The steroid hormones (estrogen and progesterone) stimulate growth, maturation and the development of new biochemical capacities in their endocrine target organs. Although it is widely accepted that steroid hormones exert major influences on the transcriptional process, the detailed mechanisms and the associated co-regulator proteins involved in gene transactivation are not yet defined in precise detail. The general objectives of our studies are to define the mechanism of steroid hormones and their receptors in regulating morphologic differentiation and biochemical specialization in target tissues. This will be accomplished by coordinating a network of investigations designed to uncover the mechanisms by which steroid receptors interact with nuclear regulatory proteins (co-activators, co-repressors, general transcription factors, chromatin modifiers, etc.) to effect target gene expression. We will emphasize experimental dissection of the protein-protein interactions which occur inside a living cell and during transcriptional process; we will define the co-regulator's role in modulating transcription and chromatin structure. In addition, we must understand the mechanisms of positive and negative regulation of receptor functional domains effected by various co-regulators. Our studies will utilize the human progesterone receptor, but to establish regulatory concepts, we will carry out selected experiments using human estrogen, thyroid hormone, and retinoic acid receptors. Cell-free binding and transcription approaches, technologies developed over the past five-year period of this grant, will be a corner stone of our methodology; all new concepts will tested finally in the milieu of the intact cell. These studies will involve aspects of nucleic acid and protein biochemistry, protein purification, cell biology and molecular endocrinology. It is expected that the understanding derived from this project will be relevant to the actions of natural sex steroid hormones relative to human physiology. The following proposed studies should also be pertinent to development of more precise theories for the biochemical mechanism of action of intracellular hormones and receptors in general.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD008188-30
Application #
6387422
Study Section
Biochemical Endocrinology Study Section (BCE)
Program Officer
Yoshinaga, Koji
Project Start
1974-09-01
Project End
2003-05-31
Budget Start
2001-06-01
Budget End
2002-05-31
Support Year
30
Fiscal Year
2001
Total Cost
$469,854
Indirect Cost
Name
Baylor College of Medicine
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
Cho, Yeon Jean; Lee, Jiyeun E; Park, Mi Jin et al. (2018) Bufalin suppresses endometriosis progression by inducing pyroptosis and apoptosis. J Endocrinol 237:255-269
Szwarc, Maria M; Kommagani, Ramakrishna; Putluri, Vasanta et al. (2018) Steroid Receptor Coactivator-2 Controls the Pentose Phosphate Pathway through RPIA in Human Endometrial Cancer Cells. Sci Rep 8:13134
Gates, Leah A; Gu, Guowei; Chen, Yue et al. (2018) Proteomic profiling identifies key coactivators utilized by mutant ER? proteins as potential new therapeutic targets. Oncogene 37:4581-4598
Camden, Alison J; Szwarc, Maria M; Chadchan, Sangappa B et al. (2017) Growth regulation by estrogen in breast cancer 1 (GREB1) is a novel progesterone-responsive gene required for human endometrial stromal decidualization. Mol Hum Reprod 23:646-653
Zhang, Zheng; Nikolai, Bryan C; Gates, Leah A et al. (2017) Crosstalk between histone modifications indicates that inhibition of arginine methyltransferase CARM1 activity reverses HIV latency. Nucleic Acids Res 45:9348-9360
Geng, C; Kaochar, S; Li, M et al. (2017) SPOP regulates prostate epithelial cell proliferation and promotes ubiquitination and turnover of c-MYC oncoprotein. Oncogene 36:4767-4777
Gates, Leah A; Shi, Jiejun; Rohira, Aarti D et al. (2017) Acetylation on histone H3 lysine 9 mediates a switch from transcription initiation to elongation. J Biol Chem 292:14456-14472
Xu, Yong; O'Malley, Bert W; Elmquist, Joel K (2017) Brain nuclear receptors and body weight regulation. J Clin Invest 127:1172-1180
Yi, Ping; Wang, Zhao; Feng, Qin et al. (2017) Structural and Functional Impacts of ER Coactivator Sequential Recruitment. Mol Cell 67:733-743.e4
Gates, Leah A; Foulds, Charles E; O'Malley, Bert W (2017) Histone Marks in the 'Driver's Seat': Functional Roles in Steering the Transcription Cycle. Trends Biochem Sci 42:977-989

Showing the most recent 10 out of 81 publications