Nucleolar localization of nucleophosmin/B23 requires GTP

Rick A. Finch, Ganapathi R. Revankar, Pui K. Chan

Research output: Contribution to journalArticlepeer-review

44 Scopus citations

Abstract

Incubation of HeLa cells with the IMP dehydrogenase inhibitors: ribavirin (100 μM, 4 h), tiazofurin (100 μM, 4 h), selenazofurin (100 μM, 4 h), or mycophenolic acid (10 μM, 4 h) resulted in ∼70% reduction in cellular GTP pools and shifting of nucleophosmin/B23 from nucleoli to nucleoplasm as detected by immunofluorescence (B23-translocation). Enzyme-linked immunosorbent assay and Western blot assay showed there is no loss or degradation of nucleophosmin/B23 protein during drug treatment. This translocation effect could be prevented by co-incubation with guanosine (100 μM) or reversed by addition of guanosine (100 μM) to the culture medium after B23-translocation had been induced by these inhibitors. Under these conditions of guanosine supplementation, cellular GTP pool concentrations were maintained at the control level. These results indicate that localization of nucleophosmin/B23 into the nucleolus is dependent on the cellular GTP level.

Original languageEnglish (US)
Pages (from-to)5823-5827
Number of pages5
JournalJournal of Biological Chemistry
Volume268
Issue number8
StatePublished - Mar 15 1993

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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