Tsc13p is required for fatty acid elongation and localizes to a novel structure at the nuclear-vacuolar interface in Saccharomyces cerevisiae

Mol Cell Biol. 2001 Jan;21(1):109-25. doi: 10.1128/MCB.21.1.109-125.2001.

Abstract

The TSC13/YDL015c gene was identified in a screen for suppressors of the calcium sensitivity of csg2Delta mutants that are defective in sphingolipid synthesis. The fatty acid moiety of sphingolipids in Saccharomyces cerevisiae is a very long chain fatty acid (VLCFA) that is synthesized by a microsomal enzyme system that lengthens the palmitate produced by cytosolic fatty acid synthase by two carbon units in each cycle of elongation. The TSC13 gene encodes a protein required for elongation, possibly the enoyl reductase that catalyzes the last step in each cycle of elongation. The tsc13 mutant accumulates high levels of long-chain bases as well as ceramides that harbor fatty acids with chain lengths shorter than 26 carbons. These phenotypes are exacerbated by the deletion of either the ELO2 or ELO3 gene, both of which have previously been shown to be required for VLCFA synthesis. Compromising the synthesis of malonyl coenzyme A (malonyl-CoA) by inactivating acetyl-CoA carboxylase in a tsc13 mutant is lethal, further supporting a role of Tsc13p in VLCFA synthesis. Tsc13p coimmunoprecipitates with Elo2p and Elo3p, suggesting that the elongating proteins are organized in a complex. Tsc13p localizes to the endoplasmic reticulum and is highly enriched in a novel structure marking nuclear-vacuolar junctions.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acetyltransferases
  • Amino Acid Sequence
  • Cell Nucleus / chemistry*
  • Cell Nucleus / enzymology
  • Cell Polarity
  • Ceramides / metabolism
  • Cloning, Molecular
  • Conserved Sequence / genetics
  • Endoplasmic Reticulum / chemistry
  • Endoplasmic Reticulum / enzymology
  • Enoyl-(Acyl-Carrier-Protein) Reductase (NADH)
  • Fatty Acids / biosynthesis*
  • Fatty Acids / chemistry
  • Fatty Acids / metabolism
  • Fungal Proteins / chemistry
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism*
  • Humans
  • Membrane Proteins*
  • Molecular Sequence Data
  • Mutation
  • Oxidoreductases / chemistry
  • Oxidoreductases / genetics
  • Oxidoreductases / metabolism
  • Oxidoreductases Acting on CH-CH Group Donors
  • Phenotype
  • Precipitin Tests
  • Protein Binding
  • Recombinant Fusion Proteins / chemistry
  • Recombinant Fusion Proteins / metabolism
  • Saccharomyces cerevisiae / cytology*
  • Saccharomyces cerevisiae / enzymology
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins*
  • Sphingolipids / biosynthesis
  • Sphingolipids / chemistry
  • Sphingolipids / metabolism
  • Vacuoles / chemistry*
  • Vacuoles / enzymology

Substances

  • Ceramides
  • Fatty Acids
  • Fungal Proteins
  • Membrane Proteins
  • Recombinant Fusion Proteins
  • Saccharomyces cerevisiae Proteins
  • Sphingolipids
  • Oxidoreductases
  • Oxidoreductases Acting on CH-CH Group Donors
  • TSC13 protein, S cerevisiae
  • Enoyl-(Acyl-Carrier-Protein) Reductase (NADH)
  • Acetyltransferases
  • ELO2 protein, S cerevisiae
  • SUR4 protein, S cerevisiae