Lifespan changes: From wild type to hsf-1;old-1
20
HT115; OP53
16.8
-27.59%
hsf-1(RNAi) also suppressed longevity associated with other components of the insulin-like signaling pathway including OLD overexpressing animals.
Double mutant hsf-1(RNAi);old-1(zls3000) has a lifespan of 16.8 days, while single mutant hsf-1(RNAi) has a lifespan of 17.9 days, single mutant old-1(zls3000) has a lifespan of 28.0 days and wild type has a lifespan of 23.2 days.
Enhancer, opposite lifespan effects
Morley JF, Morimoto RI, 2004, Regulation of longevity in Caenorhabditis elegans by heat shock factor and molecular chaperones. Mol Biol Cell. 15(2):657-64 14668486 Click here to select all mutants from this PubMed ID in the graph
Heat Shock Factor
Locus: CELE_Y53C10A.12
Wormbase description: hsf-1 encodes the C. elegans heat-shock transcription factor ortholog; HSF-1 functions as a transcriptional regulator of stress-induced gene expression whose activity is required for heat-shock and proteotoxicity response, larval development, innate immunity, and regulation of adult lifespan; HSF-1 binds bovine calmodulin in vitro in a calcium-dependent manner.
Tyrosine-protein kinase receptor old-1
Locus: CELE_C08H9.5
Wormbase description: old-1 encodes a receptor protein tyrosine kinase; old-1 plays a role in stress resistance and regulation of adult lifespan; Murakami and Johnson showed that old-1 mRNA levels are upregulated in response to stress and in daf-2 and age-1 mutant backgrounds and that overexpression of old-1 in wild-type animals results in extended lifespan and increased resistance to heat and UV irradiation; in contrast, Murphy et al., showed that old-1 expression is downregulated in daf-2 mutants and that old-1(RNAi) in an rrf-3 mutant background slightly extends lifespan; an OLD-1::GFP fusion protein is expressed in the anterior region of worms, in neuronal, hypodermal, and pharyngeal tissues, as well as in the proximal region of the male gonad; expression is visible in young adults and appears to increase as animals age and in response to heat, starvation, or UV irradiation.
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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