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A novel long noncoding RNA Linc-ASEN represses cellular senescence through multileveled reduction of p21 expression

Cell Death Differ. 2019; 
Lee HC, Kang D, Han N, Lee Y, Hwang HJ, Lee SB, You JS, Min BS, Park HJ, Ko YG, Gorospe M, Lee JS
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Proteins, Expression, Isolation and Analysis For IP and ChIP, cells were lysed in NET-2 buffer containing 100 U of RNase Inhibitor (Invitrogen) and precleared with protein G-Resin (GenScript, Piscataway, NJ, USA) or A-Sepharose beads (GE Healthcare Bio-Science AB, Uppsala, Sweden). Get A Quote

摘要

Long noncoding RNAs (lncRNAs) regulating diverse cellular processes implicate in many diseases. However, the function of lncRNAs in cellular senescence remains largely unknown. Here we identify a novel long intergenic noncoding RNA Linc-ASEN expresses in prematurely senescent cells. We find that Linc-ASEN associates with UPF1 by RNA pulldown mass spectrometry analysis, and represses cellular senescence by reducing p21 production transcriptionally and posttranscriptionally. Mechanistically, the Linc-ASEN-UPF1 complex suppressed p21 transcription by recruiting Polycomb Repressive Complex 1 (PRC1) and PRC2 to the p21 locus, and thereby preventing binding of the transcriptional activator p53 on the p21 promoter thr... More

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