The overall goal of this proposal is to define the control mechanisms that confer endometrial tissue specificity to the expression of the uteroferrin (UF) gene during pregnancy in the pig. The molecular basis for the interaction of cis-acting elements located 5' of the UF gene with nuclear transacting factors to achieve high levels of transcription in the uterus will be analyzed to provide further understanding of the mechanisms involved in the appropriate expression of endometrial genes, whose products are essential for embryonic, fetal and placental development, uterine growth and tissue remodelling. The endometrial-specific response element (ESRE), which represents the sequences conferring endometrial-specific expression of the UF gene, will be identified by deletion mapping and linker-scanning mutagenesis of the UF gene 5' flanking region and analysis of the corresponding mutated fragments for UF promoter activity. Studies will utilize a transient expression system in the hormone-responsive endometrial epithelial cell line (HRE-H9), which supports UF gene promoter activity. The transacting factor (binding protein) that binds to ESRE will be characterized in uterine endometrium and in non-UF expressing tissues of pregnant gilts to define the specificity of their binding interactions. The ESRE will be used as probe to isolate the complementary DNA (cDNA) corresponding to the transacting factor from a lambda gt11 porcine endometrial expression library. This clone will be characterized by standard molecular biology techniques to deduce the amino acid sequence of the ESRE-binding protein and used as probe in Northern blot analysis to evaluate the pattern of expression of the mRNA encoding this protein relative to that of UF, during uterine and fetal development and as a function of hormonal status in gilts. Finally, the cDNA for ESRE-binding protein and the UF-CAT chimeric gene will be co- expressed in HRE-H9 cells and in non-UF expressing cells (i.e. AKR-2B and JEG-3) to demonstrate the functional ability of the transacting factor in the endometrial-specific expression of the UF gene. Uteroferrin gene is an excellent candidate gene to elucidate the mechanisms involved in the control of uterine gene expression. Results from these studies will clarify essential mechanisms underlying maternal-fetal interactions during critical periods of conceptus and fetal development.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD021961-07
Application #
3321119
Study Section
Human Embryology and Development Subcommittee 1 (HED)
Project Start
1986-07-01
Project End
1996-06-30
Budget Start
1992-07-01
Budget End
1993-06-30
Support Year
7
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of Florida
Department
Type
Schools of Earth Sciences/Natur
DUNS #
073130411
City
Gainesville
State
FL
Country
United States
Zip Code
32611
Heard, Melissa E; Melnyk, Stepan B; Simmen, Frank A et al. (2016) High-Fat Diet Promotion of Endometriosis in an Immunocompetent Mouse Model is Associated With Altered Peripheral and Ectopic Lesion Redox and Inflammatory Status. Endocrinology 157:2870-82
Heard, Melissa E; Velarde, Michael C; Giudice, Linda C et al. (2015) Krüppel-Like Factor 13 Deficiency in Uterine Endometrial Cells Contributes to Defective Steroid Hormone Receptor Signaling but Not Lesion Establishment in a Mouse Model of Endometriosis. Biol Reprod 92:140
Simmen, Rosalia C M; Heard, Melissa E; Simmen, Angela M et al. (2015) The Krüppel-like factors in female reproductive system pathologies. J Mol Endocrinol 54:R89-R101
Pabona, John Mark P; Zhang, Daying; Ginsburg, David S et al. (2015) Prolonged pregnancy in women is associated with attenuated myometrial expression of progesterone receptor co-regulator Krüppel-like Factor 9. J Clin Endocrinol Metab 100:166-74
Heard, Melissa E; Simmons, Christian D; Simmen, Frank A et al. (2014) Krüppel-like factor 9 deficiency in uterine endometrial cells promotes ectopic lesion establishment associated with activated notch and hedgehog signaling in a mouse model of endometriosis. Endocrinology 155:1532-46
Pabona, John Mark P; Simmen, Frank A; Nikiforov, Mikhail A et al. (2012) Krüppel-like factor 9 and progesterone receptor coregulation of decidualizing endometrial stromal cells: implications for the pathogenesis of endometriosis. J Clin Endocrinol Metab 97:E376-92
Heard, Melissa E; Pabona, John Mark P; Clayberger, Carol et al. (2012) The reproductive phenotype of mice null for transcription factor Krüppel-like factor 13 suggests compensatory function of family member Krüppel-like factor 9 in the peri-implantation uterus. Biol Reprod 87:115
Simmen, Frank A; Simmen, Rosalia C M (2011) The maternal womb: a novel target for cancer prevention in the era of the obesity pandemic? Eur J Cancer Prev 20:539-48
Simmons, Christian D; Pabona, John Mark P; Heard, Melissa E et al. (2011) Krüppel-like factor 9 loss-of-expression in human endometrial carcinoma links altered expression of growth-regulatory genes with aberrant proliferative response to estrogen. Biol Reprod 85:378-85
Simmons, C D; Pabona, J M P; Zeng, Z et al. (2010) Response of adult mouse uterus to early disruption of estrogen receptor-alpha signaling is influenced by Krüppel-like factor 9. J Endocrinol 205:147-57

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