Department of Molecular Biology and Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA.
Department of Biological Sciences, University of New Orleans, New Orleans, LA, USA.
Nat Aging. 2023 Jan;3(1):47-63. doi: 10.1038/s43587-022-00329-2. Epub 2023 Jan 9.
The reproductive system regulates somatic aging through competing anti- and pro-aging signals. Germline removal extends somatic lifespan through conserved pathways including insulin and mammalian target-of-rapamycin signaling, while germline hyperactivity shortens lifespan through unknown mechanisms. Here we show that mating-induced germline hyperactivity downregulates piRNAs, in turn desilencing their targets, including the Hedgehog-like ligand-encoding genes wrt-1 and wrt-10, ultimately causing somatic collapse and death. Germline-produced Hedgehog signals require PTR-6 and PTR-16 receptors for mating-induced shrinking and death. Our results reveal an unconventional role of the piRNA pathway in transcriptional regulation of Hedgehog signaling and a new role of Hedgehog signaling in the regulation of longevity and somatic maintenance: Hedgehog signaling is controlled by the tunable piRNA pathway to encode the previously unknown germline-to-soma pro-aging signal. Mating-induced piRNA downregulation in the germline and subsequent Hedgehog signaling to the soma enable the animal to tune somatic resource allocation to germline needs, optimizing reproductive timing and survival.
生殖系统通过竞争的抗衰老和促衰老信号来调节体衰老。生殖系去除通过包括胰岛素和哺乳动物雷帕霉素靶蛋白信号在内的保守途径延长体寿命,而生殖系过度活跃通过未知机制缩短寿命。在这里,我们表明交配诱导的生殖系过度活跃会下调 piRNA,进而使它们的靶基因失活,包括 Hedgehog 样配体编码基因 wrt-1 和 wrt-10,最终导致体细胞崩溃和死亡。生殖系产生的 Hedgehog 信号需要 PTR-6 和 PTR-16 受体来诱导交配诱导的收缩和死亡。我们的结果揭示了 piRNA 途径在 Hedgehog 信号转录调控中的一种非传统作用,以及 Hedgehog 信号在长寿和体细胞维持中的新作用:Hedgehog 信号受可调节的 piRNA 途径控制,以编码先前未知的生殖系到体的促衰老信号。交配诱导的生殖系中 piRNA 的下调,以及随后 Hedgehog 信号向体细胞的传递,使动物能够调节体细胞资源分配以满足生殖系的需要,从而优化生殖时机和生存。