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Recycling of triacylglycerols for phospholipid synthesis

Recycling of triacylglycerols for phospholipid synthesis

Regina Leber (ORCID: 0000-0001-5306-5834)
  • Grant DOI 10.55776/P19041
  • Funding program Principal Investigator Projects
  • Status ended
  • Start September 1, 2006
  • End December 31, 2009
  • Funding amount € 205,538

Disciplines

Biology (100%)

Keywords

    Triacylglycerols, Phospholipids, Lipid droplets, Yeast, Recycling, Disease

Abstract Final report

Lipid disorders are a main focus of biomedical research. A massive deposit of fat (triacylglycerols) in fatty tissue and of cholesterol on the artery walls can lead to obesity, cardiovascular diseases and non-insulin-dependent diabetes. Despite this negative image, fat is essential for the normal development of multiple organs and the central nervous system in mammals. A selective degradation of triacylglycerols provides lipid precursors for membrane lipid synthesis in non-fatty tissues. A defect in this recycling process can lead to severe diseases e.g. Chanarin-Dorfman syndrome. This project aims on understanding the recycling process of fat for membrane lipid synthesis. The Chanarin- Dorfman syndrome is caused by a defect in CGI-58. The function of this protein is unknown, however, there are three yeast proteins showing homology to the mammalian CGI-58 protein. Based on structural similarities to mammalian cells, the unicellular yeast Saccharomyces cerevisiae is a well-established model system for studying cellular processes of complex eukaryotic organisms. Data obtained from studies with yeast mutant cells and proteins will contribute to the understanding of the molecular basis of diseases caused by a defect in fat recycling.

Lipid disorders are a main focus of biomedical research. A massive deposit of fat (triacylglycerols) in fatty tissue and of cholesterol on the artery walls can lead to obesity, cardiovascular diseases and non-insulin-dependent diabetes. Despite this negative image, fat is essential for the normal development of multiple organs and the central nervous system in mammals. A selective degradation of triacylglycerols provides lipid precursors for membrane lipid synthesis in non-fatty tissues. A defect in this recycling process can lead to severe diseases e.g. Chanarin- Dorfman syndrome. This project aims on understanding the recycling process of fat for membrane lipid synthesis. The Chanarin- Dorfman syndrome is caused by a defect in CGI-58. The function of this protein is unknown, however, there are three yeast proteins showing homology to the mammalian CGI-58 protein. Based on structural similarities to mammalian cells, the unicellular yeast Saccharomyces cerevisiae is a well-established model system for studying cellular processes of complex eukaryotic organisms. Data obtained from studies with yeast mutant cells and proteins will contribute to the understanding of the molecular basis of diseases caused by a defect in fat recycling.

Research institution(s)
  • Universität Graz - 100%

Research Output

  • 173 Citations
  • 2 Publications
Publications
  • 2009
    Title Identification of a Cardiolipin-specific Phospholipase Encoded by the Gene CLD1 (YGR110W) in Yeast*
    DOI 10.1074/jbc.m805511200
    Type Journal Article
    Author Beranek A
    Journal Journal of Biological Chemistry
    Pages 11572-11578
    Link Publication
  • 2010
    Title Identification of Yju3p as functional orthologue of mammalian monoglyceride lipase in the yeast Saccharomyces cerevisiae
    DOI 10.1016/j.bbalip.2010.06.001
    Type Journal Article
    Author Heier C
    Journal Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids
    Pages 1063-1071
    Link Publication

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