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10.1038/ncomms14632

http://scihub22266oqcxt.onion/10.1038/ncomms14632
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C5344980!5344980!28272405
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suck abstract from ncbi


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pmid28272405      Nat+Commun 2017 ; 8 (ä): ä
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  • PARP1 promotes gene expression at the post-transcriptional level by modulating the RNA-binding protein HuR #MMPMID28272405
  • Ke Y; Han Y; Guo X; Wen J; Wang K; Jiang X; Tian X; Ba X; Boldogh I; Zeng X
  • Nat Commun 2017[]; 8 (ä): ä PMID28272405show ga
  • Poly(ADP-ribosyl)ation (PARylation) is mainly catalysed by poly-ADP-ribose polymerase 1 (PARP1), whose role in gene transcription modulation has been well established. Here we show that, in response to LPS exposure, PARP1 interacts with the adenylateuridylate-rich element-binding protein embryonic lethal abnormal vision-like 1 (Elavl1)/human antigen R (HuR), resulting in its PARylation, primarily at site D226. PARP inhibition and the D226 mutation impair HuR's PARylation, nucleocytoplasmic shuttling and mRNA binding. Increases in mRNA level or stability of pro-inflammatory cytokines/chemokines are abolished by PARP1 ablation or inhibition, or blocked in D226A HuR-expressing cells. The present study demonstrates a mechanism to regulate gene expression at the post-transcriptional level, and suggests that blocking the interaction of PARP1 with HuR could be a strategy to treat inflammation-related diseases that involve increased mRNA stability.
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