|
|
|
|
A more recent version of this article appeared on February 1, 2006
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Submitted on April 25, 2005
Revised on November 23, 2005
Accepted on November 28, 2005
*Department of Biochemistry of Membranes, Bijvoet Institute and Institute of Biomembranes, Utrecht University, 3584 CH Utrecht, The Netherlands;
Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854;
Department of Biomolecular Mass Spectrometry, Bijvoet Center for Biomolecular Research and Institute for Pharmaceutical Sciences, 3584 CA Utrecht, The Netherlands;
Department of Biological Sciences, Duquesne University, Pittsburgh, PA 15282; ||Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853
Monitoring Editor: Sean Munro
To study the consequences of depleting the major membrane phospholipid phosphatidylcholine (PC), exponentially growing cells of a yeast cho2opi3 double deletion mutant were transferred from medium containing choline to choline-free medium. Cell growth did not cease until the PC level had dropped below 2% of total phospholipids after 4-5 generations. Increasing contents of phosphatidylethanolamine (PE) and phosphatidylinositol (PI) made up for the loss of PC. During PC depletion the remaining PC was subject to acyl chain remodeling with monounsaturated species replacing diunsaturated species, as shown by mass spectrometry. The remodeling of PC did not require turnover by the SPO14-encoded phospholipase D. The changes in the PC species profile were found to reflect an overall shift in the cellular acyl chain composition that exhibited a 40% increase in the ratio of C16 over C18 acyl chains, and a 10% increase in the degree of saturation. The shift was stronger in the phospholipid than in the neutral lipid fraction, and strongest in the species profile of PE. The shortening and increased saturation of the PE acyl chains were shown to decrease the nonbilayer propensity of PE. The results point to a regulatory mechanism in yeast that maintains intrinsic membrane curvature in an optimal range.
This article has been cited by other articles:
![]() |
L. Pineau, L. Bonifait, J.-M. Berjeaud, P. Alimardani-Theuil, T. Berges, and T. Ferreira A Lipid-mediated Quality Control Process in the Golgi Apparatus in Yeast Mol. Biol. Cell, March 1, 2008; 19(3): 807 - 821. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. de Wilde, R. Mohren, S. van den Berg, M. Boekschoten, K. W.-V. Dijk, P. de Groot, M. Muller, E. Mariman, and E. Smit Short-term high fat-feeding results in morphological and metabolic adaptations in the skeletal muscle of C57BL/6J mice Physiol Genomics, February 19, 2008; 32(3): 360 - 369. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Kainu, M. Hermansson, and P. Somerharju Electrospray Ionization Mass Spectrometry and Exogenous Heavy Isotope-labeled Lipid Species Provide Detailed Information on Aminophospholipid Acyl Chain Remodeling J. Biol. Chem., February 8, 2008; 283(6): 3676 - 3687. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. H. Loukin, C. Kung, and Y. Saimi Lipid perturbations sensitize osmotic down-shock activated Ca2+ influx, a yeast "deletome" analysis FASEB J, June 1, 2007; 21(8): 1813 - 1820. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Binder, G. Liebisch, T. Langmann, and G. Schmitz Metabolic Profiling of Glycerophospholipid Synthesis in Fibroblasts Loaded with Free Cholesterol and Modified Low Density Lipoproteins J. Biol. Chem., August 4, 2006; 281(31): 21869 - 21877. [Abstract] [Full Text] [PDF] |
||||