Members of the steroid/thyroid receptor superfamily have been shown to be important for the regulation of target genes essential for cellular differentiation and development. Preliminary results obtained have indicated that the chicken ovalbumin upstream promoter element transcription factors (COUP-TFs), members of the receptor superfamily, down regulate the activities of other members in the gene family, especially, thyroid, vitamin D and retinoic acid receptors. In addition to the negative regulatory activity, COUP-TFs also have the potential to activate target genes. Taken together, they support the idea that COUP-TFs play a primordial role in modulating gene activities in this family and thus directly or indirectly regulating development and differentiation. The long term goal of our laboratory is to define the biological function of these """"""""orphan"""""""" receptors. Before, one can reach that goal, one has to dissect the mechanism of COUP-TFs on gene regulation and the interplay between members of the steroid/thyroid hormone receptor superfamily. In this application, we design experiments by using various in vitro methodologies to elucidate the complex regulatory mechanism by COUP-TFs. The results obtained will be complemented by the in vivo studies on the effect of gene activities when COUP-TF gene activities are up- or down-regulated. It is expected that the understanding derived from this project will be relevant to the biology of development and differentiation. The proposed studies should also be pertinent to development of more precise theories for the biochemical mechanism of action of hormone in general and more specifically, thyroid, retinoic acid and vitamin D.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK045641-03
Application #
2144846
Study Section
Biochemical Endocrinology Study Section (BCE)
Project Start
1992-09-30
Project End
1995-09-29
Budget Start
1994-09-30
Budget End
1995-09-29
Support Year
3
Fiscal Year
1994
Total Cost
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
Wetendorf, Margeaux; Wu, San-Pin; Wang, Xiaoqiu et al. (2017) Decreased epithelial progesterone receptor A at the window of receptivity is required for preparation of the endometrium for embryo attachment. Biol Reprod 96:313-326
Zhao, Fei; Franco, Heather L; Rodriguez, Karina F et al. (2017) Elimination of the male reproductive tract in the female embryo is promoted by COUP-TFII in mice. Science 357:717-720
Xie, Xin; Wu, San-Pin; Tsai, Ming-Jer et al. (2017) The Role of COUP-TFII in Striated Muscle Development and Disease. Curr Top Dev Biol 125:375-403
Lee, Hui-Ju; Kao, Chung-Yang; Lin, Shih-Chieh et al. (2017) Dysregulation of nuclear receptor COUP-TFII impairs skeletal muscle development. Sci Rep 7:3136
Wang, Leiming; Xu, Mafei; Qin, Jun et al. (2016) MPC1, a key gene in cancer metabolism, is regulated by COUPTFII in human prostate cancer. Oncotarget 7:14673-83
Xie, Xin; Tsai, Sophia Y; Tsai, Ming-Jer (2016) COUP-TFII regulates satellite cell function and muscular dystrophy. J Clin Invest 126:3929-3941
Wu, San-Pin; Yu, Cheng-Tai; Tsai, Sophia Y et al. (2016) Choose your destiny: Make a cell fate decision with COUP-TFII. J Steroid Biochem Mol Biol 157:7-12
Lin, Shih-Chieh; Kao, Chung-Yang; Lee, Hui-Ju et al. (2016) Dysregulation of miRNAs-COUP-TFII-FOXM1-CENPF axis contributes to the metastasis of prostate cancer. Nat Commun 7:11418
Wu, San-Pin; Kao, Chung-Yang; Wang, Leiming et al. (2015) Increased COUP-TFII expression in adult hearts induces mitochondrial dysfunction resulting in heart failure. Nat Commun 6:8245
Tang, Ke; Tsai, Sophia Y; Tsai, Ming-Jer (2015) COUP-TFs and eye development. Biochim Biophys Acta 1849:201-9

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