daf-2;end-1

Lifespan changes: From wild type to daf-2;end-1

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Genetic mutants with daf-2, end-1 alterations

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

    20

  • Diet

    HT115

  • Lifespan (days)

    27.0

  • Lifespan change (compared to wild type)

    103.01%

  • Lifespan comparisons

    Double mutant daf-2(e1370);end-1(RNAi) has a lifespan of 27.0 days, while single mutant end-1(RNAi) has a lifespan of 13.0 days, single mutant daf-2(e1370) has a lifespan of 33.9 days and wild type has a lifespan of 13.3 days.

  • Type of interaction
    See methods

    Opposite lifespan effects of single mutants

  • Citation
    View abstract

    Budovskaya YV et al., 2008, An elt-3/elt-5/elt-6 GATA transcription circuit guides aging in C. elegans. Cell. 134(2):291-303 PubMed 18662544 Click here to select all mutants from this PubMed ID in the graph

  • Temperature °C

    20

  • Diet

    HT115

  • Lifespan (days)

    15.5

  • Lifespan change (compared to wild type)

    6.16%

  • Lifespan comparisons

    Double mutant daf-2(e1370);end-1(RNAi) has a lifespan of 15.5 days, while single mutant end-1(RNAi) has a lifespan of 13.7 days, single mutant daf-2(e1370) has a lifespan of 30.7 days and wild type has a lifespan of 14.6 days.

  • Type of interaction
    See methods

    Opposite lifespan effects of single mutants

  • Citation
    View abstract

    Budovskaya YV et al., 2008, An elt-3/elt-5/elt-6 GATA transcription circuit guides aging in C. elegans. Cell. 134(2):291-303 PubMed 18662544 Click here to select all mutants from this PubMed ID in the graph

Search genes: daf-2 end-1
  • 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.


  • Entrez ID
  • Symbol
  • GenAge
  • Wormbase ID

ENDoderm determining


Locus: CELE_F58E10.2


Wormbase description: end-1 encodes a GATA-type transcription factor paralogous to end-3; during early embryonic development, end-1 functions redundnatly with end-3 to specify endodermal fate; when expressed ectopically, however, END-1 is sufficient to initiate endoderm differentiation; END-1 expression bypasses requirement for maternal SKN-1 and the maternal Wnt signaling pathway in endoderm formation and END-1 activates endoderm differentiation in isolated Xenopus ectoderm; END-1 binds to the canonical target DNA sequence WGATAR with specificity similar to GATA-1 and D4 transcription factors; END-1 is expressed in the early E lineage.


Orthologs of daf-2;end-1 in SynergyAge
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Orthologs of daf-2 in SynergyAge
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Species Gene
Drosophila melanogaster InR
Orthologs of end-1 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