Lifespan changes: From wild type to cdk-2;daf-16
20
NGM
18.4
-2.13%
The dramatic lifespan extension associated with knockdown of cdk-2 was not fully eliminated in daf-16(mgDf47) null mutants indicating that DAF-16 is central for the influence of cell cycle regulators on longevity.
Double mutant cdk-2(RNAi);daf-16(mgDf47) has a lifespan of 18.4 days, while single mutant cdk-2(RNAi) has a lifespan of 24.1 days, single mutant daf-16(mgDf47) has a lifespan of 16.8 days and wild type has a lifespan of 18.8 days.
Opposite lifespan effects of single mutants
Dottermusch M et al., 2016, Cell cycle controls stress response and longevity in C. elegans. Aging (Albany NY). 8(9):2100-2126 27668945 Click here to select all mutants from this PubMed ID in the graph
20
NGM
17.3
-5.46%
The dramatic lifespan extension associated with knockdown of cdk-2 was not fully eliminated in daf-16(mgDf47) null mutants indicating that DAF-16 is central for the influence of cell cycle regulators on longevity.
Double mutant cdk-2(RNAi);daf-16(mgDf47) has a lifespan of 17.3 days, while single mutant cdk-2(RNAi) has a lifespan of 25.6 days, single mutant daf-16(mgDf47) has a lifespan of 15.9 days and wild type has a lifespan of 18.3 days.
Opposite lifespan effects of single mutants
Dottermusch M et al., 2016, Cell cycle controls stress response and longevity in C. elegans. Aging (Albany NY). 8(9):2100-2126 27668945 Click here to select all mutants from this PubMed ID in the graph
20
NGM
20.0
3.63%
The dramatic lifespan extension associated with knockdown of cdk-2 was not fully eliminated in daf-16(mgDf47) null mutants indicating that DAF-16 is central for the influence of cell cycle regulators on longevity.
Double mutant cdk-2(RNAi);daf-16(mgDf47) has a lifespan of 20.0 days, while single mutant cdk-2(RNAi) has a lifespan of 22.7 days, single mutant daf-16(mgDf47) has a lifespan of 17.9 days and wild type has a lifespan of 19.3 days.
Opposite lifespan effects of single mutants
Dottermusch M et al., 2016, Cell cycle controls stress response and longevity in C. elegans. Aging (Albany NY). 8(9):2100-2126 27668945 Click here to select all mutants from this PubMed ID in the graph
Cyclin-Dependent Kinase family;Cyclin-dependent kinase 2
Locus: CELE_K03E5.3
Wormbase description: cdk-2 encodes the C. elegans ortholog of cyclin-dependent kinase 2; along with CYE-1 (cyclin E), CDK-2 is required for the G1/S transition in somatic cells, centrosome assembly and polarity establishment in the embryo, proliferation of germ cells, and suppression of terminal differentiation in quiescent cells after asymmetric division; CYE-1 and CDK-2 also regulate the germline mitosis/meiosis decision through post-translational regulation of GLD-1, likely direct phosphorylation.
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.
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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