A new research paper was published in\u00a0Volume 18 of\u00a0Aging-US\u00a0on February 10, 2026, titled “Aging-associated mitochondrial circular RNAs.”<\/p>\n
Led by first author Hyejin Mun from the\u00a0University of Oklahoma\u00a0– with corresponding authors Je-Hyun Yoon from the\u00a0University of Oklahoma\u00a0and Young-Kook Kim from\u00a0Chonnam National University Medical School\u00a0– the study profiles mitochondrial circular RNAs in Peripheral Blood Mononuclear Cells (PBMCs) from young and old human cohorts and probes how mitochondrial circRNAs and the mitochondrial RNA-binding protein GRSF1 relate to mitochondrial metabolism and cellular senescence.<\/p>\n
Using total RNA sequencing of PBMCs from young and old donors and complementary cell-based experiments, the authors report that a large fraction of circular RNA junctions originates from the mitochondrial genome, with MT-RNR2 producing the most abundant circular junctions. They show that circMT-RNR2 levels are depleted in older cohorts and in replicative senescence of human fibroblasts, and that the mitochondria-localized RNA-binding protein GRSF1 interacts with both linear and circular MT-RNR2. Loss of GRSF1 reduced circMT-RNR2 levels, decreased mitochondrial TCA intermediates (fumarate and succinate), and accelerated cellular senescence and mitochondrial dysfunction – findings that link mitochondrial circRNAs to mitochondrial energetics and proliferative status in younger cells.\u00a0<\/p>\n
“Taken together, our findings demonstrate the existence and possible function of circular MT-RNR2 during human aging and senescence, implicating its role in promoting the TCA cycle.”<\/p>\n
The authors note key limitations and outline next steps: clarifying the biogenesis mechanism of mitochondrial circular RNAs (including whether trans-splicing contributes), mapping direct interactions between mitochondrial transcripts and metabolic enzymes, and performing mechanistic studies (in vivo and in additional human cohorts) to test how circMT-RNR2 and GRSF1 influence mitochondrial energetics and organismal aging. These follow-ups will determine whether mitochondrial circular RNAs are actionable targets for modulating mitochondrial metabolism or delaying aspects of cellular aging.\u00a0<\/p>\n
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