Cargando…

Orphan nuclear receptor ftz-f1 (NR5A3) promotes egg chamber survival in the Drosophila ovary

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 rece...

Descripción completa

Detalles Bibliográficos
Autores principales: Beachum, Allison N, Whitehead, Kaitlin M, McDonald, Samantha I, Phipps, Daniel N, Berghout, Hanna E, Ables, Elizabeth T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022936/
https://www.ncbi.nlm.nih.gov/pubmed/33693603
http://dx.doi.org/10.1093/g3journal/jkab003
_version_ 1783675030372089856
author Beachum, Allison N
Whitehead, Kaitlin M
McDonald, Samantha I
Phipps, Daniel N
Berghout, Hanna E
Ables, Elizabeth T
author_facet Beachum, Allison N
Whitehead, Kaitlin M
McDonald, Samantha I
Phipps, Daniel N
Berghout, Hanna E
Ables, Elizabeth T
author_sort Beachum, Allison N
collection PubMed
description 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.
format Online
Article
Text
id pubmed-8022936
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-80229362021-04-09 Orphan nuclear receptor ftz-f1 (NR5A3) promotes egg chamber survival in the Drosophila ovary Beachum, Allison N Whitehead, Kaitlin M McDonald, Samantha I Phipps, Daniel N Berghout, Hanna E Ables, Elizabeth T G3 (Bethesda) Investigation 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. Oxford University Press 2021-01-23 /pmc/articles/PMC8022936/ /pubmed/33693603 http://dx.doi.org/10.1093/g3journal/jkab003 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigation
Beachum, Allison N
Whitehead, Kaitlin M
McDonald, Samantha I
Phipps, Daniel N
Berghout, Hanna E
Ables, Elizabeth T
Orphan nuclear receptor ftz-f1 (NR5A3) promotes egg chamber survival in the Drosophila ovary
title Orphan nuclear receptor ftz-f1 (NR5A3) promotes egg chamber survival in the Drosophila ovary
title_full Orphan nuclear receptor ftz-f1 (NR5A3) promotes egg chamber survival in the Drosophila ovary
title_fullStr Orphan nuclear receptor ftz-f1 (NR5A3) promotes egg chamber survival in the Drosophila ovary
title_full_unstemmed Orphan nuclear receptor ftz-f1 (NR5A3) promotes egg chamber survival in the Drosophila ovary
title_short Orphan nuclear receptor ftz-f1 (NR5A3) promotes egg chamber survival in the Drosophila ovary
title_sort orphan nuclear receptor ftz-f1 (nr5a3) promotes egg chamber survival in the drosophila ovary
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022936/
https://www.ncbi.nlm.nih.gov/pubmed/33693603
http://dx.doi.org/10.1093/g3journal/jkab003
work_keys_str_mv AT beachumallisonn orphannuclearreceptorftzf1nr5a3promoteseggchambersurvivalinthedrosophilaovary
AT whiteheadkaitlinm orphannuclearreceptorftzf1nr5a3promoteseggchambersurvivalinthedrosophilaovary
AT mcdonaldsamanthai orphannuclearreceptorftzf1nr5a3promoteseggchambersurvivalinthedrosophilaovary
AT phippsdanieln orphannuclearreceptorftzf1nr5a3promoteseggchambersurvivalinthedrosophilaovary
AT berghouthannae orphannuclearreceptorftzf1nr5a3promoteseggchambersurvivalinthedrosophilaovary
AT ableselizabetht orphannuclearreceptorftzf1nr5a3promoteseggchambersurvivalinthedrosophilaovary