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

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作者
Je-Hyun Yoon
Kotb Abdelmohsen
Jiyoung Kim
Xiaoling Yang
Jennifer L. Martindale
Kumiko Tominaga-Yamanaka
Elizabeth J. White
Arturo V. Orjalo
John L. Rinn
Stefan G. Kreft
Gerald M. Wilson
Myriam Gorospe
机构
[1] Laboratory of Genetics,Department of Biochemistry and Molecular Biology and Marlene and Stewart Greenebaum Cancer Center
[2] National Institute on Aging-Intramural Research Program,Department of Stem Cell and Regenerative Biology
[3] NIH,Department of Biology
[4] University of Maryland School of Medicine,undefined
[5] Biosearch Technologies,undefined
[6] Inc.,undefined
[7] Harvard University,undefined
[8] University of Konstanz,undefined
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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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