AcyI-CoA synthetase (ACS) catalyzes the ligation of fatty acids to CoA yielding acyI-CoA, thus completing the initial step in fatty acid metabolism. Three isoforms of ACS predominate in rat liver with each isoform having different subcellular locations and substrate preferences, which suggests distinct roles of each isoform in partitioning fatty acids to distinct metabolic pathways. However, the function of each isoform in fatty acid metabolism has not be elucidated. Additionally, polyunsaturated fatty acids induce gene expression of enzymes involved in fatty acid oxidation and suppress genes involved in lipogenesis by upregulating peroxisome proliferators-activated receptor alpha and down-regulating sterol regulatory element binding protein-lc. In contrast, acyI-CoAs antagonize the actions of fatty acids on gene expression and upregulate genes encoding opposing pathways. Thus, we propose that controlling the conversion of fatty acids to acyI-CoAs and their pool size may be a critical step in regulating gene expression. Since ACS catalyzes this reaction, it is a novel target to regulate gene expression. The proposed research will use RNA interference to define the roles of ACS 1, 4 and 5 in hepatic fatty acid metabolism and gene expression.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32DK068993-01
Application #
6835023
Study Section
Special Emphasis Panel (ZRG1-F10 (21))
Program Officer
Podskalny, Judith M,
Project Start
2004-09-01
Project End
2007-08-31
Budget Start
2004-09-01
Budget End
2005-08-31
Support Year
1
Fiscal Year
2004
Total Cost
$42,976
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
Schools of Public Health
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Stapleton, Cliona M; Mashek, Douglas G; Wang, Shuli et al. (2011) Lysophosphatidic acid activates peroxisome proliferator activated receptor-? in CHO cells that over-express glycerol 3-phosphate acyltransferase-1. PLoS One 6:e18932
Mashek, Douglas G; Coleman, Rosalind A (2006) Cellular fatty acid uptake: the contribution of metabolism. Curr Opin Lipidol 17:274-8
Mashek, Douglas G; McKenzie, Michelle A; Van Horn, Cynthia G et al. (2006) Rat long chain acyl-CoA synthetase 5 increases fatty acid uptake and partitioning to cellular triacylglycerol in McArdle-RH7777 cells. J Biol Chem 281:945-50
Mashek, Douglas G; Li, Lei O; Coleman, Rosalind A (2006) Rat long-chain acyl-CoA synthetase mRNA, protein, and activity vary in tissue distribution and in response to diet. J Lipid Res 47:2004-10