![]()
|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Papers In Press, published online ahead of print December 29, 2003
Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425
Corresponding Author: hannun{at}musc.edu
Sphingomyelinases (SMases) generate ceramides which are known to regulate cell cycle and growth. Only one enzyme that belongs to the extended family of SMases is present in S. cerevisiae, Isc1p; however, little is known about its regulation or physiologic function. Deletion of ISC1 in S. cerevisiae resulted in a growth defect, and the slow growth phenotype was rescued by plasmid-borne expression of Isc1, confirming its role in growth. The levels of phytoceramide exhibited an Isc1p-dependent increase of ~4 fold after 24 h of growth. In addition, the specific activity of Isc1p was significantly elevated (>3 fold) between the early logarithmic and the late logarithmic/start of stationary phases of growth. The activation of the enzyme was not associated with increased levels of the protein, indicating that the mechanism is independent of transcription/translation. Interestingly, this activation was lost upon delipidation of the enzyme, raising the possibility of regulation by associated lipids. Confocal microscopy revealed that the enzyme was predominantly in the ER during early growth, but became associated with mitochondria in late logarithmic growth. These results were also supported by differential centrifugation and isolation of mitochondria, and further confirmed in mitochondria purified using sucrose gradients at the different stages of growth. These results reveal that the activity and localization of Isc1p are regulated in a growth-dependent manner. A novel mechanism for activation of Isc1p through localization to mitochondria is proposed. The results also suggest a role for Isc1p-generated ceramides in optimal regulation of growth.
J. Biol. Chem, 10.1074/jbc.M309586200
Submitted on August 28, 2003
Revised on December 19, 2003
Accepted on December 22, 2003
Activation and localization of Inositol phosphosphingolipid phospholipase C, Isc1p, to the mitochondria during growth of S. cerevisiae
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
![]() |
R. C. Dickson Thematic Review Series: Sphingolipids. New insights into sphingolipid metabolism and function in budding yeast J. Lipid Res., May 1, 2008; 49(5): 909 - 921. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Matmati and Y. A. Hannun Thematic Review Series: Sphingolipids. ISC1 (inositol phosphosphingolipid-phospholipase C), the yeast homologue of neutral sphingomyelinases J. Lipid Res., May 1, 2008; 49(5): 922 - 928. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Almeida, M. Marques, D. Mojzita, M. A. Amorim, R. D. Silva, B. Almeida, P. Rodrigues, P. Ludovico, S. Hohmann, P. Moradas-Ferreira, et al. Isc1p Plays a Key Role in Hydrogen Peroxide Resistance and Chronological Lifespan through Modulation of Iron Levels and Apoptosis Mol. Biol. Cell, March 1, 2008; 19(3): 865 - 876. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Su and W. Dowhan Translational Regulation of Nuclear Gene COX4 Expression by Mitochondrial Content of Phosphatidylglycerol and Cardiolipin in Saccharomyces cerevisiae Mol. Cell. Biol., February 1, 2006; 26(3): 743 - 753. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Vaena de Avalos, X. Su, M. Zhang, Y. Okamoto, W. Dowhan, and Y. A. Hannun The Phosphatidylglycerol/Cardiolipin Biosynthetic Pathway Is Required for the Activation of Inositol Phosphosphingolipid Phospholipase C, Isc1p, during Growth of Saccharomyces cerevisiae J. Biol. Chem., February 25, 2005; 280(8): 7170 - 7177. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| All ASBMB Journals | Molecular and Cellular Proteomics |
| Journal of Lipid Research | ASBMB Today |