henhaobio
Sign in

bioRxivGeneticsPreprint

Timing of TORC1 inhibition dictates Pol III involvement in longevity in Caenorhabditis elegans

Yasir MalikiD, Isabel Gonçalves SilvaiD, Rene Rivera DiazgranadosiD, Colin SelmaniD, Nazif AliciD, Jennifer M. A. TulletiD

PDFDOI

Abstract

Organismal growth and lifespan are inextricably linked. Target of Rapamycin (TOR) signalling regulates protein production for growth and development, but if reduced extends lifespan across species. Reduction of the enzyme RNA polymerase III, which transcribes tRNAs and 5S rRNA, also extends longevity. Here, we identify a temporal genetic relationship between TOR and Pol III in C. elegans, showing that they collaborate to regulate progeny production and lifespan. Interestingly, the lifespan interaction between Pol III and TOR is only revealed when TOR signaling is reduced specifically in adulthood demonstrating the importance of timing to control TOR regulated developmental vs adult programs. Additionally, we show that Pol III acts in C. elegans muscle to promote both longevity and healthspan and that reducing Pol III even in late adulthood is sufficient to extend lifespan. This demonstrates the importance of Pol III for lifespan and age-related health in adult C. elegans.

Citations
0

Reproducibility ledger

Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.

Sign in to file a reproducibility report.

Similarity Map
SelectedSame fieldCross-field
THISSmith '21Lin '26Zhang '19Detienne '18Das '23Wang '25
70% semantic matchGenetics
Hannah J. Smith, Anne Lanjuin, Arpit Sharma+4 more·bioRxiv·Aug 12, 2021· 3 citations