daf-3;daf-9

Lifespan changes: From wild type to daf-3;daf-9

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Genetic mutants with daf-3, daf-9 alterations

    Names of genes are ordered alphabetically. For the order of interventions, please see the specific paper.
  • Temperature °C

    15

  • Lifespan (days)

    37.5

  • Lifespan change (compared to wild type)

    79.43%

  • Phenotype

    daf-3(e1376) has a wild-type life span, but it greatly enhanced the life span of daf-9(e1406) mutants. The mean life span of the double mutant was increased by 80%.

  • Lifespan comparisons

    Double mutant daf-3(e1376);daf-9(e1406) has a lifespan of 37.5 days, while single mutant daf-3(e1376) has a lifespan of 22.3 days, single mutant daf-9(e1406) has a lifespan of 27.7 days and wild type has a lifespan of 20.9 days.

  • Type of interaction
    See methods

    Synergistic (positive)

  • Citation
    View abstract

    Jia K et al., 2002, DAF-9, a cytochrome P450 regulating C. elegans larval development and adult longevity. Development. 129(1):221-31 PubMed 11782415 Click here to select all mutants from this PubMed ID in the graph

Search genes: daf-3 daf-9
  • Entrez ID
  • Symbol
  • GenAge
  • Wormbase ID

Dwarfin sma;hypothetical protein


Locus: CELE_F25E2.5


Wormbase description: daf-3 encodes a co-SMAD protein that is most closely related to Drosophila Medea and the vertebrate Smad4 proteins; DAF-3 functions as a transcriptional regulator that is required for formation of the alternative dauer larval stage as well as for regulation of pharyngeal gene expression during non-dauer development; DAF-3 activity is antagonized by signaling through the DAF-7/TGF-beta pathway which promotes reproductive growth; in yeast two-hybrid studies, DAF-3 interacts with SMA-3, another Smad protein that does not appear to have a role in dauer formation; in vitro, DAF-3 binds the organ-specific C subelement in the promoter of the pharyngeal muscle-specific myosin myo-2 and in vivo, suppresses the enhancer activity of this element during larval development; a DAF-3::GFP fusion protein is expressed in many tissues that undergo remodeling during dauer development, including the gut, nervous system and pharynx; DAF-3 localizes predominantly to the cytoplasm, but is also found in the nucleus in association with mitotic chromosomes.


  • Entrez ID
  • Symbol
  • GenAge
  • Wormbase ID

Cytochrome P450 daf-9


Locus: CELE_T13C5.1


Wormbase description: daf-9 encodes a cytochrome P450 of the CYP2 subfamily that by homology is predicted to function as a steroidogenic or fatty acid hydroxylase; DAF-9 likely functions cell nonautonomously in hypodermal and neuronal cells to produce, for the DAF-12 nuclear receptor, a lipophilic hormone whose presence is necessary for bypassing entry into the alternative L3/dauer larval stage and promoting reproductive development; in regulating dauer formation, daf-9 acts downstream of the DAF-2/insulin/IGF receptor and the DAF-7/TGFbeta ligand, suggesting that at least two of the signaling pathways that control dauer formation converge, in part, upon daf-9; in addition, daf-9 activity is required for gonadal cell migration; a DAF-9::GFP fusion is expressed in the XXXL/R head cells at all developmental stages, in hypodermal cells from the L2 to L4 larval stages, and in the spermatheca of adult hermaphrodites.


Orthologs of daf-3;daf-9 in SynergyAge
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Orthologs of daf-3 in SynergyAge
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Orthologs of daf-9 in SynergyAge
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About

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.

Read more about SynergyAge database

How to cite us

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

Contact
Robi Tacutu, Ph.D.
Head: Systems Biology of Aging Group, Bioinformatics & Structural Biochemistry Department
Institute of Biochemistry, Ground floor
Splaiul Independentei 296, Bucharest, Romania
Email:

Group webpage: www.aging-research.group