Lifespan changes: From wild type to ifg-1;unc-70
25
NGM
25.3
7.20%
Double mutant ifg-1(cxTi9279);unc-70(RNAi) has a lifespan of 25.3 days, while single mutant unc-70(RNAi) has a lifespan of 22.1 days, single mutant ifg-1(cxTi9279) has a lifespan of 29.0 days and wild type has a lifespan of 23.6 days.
Opposite lifespan effects of single mutants
Rogers AN et al., 2011, Life span extension via eIF4G inhibition is mediated by posttranscriptional remodeling of stress response gene expression in C. elegans. Cell Metab. 14(1):55-66 21723504 Click here to select all mutants from this PubMed ID in the graph
25
NGM
22.0
8.37%
Double mutant ifg-1(cxTi9279);unc-70(RNAi) has a lifespan of 22.0 days, while single mutant unc-70(RNAi) has a lifespan of 19.2 days, single mutant ifg-1(cxTi9279) has a lifespan of 27.8 days and wild type has a lifespan of 20.3 days.
Opposite lifespan effects of single mutants
Rogers AN et al., 2011, Life span extension via eIF4G inhibition is mediated by posttranscriptional remodeling of stress response gene expression in C. elegans. Cell Metab. 14(1):55-66 21723504 Click here to select all mutants from this PubMed ID in the graph
Initiation Factor 4G (eIF4G) family
Locus: CELE_M110.4
Wormbase description: ifg-1 encodes, by alternative splicing, two orthologs of the translation initiation factor 4F, ribosome/mRNA-bridging subunit (eIF-4G); by homology, IFG-1 is predicted to function in poly(A) tail-dependent translation initiation; loss of ifg-1 activity in adult animals extends lifespan.
Spectrin beta chain
Locus: CELE_K11C4.3
Wormbase description: unc-70 encodes two isoforms of a beta-spectrin ortholog required for normal body curvature and shape, normal movement, and correct localization of the alpha-spectrin SPC-1; the predominant UNC-70 isoform is expressed in all embryonic cells except the intestine, at the plasma membrane at sites of intercellular contact; UNC-70 becomes largely restricted to muscles and neurons from hatching to adulthood, with expression in adult spermetheca and hypodermis as well; conversely, the minor isoform is predominantly expressed in gut, and is also apposed to intercellular membrane junctions in embryos; sma-1 mutations (which impair the one beta-H-spectrin ortholog in C. elegans) enhance the unc-70 phenotype; UNC-70 is dispensable for viability (under undemanding laboratory culture conditions).
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