Evidence that Ha-Ras mediates two distinguishable intracellular signals activated by v-Src

  • Sajjad A. Qureshi
  • , Konstantina Alexandropoulos
  • , Myunghi Rim
  • , Cecil K. Joseph
  • , Joseph T. Bruder
  • , Ulf R. Rapp
  • , David A. Foster

Research output: Contribution to journalArticlepeer-review

36 Scopus citations

Abstract

v-Src activates promoters under the control of 12-O-tetradecanoylphorbol-13-acetate (TPA) response elements (TREs) and serum response elements (SREs) via two distinguishable intracellular signaling mechanisms. The induction of TRE- and SRE-mediated gene expression by v-Src could be distinguished by a differential sensitivity to depleting cells of protein kinase C (PKC) and to a dominant negative Raf-1 mutant. Thus, PKC depletion and the dominant negative Raf-1 mutant were able to distinguish two intracellular signaling mechanisms activated by v-Src. Both of these v-Src-induced intracellular signals were sensitive to a dominant negative mutant of Ha-Ras. These data suggest that Ha-Ras functions to coordinately regulate multiple intracellular signaling mechanisms activated by v-Src.

Original languageEnglish
Pages (from-to)17635-17639
Number of pages5
JournalJournal of Biological Chemistry
Volume267
Issue number25
StatePublished - 5 Sep 1992
Externally publishedYes

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