D2030.4;daf-16

Lifespan changes: From wild type to D2030.4;daf-16

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Genetic mutants with D2030.4, daf-16 alterations

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

    20

  • Diet

    NGM

  • Lifespan (days)

    21.5

  • Lifespan change (compared to wild type)

    11.98%

  • Phenotype

    RNAi inactivation of a D2030.4 gene, key to mitochondrial function, markedly extended C. elegans lifespan on both daf-16 (mgDf47) and wild type.

  • Lifespan comparisons

    Double mutant D2030.4(RNAi);daf-16(mgDf47) has a lifespan of 21.5 days, while single mutant D2030.4(RNAi) has a lifespan of 27.4 days, single mutant daf-16(mgDf47) has a lifespan of 12.5 days and wild type has a lifespan of 19.2 days.

  • Type of interaction
    See methods

    Opposite lifespan effects of single mutants

  • Citation
    View abstract

    Lee SS et al., 2003, A systematic RNAi screen identifies a critical role for mitochondria in C. elegans longevity. Nat Genet. 33(1):40-8 PubMed 12447374 Click here to select all mutants from this PubMed ID in the graph

Search genes: D2030.4 daf-16
  • Entrez ID
  • Symbol
  • GenAge
  • Wormbase ID

NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 7


Locus: CELE_D2030.4


Wormbase description: D2030.4 encodes the C. elegans ortholog of the NDUFB7/B18 subunit of the mitochondrial NADH dehydrogenase (ubiquinone) complex (complex I).


  • Entrez ID
  • Symbol
  • GenAge
  • Wormbase ID

Forkhead box protein O;hypothetical protein


Locus: CELE_R13H8.1


Wormbase description: daf-16 encodes the sole C. elegans forkhead box O (FOXO) homologue; DAF-16 functions as a transcription factor that acts in the insulin/IGF-1-mediated signaling (IIS) pathway that regulates dauer formation, longevity, fat metabolism, stress response, and innate immunity; DAF-16 regulates these various processes through isoform-specific expression, isoform-specific regulation by different AKT kinases, and differential regulation of target genes; DAF-16 can interact with the CBP-1 transcription cofactor in vitro, and interacts genetically with other genes in the insulin signaling and with daf-12, which encodes a nuclear hormone receptor; DAF-16 is activated in response to DNA damage during development and co-regulated by EGL-27, alleviates DNA-damage-induced developmental arrest by inducing DAF-16-associated element (DAE)-regulated genes; DAF-16 is broadly expressed but displays isoform-specific tissue enrichment; DAF-16 localizes to both the cytoplasm and the nucleus, with the ratio between the two an important regulator of function.


Orthologs of D2030.4;daf-16 in SynergyAge
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Orthologs of D2030.4 in SynergyAge
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Orthologs of daf-16 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