In the yeast Saccharomyces cerevisiae, CTP, the CTP synthetase reaction product, is a precursor of phospholipids that are synthesized by the CDP-diacylglycerol and Kennedy (CDP-choline) pathways as well as all membrane phospholipids. Studies performed during the current grant period showed that CTP synthetase activity plays a regulatory role in the utilization of the pathways used for the synthesis of phosphatidylcholine. CTP synthetase was purified, characterized, and shown to be activated by phosphorylation via protein kinase A and protein kinase C and inhibited by CTP. In this competitive continuation grant application we propose molecular genetic and biochemical studies that are expected to provide insight into the regulation of CTP synthetase activity by phosphorylation and by CTP product inhibition and into the physiological relevance of this regulation with respect to phospholipid synthesis. They propose to examine the hypothesis that the regulation of CTP synthetase activity by phosphorylation involves the nucleotide-dependent tetramerization of the enzyme. CTP synthetase mutants will be isolated with altered protein kinase A and protein kinase C phosphorylation sites. These mutants will be used for physiological and biochemical studies to examine the effects of phosphorylation on the regulation of CTP synthetase activity. The effects of this regulation of phospholipid synthesis will be propose to isolate mutants that are defective in a proposed CTP binding site in CTP synthetase. These mutants will be used for physiological and biuochemical studies to examine the regulation of CTP synthetase activity by CTP product inhibition. The effect of this regulation on phospholipid synthesis will be examined. The results from the proposed studies should be relevant to higher eukaryotic organisms and be of great interest to, and complement the work of, other investigators in the field of phospholipid metabolism. This work should also be relevant to other aspects of macromolecular synthesis that are dependent on CTP as a precursor.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM050679-06
Application #
2910135
Study Section
Physiological Chemistry Study Section (PC)
Project Start
1994-05-01
Project End
2001-04-30
Budget Start
1999-05-01
Budget End
2000-04-30
Support Year
6
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Rutgers University
Department
Nutrition
Type
Schools of Earth Sciences/Natur
DUNS #
038633251
City
New Brunswick
State
NJ
Country
United States
Zip Code
08901
Su, Wen-Min; Han, Gil-Soo; Dey, Prabuddha et al. (2018) Protein kinase A phosphorylates the Nem1-Spo7 protein phosphatase complex that regulates the phosphorylation state of the phosphatidate phosphatase Pah1 in yeast. J Biol Chem 293:15801-15814
Carman, George M; Han, Gil-Soo (2018) Phosphatidate phosphatase regulates membrane phospholipid synthesis via phosphatidylserine synthase. Adv Biol Regul 67:49-58
Carman, George M (2018) Discoveries of the phosphatidate phosphatase genes in yeast published in the Journal of Biological Chemistry. J Biol Chem :
Dey, Prabuddha; Su, Wen-Min; Han, Gil-Soo et al. (2017) Phosphorylation of lipid metabolic enzymes by yeast protein kinase C requires phosphatidylserine and diacylglycerol. J Lipid Res 58:742-751
Hsieh, Lu-Sheng; Su, Wen-Min; Han, Gil-Soo et al. (2016) Phosphorylation of Yeast Pah1 Phosphatidate Phosphatase by Casein Kinase II Regulates Its Function in Lipid Metabolism. J Biol Chem 291:9974-90
Qiu, Yixuan; Hassaninasab, Azam; Han, Gil-Soo et al. (2016) Phosphorylation of Dgk1 Diacylglycerol Kinase by Casein Kinase II Regulates Phosphatidic Acid Production in Saccharomyces cerevisiae. J Biol Chem 291:26455-26467
Hsieh, Lu-Sheng; Su, Wen-Min; Han, Gil-Soo et al. (2015) Phosphorylation regulates the ubiquitin-independent degradation of yeast Pah1 phosphatidate phosphatase by the 20S proteasome. J Biol Chem 290:11467-78
Sahu-Osen, Anita; Montero-Moran, Gabriela; Schittmayer, Matthias et al. (2015) CGI-58/ABHD5 is phosphorylated on Ser239 by protein kinase A: control of subcellular localization. J Lipid Res 56:109-21
Barbosa, Antonio Daniel; Sembongi, Hiroshi; Su, Wen-Min et al. (2015) Lipid partitioning at the nuclear envelope controls membrane biogenesis. Mol Biol Cell 26:3641-57
Su, Wen-Min; Han, Gil-Soo; Carman, George M (2014) Yeast Nem1-Spo7 protein phosphatase activity on Pah1 phosphatidate phosphatase is specific for the Pho85-Pho80 protein kinase phosphorylation sites. J Biol Chem 289:34699-708

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