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Journal Article

Co-chaperone p23 Regulates C. elegans Lifespan in Response to Temperature

MPS-Authors

Horikawa,  M.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Sural,  S.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Hsu,  A. L.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Antebi,  A.
Max Planck Institute for Biology of Ageing, Max Planck Society;

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Citation

Horikawa, M., Sural, S., Hsu, A. L., & Antebi, A. (2015). Co-chaperone p23 Regulates C. elegans Lifespan in Response to Temperature. PLoS Genet, 11(4), e1005023. doi:10.1371/journal.pgen.1005023.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0028-590E-5
Abstract
Temperature potently modulates various physiologic processes including organismal motility, growth rate, reproduction, and ageing. In ectotherms, longevity varies inversely with temperature, with animals living shorter at higher temperatures. Thermal effects on lifespan and other processes are ascribed to passive changes in metabolic rate, but recent evidence also suggests a regulated process. Here, we demonstrate that in response to temperature, daf-41/ZC395.10, the C. elegans homolog of p23 co-chaperone/prostaglandin E synthase-3, governs entry into the long-lived dauer diapause and regulates adult lifespan. daf-41 deletion triggers constitutive entry into the dauer diapause at elevated temperature dependent on neurosensory machinery (daf-10/IFT122), insulin/IGF-1 signaling (daf-16/FOXO), and steroidal signaling (daf-12/FXR). Surprisingly, daf-41 mutation alters the longevity response to temperature, living longer than wild-type at 25 degrees C but shorter than wild-type at 15 degrees C. Longevity phenotypes at 25 degrees C work through daf-16/FOXO and heat shock factor hsf-1, while short lived phenotypes converge on daf-16/FOXO and depend on the daf-12/FXR steroid receptor. Correlatively daf-41 affected expression of DAF-16 and HSF-1 target genes at high temperature, and nuclear extracts from daf-41 animals showed increased occupancy of the heat shock response element. Our studies suggest that daf-41/p23 modulates key transcriptional changes in longevity pathways in response to temperature.