Lifespan changes: From wild type to ddl-1;hsf-1
20
13.2
-20.00%
RNAi treatment of ddl-1 failed to produce any significant lifespan extension on hsf-1(sy441) mutants, while reducing expression of ddl-1 by RNAi extends lifespan in wild type. This finding suggests that hsf-1 is required for the extended lifespan observed in ddl-1 RNAi treated animals.
Double mutant ddl-1(RNAi);hsf-1(sy441) has a lifespan of 13.2 days, while single mutant ddl-1(RNAi) has a lifespan of 18.4 days, single mutant hsf-1(sy441) has a lifespan of 13.5 days and wild type has a lifespan of 16.5 days.
Opposite lifespan effects of single mutants
Chiang WC et al., 2012, HSF-1 regulators DDL-1/2 link insulin-like signaling to heat-shock responses and modulation of longevity. Cell. 148(1-2):322-34 22265419 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.
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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