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Hierarchical recruitment into nascent ribosomes of assembly factors required for 27SB pre-rRNA processing in Saccharomyces cerevisiae

机译:在酿酒酵母中将27SB pre-rRNA加工所需的组装因子分级募集到新生核糖体中

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摘要

To better define the roles of assembly factors required for eukaryotic ribosome biogenesis, we have focused on one specific step in maturation of yeast 60 S ribosomal subunits: processing of 27SB pre-ribosomal RNA. At least 14 assembly factors, the ‘B-factor’ proteins, are required for this step. These include most of the major functional classes of assembly factors: RNA-binding proteins, scaffolding protein, DEAD-box ATPases and GTPases. We have investigated the mechanisms by which these factors associate with assembling ribosomes. Our data establish a recruitment model in which assembly of the B-factors into nascent ribosomes ultimately leads to the recruitment of the GTPase Nog2. A more detailed analysis suggests that this occurs in a hierarchical manner via two largely independent recruiting pathways that converge on Nog2. Understanding recruitment has allowed us to better determine the order of association of all assembly factors functioning in one step of ribosome assembly. Furthermore, we have identified a novel subcomplex composed of the B-factors Nop2 and Nip7. Finally, we identified a means by which this step in ribosome biogenesis is regulated in concert with cell growth via the TOR protein kinase pathway. Inhibition of TOR kinase decreases association of Rpf2, Spb4, Nog1 and Nog2 with pre-ribosomes.
机译:为了更好地定义真核生物核糖体生物合成所需的装配因子的作用,我们集中于酵母60 S核糖体亚基成熟的一个特定步骤:27SB前核糖体RNA的加工。此步骤至少需要14个组装因子,即“ B因子”蛋白。这些包括装配因子的大多数主要功能类别:RNA结合蛋白,支架蛋白,DEAD-box ATPase和GTPases。我们已经研究了这些因素与组装核糖体有关的机制。我们的数据建立了一个募集模型,其中将B因子组装到新生核糖体中最终导致了GTPase Nog2的募集。更详细的分析表明,这是通过两个在Nog2上汇聚的基本上独立的募集途径以分级方式发生的。了解募集使我们能够更好地确定在核糖体组装的一个步骤中起作用的所有组装因子的关联顺序。此外,我们已经确定了由B因子Nop2和Nip7组成的新型亚复合物。最后,我们确定了通过TOR蛋白激酶途径与细胞生长协同调节核糖体生物发生这一步骤的方法。 TOR激酶的抑制作用可降低Rpf2,Sb4,Nog1和Nog2与前核糖体的结合。

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