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Kubon, D.

Publications and source records attributed to Kubon, D..

2 recordsLinked to original sources

PARP6-dependent vimentin ADP-ribosylation prevents myofibroblast activation in cardiac fibrosis

Cardiac fibrosis is a central driver of adverse remodeling during heart failure, yet the post-translational regulation of myofibroblast activation remains poorly defined. Here, we identified PARP6 as a mono-ADP-ribosyltransferase that repressed myofibroblast activation through the ADP-ribosylation of vimentin. PARP6 expression was reduced in failing human hearts and Parp6 haploinsufficiency in mice was sufficient to induce cardiac fibrosis. At the cellular level, PARP6 ADP-ribosylated vimentin thereby limiting actin stress fiber formation. Mechanistically, PARP6 inhibition enhanced RhoA activation and vimentin-RhoA complex formation, thus activating the RhoA-ROCK-LIMK-cofilin pathway. Consistently, Parp6 haploinsufficiency was associated with increased cofilin phosphorylation in mice hearts. In primary cardiac fibroblasts, PARP6 inhibition promoted RhoA-dependent actin stress fiber accumulation and induced myofibrotic protein expression. Together, these findings define a PARP6-vimentin(ADP-ribosylation)-RhoA axis that restrained contractility-driven fibroblast activation, indicating a cardioprotective role of PARP6 with potential therapeutic relevance for fibrotic heart disease.

molecular biology↗

PARP14 mediated SQSTM1/p62 cysteine ADP-ribosylation is counteracted by the SARS-CoV-2 macrodomain

Interferon-induced ADP-ribosyltransferases are emerging regulators of cellular innate immunity, yet the relevant substrates and downstream effects remain incompletely defined. Here, we mapped the PARP14-dependent ADP-ribosylome in lung epithelial cancer cells and identified the selective autophagy adaptor SQSTM1/p62, along with multiple innate immune regulators, as IFN-dependent MARylation substrates. Site-resolved analysis revealed that PARP14-dependent MARylation is strongly enriched on cysteine residues, including defined cysteine acceptor sites within p62. PARP14-dependent MARylation is localized to cytoplasmic p62 foci that colocalize with diverse ubiquitin species. Furthermore, our results indicate that TRIM21 limits the autophagic degradation of p62, suggesting that the identified p62 foci may have degradation-independent roles. Consistent with this, both PARP14 and p62 support inflammatory gene expression, linking PARP14-dependent MARylation to innate immune regulation. Together, our findings identify p62 foci as sites of PARP14-dependent ADP-ribosylation and suggest a functional link between interferon signaling, ubiquitin-associated protein assemblies, and MARylation-dependent innate immune regulation.

molecular biology↗