aco-2;daf-2

Lifespan changes: From wild type to aco-2;daf-2

There is no network for this step.
Fullscreen mode
Hide graph
Legend

Genetic mutants with aco-2, daf-2 alterations

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

    20

  • Diet

    OP50

  • Lifespan (days)

    46.57

  • Lifespan comparisons

    Double mutant aco-2(RNAi);daf-2(e1370) has a lifespan of 46.57 days, while single mutant daf-2(e1370) has a lifespan of 46.57 days.

  • Citation
    View abstract

    Dong MQ et al., 2007, Quantitative mass spectrometry identifies insulin signaling targets in C. elegans. Science. 317(5838):660-3 PubMed 17673661 Click here to select all mutants from this PubMed ID in the graph

  • Temperature °C

    20

  • Diet

    OP50

  • Lifespan (days)

    61.3

  • Lifespan comparisons

    Double mutant aco-2(RNAi);daf-2(e1370) has a lifespan of 61.3 days, while single mutant daf-2(e1370) has a lifespan of 47.7 days.

  • Citation
    View abstract

    Dong MQ et al., 2007, Quantitative mass spectrometry identifies insulin signaling targets in C. elegans. Science. 317(5838):660-3 PubMed 17673661 Click here to select all mutants from this PubMed ID in the graph

Search genes: aco-2 daf-2
  • Entrez ID
  • Symbol
  • GenAge
  • Wormbase ID

Probable aconitate hydratase, mitochondrial


Locus: CELE_F54H12.1


Wormbase description: aco-2 encodes an aconitase homolog that is required for embryonic viability, fertility, locomotion, and vulval morphogenesis, and perhaps for normal lifespan.


  • Entrez ID
  • Symbol
  • GenAge
  • Wormbase ID

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.


Orthologs of aco-2;daf-2 in SynergyAge
Show in SynergyAge
Species Gene
Orthologs of aco-2 in SynergyAge
Show in SynergyAge
Species Gene
Orthologs of daf-2 in SynergyAge
Show in SynergyAge
Species Gene
Drosophila melanogaster InR
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