Abstract
Heat shock factor 1 (HSF-1) and forkhead box O (FOXO) are key transcription factors that protect cells from various stresses. In Caenorhabditis elegans, HSF-1 and FOXO together promote a long life span when insulin/IGF-1 signaling (IIS) is reduced. However, it remains poorly understood how HSF-1 and FOXO cooperate to confer IIS-mediated longevity. Here, we show that prefoldin 6 (PFD-6), a component of the molecular chaperone prefoldin-like complex, relays longevity response from HSF-1 to FOXO under reduced IIS. We found that PFD-6 was specifically required for reduced IIS-mediated longevity by acting in the intestine and hypodermis. We showed that HSF-1 increased the levels of PFD-6 proteins, which in turn directly bound FOXO and enhanced its transcriptional activity. Our work suggests that the prefoldin-like chaperone complex mediates longevity response from HSF-1 to FOXO to increase the life span in animals with reduced IIS.
Original language | English |
---|---|
Pages (from-to) | 1562-1575 |
Number of pages | 14 |
Journal | Genes and Development |
Volume | 32 |
Issue number | 23-24 |
DOIs | |
State | Published - 1 Dec 2018 |
Bibliographical note
Publisher Copyright:© 2018 Son et al.
Keywords
- Aging
- C.elegans
- DAF-16/FOXO
- HSF-1/HSF1
- PFD-6/PFDN6