Lifespan changes: From wild type to daf-2;sod-2;sod-3
20
56.3
148.02%
The sod-2(sj173); daf-2(e1370); sod-3(sj134) triple mutant lived longer than the daf-2(e1370) mutant, similarly to the daf-2(e1370); sod-3(sj134) double mutant, demonstrating that sod-3 is epistatic to sod-2 in Age.
Triple mutant daf-2(e1370);sod-2(sj173);sod-3(sj134) has a lifespan of 56.3 days, while double mutant daf-2(e1370);sod-3(sj134) has a lifespan of 57.3 days, single mutant sod-2(sj173) has a lifespan of 22.5 days and wild type has a lifespan of 22.7 days.
Contains dependence
Honda Y et al., 2008, Modulation of longevity and diapause by redox regulation mechanisms under the insulin-like signaling control in Caenorhabditis elegans. Exp Gerontol. 43(6):520-9 18406553 Click here to select all mutants from this PubMed ID in the graph
Insulin-like receptor subunit beta;Receptor protein-tyrosine kinase;hypothetical protein
Locus: CELE_Y55D5A.5
Wormbase description: daf-2 encodes a receptor tyrosine kinase that is the C. elegans insulin/IGF receptor ortholog; DAF-2 activity is required for a number of processes in C. elegans, including embryonic and larval development, formation of the developmentally arrested dauer larval stage (diapause), larval developmental timing, adult longevity, reproduction, fat storage, salt chemotaxis learning, and stress resistance, including response to high temperature, oxidative stress, and bacterial infection; DAF-2 signals through a conserved PI 3-kinase pathway to negatively regulate the activity of DAF-16, a Forkhead-related transcription factor, by inducing its phosphorylation and nuclear exclusion; in addition, DAF-2 negatively regulates the nuclear localization, and hence transcriptional activity, of SKN-1 in intestinal nuclei; amongst the 38 predicted insulin-like molecules in C. elegans, genetic and microarray analyses suggest that at least DAF-28, INS-1, and INS-7 are likely DAF-2 ligands; genetic mosaic and tissue-specific promoter studies indicate that daf-2 can function cell nonautonomously and within multiple cell types to influence dauer formation and adult lifespan, likely by regulating the production of secondary endocrine signals that coordinate growth and longevity throughout the animal; temporal analysis of daf-2 function indicates that daf-2 regulates lifespan, reproduction, and diapause independently, at distinct times during the animal's life cycle.
Superoxide dismutase [Mn] 1, mitochondrial
Locus: CELE_F10D11.1
Wormbase description: sod-2 encodes a iron/manganese superoxide dismutase, predicted to be mitochondrial, that might defend against oxidative stress and promote normal lifespan; sod-2 mRNA levels are diminished by mutation of daf-16, and heterologously expressed SOD-2 in E. coli protects against methyl viologen-induced oxidative stress.
Superoxide dismutase [Mn] 2, mitochondrial
Locus: CELE_C08A9.1
Wormbase description: sod-3 encodes a iron/manganese superoxide dismutase, predicted to be mitochondrial, that might defend against oxidative stress and promote normal lifespan; sod-3 mRNA levels are diminished by mutation of daf-16 and chromatin immunoprecipitation (ChIP) studies demonstrate that DAF-16 can directly bind the sod-3 promoter; heterologously expressed SOD-3 in E. coli protects against methyl viologen-induced oxidative stress.
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Species | Gene |
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Species | Gene |
Drosophila melanogaster | InR |
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Species | Gene |
Drosophila melanogaster | Sod2 |
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Species | Gene |
Drosophila melanogaster | Sod2 |
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