Year: 2026
Type: preprint
Abstract: Through mitochondrial outer membrane permeabilization (MOMP), mitochondria are central to apoptosis. MOMP is pro-inflammatory, impacting diverse processes including anti-tumor immunity and cellular senescence. Despite this, how damaged mitochondria activate inflammation remains unclear. Recent studies have shown that following MOMP, mitochondria are extensively ubiquitinated activating pro-inflammatory NF-κB signaling. We identify the E3 ligase, RNF213, as essential for pro-inflammatory mitochondrial ubiquitination following MOMP. RNF213 has an established role in pro-inflammatory, cell-autonomous immunity to bacteria and other pathogens. We discover that RNF213 is required for mitochondrial M1-linked (linear) ubiquitination. Interestingly, this was found to be independent of the canonical M1-ubiquitin ligase complex LUBAC. RNF213 can directly catalyze M1-linked ubiquitination. By promoting mitochondrial M1-linked ubiquitination, RNF213 initiates the recruitment of the essential NF-κB adaptor molecule, NEMO, and subsequently activates pro-inflammatory NF-κB signaling. Collectively, our findings highlight striking similarities between how cells detect damaged mitochondria and intracellular pathogens, leading to inflammation.
Authors: Rosalie Heilig, Hannah Glover, Charlotte E L Mellor, Catherine Cloix, Michael J Mcilwraith, Lyndsey Flanagan, Nikki Paul, Peter Thomason, Bodhayan Prasad, Asma Ahmed, Hugo Dupuis, Destiny Dalseno, Leah Smith, James Hamilton, Ella Hall-Younger, Esmee Vringer, Lori Buetow, Alba Roca-Portoles, Alfredo Montes Gomes, Graeme Clark, Annabel Black, Sergio Lilla, Sara Zanivan, Leo Carlin, Vignir Helgason, Danny Huang, Stephen WG Tait
Language: English
Topic: NF-κB Signaling Pathways
Subfield: Cancer Research
Domain: Life Sciences
Open Access status: green
OpenAlex ID: W7214013385