Ribonucleotide incorporation into mitochondrial DNA drives inflammation

• 成果类型: Article
• 署名作者: Bahat, Amir; Milenkovic, Dusanka; Cors, Eileen; Barnett, Mabel; Niftullayev, Sadig; Katsalifis, Athanasios; Schwill, Marc; Kirschner, Petra; Macvicar, Thomas; Giavalisco, Patrick; Jenninger, Louise; Clausen, Anders R.; Paupe, Vincent; Prudent, Julien; Larsson, Nils-Goran; Rogg, Manuel; Schell, Christoph; Muylaert, Isabella; Lekholm, Erik; Nolte, Hendrik; Falkenberg, Maria; Langer, Thomas
• 署名单位: Max Planck Society; University of Gothenburg; University of Cambridge; Karolinska Institutet; University of Freiburg; University of Cologne
• 刊物名称: NATURE
• ISSN/ISSBN: 0028-0836; 1476-4687
• DOI: 10.1038/s41586-025-09541-7
• 发表日期: 2025-11-20
• 关键词: mass-spectrometry; mtdna; mutations; replication; release

摘要

Metabolic dysregulation can lead to inflammatory responses1,2. Imbalanced nucleotide synthesis triggers the release of mitochondrial DNA (mtDNA) to the cytosol and an innate immune response through cGAS-STING signalling3. However, how nucleotide deficiency drives mtDNA-dependent inflammation has not been elucidated. Here we show that nucleotide imbalance leads to an increased misincorporation of ribonucleotides into mtDNA during age-dependent renal inflammation in a mouse model lacking the mitochondrial exonuclease MGME14, in various tissues of aged mice and in cells lacking the mitochondrial i-AAA protease YME1L. Similarly, reduced deoxyribonucleotide synthesis increases the ribonucleotide content of mtDNA in cell-cycle-arrested senescent cells. This leads to mtDNA release into the cytosol, cGAS-STING activation and the mtDNA-dependent senescence-associated secretory phenotype (SASP), which can be suppressed by exogenously added deoxyribonucleosides. Our results highlight the sensitivity of mtDNA to aberrant ribonucleotide incorporation and show that imbalanced nucleotide metabolism leads to age- and mtDNA-dependent inflammatory responses and SASP in senescence.