Lifespan changes: From wild type to daf-16;daf-7
20
11.8
-28.92%
Double mutant daf-16(RNAi);daf-7(e1372) has a lifespan of 11.8 days, while single mutant daf-7(e1372) has a lifespan of 17.1 days, single mutant daf-16(RNAi) has a lifespan of 12.1 days and wild type has a lifespan of 16.6 days.
Opposite lifespan effects of single mutants
Shaw WM et al., 2007, The C. elegans TGF-beta Dauer pathway regulates longevity via insulin signaling. Curr Biol. 17(19):1635-45 17900898 Click here to select all mutants from this PubMed ID in the graph
20
18.2
-3.70%
Loss of daf-16 activity completely suppressed the longevity phenotype of daf-7(-) mutants or RNAi
Double mutant daf-16(mu86);daf-7(RNAi) has a lifespan of 18.2 days, while single mutant daf-7(RNAi) has a lifespan of 21 days, single mutant daf-16(mu86) has a lifespan of 18 days and wild type has a lifespan of 18.9 days.
Opposite lifespan effects of single mutants
Shaw WM et al., 2007, The C. elegans TGF-beta Dauer pathway regulates longevity via insulin signaling. Curr Biol. 17(19):1635-45 17900898 Click here to select all mutants from this PubMed ID in the graph
20
15.4
-7.23%
Loss of daf-16 activity completely suppressed the longevity phenotype of daf-7(-) mutants or RNAi
Double mutant daf-16(mu86);daf-7(RNAi) has a lifespan of 15.4 days, while single mutant daf-7(RNAi) has a lifespan of 20.3 days, single mutant daf-16(mu86) has a lifespan of 16.2 days and wild type has a lifespan of 16.6 days.
Opposite lifespan effects of single mutants
Shaw WM et al., 2007, The C. elegans TGF-beta Dauer pathway regulates longevity via insulin signaling. Curr Biol. 17(19):1635-45 17900898 Click here to select all mutants from this PubMed ID in the graph
20
13.0
-13.33%
Loss of daf-16 activity completely suppressed the longevity phenotype of daf-7(-) mutants or RNAi
Double mutant daf-16(mu86);daf-7(e1372) has a lifespan of 13 days, while single mutant daf-7(e1372) has a lifespan of 17.5 days, single mutant daf-16(mu86) has a lifespan of 12.6 days and wild type has a lifespan of 16.4 days.
Opposite lifespan effects of single mutants
Shaw WM et al., 2007, The C. elegans TGF-beta Dauer pathway regulates longevity via insulin signaling. Curr Biol. 17(19):1635-45 17900898 Click here to select all mutants from this PubMed ID in the graph
Forkhead box protein O;hypothetical protein
Locus: CELE_R13H8.1
Wormbase description: daf-16 encodes the sole C. elegans forkhead box O (FOXO) homologue; DAF-16 functions as a transcription factor that acts in the insulin/IGF-1-mediated signaling (IIS) pathway that regulates dauer formation, longevity, fat metabolism, stress response, and innate immunity; DAF-16 regulates these various processes through isoform-specific expression, isoform-specific regulation by different AKT kinases, and differential regulation of target genes; DAF-16 can interact with the CBP-1 transcription cofactor in vitro, and interacts genetically with other genes in the insulin signaling and with daf-12, which encodes a nuclear hormone receptor; DAF-16 is activated in response to DNA damage during development and co-regulated by EGL-27, alleviates DNA-damage-induced developmental arrest by inducing DAF-16-associated element (DAE)-regulated genes; DAF-16 is broadly expressed but displays isoform-specific tissue enrichment; DAF-16 localizes to both the cytoplasm and the nucleus, with the ratio between the two an important regulator of function.
Dauer larva development regulatory growth factor daf-7
Locus: CELE_B0412.2
Wormbase description: daf-7 encodes a member of the transforming growth factor beta superfamily; in C. elegans, DAF-7 functions as part of a signaling pathway that interprets environmental conditions to regulate energy-balance pathways that affect dauer larval formation, fat metabolism, egg laying, pathogen avoidance behavior, and feeding behavior; daf-7 reporter gene fusions are expressed in the ASI, ADE, and OLQ neurons, and daf-7 expression is induced in both ASI and ASJ chemosensory neurons in response to the pathogenic bacterial strain Pseudomonas aeruginosa PA14.
Show in SynergyAge | |
---|---|
Species | Gene |
Show in SynergyAge | |
---|---|
Species | Gene |
Show in SynergyAge | |
---|---|
Species | Gene |
SynergyAge database hosts high-quality, manually curated information about the synergistic and antagonistic lifespan effects of genetic interventions in model organisms, also allowing users to explore the longevity relationships between genes in a visual way.
If you would like to cite this database please use:
Bunu, G., Toren, D., Ion, C. et al. SynergyAge, a curated database for synergistic and antagonistic interactions of longevity-associated genes. Sci Data 7, 366 (2020). https://doi.org/10.1038/s41597-020-00710-z
Group webpage: www.aging-research.group