Regulation of synthesis and turnover of an interferon-inducible mRNA

Mol Cell Biol. 1986 Jun;6(6):2062-7. doi: 10.1128/mcb.6.6.2062-2067.1986.

Abstract

Regulation of synthesis and turnover of an interferon (IFN)-inducible mRNA, mRNA 561, in HeLa monolayer cells was studied. Cytoplasmic levels of this mRNA were estimated by hybridization analyses with a cDNA clone that we have isolated as a probe. IFN-alpha A induced a high level of this mRNA in a transient fashion, whereas no induction was observed in response to IFN-gamma. Surprisingly little mRNA 561 was induced in cells treated simultaneously with IFN-alpha A and an inhibitor of protein synthesis, suggesting that in addition to IFN-alpha A, an interferon-inducible protein was needed for induction of this mRNA. Apparently this putative protein could be induced by IFN-gamma as well. Thus, although little mRNA 561 was synthesized in cells treated either with IFN-gamma alone or with IFN-alpha A and cycloheximide, a large quantity of this mRNA was induced in cells which had been pretreated with IFN-gamma and then treated with IFN-alpha A and cycloheximide. Once mRNA 561 was induced by IFN-alpha A, it turned over rapidly. This rapid turnover could be blocked by actinomycin D or cycloheximide indicating that another IFN-inducible protein may mediate this process.

Publication types

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

MeSH terms

  • Cell Adhesion
  • Cloning, Molecular
  • Cycloheximide / pharmacology
  • HeLa Cells
  • Humans
  • Interferon Type I / pharmacology*
  • Interferon-gamma / pharmacology
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism
  • Transcription, Genetic / drug effects

Substances

  • Interferon Type I
  • RNA, Messenger
  • Interferon-gamma
  • Cycloheximide