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Orphan nuclear receptorftz-f1 (NR5A3)promotes egg chamber survival in theDrosophilaovary
Author(s) -
Allison N. Beachum,
Kaitlin M. Whitehead,
Samantha I McDonald,
Daniel N. Phipps,
Hanna E Berghout,
Elizabeth T. Ables
Publication year - 2021
Publication title -
g3 genes genomes genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.468
H-Index - 66
ISSN - 2160-1836
DOI - 10.1093/g3journal/jkab003
Subject(s) - biology , gametogenesis , oogenesis , nuclear receptor , germline , microbiology and biotechnology , oocyte , somatic cell , drosophila melanogaster , gonad , gamete , ovary , genetics , endocrinology , embryogenesis , embryo , transcription factor , sperm , gene
Gamete production in mammals and insects is controlled by cell signaling pathways that facilitate communication between germ cells and somatic cells. Nuclear receptor signaling is a key mediator of many aspects of reproduction, including gametogenesis. For example, the NR5A subfamily of nuclear receptors is essential for gonad development and sex steroid production in mammals. Despite the original identification of the NR5A subfamily in the model insect Drosophila melanogaster, it has been unclear whether Drosophila NR5A receptors directly control oocyte production. Ftz-f1 is expressed throughout the ovary, including in germline stem cells, germline cysts, and several populations of somatic cells. We show that ftz-f1 is required in follicle cells prior to stage 10 to promote egg chamber survival at the mid-oogenesis checkpoint. Our data suggest that egg chamber death in the absence of ftz-f1 is due, at least in part, to failure of follicle cells to exit the mitotic cell cycle or failure to accumulate oocyte-specific factors in the germline. Taken together, these results show that, as in mammals, the NR5A subfamily promotes maximal reproductive output in Drosophila. Our data underscore the importance of nuclear receptors in the control of reproduction and highlight the utility of Drosophila oogenesis as a key model for unraveling the complexity of nuclear receptor signaling in gametogenesis.

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