Lysosomes signal through the epigenome to regulate longevity across generations

The epigenome is sensitive to metabolic inputs and is crucial for aging. Lysosomes act as a signaling hub to sense metabolic cues and regulate longevity. We found that lysosomal metabolic pathways signal through the epigenome to regulate transgenerational longevity in <i>Caenorhabditis elegans</i>. Activation of lysosomal lipid signaling and lysosomal adenosine monophosphate-activated protein kinase (AMPK) or reduction of lysosomal mechanistic target of rapamycin (mTOR) signaling increased the expression of a histone H3.3 variant and increased its methylation on K79, leading to life-span extension across multiple generations. This transgenerational prolongevity effect required intestine-to-germline transportation of histone H3.3 and a germline-specific H3K79 methyltransferase and was recapitulated by overexpressing H3.3 or the H3K79 methyltransferase. Thus, signals from a lysosome affect the epigenome and link the soma and germ line to mediate transgenerational inheritance of longevity.

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Publication Details

Journal
Science
Published
2025-09-25
DOI
https://doi.org/10.1126/science.adn8754
Citations
9
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
Field-Weighted Citation Impact
8.58
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article

Lysosomes signal through the epigenome to regulate longevity across generations

Meng Carla Wang, Weiwei Dang, Qinghao Zhang
9 citations
Science
Genetics, Aging, and Longevity in Model Organisms
8.58
article

Lysosomes signal through the epigenome to regulate longevity across generations

Meng Carla Wang, Weiwei Dang, Qinghao Zhang
article en
9 citations

Abstract

The epigenome is sensitive to metabolic inputs and is crucial for aging. Lysosomes act as a signaling hub to sense metabolic cues and regulate longevity. We found that lysosomal metabolic pathways signal through the epigenome to regulate transgenerational longevity in <i>Caenorhabditis elegans</i>. Activation of lysosomal lipid signaling and lysosomal adenosine monophosphate-activated protein kinase (AMPK) or reduction of lysosomal mechanistic target of rapamycin (mTOR) signaling increased the expression of a histone H3.3 variant and increased its methylation on K79, leading to life-span extension across multiple generations. This transgenerational prolongevity effect required intestine-to-germline transportation of histone H3.3 and a germline-specific H3K79 methyltransferase and was recapitulated by overexpressing H3.3 or the H3K79 methyltransferase. Thus, signals from a lysosome affect the epigenome and link the soma and germ line to mediate transgenerational inheritance of longevity.

ScienceVol. 389(6767)
Howard Hughes Medical Institute (US), Baylor College of Medicine (US), Janelia Research Campus (US)
Openalex Percentile: Top 2%
Genetics, Aging, and Longevity in Model Organisms
8.58
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