Cytosolic Accumulation of Small Nucleolar RNAs (snoRNAs) Is Dynamically Regulated by NADPH Oxidase |
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Authors: | Christopher L. Holley Melissa W. Li Benjamin S. Scruggs Scot J. Matkovich Daniel S. Ory Jean E. Schaffer |
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Affiliation: | From the ‡Diabetic Cardiovascular Disease Center and ;§Center for Pharmacogenomics, Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missiouri 63110 |
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Abstract: | 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. |
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Keywords: | Intracellular Trafficking Molecular Cell Biology NADPH Oxidase Reactive Oxygen Species (ROS) Small Nucleolar RNA (snoRNA) Subcellular Fractionation Doxorubicin |
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