Estrogens and progestins are two key components in mammalian reproduction. hese hormones with their receptors provide an interlocking and coordinated syste that regulates several tissues critical for female reproduction. One essential requirement in this system is for the estrogen/receptor complex to regulate he availability of the progesterone receptor (PR). In a strain of cells devel ed in our laboratory, Rat1+ER cells, the estrogen receptor (ER) complex is nec sary and sufficient to cause the expression of the previously silent PR gene. T s takes place in a cell that normally does not express either the ER or PR ge s. It appears to be dependent on the stable transfection of the cells with the R because transient transfection does not yield the same results. These cell provide a unique system for studying the new expression of an estrogen-regu ted gene. It should also make possible quantitative studies on the time course f the induction of the PR gene as well as the relationship of estrogen occupa y of the ER to the response of the PR gene. Since the response of the PR gene apparently involves some changes in the accessibility of the regulatory regions of the PR gene to the ER, changes i chromatin structure will also be a focus of our studies. Again, the time c rse of change in chromatin structure in relationship to changes in transcriptio rate of the PR gene will be a major area of study. Finally, all the studies noted above have as a key component the interactio of the ER with regulatory sequences of DNA or estrogen response elements (ERE) Studies of the interaction of the ER with EREs have been limited by the availability of physical techniques that are useful using low concentration of receptor and that can give kinetic measurements of the interaction of the receptor with the DNA. Fluorescent anisotropic spectrophotometry appears t be a procedure of promise that we will use to study DNA/receptor interactions.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD008192-26
Application #
2673394
Study Section
Biochemical Endocrinology Study Section (BCE)
Project Start
1978-05-01
Project End
1999-07-31
Budget Start
1998-08-01
Budget End
1999-07-31
Support Year
26
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Biochemistry
Type
Schools of Earth Sciences/Natur
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Gorski, J; Hansen, J C (1987) The ""one and only"" step model of estrogen action. Steroids 49:461-75