Farnesylated proteins and cell cycle progression

J Cell Biochem Suppl. 2001:Suppl 37:64-70. doi: 10.1002/jcb.10067.

Abstract

Post-translational modification of proteins by the addition of a farnesyl group is critical for the function of a number of proteins involved in signal transduction. Farnesylation facilitates their membrane association and also promotes protein-protein interaction. Recently, progress has been made in understanding the biological significance of farnesylation. First, effects of farnesyltransferase inhibitors (FTIs) on cancer cells have been examined using a variety of human cancer cells. This study showed that one of the major effects of FTIs is to alter cell cycle progression. Both G0/G1 enrichment and G2/M accumulation were observed depending on the cell line examined. Second, a number of novel farnesylated proteins have been characterized. Of these, Rheb and CENP-E,F are of particular interest. Rheb, a novel member of the Ras superfamily G-proteins, may play a role in the G1 phase of the cell cycle. CENP-E,F are centromere associated motors that play critical roles in mitosis. These results suggest important contributions of farnesylated proteins in the regulation of cell cycle progression.

Publication types

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

MeSH terms

  • Alkyl and Aryl Transferases / antagonists & inhibitors
  • Alkyl and Aryl Transferases / metabolism*
  • Animals
  • Cell Cycle / drug effects
  • Cell Cycle / physiology*
  • Chromosomal Proteins, Non-Histone / metabolism
  • Enzyme Inhibitors / pharmacology
  • Farnesyltranstransferase
  • G1 Phase / drug effects
  • G1 Phase / physiology
  • Humans
  • Microfilament Proteins
  • Monomeric GTP-Binding Proteins / metabolism
  • Neuropeptides / metabolism
  • Protein Prenylation / physiology*
  • Quinolones / pharmacology
  • Ras Homolog Enriched in Brain Protein
  • Resting Phase, Cell Cycle / drug effects
  • Resting Phase, Cell Cycle / physiology
  • Tumor Cells, Cultured

Substances

  • Chromosomal Proteins, Non-Histone
  • Enzyme Inhibitors
  • Microfilament Proteins
  • Neuropeptides
  • Quinolones
  • RHEB protein, human
  • Ras Homolog Enriched in Brain Protein
  • centromere protein E
  • centromere protein F
  • Alkyl and Aryl Transferases
  • Farnesyltranstransferase
  • Monomeric GTP-Binding Proteins
  • tipifarnib