Cullinan Sara B, Gordan John D, Jin Jianping, Harper J Wade, Diehl J Alan
The Leonard and Madlyn Abramson Family Cancer Research Institute and Cancer Center, Department of Cancer Biology, University of Pennsylvania Cancer Center, 454 BRB II/III, 421 Curie Blvd., Philadelphia, PA 19104, USA.
Mol Cell Biol. 2004 Oct;24(19):8477-86. doi: 10.1128/MCB.24.19.8477-8486.2004.
The Nrf2 transcription factor promotes survival following cellular insults that trigger oxidative damage. Nrf2 activity is opposed by the BTB/POZ domain protein Keap1. Keap1 is proposed to regulate Nrf2 activity strictly through its capacity to inhibit Nrf2 nuclear import. Recent work suggests that inhibition of Nrf2 may also depend upon ubiquitin-mediated proteolysis. To address the contribution of Keap1-dependent sequestration versus Nrf2 proteolysis, we identified the E3 ligase that regulates Nrf2 ubiquitination. We demonstrate that Keap1 is not solely a cytosolic anchor; rather, Keap1 is an adaptor that bridges Nrf2 to Cul3. We demonstrate that Cul3-Keap1 complexes regulate Nrf2 polyubiquitination both in vitro and in vivo. Inhibition of either Keap1 or Cul3 increases Nrf2 nuclear accumulation, leading to promiscuous activation of Nrf2-dependent gene expression. Our data demonstrate that Keap1 restrains Nrf2 activity via its capacity to target Nrf2 to a cytoplasmic Cul3-based E3 ligase and suggest a model in which Keap1 coordinately regulates both Nrf2 accumulation and access to target genes.
Nrf2转录因子在引发氧化损伤的细胞损伤后促进细胞存活。Nrf2的活性受到BTB/POZ结构域蛋白Keap1的拮抗。有人提出,Keap1严格通过其抑制Nrf2核输入的能力来调节Nrf2的活性。最近的研究表明,对Nrf2的抑制也可能取决于泛素介导的蛋白水解作用。为了探讨Keap1依赖性隔离与Nrf2蛋白水解的作用,我们鉴定了调节Nrf2泛素化的E3连接酶。我们证明,Keap1不仅仅是一种胞质锚定蛋白;相反,Keap1是一种衔接蛋白,可将Nrf2与Cul3连接起来。我们证明,Cul3-Keap1复合物在体外和体内均调节Nrf2的多聚泛素化。抑制Keap1或Cul3都会增加Nrf2的核积累,导致Nrf2依赖性基因表达的过度激活。我们的数据表明,Keap1通过将Nrf2靶向基于Cul3的胞质E3连接酶的能力来抑制Nrf2的活性,并提出了一个模型,其中Keap1协调调节Nrf2的积累及其对靶基因的作用。