The memory of neuronal mitochondrial stress is inherited transgenerationally via elevated mitochondrial DNA levels

The memory of stresses experienced by parents can be passed on to descendants as a forecast of the challenges to come. Here, we discovered that the neuronal mitochondrial perturbation-induced systemic mitochondrial unfolded protein response (UPR mt ) in Caenorhabditis elegans can be transmitted to o...

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Veröffentlicht in:Nature cell biology 2021-08, Vol.23 (8), p.870-880
Hauptverfasser: Zhang, Qian, Wang, Zihao, Zhang, Wenfeng, Wen, Qingbo, Li, Xinyu, Zhou, Jun, Wu, Xueying, Guo, Yongqing, Liu, Yangli, Wei, Changshuo, Qian, Wenfeng, Tian, Ye
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Sprache:eng
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Zusammenfassung:The memory of stresses experienced by parents can be passed on to descendants as a forecast of the challenges to come. Here, we discovered that the neuronal mitochondrial perturbation-induced systemic mitochondrial unfolded protein response (UPR mt ) in Caenorhabditis elegans can be transmitted to offspring over multiple generations. The transgenerational activation of UPR mt is mediated by maternal inheritance of elevated levels of mitochondrial DNA (mtDNA), which causes the proteostasis stress within mitochondria. Furthermore, results from intercrossing studies using wild C. elegans strains further support that maternal inheritance of higher levels of mtDNA can induce the UPR mt in descendants. The mitokine Wnt signalling pathway is required for the transmission of elevated mtDNA levels across generations, thereby conferring lifespan extension and stress resistance to offspring. Collectively, our results reveal that the nervous system can transmit stress signals across generations by increasing mtDNA in the germline, enabling descendants to better cope with anticipated challenges. Zhang et al. report that the systemic mitochondrial unfolded protein response triggered by neuronal mitochondrial stress can be transmitted across multiple generations in Caenorhabditis elegans via a mechanism involving elevation in mitochondrial DNA levels in oocytes.
ISSN:1465-7392
1476-4679
DOI:10.1038/s41556-021-00724-8