cye-1;mes-1

Lifespan changes: From wild type to cye-1;mes-1

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Genetic mutants with cye-1, mes-1 alterations

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

    20

  • Diet

    NGM

  • Lifespan (days)

    22.1

  • Lifespan change (compared to wild type)

    19.46%

  • Phenotype

    Knockdown of cye-1(RNAi) was able to extend the lifespan of fertile mes-1(bn7) worms (21%).

  • Lifespan comparisons

    Double mutant cye-1(RNAi);mes-1(bn7) has a lifespan of 22.1 days, while single mutant cye-1(RNAi) has a lifespan of 23.4 days, single mutant mes-1(bn7) has a lifespan of 18.1 days and wild type has a lifespan of 18.5 days.

  • Type of interaction
    See methods

    Opposite lifespan effects of single mutants

  • Citation
    View abstract

    Dottermusch M et al., 2016, Cell cycle controls stress response and longevity in C. elegans. Aging (Albany NY). 8(9):2100-2126 PubMed 27668945 Click here to select all mutants from this PubMed ID in the graph

  • Temperature °C

    20

  • Diet

    NGM

  • Lifespan (days)

    23.7

  • Lifespan change (compared to wild type)

    25.40%

  • Phenotype

    Knockdown of cye-1(RNAi) was not able to extend the lifespan of sterile mes-1(bn7) animals.

  • Lifespan comparisons

    Double mutant cye-1(RNAi);mes-1(bn7) has a lifespan of 23.7 days, while single mutant cye-1(RNAi) has a lifespan of 24.2 days, single mutant mes-1(bn7) has a lifespan of 24.2 days and wild type has a lifespan of 18.9 days.

  • Type of interaction
    See methods

    Antagonistic (positive)

  • Citation
    View abstract

    Dottermusch M et al., 2016, Cell cycle controls stress response and longevity in C. elegans. Aging (Albany NY). 8(9):2100-2126 PubMed 27668945 Click here to select all mutants from this PubMed ID in the graph

  • Temperature °C

    20

  • Diet

    NGM

  • Lifespan (days)

    22.0

  • Lifespan change (compared to wild type)

    13.99%

  • Phenotype

    Knockdown of cye-1(RNAi) was able to extend the lifespan of fertile mes-1(bn7) worms (21%).

  • Lifespan comparisons

    Double mutant cye-1(RNAi);mes-1(bn7) has a lifespan of 22.0 days, while single mutant cye-1(RNAi) has a lifespan of 25.2 days, single mutant mes-1(bn7) has a lifespan of 18.4 days and wild type has a lifespan of 19.3 days.

  • Type of interaction
    See methods

    Opposite lifespan effects of single mutants

  • Citation
    View abstract

    Dottermusch M et al., 2016, Cell cycle controls stress response and longevity in C. elegans. Aging (Albany NY). 8(9):2100-2126 PubMed 27668945 Click here to select all mutants from this PubMed ID in the graph

  • Temperature °C

    20

  • Diet

    NGM

  • Lifespan (days)

    24.3

  • Lifespan change (compared to wild type)

    25.91%

  • Phenotype

    Knockdown of cye-1(RNAi) was not able to extend the lifespan of sterile mes-1(bn7) animals.

  • Lifespan comparisons

    Double mutant cye-1(RNAi);mes-1(bn7) has a lifespan of 24.3 days, while single mutant cye-1(RNAi) has a lifespan of 25.2 days, single mutant mes-1(bn7) has a lifespan of 24.5 days and wild type has a lifespan of 19.3 days.

  • Type of interaction
    See methods

    Antagonistic (positive)

  • Citation
    View abstract

    Dottermusch M et al., 2016, Cell cycle controls stress response and longevity in C. elegans. Aging (Albany NY). 8(9):2100-2126 PubMed 27668945 Click here to select all mutants from this PubMed ID in the graph

  • Temperature °C

    20

  • Diet

    NGM

  • Lifespan (days)

    23.1

  • Lifespan change (compared to wild type)

    24.86%

  • Phenotype

    Knockdown of cye-1(RNAi) was not able to extend the lifespan of sterile mes-1(bn7) animals.

  • Lifespan comparisons

    Double mutant cye-1(RNAi);mes-1(bn7) has a lifespan of 23.1 days, while single mutant cye-1(RNAi) has a lifespan of 23.4 days, single mutant mes-1(bn7) has a lifespan of 23.9 days and wild type has a lifespan of 18.5 days.

  • Type of interaction
    See methods

    Antagonistic (positive)

  • Citation
    View abstract

    Dottermusch M et al., 2016, Cell cycle controls stress response and longevity in C. elegans. Aging (Albany NY). 8(9):2100-2126 PubMed 27668945 Click here to select all mutants from this PubMed ID in the graph

Search genes: cye-1 mes-1
  • Entrez ID
  • Symbol
  • GenAge
  • Wormbase ID

G1/S-specific cyclin-E


Locus: CELE_C37A2.4


Wormbase description: cye-1 encodes the sole C. elegans E-type cyclin; CYE-1 is required for progression through the mitotic cell cycle during embryonic, larval, and germline development; cye-1 is also required for endoreduplication in intestinal cells; CYE-1 is expressed ubiquitously in nuclei during embryonic development and postembryonically in proliferating blast cells, including germline stem cells; in the germline, CYE-1 levels are negatively regulated in meiotic cells by a CUL-1, SKR-1/2, PROM-1 SCF ubiquitin ligase.


  • Entrez ID
  • Symbol
  • GenAge
  • Wormbase ID

Protein mes-1


Locus: CELE_F54F7.5


Wormbase description: The mes-1 gene encodes a receptor tyrosine kinase-like protein that is required for unequal cell divisions in the early embryonic germline; during embryonic cell divisions, mes-1 is involved in positioning of the early mitotic spindle and of associated P granules.


Orthologs of cye-1;mes-1 in SynergyAge
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Species Gene
Orthologs of cye-1 in SynergyAge
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Species Gene
Orthologs of mes-1 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