FB2026_03 , released September 17, 2026
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Citation
Neitzel, L.R., Broadus, M.R., Zhang, N., Sawyer, L., Wallace, H.A., Merkle, J.A., Jodoin, J.N., Sitaram, P., Crispi, E.E., Rork, W., Lee, L.A., Pan, D., Gould, K.L., Page-McCaw, A., Lee, E. (2018). Characterization of a cdc14 null allele in Drosophila melanogaster.  Biol. Open 7(7): bio035394.
FlyBase ID
FBrf0239420
Publication Type
Research paper
Abstract
Cdc14 is an evolutionarily conserved serine/threonine phosphatase. Originally identified in Saccharomyces cerevisiae as a cell cycle regulator, its role in other eukaryotic organisms remains unclear. In Drosophila melanogaster, Cdc14 is encoded by a single gene, thus facilitating its study. We found that Cdc14 expression is highest in the testis of adult flies and that cdc14 null flies are viable. cdc14 null female and male flies do not display altered fertility. cdc14 null males, however, exhibit decreased sperm competitiveness. Previous studies have shown that Cdc14 plays a role in ciliogenesis during zebrafish development. In Drosophila, sensory neurons are ciliated. We found that the Drosophila cdc14 null mutants have defects in chemosensation and mechanosensation as indicated by decreased avoidance of repellant substances and decreased response to touch. In addition, we show that cdc14 null mutants have defects in lipid metabolism and resistance to starvation. These studies highlight the diversity of Cdc14 function in eukaryotes despite its structural conservation.
PubMed ID
PubMed Central ID
PMC6078348 (PMC) (EuropePMC)
Related Publication(s)
Erratum

Correction: Characterization of a cdc14 null allele in Drosophila melanogaster (doi:10.1242/bio.035394).
Neitzel et al., 2018, Biol. Open 7(8): bio037705 [FBrf0239842]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Biol. Open
    Title
    Biology open
    ISBN/ISSN
    2046-6390
    Data From Reference
    Alleles (5)
    Genes (3)
    Natural transposons (1)
    Insertions (1)
    Experimental Tools (3)
    Transgenic Constructs (4)