In the last two funding cycles, the investigators of this Program Project Grant (PPG) have largely relied on genetically manipulated mice (GMM) to study the physiological and pathological roles of genes in the steroid receptor coactivator (SRC) family and the nuclear receptor COUP-TFII in organ function and metabolism. The high quality of mouse services provided by Core A has played an essential role in the great success of this PPG. In the next funding cycle, all projects of this PPG will continue to be heavily dependent on the usage of GMM. More than 18 mouse lines will be used and thousands of GMM will be needed for the proposed studies of this PPG. Therefore, the role of Core A remains essential for the continued success of this PPG. Core A is dedicated to this PPG by achieving 3 major objectives. 1) Core A will use its specialized and state-of-the-art expertise, equipment and facilities to provide essential high quality mouse services to support all projects of this PPG. Core A has a high quality mouse service team with adequate expertise, equipment and facilities for generation of new transgenic/knockout mouse lines, for breeding and maintenance of all existing mouse lines and for performance of mouse genotype analysis. Core A will provide age, sex and genotype-matched mice to individual investigators of this PPG for their experiments. 2) Core A will provide assistance to all projects of this PPG for mouse phenotypic characterization. Core A will use its expertise to assist investigators of this PPG to characterize mouse metabolic phenotypes. Specifically, Core A can help investigators to perform animal surgeries, organ dissections, tail vein injection, special diet feeding, analysis of circadian physiology-regulated metabolism. Clams assays, etc. 3) Core A will integrate efficient usage of animal resources by all projects of this PPG. Core A will minimize the total cost of animal experiments in this PPG by consolidating the usage of equipment, expertise and animal resources. Core A will also ensure the efficient usage of animal resources with appropriate ethical care. In addition, Core A will serve as a resource for execution and training in the use of all animal manipulations needed in this PPG and oversee the human care and use of experimental animals. Core A will minimize the total cost of animal experiments in this PPG by consolidating the usage of equipment, expertise and animal resources. Core A will also ensure the efficient usage of animal resources with appropriate ethical care.

Public Health Relevance

Because many experiments can not be done in human and because many gene functions and pathways regulating energy balance and metabolic rate are similar in human and mouse, genetically manipulated mouse models become essential for this PPG to study the roles and mechanisms of coregulators and nuclear receptors in metabolic diseases. Core A will generate and maintain all mouse models and provide high quality mouse services to guarantee the success of this PPG.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Program Projects (P01)
Project #
5P01DK059820-12
Application #
8545167
Study Section
Special Emphasis Panel (ZDK1-GRB-D)
Project Start
Project End
Budget Start
2013-07-01
Budget End
2014-06-30
Support Year
12
Fiscal Year
2013
Total Cost
$267,690
Indirect Cost
$96,030
Name
Baylor College of Medicine
Department
Type
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Xie, Xin; Tsai, Sophia Y; Tsai, Ming-Jer (2016) COUP-TFII regulates satellite cell function and muscular dystrophy. J Clin Invest 126:3929-3941
Vasquez, Yasmin M; Wu, San-Pin; Anderson, Matthew L et al. (2016) Endometrial Expression of Steroidogenic Factor 1 Promotes Cystic Glandular Morphogenesis. Mol Endocrinol 30:518-32
Wang, Lei; Lonard, David M; O'Malley, Bert W (2016) The Role of Steroid Receptor Coactivators in Hormone Dependent Cancers and Their Potential as Therapeutic Targets. Horm Cancer 7:229-35
Xu, Y; Qin, L; Sun, T et al. (2016) Twist1 promotes breast cancer invasion and metastasis by silencing Foxa1 expression. Oncogene :
Song, Xianzhou; Chen, Jianwei; Zhao, Mingkun et al. (2016) Development of potent small-molecule inhibitors to drug the undruggable steroid receptor coactivator-3. Proc Natl Acad Sci U S A 113:4970-5
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
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
Fleet, Tiffany; Stashi, Erin; Zhu, Bokai et al. (2016) Genetic and Environmental Models of Circadian Disruption Link SRC-2 Function to Hepatic Pathology. J Biol Rhythms 31:443-60
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
Fleet, Tiffany; Zhang, Bin; Lin, Fumin et al. (2015) SRC-2 orchestrates polygenic inputs for fine-tuning glucose homeostasis. Proc Natl Acad Sci U S A 112:E6068-77

Showing the most recent 10 out of 172 publications