Our long-term objective is to understand the complex interrelationship between phospholipid, sphingolipid metabolism and metabolic signaling in vivo. Intermediates of phospholipid (PL) and sphingolipid (SL) metabolism serve as second messengers for a number of signaling cascades including activation of G-protein-coupled receptors such as adrenaline, thrombin, etc., as well as receptor tyrosine kinases by growth factors. They mediate a number of processes ranging from protein secretion to activation of apoptosis. We have initiated studies to understand different aspects of lipid signaling in Drosophila. Lipid Reservoirs and Signaling. Sphingomyelin (or phosphorylethanolamine ceramide in flies) could serve as a reservoir for several lipid messengers such as ceramide, ceramide 1-phosphate, sphingosine, and sphingosine 1-phosphate. We have initiated studies to delineate the in vivo role of some of the enzymes of the putative 'Sphingomyelin Cycle'. We have begun by identifying homolgous genes in Drosophila. We are using transgenic and mutagenic studies to analyse the importance of such a pathway in Drosophila. Lipid Distribution and Signaling. PL and SL at the plasma membrane play an important role in stimulus-response coupling, cell differentiation, movement, and exo- and endocytosis. They are asymmetrically distributed in biological membranes, and different proteins catalyzing uni- and bi-directional movements of lipids perpetuate asymmetry. Our current efforts focus on scramblase, a protein proposed to be involved in bi-directional transbilayer movement of phospholipids. We have recently completed a genetic screen and obtained Drosophila flies lacking a scramblase protein. We have begun phenotypic analyses of these mutant flies. We anticipate that a combination of genetic, molecular, and biochemical approaches in Drosophila will define the important players involved in PL, SL signaling in their normal cellular environment.

Agency
National Institute of Health (NIH)
Institute
Division of Basic Sciences - NCI (NCI)
Type
Intramural Research (Z01)
Project #
1Z01BC010331-02
Application #
6559214
Study Section
(RCGL)
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Basic Sciences
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Rao, Raghavendra Pralhada; Acharya, Jairaj K (2008) Sphingolipids and membrane biology as determined from genetic models. Prostaglandins Other Lipid Mediat 85:1-16
Rao, Raghavendra Pralhada; Yuan, Changqing; Allegood, Jeremy C et al. (2007) Ceramide transfer protein function is essential for normal oxidative stress response and lifespan. Proc Natl Acad Sci U S A 104:11364-9
Acharya, Usha; Edwards, Michael Beth; Jorquera, Ramon A et al. (2006) Drosophila melanogaster Scramblases modulate synaptic transmission. J Cell Biol 173:69-82
Acharya, U; Acharya, J K (2005) Enzymes of sphingolipid metabolism in Drosophila melanogaster. Cell Mol Life Sci 62:128-42
Acharya, Usha; Mowen, Michael Beth; Nagashima, Kunio et al. (2004) Ceramidase expression facilitates membrane turnover and endocytosis of rhodopsin in photoreceptors. Proc Natl Acad Sci U S A 101:1922-6
Rohrbough, Jeffrey; Rushton, Emma; Palanker, Laura et al. (2004) Ceramidase regulates synaptic vesicle exocytosis and trafficking. J Neurosci 24:7789-803
Acharya, Usha; Patel, Shetal; Koundakjian, Edmund et al. (2003) Modulating sphingolipid biosynthetic pathway rescues photoreceptor degeneration. Science 299:1740-3