FB2024_03 , released June 25, 2024
Reference Report
Open Close
Reference
Citation
Hinson, S., Pettus, J., Nagoshi, R.N. (1999). Regulatory and functional interactions between ovarian tumor and ovo during Drosophila oogenesis.  Mech. Dev. 88(1): 3--14.
FlyBase ID
FBrf0111908
Publication Type
Research paper
Abstract
The ovo and ovarian tumor genes are required during early and late stages of Drosophila oogenesis. The ovo product, a zinc-finger transcription factor, can bind to sites and influence the level of expression of the ovarian tumor promoter. Our examination of ovo null mutant organelles demonstrate that it is required for the differentiation of XX germ cells during larval gonial stages, in addition to its known role in maintaining germ cell numbers. In contrast, ovarian tumor is required during pupal and adult stages for the cystocyte divisions that give rise to the egg chamber. Studies on sexually transformed flies indicate that both the ovo and ovarian tumor null mutant phenotypes are distinctive from and more severe than the germline defects produced when male germ cells develop in female soma. This suggests that ovo and ovarian tumor have oogenic functions other than their putative role in germline sex determination. We also demonstrate that the regulation of ovarian tumor by ovo is stage-specific, as ovarian tumor promoter activity does not require ovo during larval stages but becomes ovo-dependent in the adult ovary. This coincides with when the ovarian tumor promoter becomes responsive to sex-specific signals from the soma suggesting a convergence of somatic and germline regulatory pathways on ovarian tumor during oogenesis.
PubMed ID
PubMed Central ID
Associated Information
Comments
Associated Files
Other Information
Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Mech. Dev.
    Title
    Mechanisms of Development
    Publication Year
    1990-
    ISBN/ISSN
    0925-4773
    Data From Reference
    Aberrations (1)
    Alleles (14)
    Genes (10)
    Insertions (1)
    Experimental Tools (1)
    Transgenic Constructs (4)