The overall goal of the proposed research is to understand the molecular events which permit the regulated, coordinate expression of the pituitary glycoprotein hormone genes, lutropin (LH), follitropin (FSH) and thyrotropin (TSH). Besides being important physiologically for reproduction and metabolic regulation, these proteins provide a good model system for analysis of gene expression of subunit proteins. All three proteins contain a common alpha subunit and a different beta subunit. Initially cDNAs will be isolated for FSH-beta; cDNAs are already available for the other subunits. The cloned cDNAs will be used to study the regulation of subunit mRNA levels, gene transcription and gene structure. Particular attention will be focused on the relationship of alpha subunit gene structure and expression to the structure and expression of the beta subunits. In addition, the interaction of steroid and thyroid hormone receptors with the subunit gene sequences will be examined to gain further insight into DNA sequences possibly involved in regulating gene expression. The function of putative regulatory DNA sequences will then be tested by construction of fusion genes which will be transfected into suitable cells. Finally, an effort will be made to identify protein factors which interact with the glycoprotein hormone genes to facilitate their appropriate expression. These studies should provide increased understanding of the molecular machinery responsible for the regulated expression of the genes for subunit proteins.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
1R01DK036407-01
Application #
3234768
Study Section
Endocrinology Study Section (END)
Project Start
1986-02-01
Project End
1989-01-31
Budget Start
1986-02-01
Budget End
1987-01-31
Support Year
1
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Iowa
Department
Type
Schools of Medicine
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
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Howard, P W; Maurer, R A (2001) A point mutation in the LIM domain of Lhx3 reduces activation of the glycoprotein hormone alpha-subunit promoter. J Biol Chem 276:19020-6
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Glenn, D J; Maurer, R A (1999) MRG1 binds to the LIM domain of Lhx2 and may function as a coactivator to stimulate glycoprotein hormone alpha-subunit gene expression. J Biol Chem 274:36159-67
Roberson, M S; Misra-Press, A; Laurance, M E et al. (1995) A role for mitogen-activated protein kinase in mediating activation of the glycoprotein hormone alpha-subunit promoter by gonadotropin-releasing hormone. Mol Cell Biol 15:3531-9
Kim, D S; Ahn, S K; Yoon, J H et al. (1994) Involvement of a cAMP-responsive DNA element in mediating TRH responsiveness of the human thyrotropin alpha-subunit gene. Mol Endocrinol 8:528-36
Roberson, M S; Schoderbek, W E; Tremml, G et al. (1994) Activation of the glycoprotein hormone alpha-subunit promoter by a LIM-homeodomain transcription factor. Mol Cell Biol 14:2985-93
Schoderbek, W E; Roberson, M S; Maurer, R A (1993) Two different DNA elements mediate gonadotropin releasing hormone effects on expression of the glycoprotein hormone alpha-subunit gene. J Biol Chem 268:3903-10
Markkula, M A; Hamalainen, T M; Zhang, F et al. (1993) The FSH beta-subunit promoter directs the expression of Herpes simplex virus type 1 thymidine kinase to the testis of transgenic mice. Mol Cell Endocrinol 96:25-36
Sun, P; Schoderbek, W E; Maurer, R A (1992) Phosphorylation of cyclic adenosine 3',5'-monophosphate (cAMP) response element-binding protein isoforms by the cAMP-dependent protein kinase. Mol Endocrinol 6:1858-66

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