Literature DB >> 15226447

Diazaborine treatment of yeast cells inhibits maturation of the 60S ribosomal subunit.

Brigitte Pertschy1, Gertrude Zisser, Hermine Schein, René Köffel, Gernot Rauch, Karlheinz Grillitsch, Christina Morgenstern, Michael Durchschlag, Gregor Högenauer, Helmut Bergler.   

Abstract

Diazaborine treatment of yeast cells was shown previously to cause accumulation of aberrant, 3'-elongated mRNAs. Here we demonstrate that the drug inhibits maturation of rRNAs for the large ribosomal subunit. Pulse-chase analyses showed that the processing of the 27S pre-rRNA to consecutive species was blocked in the drug-treated wild-type strain. The steady-state level of the 7S pre-rRNA was clearly reduced after short-term treatment with the inhibitor. At the same time an increase of the 35S pre-rRNA was observed. Longer incubation with the inhibitor resulted in a decrease of the 27S precursor. Primer extension assays showed that an early step in 27S pre-rRNA processing is inhibited, which results in an accumulation of the 27SA2 pre-rRNA and a strong decrease of the 27SA3, 27SB1L, and 27SB1S precursors. The rRNA processing pattern observed after diazaborine treatment resembles that reported after depletion of the RNA binding protein Nop4p/Nop77p. This protein is essential for correct pre-27S rRNA processing. Using a green fluorescent protein-Nop4 fusion, we found that diazaborine treatment causes, within minutes, a rapid redistribution of the protein from the nucleolus to the periphery of the nucleus, which provides a possible explanation for the effect of diazaborine on rRNA processing.

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Year:  2004        PMID: 15226447      PMCID: PMC434233          DOI: 10.1128/MCB.24.14.6476-6487.2004

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  51 in total

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4.  Diazaborine treatment of Baker's yeast results in stabilization of aberrant mRNAs.

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Journal:  J Biol Chem       Date:  2001-07-26       Impact factor: 5.157

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7.  The drug diazaborine blocks ribosome biogenesis by inhibiting the AAA-ATPase Drg1.

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