Abstract
Although mammalian long non-coding (lnc)RNAs are best known for modulating transcription, their post-transcriptional influence on mRNA splicing, stability and translation is emerging. Here we report a post-translational function for the lncRNA HOTAIR as an inducer of ubiquitin-mediated proteolysis. HOTAIR associates with E3 ubiquitin ligases bearing RNA-binding domains, Dzip3 and Mex3b, as well as with their respective ubiquitination substrates, Ataxin-1 and Snurportin-1. In this manner, HOTAIR facilitates the ubiquitination of Ataxin-1 by Dzip3 and Snurportin-1 by Mex3b in cells and in vitro, and accelerates their degradation. HOTAIR levels are highly upregulated in senescent cells, causing rapid decay of targets Ataxin-1 and Snurportin-1, and preventing premature senescence. These results uncover a role for a lncRNA, HOTAIR, as a platform for protein ubiquitination.
Publication types
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Research Support, N.I.H., Extramural
MeSH terms
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Argonaute Proteins / metabolism
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Ataxin-1
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Ataxins
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Cellular Senescence / genetics
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ELAV Proteins / metabolism
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HeLa Cells
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Humans
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Nerve Tissue Proteins / metabolism
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Nuclear Proteins / metabolism
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Proteins / genetics
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Proteins / metabolism*
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RNA Cap-Binding Proteins / metabolism
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RNA Stability
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RNA, Long Noncoding / metabolism*
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RNA-Binding Proteins / genetics
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RNA-Binding Proteins / metabolism
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Receptors, Cytoplasmic and Nuclear / metabolism
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Ubiquitin-Protein Ligases / genetics
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Ubiquitin-Protein Ligases / metabolism
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Ubiquitination*
Substances
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AGO2 protein, human
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ATXN1 protein, human
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Argonaute Proteins
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Ataxin-1
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Ataxins
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ELAV Proteins
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HOTAIR long untranslated RNA, human
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Nerve Tissue Proteins
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Nuclear Proteins
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Proteins
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RNA Cap-Binding Proteins
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RNA, Long Noncoding
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RNA-Binding Proteins
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Receptors, Cytoplasmic and Nuclear
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SNUPN protein, human
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DZIP3 protein, human
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Ubiquitin-Protein Ligases