The Mediator complex subunit Med19 extends healthy lifespan in Drosophila by preventing cellular and organismal frailty

Payet, A.; Guillou, E.; Bernat-Fabre, S.; Dromard-Berthezene, C.; Contreras, X.; Rivero, A.; Jullien, D.; BOURBON, H.-M.; FRENDO, J.-L.; Sengenes, C.; BOUBE, M.

doi:10.1101/2025.06.18.659864

bioRxiv · 10.1101/2025.06.18.659864

The Mediator complex subunit Med19 extends healthy lifespan in Drosophila by preventing cellular and organismal frailty

Payet, A.·Guillou, E.·Bernat-Fabre, S.·Dromard-Berthezene, C.·Contreras, X.·Rivero, A.·Jullien, D.·BOURBON, H.-M.·FRENDO, J.-L.·Sengenes, C.·BOUBE, M.

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Abstract

Aging involves a progressive decline in physiological functions, often marked by the onset of a "frailty point" just before survival rates decrease rapidly. Here, we investigate how the Mediator subunit Med19 modulates this transition in Drosophila. We find that upregulating Med19 extends the median lifespan by nearly 90% and postpones the onset of accelerated mortality, suggesting that Med19 helps preserve the resilience phase of aging. In contrast, Med19 downregulation sharply reduces both median and maximum lifespan, advancing the frailty threshold. We show that Med19 knockdown increases fly vulnerability to environmental insults such as oxidative and genotoxic challenges whereas Med19 upregulation helps them resist these stresses, underscoring Med19s protective role in maintaining genomic integrity. We link these phenotypes to altered stress-response pathways at the cellular level: Med19-depleted cells show a compensatory upregulation of genes involved in iron-sulfur cluster biogenesis, glutathione metabolism, and DNA damage repair. At the cellular level, Med19 depletion triggers a "loser" phenotype in cell competition assays, activating the JNK pathway and undergoing apoptosis, highlighting a form of "cellular frailty" that parallels organismal frailty. Finally, we found that the Med19 protein level naturally decreases with age and showed that restoring Med19 expression in aged flies increases fitness and delays the onset of frailty even in older, "frail" individuals, underscoring its significance as an aging regulator. Altogether, our findings establish Med19 as a crucial mediator of lifespan and stress resilience, suggesting it acts as a rheostat that modulates the transition from healthy aging to frailty in Drosophila. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=180 HEIGHT=200 SRC="FIGDIR/small/659864v1_ufig1.gif" ALT="Figure 1"> View larger version (54K): org.highwire.dtl.DTLVardef@1a5e398org.highwire.dtl.DTLVardef@14658org.highwire.dtl.DTLVardef@1b14089org.highwire.dtl.DTLVardef@41060_HPS_FORMAT_FIGEXP M_FIG C_FIG Highlights- At the organismal level, Med19 upregulation extends Drosophila lifespan by 90%, delays the onset of frailty and enhances oxidative and DNA damage stress resistance, while its depletion has the opposite effect. - Med19 depletion alters the expression of stress response genes and induces a loser-cell phenotype in cell competition assays revealing its crucial function in controlling cellular fitness. - Med19 protein levels naturally decline with age, and its restoration in aged flies improves both healthspan and lifespan.

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Payet, A., Guillou, E., Bernat-Fabre, S., Dromard-Berthezene, C., Contreras, X., Rivero, A., Jullien, D., BOURBON, H.-M., FRENDO, J.-L., Sengenes, C., BOUBE, M.. 2025-06-18. The Mediator complex subunit Med19 extends healthy lifespan in Drosophila by preventing cellular and organismal frailty. https://doi.org/10.1101/2025.06.18.659864

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