Lifespan changes: From wild type to cye-1;daf-9
20
NGM
19.7
-1.01%
The lifespan extension of cye-1(RNAi) was strongly suppressed in the daf-9(rh50) mutant background.
Double mutant cye-1(RNAi);daf-9(rh50) has a lifespan of 19.7 days, while single mutant cye-1(RNAi) has a lifespan of 24.0 days, single mutant daf-9(rh50) has a lifespan of 18.5 days and wild type has a lifespan of 19.9 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
20
NGM
19.5
-4.41%
The lifespan extension of cye-1(RNAi) was strongly suppressed in the daf-9(rh50) mutant background.
Double mutant cye-1(RNAi);daf-9(rh50) has a lifespan of 19.5 days, while single mutant cye-1(RNAi) has a lifespan of 24.3 days, single mutant daf-9(rh50) has a lifespan of 18.3 days and wild type has a lifespan of 20.4 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
19.9
3.11%
The lifespan extension of cye-1(RNAi) was strongly suppressed in the daf-9(rh50) mutant background.
Double mutant cye-1(RNAi);daf-9(rh50) has a lifespan of 19.9 days, while single mutant cye-1(RNAi) has a lifespan of 23.6 days, single mutant daf-9(rh50) has a lifespan of 18.8 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
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.
Cytochrome P450 daf-9
Locus: CELE_T13C5.1
Wormbase description: daf-9 encodes a cytochrome P450 of the CYP2 subfamily that by homology is predicted to function as a steroidogenic or fatty acid hydroxylase; DAF-9 likely functions cell nonautonomously in hypodermal and neuronal cells to produce, for the DAF-12 nuclear receptor, a lipophilic hormone whose presence is necessary for bypassing entry into the alternative L3/dauer larval stage and promoting reproductive development; in regulating dauer formation, daf-9 acts downstream of the DAF-2/insulin/IGF receptor and the DAF-7/TGFbeta ligand, suggesting that at least two of the signaling pathways that control dauer formation converge, in part, upon daf-9; in addition, daf-9 activity is required for gonadal cell migration; a DAF-9::GFP fusion is expressed in the XXXL/R head cells at all developmental stages, in hypodermal cells from the L2 to L4 larval stages, and in the spermatheca of adult hermaphrodites.
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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