The NBDY Microprotein Regulates Cellular RNA Decapping
Proteogenomic identification of translated small open reading frames in humans has revealed thousands of microproteins, or polypeptides of fewer than 100 amino acids, that were previously invisible to geneticists. Hundreds of microproteins have been shown to be essential for cell growth and prolifer...
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Published in | Biochemistry (Easton) Vol. 59; no. 42; pp. 4131 - 4142 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Chemical Society
27.10.2020
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Subjects | |
Online Access | Get full text |
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Summary: | Proteogenomic identification of translated small open reading frames in humans has revealed thousands of microproteins, or polypeptides of fewer than 100 amino acids, that were previously invisible to geneticists. Hundreds of microproteins have been shown to be essential for cell growth and proliferation, and many regulate macromolecular complexes. One such regulatory microprotein is NBDY, a 68-amino acid component of the human cytoplasmic RNA decapping complex. Heterologously expressed NBDY was previously reported to regulate cytoplasmic ribonucleoprotein granules known as P-bodies and reporter gene stability, but the global effect of endogenous NBDY on the cellular transcriptome remained undefined. In this work, we demonstrate that endogenous NBDY directly interacts with the human RNA decapping complex through EDC4 and DCP1A and localizes to P-bodies. Global profiling of RNA stability changes in NBDY knockout (KO) cells reveals dysregulated stability of more than 1400 transcripts. DCP2 substrate transcript half-lives are both increased and decreased in NBDY KO cells, which correlates with 5′ UTR length. NBDY deletion additionally alters the stability of non-DCP2 target transcripts, possibly as a result of downregulated expression of nonsense-mediated decay factors in NBDY KO cells. We present a comprehensive model of the regulation of RNA stability by NBDY. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Z.N. and Y.L. designed and performed experiments and analyzed data. J.A.S. and M.D.S. performed and analyzed TimeLapse-seq experiments. S.S. generated NBDY rescue cell lines and performed experiments. A.K. performed experiments. S.M. and E.V. provided purified full-length EDC4 protein. S.A.S. conceived the project, designed experiments, and analyzed data. Z.N., Y.L., and S.A.S. wrote the manuscript, and all authors edited and approved the final version of the manuscript. Author Contributions |
ISSN: | 0006-2960 1520-4995 1520-4995 |
DOI: | 10.1021/acs.biochem.0c00672 |