The long term objective is to understand the physiology of the insulin-like growth factor system. The IGF system is essential to normal growth and development. Defects in the various components of the IGF system have been identified in cancer, diabetes and undernutrition. In addition to the classical interaction with receptors, IGF-I and IGF-II the ligands of the IGF system associate with six soluble carrier proteins called insulin-like growth factor binding protein (IGFBP1-6). Postnatally, the functional IGF transporting unit is actually a ternary complex formed by association of IGF with IGFBP-3 and a third protein called acid-labile subunit (ALS). The focus of this application is on ALS because current evidence suggests that ALS determines surum levels of IGF-I and -II and their delivery to target tissue. Growth hormone is a major factor controlling the circulating levels of ALS. The mechanisms underlying this regulation, however, have not been defined. This proposal addresses the nature of growth hormone regulation of ALS and its role in vivo.
The specific aims and methods are: 1. To determine themechanism by which growth hormone regulates the abundance of ALS mRNA in the liver of mice. This will be done by comparing in liver the abundance of ALS mRNA and the rate of transcription of the gene under different growth hormone status. 2. To define the cis-elements in the 5' upstream region of the ALS gene that mediate the growth hormone and basal activation of transcription. This will be done by transfecting into liver cells luciferase minigenes driven by the promoter of the ALS gene. 3. To study the fuction of the ALS protein in vivo. This will be done by obtaineng and studying mice in which the ALS protein is absent. These mice iwll be created by the gene knockout approach.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK051624-03
Application #
2905903
Study Section
Endocrinology Study Section (END)
Program Officer
Sato, Sheryl M
Project Start
1997-09-26
Project End
2002-06-30
Budget Start
1999-07-01
Budget End
2000-06-30
Support Year
3
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Cornell University
Department
Veterinary Sciences
Type
Schools of Earth Sciences/Natur
DUNS #
City
Ithaca
State
NY
Country
United States
Zip Code
14850
Ueki, Iori; Giesy, Sarah L; Harvatine, Kevin J et al. (2009) The acid-labile subunit is required for full effects of exogenous growth hormone on growth and carbohydrate metabolism. Endocrinology 150:3145-52
Gu, Feng; Dube, Nadia; Kim, Jin Wook et al. (2003) Protein tyrosine phosphatase 1B attenuates growth hormone-mediated JAK2-STAT signaling. Mol Cell Biol 23:3753-62
Suwanichkul, A; Boisclair, Y R; Olney, R C et al. (2000) Conservation of a growth hormone-responsive promoter element in the human and mouse acid-labile subunit genes. Endocrinology 141:833-8