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      Scaffold function of long non-coding RNA HOTAIR in protein ubiquitination.

      Nature Communications
      Argonaute Proteins, metabolism, Cell Aging, genetics, HeLa Cells, Hu Paraneoplastic Encephalomyelitis Antigens, Humans, Nerve Tissue Proteins, Nuclear Proteins, Proteins, RNA Cap-Binding Proteins, RNA Stability, RNA, Long Noncoding, RNA-Binding Proteins, Receptors, Cytoplasmic and Nuclear, Ubiquitin-Protein Ligases, Ubiquitination

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          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.

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