化与Nrf2稳定和核积累同时发生。相比之下,BMCC未诱导Keap1多聚泛素化。我们的结果表明,Nrf2激活是通过Keap1的多聚泛素化来调节的,而这又由Keap1中央连接域亲电试剂修饰的特定模式触发。这些结果表明,Keap1加合物触发了Cul3依赖性泛素化从Nrf2向Keap1的转换,从而导致Nrf2激活。

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