Institut für Biochemie, Genetik und Mikrobiologie, University of Regensburg, Universitätsstr. 31, 93053 Regensburg, Germany.
Nucleic Acids Res. 2010 May;38(9):3068-80. doi: 10.1093/nar/gkp1244. Epub 2010 Jan 25.
Formation of eukaryotic ribosomes requires more than 150 biogenesis factors which transiently interact with the nascent ribosomal subunits. Previously, many pre-ribosomal intermediates could be distinguished by their protein composition and rRNA precursor (pre-rRNA) content. We purified complexes of ribosome biogenesis factors from yeast cells in which de novo synthesis of rRNA precursors was down-regulated by genetic means. We compared the protein composition of these largely pre-rRNA free assemblies with the one of analogous pre-ribosomal preparations by semi-quantitative mass spectrometry. The experimental setup minimizes the possibility that the analysed pre-rRNA free protein modules were derived from (partially) disrupted pre-ribosomal particles and provides thereby strong evidence for their pre-ribosome independent existence. In support of the validity of this approach (i) the predicted composition of the analysed protein modules was in agreement with previously described rRNA-free complexes and (ii) in most of the cases we could identify new candidate members of reported protein modules. An unexpected outcome of these analyses was that free large ribosomal subunits are associated with a specific set of ribosome biogenesis factors in cells where neo-production of nascent ribosomes was blocked. The data presented strengthen the idea that assembly of eukaryotic pre-ribosomal particles can result from transient association of distinct building blocks.
真核生物核糖体的形成需要 150 多种生物发生因子,这些因子与新生核糖体亚基短暂相互作用。以前,许多核糖体前体可以通过其蛋白质组成和 rRNA 前体(pre-rRNA)含量来区分。我们通过遗传手段下调酵母细胞中 rRNA 前体的从头合成,从这些细胞中纯化核糖体生物发生因子复合物。我们通过半定量质谱法比较了这些基本上无 pre-rRNA 的组装体与类似的 pre-ribosomal 制剂的蛋白质组成。该实验方案最大限度地减少了分析的无 pre-rRNA 蛋白模块源自(部分)破坏的 pre-ribosomal 颗粒的可能性,从而为它们的 pre-ribosome 独立存在提供了有力证据。为了支持这种方法的有效性(i)分析的蛋白模块的预测组成与之前描述的无 rRNA 复合物一致,(ii)在大多数情况下,我们可以鉴定出报道的蛋白模块的新候选成员。这些分析的一个意外结果是,在新生核糖体的新合成被阻断的细胞中,游离的大亚基核糖体与一组特定的核糖体生物发生因子相关。所提出的观点认为,真核生物 pre-ribosomal 颗粒的组装可以由不同构建块的短暂缔合来实现。