INSERM U827, 34000, Montpellier, France.
Cell Mol Life Sci. 2010 Jul;67(13):2297-309. doi: 10.1007/s00018-010-0336-4. Epub 2010 Mar 23.
A few studies have clearly indicated that oxidative stress suppresses the cystic fibrosis transmembrane conductance receptor (CFTR) function and expression. However, the mechanisms by which this occurs are still poorly understood. To clarify this effect, we investigated the role of NF-E2-related factor 2 (Nrf2) transcription factor, a key cellular sensor of oxidative stress. A conserved antioxidant response element (ARE) in the CFTR minimal promoter, which binds Nrf2, has been identified. Surprisingly, Nrf2 exerts an unexpected repressive role on the CFTR gene promoter activity. To decipher the molecular mechanisms involved, we evaluated the role of YY1 in the Nrf2-mediated transcriptional activity and showed cooperation between these two factors. We demonstrated that Nrf2 promotes YY1 nuclear localization and increases its binding to the CFTR promoter. To our knowledge, this study is the first to report a repressor role of Nrf2 through the cooperation with YY1 and contributes to clarify the cascade events leading to the oxidative stress-suppressed CFTR expression.
已有一些研究明确指出,氧化应激会抑制囊性纤维化跨膜电导调节因子(CFTR)的功能和表达。然而,其具体机制仍知之甚少。为了阐明这一效应,我们研究了 NF-E2 相关因子 2(Nrf2)转录因子的作用,该转录因子是氧化应激的关键细胞传感器。在 CFTR 最小启动子中已经鉴定出一个保守的抗氧化反应元件(ARE),它可以与 Nrf2 结合。令人惊讶的是,Nrf2 对 CFTR 基因启动子活性产生了意想不到的抑制作用。为了解释所涉及的分子机制,我们评估了 YY1 在 Nrf2 介导的转录活性中的作用,并表明这两个因素之间存在合作。我们证明,Nrf2 促进 YY1 的核定位,并增加其与 CFTR 启动子的结合。据我们所知,这项研究首次报道了 Nrf2 通过与 YY1 的合作发挥抑制作用,并有助于阐明导致氧化应激抑制 CFTR 表达的级联事件。