首页> 外文期刊>Nucleic Acids Research >Stabilization of the methyl-CpG binding protein ZBTB38 by the deubiquitinase USP9X limits the occurrence and toxicity of oxidative stress in human cells
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Stabilization of the methyl-CpG binding protein ZBTB38 by the deubiquitinase USP9X limits the occurrence and toxicity of oxidative stress in human cells

机译:脱硫酶USP9X稳定甲基-CPG结合蛋白ZBTB38限制了人细胞中氧化应激的发生和毒性

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Reactive oxygen species (ROS) are a byproduct of cell metabolism, and can also arise from environmental sources, such as toxins or radiation. Depending on dose and context, ROS have both beneficial and deleterious roles in mammalian development and disease, therefore it is crucial to understand how these molecules are generated, sensed, and detoxified. The question of how oxidative stress connects to the epigenome, in particular, is important yet incompletely understood. Here we show that an epigenetic regulator, the methyl-CpG-binding protein ZBTB38, limits the basal cellular production of ROS, is induced by ROS, and is required to mount a proper response to oxidative stress. Molecularly, these functions depend on a deubiquitinase, USP9X, which interacts with ZBTB38, deubiquitinates it, and stabilizes it. We find that USP9X is itself stabilized by oxidative stress, and is required together with ZBTB38 to limit the basal generation of ROS, as well as the toxicity of an acute oxidative stress. Our data uncover a new nuclear target of USP9X, show that the USP9X/ZBTB38 axis limits, senses and detoxifies ROS, and provide a molecular link between oxidative stress and the epigenome.
机译:反应性氧物质(ROS)是细胞代谢的副产物,并且也可以从环境源产生,例如毒素或辐射。根据剂量和背景,ROS在哺乳动物的发展和疾病中具有有益和有害的作用,因此了解如何产生,感测和解毒。氧化应激如何连接到外形内蛋白组的问题是重要的,但重要的是不完全理解。在这里,我们表明,由ROS诱导了表观遗传调节剂,甲基-CPG结合蛋白ZBTB38限制了ROS的基础细胞生成,并且需要安装适当的氧化应激。分子量,这些功能依赖于脱硫结酶U​​SP9x,其与ZBTB38相互作用,脱硫酯,并稳定它。我们发现USP9X本身通过氧化应激稳定,并且是与ZBTB38一起稳定的,以限制ROS的基础产生,以及急性氧化应激的毒性。我们的数据揭示了USP9X的新核目标,表明USP9X / ZBTB38轴限制,感测和排毒ROS,并提供氧化应激和外延蛋白之间的分子链。

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