Lifespan changes: From wild type to age-1;drp-1
20
40.72
111.97%
The extended longevity and the sensitivity to heat stress of the age1;drp-1 mutant compared to the age-1 mutant can be rescued by introduction of a transgene overexpressing drp-1. drp-1 RNAi affects mitochondrial morphology in muscle cells of the body wall. Both age-1 and daf-2 mutants treated with drp-1 RNAi showed substantial further increase in mean lifespan (>65% compared to age-1 and daf-2 single mutant on control RNAi).
Double mutant age-1(hx546);drp-1(RNAi) has a lifespan of 40.72 days, while single mutant drp-1(RNAi) has a lifespan of 19.27 days, single mutant age-1(hx546) has a lifespan of 26.89 days and wild type has a lifespan of 19.21 days.
Synergistic (positive)
Yang CC et al., 2011, The dynamin-related protein DRP-1 and the insulin signaling pathway cooperate to modulate Caenorhabditis elegans longevity. Aging Cell. 10(4):724-8 21463460 Click here to select all mutants from this PubMed ID in the graph
20
33.49
121.06%
age-1;drp-1 and daf-2;drp-1 mutants exhibited a >75% increase in mean lifespan and an extension by up to 30 days in maximum lifespan when compared to their single mutant counterparts.
Double mutant age-1(hx546);drp-1(tm1108) has a lifespan of 33.49 days, while single mutant age-1(hx546) has a lifespan of 26.87 days, single mutant drp-1(tm1108) has a lifespan of 15.44 days and wild type has a lifespan of 15.15 days.
Synergistic (positive)
Yang CC et al., 2011, The dynamin-related protein DRP-1 and the insulin signaling pathway cooperate to modulate Caenorhabditis elegans longevity. Aging Cell. 10(4):724-8 21463460 Click here to select all mutants from this PubMed ID in the graph
20
37.76
149.24%
age-1;drp-1 and daf-2;drp-1 mutants exhibited a >75% increase in mean lifespan and an extension by up to 30 days in maximum lifespan when compared to their single mutant counterparts.
Double mutant age-1(hx546);drp-1(tm1108) has a lifespan of 37.76 days, while single mutant drp-1(tm1108) has a lifespan of 15.44 days, single mutant age-1(hx546) has a lifespan of 26.87 days and wild type has a lifespan of 15.15 days.
Synergistic (positive)
Yang CC et al., 2011, The dynamin-related protein DRP-1 and the insulin signaling pathway cooperate to modulate Caenorhabditis elegans longevity. Aging Cell. 10(4):724-8 21463460 Click here to select all mutants from this PubMed ID in the graph
Phosphatidylinositol 3-kinase age-1;hypothetical protein
Locus: CELE_B0334.8
Wormbase description: age-1 encodes the C. elegans ortholog of the phosphoinositide 3-kinase (PI3K) p110 catalytic subunit; AGE-1, supplied maternally and embryonically, is a central component of the C. elegans insulin-like signaling pathway, lying downstream of the DAF-2/insulin receptor and upstream of both the PDK-1 and AKT-1/AKT-2 kinases and the DAF-16 forkhead type transcription factor, whose negative regulation is the key output of the insulin signaling pathway; in accordance with its role in insulin signaling, AGE-1 activity is required for regulation of metabolism, life span, dauer formation, stress resistance, salt chemotaxis learning, fertility, and embryonic development; although the age-1 expression pattern has not yet been reported, ectopic expression studies indicate that pan-neuronal age-1 expression is sufficient to rescue life-span defects, while neuronal, intestinal, or muscle expression can partially rescue dauer formation, and neuronal or muscle expression can rescue metabolic defects.
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Species | Gene |
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Species | Gene |
Drosophila melanogaster | Pi3K92E |
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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