daf-16 integrates developmental and environmental inputs to mediate aging in the nematode Caenorhabditis elegans.
By S. Henderson, T. Johnson. Current Biology, 2001
926 citations recorded by the source corpus.
Subfields: Aging
View Paper: https://www.semanticscholar.org/paper/5ec128236f4eae34848ab2c62dead6698d40c442
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Citations in the corpus
- FOXO transcription factors at the interface between longevity and tumor suppression (2005, background): “In worms, flies, and mammalian cells, stress stimuli trigger the relocalization of FOXO to the nucleus (Henderson and Johnson, 2001; Lin et al., 2001; Wang et al., 2003; Brunet et al., 2004; Essers et al., 2004).”
- The C. elegans TGF-β Dauer Pathway Regulates Longevity via Insulin Signaling (2007, positive): “When daf-2 insulin receptor signaling is abrogated, DAF-16/FOXO becomes nuclearly localized [18, 19], and mutations in daf-18, the PTEN phosphatase that opposes insulin/PI-3-kinase signaling, promote cytoplasmic retention of DAF-16 [18].”
- FOXO transcription factor activation by oxidative stress mediated by the small GTPase Ral and JNK (2004, background): “In C. elegans, a variety of stresses including oxidative stress have been shown to induce translocation of DAF-16/ GFP from the cytosol to the nucleus (Henderson and Johnson, 2001).”
- Lifespan extension by conditions that inhibit translation in Caenorhabditis elegans (2007, background): “Moreover, DAF-16 regulates many stress-response genes (Honda & Honda, 1999; McElwee et al., 2003; Murphy et al., 2003) and DAF-16 is known to be activated by environmental stress (Henderson & Johnson, 2001; Lin et al., 2001).”
- p38 MAPK Regulates Expression of Immune Response Genes and Contributes to Longevity in C. elegans (2006, background): “How does the PMK-1 pathway interact with the DAF-2–DAF-16 pathway?”
- The plasticity of aging: insights from long-lived mutants. (2005, background): “Heat shock triggers DAF-16 nuclear lotcalization (Henderson and Johnson, 2001; Lin et al., h2001), and DAF-16 is required for the full expression aof certain heat-shock genes, including the small heatwshock protein genes, following heat shock (Hsu et al., R2003).”
- SKN-1 links C. elegans mesendodermal specification to a conserved oxidative stress response. (2003, background): “…signaling reduces C. elegans lifespan by inhibiting the Foxo-type transcription factor DAF-16, which promotes longevity in part by increasing expression of ROS-resistance genes (Kenyon et al. 1993; Honda and Honda 1999; Finch and Ruvkun 2001; Henderson and Johnson 2001; Lee et al. 2003).”
- Long live FOXO: unraveling the role of FOXO proteins in aging and longevity (2015, background): “…mainly as transcriptional activators by binding the consensus core recognition motif TTGTTTAC, and their activity is inhibited by the IIS pathway (Biggs et al., 1999; Brunet et al., 1999; Henderson & Johnson, 2001; Lin et al., 2001; Calnan & Brunet, 2008; Zanella et al., 2010; Webb & Brunet, 2014).”
- An AMPK-FOXO pathway mediates longevity induced by a novel method of dietary restriction in C. elegans. (2007, background): “Activated AMPK enhances FOXO/DAF-16-dependent transcription, perhaps via direct phosphorylation, leading to resistance to oxidative stress and longevity extension (Figure 7).”