Sterol transporters at membrane contact sites regulate TORC1 and TORC2 signaling

J Cell Biol. 2017 Sep 4;216(9):2679-2689. doi: 10.1083/jcb.201610032. Epub 2017 Aug 3.

Abstract

Membrane contact sites (MCSs) function to facilitate the formation of membrane domains composed of specialized lipids, proteins, and nucleic acids. In cells, membrane domains regulate membrane dynamics and biochemical and signaling pathways. We and others identified a highly conserved family of sterol transport proteins (Ltc/Lam) localized at diverse MCSs. In this study, we describe data indicating that the yeast family members Ltc1 and Ltc3/4 function at the vacuole and plasma membrane, respectively, to create membrane domains that partition upstream regulators of the TORC1 and TORC2 signaling pathways to coordinate cellular stress responses with sterol homeostasis.

MeSH terms

  • Antiporters / genetics
  • Antiporters / metabolism*
  • Biological Transport
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Cytoskeletal Proteins
  • Endoplasmic Reticulum / enzymology
  • Mechanistic Target of Rapamycin Complex 2
  • Membrane Microdomains / enzymology*
  • Multiprotein Complexes / genetics
  • Multiprotein Complexes / metabolism*
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism
  • Saccharomyces cerevisiae / enzymology*
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Signal Transduction
  • Sterols / metabolism*
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / metabolism*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Vacuoles / enzymology

Substances

  • Antiporters
  • Carrier Proteins
  • Cytoskeletal Proteins
  • LTC1 protein, S cerevisiae
  • Multiprotein Complexes
  • RNA-Binding Proteins
  • Saccharomyces cerevisiae Proteins
  • Slm1 protein, S cerevisiae
  • Slm2 protein, S cerevisiae
  • Sterols
  • TORC1 protein complex, S cerevisiae
  • Transcription Factors
  • Mechanistic Target of Rapamycin Complex 2
  • TOR Serine-Threonine Kinases