| Literature DB >> 24371142 |
Mathias Loibl1, Isabella Klein, Michael Prattes, Claudia Schmidt, Lisa Kappel, Gertrude Zisser, Anna Gungl, Elmar Krieger, Brigitte Pertschy, Helmut Bergler.
Abstract
The drug diazaborine is the only known inhibitor of ribosome biogenesis and specifically blocks large subunit formation in eukaryotic cells. However, the target of this drug and the mechanism of inhibition were unknown. Here we identify the AAA-ATPase Drg1 as a target of diazaborine. Inhibitor binding into the second AAA domain of Drg1 requires ATP loading and results in inhibition of ATP hydrolysis in this site. As a consequence the physiological activity of Drg1, i.e. the release of Rlp24 from pre-60S particles, is blocked, and further progression of cytoplasmic preribosome maturation is prevented. Our results identify the first target of an inhibitor of ribosome biogenesis and provide the mechanism of inhibition of a key step in large ribosomal subunit formation.Entities:
Keywords: AAA-ATPases; ATPases; Diazaborine; Drug Action; Enzyme Inhibitors; Protein-Drug Interactions; Ribosome Assembly; Small Molecule Inhibitor
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Year: 2013 PMID: 24371142 PMCID: PMC3924260 DOI: 10.1074/jbc.M113.536110
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157