Secretions from oviducts are essential for preparing gametes for fertilization, processes conserved throughout the animal kingdom. However, molecular mechanisms underlying oviduct physiology are largely unknown. Recent studies from our lab have shown that secretory cells of spermathecae and parovaria, two types of glands in Drosophila female reproductive tract, are functionally homologous to secretory cells in mammalian oviducts and play essential roles for ovulation, sperm storage, and fertilization. With the wealth of genetic tools we developed and capability of rapid and precise genetic manipulation, we propose to utilize this novel Drosophila system to elucidate the conserved molecular mechanisms underlying secretory cell-regulated ovulation and sperm storage. Particularly, we will characterize the role of conserved transcription factors (NR5A-family nuclear receptor Hr39, GATA-family transcription factors Pannier and Serpent) in secretory cells for sperm storage and ovulation. We will also identify the downstream targets of these transcription factors in secretory cells to fulfill their roles and identify novel secretory factors for sperm storage using genetic screens. This work will provide a comprehensive understanding of the secretory cell physiology in female reproductive tract. The conserved nature of these signaling pathways will allow the knowledge gained from this study to be further validated in other insect species as well as in mammalian and human oviducts. Therefore, this work will ultimately reveal promising new drug targets for the alleviation of infertility, for novel contraceptive development, and for controlling malaria-bearing mosquito population, all of which are highly relevant to human health.

Public Health Relevance

Secretory cells in oviducts are essential for gamete survival and fertilization. This project utilizes a novel Drosophila model to genetically interrogate the role of conserved transcription factors in oviduct secretory cells and identify novel factors for sperm attraction and ovulation. Through this work, we will gain mechanistic insights into the precise regulation of oviduct secretions, which will aid the development of new approaches for contraception, treating infertility, and controlling malaria-bearing mosquito population.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
1R01HD097206-01A1
Application #
9885288
Study Section
Cellular, Molecular and Integrative Reproduction Study Section (CMIR)
Program Officer
Taymans, Susan
Project Start
2020-04-01
Project End
2025-03-31
Budget Start
2020-04-01
Budget End
2021-03-31
Support Year
1
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Connecticut
Department
Physiology
Type
Schools of Arts and Sciences
DUNS #
614209054
City
Storrs-Mansfield
State
CT
Country
United States
Zip Code
06269