The role of very long chain fatty acids in yeast physiology and human diseases

Autor(en): Erdbruegger, Pia
Froehlich, Florian 
Stichwörter: ACYL-COA SYNTHETASE; BETA-OXIDATION; Biochemistry & Molecular Biology; ELONGATION; fatty acid elongation; GENE ENCODES; H+-ATPASE; HEAT-STRESS; lipid homeostasis; NUCLEUS-VACUOLE JUNCTIONS; PROTEIN; PROTEOMIC ANALYSIS; SACCHAROMYCES-CEREVISIAE; sphingolipid; very long chain fatty acid
Erscheinungsdatum: 2021
Herausgeber: WALTER DE GRUYTER GMBH
Journal: BIOLOGICAL CHEMISTRY
Volumen: 402
Ausgabe: 1
Startseite: 25
Seitenende: 38
Zusammenfassung: 
Fatty acids (FAs) are a highly diverse class of molecules that can have variable chain length, number of double bonds and hydroxylation sites. FAs with 22 or more carbon atoms are described as very long chain fatty acids (VLCFAs). VLCFAs are synthesized in the endoplasmic reticulum (ER) through a four-step elongation cycle by membrane embedded enzymes. VLCFAs are precursors for the synthesis of sphingolipids (SLs) and glycerophospholipids. Besides their role as lipid constituents, VLCFAs are also found as precursors of lipid mediators. Mis-regulation of VLCFA metabolism can result in a variety of inherited diseases ranging from ichthyosis, to myopathies and demyelination. The enzymes for VLCFA biosynthesis are evolutionary conserved and many of the pioneering studies were performed in the model organism Saccharomyces cerevisiae. A growing body of evidence suggests that VLCFA metabolism is intricately regulated to maintain lipid homeostasis. In this review we will describe the metabolism of VLCFAs, how they are synthesized, transported and degraded and how these processes are regulated, focusing on budding yeast. We will review how lipid metabolism and membrane properties are affected by VLCFAs and which impact mutations in the biosynthetic genes have on physiology. We will also briefly describe diseases caused by mis-regulation of VLCFAs in human cells.
ISSN: 14316730
DOI: 10.1515/hsz-2020-0234

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