Lifespan changes: From wild type to cye-1;daf-16
20
NGM
19.2
-1.03%
daf-16(mgDf47) null mutation significantly suppressed the longevity of cye-1(RNAi).
Double mutant cye-1(RNAi);daf-16(mgDf47) has a lifespan of 19.2 days, while single mutant cye-1(RNAi) has a lifespan of 25.3 days, single mutant daf-16(mgDf47) has a lifespan of 17.2 days and wild type has a lifespan of 19.4 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
19.5
-2.99%
daf-16(mgDf47) null mutation significantly suppressed the longevity of cye-1(RNAi).
Double mutant cye-1(RNAi);daf-16(mgDf47) has a lifespan of 19.5 days, while single mutant cye-1(RNAi) has a lifespan of 26.7 days, single mutant daf-16(mgDf47) has a lifespan of 17.5 days and wild type has a lifespan of 20.1 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
18.9
0.53%
daf-16(mgDf47) null mutation significantly suppressed the longevity of cye-1(RNAi).
Double mutant cye-1(RNAi);daf-16(mgDf47) has a lifespan of 18.9 days, while single mutant cye-1(RNAi) has a lifespan of 24.2 days, single mutant daf-16(mgDf47) has a lifespan of 17.0 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
18.5
-4.15%
The longevity of cye-1(RNAi) was suppressed by daf-16(mu86) mutation.
Double mutant cye-1(RNAi);daf-16(mu86) has a lifespan of 18.5 days, while single mutant cye-1(RNAi) has a lifespan of 23.8 days, single mutant daf-16(mu86) has a lifespan of 16.3 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
20
NGM
19.5
The longevity of cye-1(RNAi) was suppressed by daf-16(mu86) mutation.
Double mutant cye-1(RNAi);daf-16(mu86) has a lifespan of 19.5 days, while single mutant cye-1(RNAi) has a lifespan of 23.7 days, single mutant daf-16(mu86) has a lifespan of 17.0 days and wild type has a lifespan of 19.5 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
19.1
-1.55%
The longevity of cye-1(RNAi) was suppressed by daf-16(mu86) mutation.
Double mutant cye-1(RNAi);daf-16(mu86) has a lifespan of 19.1 days, while single mutant cye-1(RNAi) has a lifespan of 24.5 days, single mutant daf-16(mu86) has a lifespan of 16.7 days and wild type has a lifespan of 19.4 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
16.0
-15.34%
The longevity of cye-1(RNAi) was suppressed by daf-16(mu86) mutation.
Double mutant cye-1(RNAi);daf-16(mu86) has a lifespan of 16.0 days, while single mutant cye-1(RNAi) has a lifespan of 23.5 days, single mutant daf-16(mu86) has a lifespan of 14.6 days and wild type has a lifespan of 18.9 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
G1/S-specific cyclin-E
Locus: CELE_C37A2.4
Wormbase description: cye-1 encodes the sole C. elegans E-type cyclin; CYE-1 is required for progression through the mitotic cell cycle during embryonic, larval, and germline development; cye-1 is also required for endoreduplication in intestinal cells; CYE-1 is expressed ubiquitously in nuclei during embryonic development and postembryonically in proliferating blast cells, including germline stem cells; in the germline, CYE-1 levels are negatively regulated in meiotic cells by a CUL-1, SKR-1/2, PROM-1 SCF ubiquitin ligase.
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