Lifespan changes: From wild type to daf-2;elt-1
20
HT115
32.5
122.60%
Double mutant daf-2(e1370);elt-1(RNAi) has a lifespan of 32.5 days, while single mutant elt-1(RNAi) has a lifespan of 8.9 days, single mutant daf-2(e1370) has a lifespan of 28.5 days and wild type has a lifespan of 14.6 days.
Enhancer, opposite lifespan effects
Budovskaya YV et al., 2008, An elt-3/elt-5/elt-6 GATA transcription circuit guides aging in C. elegans. Cell. 134(2):291-303 18662544 Click here to select all mutants from this PubMed ID in the graph
20
HT115
25.7
76.03%
Double mutant daf-2(e1370);elt-1(RNAi) has a lifespan of 25.7 days, while single mutant elt-1(RNAi) has a lifespan of 11.6 days, single mutant daf-2(e1370) has a lifespan of 30.7 days and wild type has a lifespan of 14.6 days.
Opposite lifespan effects of single mutants
Budovskaya YV et al., 2008, An elt-3/elt-5/elt-6 GATA transcription circuit guides aging in C. elegans. Cell. 134(2):291-303 18662544 Click here to select all mutants from this PubMed ID in the graph
20
HT115
30.7
130.83%
Double mutant daf-2(e1370);elt-1(RNAi) has a lifespan of 30.7 days, while single mutant elt-1(RNAi) has a lifespan of 12.0 days, single mutant daf-2(e1370) has a lifespan of 33.9 days and wild type has a lifespan of 13.3 days.
Opposite lifespan effects of single mutants
Budovskaya YV et al., 2008, An elt-3/elt-5/elt-6 GATA transcription circuit guides aging in C. elegans. Cell. 134(2):291-303 18662544 Click here to select all mutants from this PubMed ID in the graph
Insulin-like receptor subunit beta;Receptor protein-tyrosine kinase;hypothetical protein
Locus: CELE_Y55D5A.5
Wormbase description: daf-2 encodes a receptor tyrosine kinase that is the C. elegans insulin/IGF receptor ortholog; DAF-2 activity is required for a number of processes in C. elegans, including embryonic and larval development, formation of the developmentally arrested dauer larval stage (diapause), larval developmental timing, adult longevity, reproduction, fat storage, salt chemotaxis learning, and stress resistance, including response to high temperature, oxidative stress, and bacterial infection; DAF-2 signals through a conserved PI 3-kinase pathway to negatively regulate the activity of DAF-16, a Forkhead-related transcription factor, by inducing its phosphorylation and nuclear exclusion; in addition, DAF-2 negatively regulates the nuclear localization, and hence transcriptional activity, of SKN-1 in intestinal nuclei; amongst the 38 predicted insulin-like molecules in C. elegans, genetic and microarray analyses suggest that at least DAF-28, INS-1, and INS-7 are likely DAF-2 ligands; genetic mosaic and tissue-specific promoter studies indicate that daf-2 can function cell nonautonomously and within multiple cell types to influence dauer formation and adult lifespan, likely by regulating the production of secondary endocrine signals that coordinate growth and longevity throughout the animal; temporal analysis of daf-2 function indicates that daf-2 regulates lifespan, reproduction, and diapause independently, at distinct times during the animal's life cycle.
Erythroid-Like Transcription factor family;Transcription factor elt-1
Locus: CELE_W09C2.1
Wormbase description: elt-1 encodes a GATA-like transcription factor; elt-1 is essential for fate specification of both AB- and P1-derived epidermal (hypodermal) cells during embryogenesis; elt-1 is also required for regulation of sperm-specific gene expression in the germ line and sperm function, and ELT-1 binds a sequence-specific DNA sequence, the sperm consensus site, in vitro; ELT-1 has also been shown to activate transcription from a yeast reporter plasmid; ELT-1 is a nuclear protein and is expressed in the early embryo in blastomeres that generate major hypodermal cells and in the major hypodermal cells, themselves; elt-1 is also expressed in the sperm-producing germ line.
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Drosophila melanogaster | InR |
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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