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Author ORCID Identifier
https://orcid.org/0009-0000-3912-990X
Date Available
5-1-2028
Year of Publication
2026
Document Type
Master's Thesis
Degree Name
Master of Science in Medical Sciences (MSMS)
College
Medicine
Department/School/Program
Medical Sciences
Faculty
Misung Jo
Faculty
Richard Grondin
Abstract
Successful ovulation and subsequent formation of the corpus luteum (CL) is essential for female fertility. These processes require tightly controlled changes in the expression of a myriad of genes. Transcription factors (TFs) induced in ovulatory follicles play critical roles in regulating the expression of these genes. Studies have shed light on FOS, a subunit of AP-1, as a critical TF involved in ovulation and luteal formation. The purpose of this study was first to determine the expression of Fos and Jun family members in response to ovulatory LH/hCG, then elucidate the roles of ovarian Fos and Junb expression during the ovulatory process. Herein, we show a rapid upregulation of Fos and Jun family members in response to hCG, with peak expression occurring at 3h and 11h after hCG stimulation. We also show conditional deletion of Fos or Junb in mice results in modest subfertility, while simultaneous deletion of Fos;Junb leads to an anovulation and infertility with reduced expression of key ovulatory genes, atypical steroidogenesis, and abnormal CL formation. These data indicate the loss of one subunit can be compensated by other family members, but the simultaneous loss of both FOS and JUNB is detrimental to gene regulation, ovulation, and fertility.
Digital Object Identifier (DOI)
https://doi.org/10.13023/etd.2026.380
Archival?
Archival
Recommended Citation
Southall, Jacqueline N., "INVESTIGATING THE ROLE OF AP-1 IN MURINE OVULATION AND LUTEINIZATION VIA TARGETED DELETION OF OVARIAN FOS AND JUNB" (2026). Theses and Dissertations--Medical Sciences. 31.
https://uknowledge.uky.edu/medsci_etds/31
Included in
Medical Molecular Biology Commons, Obstetrics and Gynecology Commons, Reproductive and Urinary Physiology Commons
