eat-2;elt-3

Lifespan changes: From wild type to eat-2;elt-3

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Genetic mutants with eat-2, elt-3 alterations

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

    20

  • Diet

    HT115

  • Lifespan (days)

    11.8

  • Lifespan change (compared to wild type)

    -4.07%

  • Phenotype

    elt-3(RNAi) suppresses the longevity phenotype of eat-2(ad1116) mutants, which have a defect in pharyngeal pumping that results in dietary restriction.

  • Lifespan comparisons

    Double mutant eat-2(ade465);elt-3(RNAi) has a lifespan of 11.8 days, while single mutant elt-3(RNAi) has a lifespan of 12.1 days, single mutant eat-2(ade465) has a lifespan of 14.3 days and wild type has a lifespan of 12.3 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

Search genes: eat-2 elt-3
  • Entrez ID
  • Symbol
  • GenAge
  • Wormbase ID

Neuronal acetylcholine receptor subunit eat-2


Locus: CELE_Y48B6A.4


Wormbase description: eat-2 encodes a ligand-gated ion channel subunit most closely related to the non-alpha-subunits of nicotinic acetylcholine receptors (nAChR); EAT-2 functions postsynaptically in pharyngeal muscle to regulate the rate of pharyngeal pumping; eat-2 is also required for normal life span and defecation; a functional EAT-2::GFP fusion protein localizes to two small dots near the junction of pharyngeal muscles pm4 and pm5, which is the site of the posterior-most MC motor neuron processes and the MC synapse; eat-2 genetically interacts with eat-18, which encodes a predicted novel transmembrane protein expressed in pharyngeal muscle and required for proper function of pharyngeal nicotonic receptors.


  • Entrez ID
  • Symbol
  • GenAge
  • Wormbase ID

Erythroid-Like Transcription factor family


Locus: CELE_K02B9.4


Wormbase description: elt-3 gene encodes a GATA transcription factor; during embryogenesis, ELT-3 appears to act downstream of ELT-1, also a GATA transcription factor, in a redundant pathway controlling hypodermal cell differentiation; ELT-3 is also required for positive regulation of transcription of nlp-29, which encodes an antimicrobial peptide, in response to fungal infection and gpdh-1 in response to salt stress; in addition, ELT-3 may also play a role in regulating adult lifespan; ELT-3 is expressed in all of the major hypodermal cells except the lateral seam cells and localizes to the nucleus; elt-3 expression in the hypodermis is positively regulated by ELT-1 and negatively regulated by ELT-5 and ELT-6.


Orthologs of eat-2;elt-3 in SynergyAge
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Orthologs of eat-2 in SynergyAge
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Orthologs of elt-3 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