表观基因组
生物
细胞生物学
组蛋白
自噬
长寿
溶酶体
表观遗传学
组蛋白H3
信号转导
代谢途径
5-羟甲基胞嘧啶
磷酸化
组蛋白H2B
细胞信号
TFEB
遗传学
DNA甲基化
基因表达调控
泛素
内吞作用
激酶
甲基化
后生
组蛋白甲基化
组蛋白甲基转移酶
内吞循环
作者
Qinghao Zhang,Weiwei Dang,Meng C. Wang
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2025-09-25
卷期号:389 (6767): 1353-1360
被引量:9
标识
DOI:10.1126/science.adn8754
摘要
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 Caenorhabditis elegans. 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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