eat-2;prmt-1

Lifespan changes: From wild type to eat-2;prmt-1

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Genetic mutants with eat-2, prmt-1 alterations

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

    20

  • Diet

    OP50

  • Lifespan (days)

    20.8

  • Lifespan comparisons

    Double mutant eat-2(ad1116);prmt-1(ok2710) has a lifespan of 20.8 days, while single mutant eat-2(ad1116) has a lifespan of 21.4 days.

  • Citation
    View abstract

    Takahashi Y et al., 2011, Asymmetric arginine dimethylation determines life span in C. elegans by regulating forkhead transcription factor DAF-16. Cell Metab. 13(5):505-16 PubMed 21531333 Click here to select all mutants from this PubMed ID in the graph

Search genes: eat-2 prmt-1
  • 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

Protein arginine N-methyltransferase 1


Locus: CELE_Y113G7B.17


Wormbase description: prmt-1 encodes a type I protein arginine methyltransferase; in C. elegans, PRMT-1 positively regulates adult lifespan and is required for stress response and fat storage in the absence of DAF-2-mediated signaling; PRMT-1 is also required for proper development of myofilament structure; PRMT-1 physically interacts with, and methylates, DAF-16 thereby preventing its phosphorylation and cytoplasmic retention; in body wall muscle cells, PRMT-1 has been localized to the endoplasmic reticulum.


Orthologs of eat-2;prmt-1 in SynergyAge
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Orthologs of eat-2 in SynergyAge
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Orthologs of prmt-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