Lifespan changes: From wild type to lgg-1;LPL-4
20
OP50; HT115E
15.8
-12.22%
RNAi-mediated inhibition of lgg-1 significantly reduced the lifespan of LIPL-4 overexpressing animals, while having negligible effects on non-transgenic siblings.
Double mutant lgg-1(RNAi);LPL-4(OE) has a lifespan of 15.8 days, while single mutant lgg-1(RNAi) has a lifespan of 17.8 days, single mutant LPL-4(OE) has a lifespan of 19.2 days and wild type has a lifespan of 18.0 days.
Opposite lifespan effects of single mutants
Lapierre LR et al., 2011, Autophagy and lipid metabolism coordinately modulate life span in germline-less C. elegans. Curr Biol. 21(18):1507-14 21906946 Click here to select all mutants from this PubMed ID in the graph
20
OP50; HT115E
16.7
-9.24%
RNAi-mediated inhibition of lgg-1 significantly reduced the lifespan of LIPL-4 overexpressing animals, while having negligible effects on non-transgenic siblings.
Double mutant lgg-1(RNAi);LPL-4(OE) has a lifespan of 16.7 days, while single mutant lgg-1(RNAi) has a lifespan of 19.8 days, single mutant LPL-4(OE) has a lifespan of 22.7 days and wild type has a lifespan of 18.4 days.
Antagonistic (negative)
Lapierre LR et al., 2011, Autophagy and lipid metabolism coordinately modulate life span in germline-less C. elegans. Curr Biol. 21(18):1507-14 21906946 Click here to select all mutants from this PubMed ID in the graph
20
OP50; HT115E
18.5
RNAi-mediated inhibition of lgg-1 significantly reduced the lifespan of LIPL-4 overexpressing animals, while having negligible effects on non-transgenic siblings.
Double mutant lgg-1(RNAi);LPL-4(OE) has a lifespan of 18.5 days, while single mutant lgg-1(RNAi) has a lifespan of 18.3 days, single mutant LPL-4(OE) has a lifespan of 21.4 days and wild type has a lifespan of 18.5 days.
Opposite lifespan effects of single mutants
Lapierre LR et al., 2011, Autophagy and lipid metabolism coordinately modulate life span in germline-less C. elegans. Curr Biol. 21(18):1507-14 21906946 Click here to select all mutants from this PubMed ID in the graph
Protein lgg-1
Locus: CELE_C32D5.9
Wormbase description: lgg-1 encodes the C. elegans ortholog of Saccharomyces cerevisiae Atg8p and mammalian MAP-LC3; by homology, LGG-1 is predicted to be required for the degradation of cellular components by autophagy; loss of lgg-1 function via RNAi indicates that, like several other C. elegans genes involved in autophagy, lgg-1 is essential for normal dauer morphogenesis and life-span extension; a GFP::LGG-1 reporter fusion protein is expression in several different stages of development in multiple tissues, including the nervous system, pharynx, intestine, hypodermis, somatic gonad and vulva; under normal growth conditions, GFP::LGG-1 shows a diffuse cytoplasmic localization, but during dauer formation and in long-lived animals, GFP::LGG-1 shows a marked increase in punctate staining in hypodermal seam cells that likely reflects an increase in the number of preautophagosomal and autophagosomal structures.
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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