The goal of this proposal is to investigate the role of ICER in ovarian function. ICER functions as a transcriptional repressor and is a product of the cAMP Responsive Element Modulator (CREM) gene. The main focus of research in Dr. Molina's lab has been in providing evidence in supporting the hypothesis that ICER acts as a tumor suppressor gene product. ICER can be detected in normal cells, but is undetectable in such tumors cells like prostate tumor cells and human ovarian granulosa tumor cells. ICER is highly expressed in human ovarian tissue and its expression is induced by LH in the ovaries of immature rats. Conversely, LH reduces cyclin D2 expression and its levels are low in the rat's corpus luteum. Additionally, our lab has shown that ICER blocks PKA-induced DNA synthesis and represses the activity of cyclin D2 promoter in cultured granulosa cells. Our hypothesis is that ICER regulates ovarian granulosa cell growth and differentiation by controlling the expression of cyclin D2. This hypothesis will be tested using a transgenic mouse model in which the permissible (Tet-On) expression of ICER is restricted to ovarian granulosa cells and regulated by FSH.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
1F31HD043691-01A1
Application #
6686133
Study Section
Special Emphasis Panel (ZRG1-MBC-1 (29))
Program Officer
Taymans, Susan
Project Start
2004-02-01
Project End
2007-01-31
Budget Start
2004-02-01
Budget End
2005-01-31
Support Year
1
Fiscal Year
2003
Total Cost
$28,274
Indirect Cost
Name
University of Medicine & Dentistry of NJ
Department
Obstetrics & Gynecology
Type
Schools of Medicine
DUNS #
623946217
City
Newark
State
NJ
Country
United States
Zip Code
07107
Muñiz, Luis C; Molina, Carlos A (2016) The transcriptional repressor ICER binds to multiple loci throughout the genome. Biochem Biophys Res Commun 478:1462-5
Muniz, Luis C; Yehia, Ghassan; Memin, Elisabeth et al. (2006) Transcriptional regulation of cyclin D2 by the PKA pathway and inducible cAMP early repressor in granulosa cells. Biol Reprod 75:279-88