Prefoldin 6 mediates longevity response from heat shock factor 1 to FOXO in C. elegans

Heat shock factor 1 (HSF-1) and forkhead box O (FOXO) are key transcription factors that protect cells from various stresses. In , 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 con...

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Veröffentlicht in:Genes & development 2018-12, Vol.32 (23-24), p.1562-1575
Hauptverfasser: Son, Heehwa G, Seo, Keunhee, Seo, Mihwa, Park, Sangsoon, Ham, Seokjin, An, Seon Woo A, Choi, Eun-Seok, Lee, Yujin, Baek, Haeshim, Kim, Eunju, Ryu, Youngjae, Ha, Chang Man, Hsu, Ao-Lin, Roh, Tae-Young, Jang, Sung Key, Lee, Seung-Jae V
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Sprache:eng
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Zusammenfassung:Heat shock factor 1 (HSF-1) and forkhead box O (FOXO) are key transcription factors that protect cells from various stresses. In , 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.
ISSN:0890-9369
1549-5477
DOI:10.1101/gad.317362.118