Holley Christopher L, Li Melissa W, Scruggs Benjamin S, Matkovich Scot J, Ory Daniel S, Schaffer Jean E
From the Diabetic Cardiovascular Disease Center and.
Center for Pharmacogenomics, Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missiouri 63110.
J Biol Chem. 2015 May 1;290(18):11741-8. doi: 10.1074/jbc.M115.637413. Epub 2015 Mar 19.
Small nucleolar RNAs (snoRNAs) guide nucleotide modifications of cellular RNAs in the nucleus. We previously showed that box C/D snoRNAs from the Rpl13a locus are unexpected mediators of physiologic oxidative stress, independent of their predicted ribosomal RNA modifications. Here we demonstrate that oxidative stress induced by doxorubicin causes rapid cytoplasmic accumulation of the Rpl13a snoRNAs through a mechanism that requires superoxide and a nuclear splice variant of NADPH oxidase. RNA-sequencing analysis reveals that box C/D snoRNAs as a class are present in the cytoplasm, where their levels are dynamically regulated by NADPH oxidase. These findings suggest that snoRNAs may orchestrate the response to environmental stress through molecular interactions outside of the nucleus.
小核仁RNA(snoRNA)指导细胞核中细胞RNA的核苷酸修饰。我们之前表明,来自Rpl13a基因座的C/D盒snoRNA是生理氧化应激的意外介质,与其预测的核糖体RNA修饰无关。在这里,我们证明阿霉素诱导的氧化应激通过一种需要超氧化物和NADPH氧化酶的核剪接变体的机制,导致Rpl13a snoRNA在细胞质中快速积累。RNA测序分析表明,作为一类的C/D盒snoRNA存在于细胞质中,其水平由NADPH氧化酶动态调节。这些发现表明,snoRNA可能通过细胞核外的分子相互作用协调对环境应激的反应。