c-Fos: an AP-1 transcription factor with an additional cytoplasmic, non-genomic lipid synthesis activation capacity

Biochim Biophys Acta. 2014 Sep;1841(9):1241-6. doi: 10.1016/j.bbalip.2014.05.007. Epub 2014 Jun 2.

Abstract

The mechanisms that co-ordinately activate lipid synthesis when high rates of membrane biogenesis are needed to support cell growth are largely unknown. c-Fos, a well known AP-1 transcription factor, has emerged as a unique protein with the capacity to associate to specific enzymes of the pathway of synthesis of phospholipids at the endoplasmic reticulum and activate their synthesis to accompany genomic decisions of growth. Herein, we discuss this cytoplasmic, non-genomic effect of c-Fos in the context of other mechanisms that have been proposed to regulate lipid synthesis.

Keywords: Membrane biogenesis regulation; PI4KIIα/c-Fos association; Phospholipid synthesizing enzymes regulation; c-Fos/CDS association.

Publication types

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

MeSH terms

  • Animals
  • Cell Cycle
  • Cell Proliferation
  • Endoplasmic Reticulum / metabolism*
  • Eukaryotic Cells / cytology
  • Eukaryotic Cells / metabolism*
  • Gene Expression Regulation
  • Humans
  • Lipid Metabolism
  • Minor Histocompatibility Antigens
  • Phospholipids / biosynthesis*
  • Phospholipids / genetics
  • Phosphotransferases (Alcohol Group Acceptor) / genetics*
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism
  • Protein Binding
  • Proto-Oncogene Proteins c-fos / genetics*
  • Proto-Oncogene Proteins c-fos / metabolism
  • Signal Transduction

Substances

  • Minor Histocompatibility Antigens
  • Phospholipids
  • Proto-Oncogene Proteins c-fos
  • Phosphotransferases (Alcohol Group Acceptor)
  • phosphatidylinositol phosphate 4-kinase