ifg-1;unc-70

Lifespan changes: From wild type to ifg-1;unc-70

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Genetic mutants with ifg-1, unc-70 alterations

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

    25

  • Diet

    NGM

  • Lifespan (days)

    25.3

  • Lifespan change (compared to wild type)

    7.20%

  • Lifespan comparisons

    Double mutant ifg-1(cxTi9279);unc-70(RNAi) has a lifespan of 25.3 days, while single mutant unc-70(RNAi) has a lifespan of 22.1 days, single mutant ifg-1(cxTi9279) has a lifespan of 29.0 days and wild type has a lifespan of 23.6 days.

  • Type of interaction
    See methods

    Opposite lifespan effects of single mutants

  • Citation
    View abstract

    Rogers AN et al., 2011, Life span extension via eIF4G inhibition is mediated by posttranscriptional remodeling of stress response gene expression in C. elegans. Cell Metab. 14(1):55-66 PubMed 21723504 Click here to select all mutants from this PubMed ID in the graph

  • Temperature °C

    25

  • Diet

    NGM

  • Lifespan (days)

    22.0

  • Lifespan change (compared to wild type)

    8.37%

  • Lifespan comparisons

    Double mutant ifg-1(cxTi9279);unc-70(RNAi) has a lifespan of 22.0 days, while single mutant unc-70(RNAi) has a lifespan of 19.2 days, single mutant ifg-1(cxTi9279) has a lifespan of 27.8 days and wild type has a lifespan of 20.3 days.

  • Type of interaction
    See methods

    Opposite lifespan effects of single mutants

  • Citation
    View abstract

    Rogers AN et al., 2011, Life span extension via eIF4G inhibition is mediated by posttranscriptional remodeling of stress response gene expression in C. elegans. Cell Metab. 14(1):55-66 PubMed 21723504 Click here to select all mutants from this PubMed ID in the graph

Search genes: ifg-1 unc-70
  • Entrez ID
  • Symbol
  • GenAge
  • Wormbase ID

Initiation Factor 4G (eIF4G) family


Locus: CELE_M110.4


Wormbase description: ifg-1 encodes, by alternative splicing, two orthologs of the translation initiation factor 4F, ribosome/mRNA-bridging subunit (eIF-4G); by homology, IFG-1 is predicted to function in poly(A) tail-dependent translation initiation; loss of ifg-1 activity in adult animals extends lifespan.


  • Entrez ID
  • Symbol
  • GenAge
  • Wormbase ID

Spectrin beta chain


Locus: CELE_K11C4.3


Wormbase description: unc-70 encodes two isoforms of a beta-spectrin ortholog required for normal body curvature and shape, normal movement, and correct localization of the alpha-spectrin SPC-1; the predominant UNC-70 isoform is expressed in all embryonic cells except the intestine, at the plasma membrane at sites of intercellular contact; UNC-70 becomes largely restricted to muscles and neurons from hatching to adulthood, with expression in adult spermetheca and hypodermis as well; conversely, the minor isoform is predominantly expressed in gut, and is also apposed to intercellular membrane junctions in embryos; sma-1 mutations (which impair the one beta-H-spectrin ortholog in C. elegans) enhance the unc-70 phenotype; UNC-70 is dispensable for viability (under undemanding laboratory culture conditions).


Orthologs of ifg-1;unc-70 in SynergyAge
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Orthologs of ifg-1 in SynergyAge
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Species Gene
Orthologs of unc-70 in SynergyAge
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Species Gene
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