GTP gamma S activation of proto-oncogene expression in transiently permeabilised Swiss 3T3 fibroblasts

FEBS Lett. 1988 Jan 25;227(2):203-8. doi: 10.1016/0014-5793(88)80899-8.

Abstract

A technique of transient permeabilisation has been used to show that the introduction of guanosine 5'-O-(3-thiotriphosphate) (GTP gamma S), a non-hydrolysable analogue of GTP, into intact Swiss 3T3 fibroblasts stimulates phosphoinositide hydrolysis, cyclic AMP accumulation and the activation of c-fos and c-myc proto-oncogenes. Of a number of nucleotide triphosphates introduced into the cells, only GTP and its non-hydrolysable analogues activated inositol phosphate release, suggesting that this response is mediated by guanine nucleotide regulatory (G) protein(s). The data demonstrate that transient permeabilisation provides a method of examining the involvement of G-proteins in nuclear activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Membrane Permeability
  • Cells, Cultured
  • DNA Replication / drug effects
  • Fibroblasts / cytology
  • Fibroblasts / drug effects
  • Guanosine 5'-O-(3-Thiotriphosphate)
  • Guanosine Triphosphate / analogs & derivatives*
  • Guanosine Triphosphate / pharmacology
  • Inositol / metabolism
  • Inositol Phosphates / metabolism
  • Kinetics
  • Mice
  • Proto-Oncogenes / drug effects*
  • RNA, Messenger / drug effects
  • RNA, Messenger / genetics
  • Thionucleotides / pharmacology*
  • Transcription, Genetic / drug effects*

Substances

  • Inositol Phosphates
  • RNA, Messenger
  • Thionucleotides
  • Guanosine 5'-O-(3-Thiotriphosphate)
  • Inositol
  • Guanosine Triphosphate