首页> 美国卫生研究院文献>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:去泛素酶USP9X对甲基CpG结合蛋白ZBTB38的稳定作用限制了人体细胞氧化应激的发生和毒性

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摘要

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:活性氧(ROS)是细胞代谢的副产物,也可能来自环境来源,例如毒素或辐射。根据剂量和环境,ROS在哺乳动物的发育和疾病中既有有益作用,也有有害作用,因此了解这些分子如何产生,感测和排毒至关重要。氧化应激如何与表观基因组联系的问题尤其重要,但尚未完全理解。在这里,我们表明表观遗传调节剂,甲基-CpG结合蛋白ZBTB38,限制了ROS的基础细胞产生,被ROS诱导,并且需要对氧化应激进行适当的反应。在分子上,这些功能取决于去泛素酶USP9X,该酶与ZBTB38相互作用,使其去泛素并使其稳定。我们发现,USP9X本身可以通过氧化应激稳定,并且需要与ZBTB38一起限制ROS的基础生成以及急性氧化应激的毒性。我们的数据揭示了USP9X的新核靶标,表明USP9X / ZBTB38轴限制了ROS的作用并对其进行了解毒,并在氧化应激和表观基因组之间提供了分子联系。

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